Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54187 |
| ensemblid | ENSG00000095380.11 |
| hgncid | 19237 |
| symbol | NANS |
| name | N-acetylneuraminate synthase |
| refseq_nuc | NM_018946.4 |
| refseq_prot | NP_061819.2 |
| ensembl_nuc | ENST00000210444.6 |
| ensembl_prot | ENSP00000210444.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 98056732 |
| end | 98083077 |
| strand | + |
| ver | v1.2 |
| region | chr9:98056732-98083077 |
| region5000 | chr9:98051732-98088077 |
| regionname0 | NANS_chr9_98056732_98083077 |
| regionname5000 | NANS_chr9_98051732_98088077 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 224 | 49 | 43 | 89 | 10 | 31 | 69 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| a0002 | 0/0 | 359 | 88 | 18 | 23 | 46 | 0 | 1 | 34 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| a0003 | 0/0 | 359 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| a0004 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| a0005 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| a0006 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| a0007 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | MPLEL others(354): Show |
chr9 | 98051732 | 98088077 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 119 | 4 | 19 | 74 | 5 | 15 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0001c0003 | 0/0 | 1077 | 82 | 41 | 13 | 12 | 3 | 13 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0001c0004 | 0/0 | 1077 | 21 | 4 | 11 | 2 | 2 | 2 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0001c0013 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0001c0014 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0002c0002 | 0/0 | 1077 | 85 | 17 | 22 | 45 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0002c0006 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0002c0008 | 0/0 | 1077 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0002c0010 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0003c0005 | 0/0 | 1077 | 2 | 2 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0004c0007 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0005c0011 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0006c0012 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 | ||
| a0007c0009 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ATGCC others(1072): Show |
chr9 | 98051732 | 98088077 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0001c0001t0002 | 1/1 | 1179 | 118 | 3 | 19 | 74 | 5 | 15 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0001c0003t0001 | 0/0 | 1179 | 82 | 41 | 13 | 12 | 3 | 13 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0001c0004t0001 | 0/0 | 1179 | 10 | 4 | 4 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0001c0004t0002 | 0/0 | 1179 | 11 | 0 | 7 | 0 | 2 | 2 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0001c0013t0001 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0001c0014t0001 | 0/0 | 1179 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0002c0002t0001 | 0/0 | 1179 | 85 | 17 | 22 | 45 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0002c0006t0001 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0002c0008t0001 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0002c0010t0001 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0003c0005t0001 | 0/0 | 1179 | 2 | 2 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0004c0007t0001 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0005c0011t0001 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0006c0012t0001 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| a0007c0009t0001 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | ACAGA others(1174): Show |
chr9 | 98051732 | 98088077 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0001 | 0/0 | 14 | 1 | 4 | 5 | 2 | 2 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0004 | 1/0 | 6 | 0 | 1 | 0 | 2 | 2 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0016 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0031 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0003 | 0/0 | 6 | 4 | 1 | 0 | 1 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0014 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0012 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0013t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0001c0014t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0002 | 0/0 | 13 | 0 | 7 | 6 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0008 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0008t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0002c0010t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0003c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0003c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0004c0007t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0005c0011t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0006c0012t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| a0007c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0020 | EUR | GBR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00323 | hp2 | a0001 | c0004 | t0002 | g0012 | EUR | FIN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00438 | hp2 | a0002 | c0006 | t0001 | g0078 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0017 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0133 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0012 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0232 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01081 | hp2 | a0002 | c0008 | t0001 | g0055 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0101 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01433 | hp1 | a0001 | c0004 | t0002 | g0020 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0017 | AMR | CLM | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0137 | EUR | IBS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0130 | EUR | IBS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01943 | hp1 | a0001 | c0004 | t0002 | g0096 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02004 | hp1 | a0001 | c0004 | t0002 | g0097 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02148 | hp2 | a0001 | c0004 | t0002 | g0098 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CDX | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CDX | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0215 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0115 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02258 | hp1 | a0004 | c0007 | t0001 | g0079 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0138 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02300 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PEL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0103 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0146 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0119 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0145 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02738 | hp2 | a0001 | c0004 | t0002 | g0099 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02809 | hp1 | a0002 | c0010 | t0001 | g0082 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02818 | hp1 | a0003 | c0005 | t0001 | g0035 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | ESN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0126 | AFR | ESN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | ESN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03098 | hp1 | a0003 | c0005 | t0001 | g0034 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0216 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ESN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0155 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03540 | hp1 | a0005 | c0011 | t0001 | g0040 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0128 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0144 | SAS | STU | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0122 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0039 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0141 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0235 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0234 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG04184 | hp2 | a0001 | c0014 | t0001 | g0132 | SAS | BEB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0131 | SAS | STU | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG04204 | hp2 | a0001 | c0004 | t0002 | g0012 | SAS | STU | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0151 | SAS | STU | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | CHB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | YRI | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | YRI | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18949 | hp2 | a0006 | c0012 | t0001 | g0135 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18951 | hp2 | a0001 | c0013 | t0001 | g0114 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18998 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0110 | AFR | LWK | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | LWK | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0003 | EUR | TSI | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | GIH | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | GIH | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ACB | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | MSL | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | USA | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | USA | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18955 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | USA | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | USA | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA21309 | hp1 | a0007 | c0009 | t0001 | g0053 | AFR | LWK | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0157 | AFR | LWK | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0031 | REF | REF | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0004 | REF | REF | NANS_chr9_98051732_98088077 | NANS | chr9 | 98051732 | 98088077 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98060853 | G | C | 4 | a0002 a0004 a0005 others(1): Show |
91 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
missense_variant | MODERATE | c.204G>C | p.Glu68Asp | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/6 | 281/1179 | 204/1080 | 68/359 | chr9 | 98060853 | |||
| chr9:98060893 | G | A | 1 | a0004 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.244G>A | p.Gly82Arg | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/6 | 321/1179 | 244/1080 | 82/359 | chr9 | 98060893 | |||
| chr9:98078264 | C | T | 1 | a0003 | 2 | HG02818.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.520C>T | p.Pro174Ser | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/6 | 597/1179 | 520/1080 | 174/359 | chr9 | 98078264 | |||
| chr9:98082898 | C | T | 1 | a0005 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.923C>T | p.Thr308Ile | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 6/6 | 1000/1179 | 923/1080 | 308/359 | chr9 | 98082898 | |||
| chr9:98082925 | G | A | 1 | a0006 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.950G>A | p.Gly317Asp | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 6/6 | 1027/1179 | 950/1080 | 317/359 | chr9 | 98082925 | |||
| chr9:98082985 | T | G | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1010T>G | p.Val337Gly | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 6/6 | 1087/1179 | 1010/1080 | 337/359 | chr9 | 98082985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98056910 | C | T | 4 | a0001c0003 a0001c0013 a0001c0014 others(1): Show |
85 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(82): Show |
synonymous_variant | LOW | c.102C>T | p.Asp34Asp | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/6 | 179/1179 | 102/1080 | 34/359 | chr9 | 98056910 | |||
| chr9:98056937 | C | T | 1 | a0001c0014 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.129C>T | p.Ala43Ala | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/6 | 206/1179 | 129/1080 | 43/359 | chr9 | 98056937 | |||
| chr9:98060802 | T | C | 11 | a0001c0003 a0001c0004 a0001c0014 others(8): Show |
196 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(193): Show |
synonymous_variant | LOW | c.153T>C | p.Ala51Ala | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/6 | 230/1179 | 153/1080 | 51/359 | chr9 | 98060802 | |||
| chr9:98060868 | G | A | 1 | a0002c0006 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.219G>A | p.Ser73Ser | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/6 | 296/1179 | 219/1080 | 73/359 | chr9 | 98060868 | |||
| chr9:98080956 | T | C | 1 | a0002c0008 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.744T>C | p.Ser248Ser | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/6 | 821/1179 | 744/1080 | 248/359 | chr9 | 98080956 | |||
| chr9:98083020 | T | C | 2 | a0002c0010 a0007c0009 |
2 | HG02809.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.1045T>C | p.Leu349Leu | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 6/6 | 1122/1179 | 1045/1080 | 349/359 | chr9 | 98083020 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98056788 | T | G | 14 | a0001c0001t0001 a0001c0003t0001 a0001c0004t0001 others(11): Show |
189 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(186): Show |
5_prime_UTR_variant | MODIFIER | c.-21T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/6 | 21 | chr9 | 98056788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98057034 | G | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.132+94G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057034 | |||||||
| chr9:98057057 | G | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | NA18951.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.132+117G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057057 | |||||||
| chr9:98057060 | C | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.132+120C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057060 | |||||||
| chr9:98057104 | G | A | 1 | a0001c0003t0001g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.132+164G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057104 | |||||||
| chr9:98057369 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.132+429C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057369 | |||||||
| chr9:98057380 | G | T | 1 | a0002c0002t0001g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.132+440G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057380 | |||||||
| chr9:98057639 | C | T | 3 | a0001c0003t0001g0234 a0001c0003t0001g0235 a0001c0003t0001g0236 |
3 | HG03942.hp1 HG04184.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.132+699C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057639 | |||||||
| chr9:98057658 | G | A | 83 | a0001c0001t0001g0100 a0001c0004t0001g0013 a0001c0004t0001g0021 others(80): Show |
114 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.132+718G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057658 | |||||||
| chr9:98057795 | T | G | 1 | a0001c0001t0002g0106 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.132+855T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057795 | |||||||
| chr9:98057843 | TTATC | T | 82 | a0001c0001t0001g0100 a0001c0003t0001g0232 a0001c0004t0001g0013 others(79): Show |
113 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.132+907_132+910del others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98057843 | ||||||
| chr9:98057902 | GT | G | 144 | a0001c0001t0001g0100 a0001c0001t0002g0107 a0001c0001t0002g0108 others(141): Show |
190 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.132+977delT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98057902 | ||||||
| chr9:98057921 | G | GT | 3 | a0001c0003t0001g0155 a0001c0003t0001g0156 a0001c0003t0001g0157 |
3 | HG01891.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.132+981_132+982ins others(1): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057921 | |||||||
| chr9:98057921 | G | GTTT | 2 | a0001c0004t0001g0013 a0001c0004t0001g0101 |
4 | HG01069.hp2 HG01070.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+981_132+982ins others(3): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057921 | |||||||
| chr9:98057922 | G | GT | 63 | a0001c0001t0002g0033 a0001c0001t0002g0222 a0001c0001t0002g0223 others(60): Show |
78 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.132+1002dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98057922 | ||||||
| chr9:98057922 | G | GTT | 61 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0146 others(58): Show |
86 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.132+1001_132+1002d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98057922 | ||||||
| chr9:98057922 | G | GTTT | 22 | a0001c0001t0001g0100 a0001c0004t0001g0021 a0001c0004t0002g0012 others(19): Show |
26 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.132+1000_132+1002d others(5): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98057922 | ||||||
| chr9:98057922 | G | T | 5 | a0001c0003t0001g0155 a0001c0003t0001g0156 a0001c0003t0001g0157 others(2): Show |
7 | HG01069.hp2 HG01070.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+982G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98057922 | |||||||
| chr9:98058037 | C | T | 1 | a0001c0003t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.132+1097C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058037 | |||||||
| chr9:98058062 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.132+1122C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058062 | |||||||
| chr9:98058204 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.132+1264A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058204 | |||||||
| chr9:98058362 | T | G | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.132+1422T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058362 | |||||||
| chr9:98058389 | C | T | 62 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(59): Show |
77 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.132+1449C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058389 | |||||||
| chr9:98058746 | C | T | 69 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(66): Show |
84 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(81): Show |
intron_variant | MODIFIER | c.132+1806C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058746 | |||||||
| chr9:98058983 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.133-1799G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058983 | |||||||
| chr9:98058993 | T | C | 62 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(59): Show |
77 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.133-1789T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98058993 | |||||||
| chr9:98059000 | A | G | 1 | a0001c0003t0001g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133-1782A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059000 | |||||||
| chr9:98059029 | A | AT | 15 | a0001c0003t0001g0232 a0001c0004t0001g0013 a0001c0004t0001g0021 others(12): Show |
22 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.133-1742dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98059029 | ||||||
| chr9:98059131 | C | T | 1 | a0002c0002t0001g0083 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133-1651C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059131 | |||||||
| chr9:98059190 | A | T | 1 | a0001c0004t0001g0021 | 2 | HG00423.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.133-1592A>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059190 | |||||||
| chr9:98059286 | G | A | 2 | a0001c0001t0002g0159 a0001c0001t0002g0160 |
2 | NA18950.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.133-1496G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059286 | |||||||
| chr9:98059318 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.133-1464C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059318 | |||||||
| chr9:98059342 | C | G | 66 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(63): Show |
90 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.133-1440C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059342 | |||||||
| chr9:98059367 | A | G | 1 | a0001c0003t0001g0145 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.133-1415A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059367 | |||||||
| chr9:98059372 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.133-1410C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059372 | |||||||
| chr9:98059409 | T | G | 56 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(53): Show |
71 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.133-1373T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059409 | |||||||
| chr9:98059457 | C | T | 1 | a0001c0003t0001g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133-1325C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059457 | |||||||
| chr9:98059628 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.133-1154T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059628 | |||||||
| chr9:98059684 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.133-1098G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059684 | |||||||
| chr9:98059723 | G | GT | 6 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-1053dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr9 | 98059723 | ||||||
| chr9:98059730 | G | T | 6 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-1052G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059730 | |||||||
| chr9:98059812 | T | G | 2 | a0002c0002t0001g0046 a0002c0002t0001g0084 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.133-970T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059812 | |||||||
| chr9:98059995 | C | G | 2 | a0001c0003t0001g0143 a0001c0003t0001g0144 |
2 | HG01256.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.133-787C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98059995 | |||||||
| chr9:98060026 | T | C | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.133-756T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060026 | |||||||
| chr9:98060259 | T | C | 2 | a0002c0002t0001g0047 a0002c0002t0001g0048 |
2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.133-523T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060259 | |||||||
| chr9:98060401 | A | G | 68 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(65): Show |
83 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.133-381A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060401 | |||||||
| chr9:98060441 | T | G | 232 | a0001c0001t0001g0100 a0001c0001t0002g0001 a0001c0001t0002g0006 others(229): Show |
303 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.133-341T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060441 | |||||||
| chr9:98060558 | T | A | 54 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(51): Show |
69 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.133-224T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060558 | |||||||
| chr9:98060604 | T | G | 1 | a0002c0002t0001g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.133-178T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060604 | |||||||
| chr9:98060658 | G | A | 69 | a0001c0001t0002g0027 a0001c0003t0001g0003 a0001c0003t0001g0005 others(66): Show |
85 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(82): Show |
intron_variant | MODIFIER | c.133-124G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 1/5 | chr9 | 98060658 | |||||||
| chr9:98061077 | G | A | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+80G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061077 | |||||||
| chr9:98061078 | C | A | 55 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(52): Show |
70 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.348+81C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061078 | |||||||
| chr9:98061084 | C | G | 1 | a0001c0004t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.348+87C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061084 | |||||||
| chr9:98061088 | C | T | 1 | a0002c0010t0001g0082 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.348+91C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061088 | |||||||
| chr9:98061348 | G | A | 66 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(63): Show |
90 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.348+351G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061348 | |||||||
| chr9:98061351 | C | T | 7 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+354C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061351 | |||||||
| chr9:98061351 | CCTGTAAT others(296): Show |
C | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+360_348+662del | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98061351 | ||||||
| chr9:98061551 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02080.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.348+554A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061551 | |||||||
| chr9:98061558 | G | A | 7 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+561G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061558 | |||||||
| chr9:98061599 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.348+602G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061599 | |||||||
| chr9:98061728 | C | T | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+731C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061728 | |||||||
| chr9:98061778 | C | CA | 6 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 others(3): Show |
6 | HG01952.hp1 HG02602.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+795dupA | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98061778 | ||||||
| chr9:98061793 | TTAATAA | T | 4 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0045 others(1): Show |
4 | HG01081.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+808_348+813del others(6): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98061793 | ||||||
| chr9:98061799 | A | T | 1 | a0001c0004t0001g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.348+802A>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061799 | |||||||
| chr9:98061941 | C | A | 77 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(74): Show |
99 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.348+944C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98061941 | |||||||
| chr9:98062082 | C | T | 2 | a0002c0002t0001g0080 a0002c0002t0001g0081 |
2 | NA18965.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.348+1085C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062082 | |||||||
| chr9:98062091 | G | A | 1 | a0002c0002t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.348+1094G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062091 | |||||||
| chr9:98062210 | T | TA | 21 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0211 others(18): Show |
28 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.348+1228dupA | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98062210 | ||||||
| chr9:98062238 | A | G | 2 | a0001c0004t0001g0013 a0001c0004t0001g0101 |
4 | HG01069.hp2 HG01070.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1241A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062238 | |||||||
| chr9:98062256 | G | A | 4 | a0001c0003t0001g0116 a0001c0003t0001g0117 a0001c0003t0001g0118 others(1): Show |
4 | HG02723.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1259G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062256 | |||||||
| chr9:98062405 | T | A | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.348+1408T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062405 | |||||||
| chr9:98062468 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.348+1471T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062468 | |||||||
| chr9:98062470 | C | G | 152 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(149): Show |
198 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.348+1473C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98062470 | |||||||
| chr9:98062777 | G | GT | 69 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0161 others(66): Show |
93 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.348+1800dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98062777 | ||||||
| chr9:98062777 | G | GTT | 9 | a0002c0002t0001g0039 a0002c0002t0001g0048 a0002c0002t0001g0050 others(6): Show |
9 | HG00438.hp2 HG01192.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1799_348+1800d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98062777 | ||||||
| chr9:98062777 | GTT | G | 6 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+1799_348+1800d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98062777 | ||||||
| chr9:98062906 | TAA | T | 7 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+1915_348+1916d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98062906 | ||||||
| chr9:98063006 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+2009G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98063006 | |||||||
| chr9:98063111 | G | A | 1 | a0003c0005t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.348+2114G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98063111 | |||||||
| chr9:98063345 | T | G | 9 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+2348T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98063345 | |||||||
| chr9:98063895 | G | T | 3 | a0001c0003t0001g0219 a0001c0003t0001g0220 a0001c0003t0001g0221 |
3 | HG02451.hp2 HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.348+2898G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98063895 | |||||||
| chr9:98064017 | T | A | 6 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+3020T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064017 | |||||||
| chr9:98064097 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+3100T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064097 | |||||||
| chr9:98064205 | G | A | 6 | a0001c0003t0001g0022 a0001c0003t0001g0023 a0001c0003t0001g0116 others(3): Show |
8 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+3208G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064205 | |||||||
| chr9:98064277 | G | A | 2 | a0001c0003t0001g0022 a0002c0002t0001g0062 |
3 | HG02451.hp1 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.348+3280G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064277 | |||||||
| chr9:98064280 | G | T | 1 | a0002c0002t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.348+3283G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064280 | |||||||
| chr9:98064438 | T | G | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.348+3441T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064438 | |||||||
| chr9:98064440 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+3443G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064440 | |||||||
| chr9:98064443 | A | G | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.348+3446A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064443 | |||||||
| chr9:98064724 | G | T | 5 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0044 others(2): Show |
5 | HG01081.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+3727G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98064724 | |||||||
| chr9:98065174 | C | T | 1 | a0001c0001t0002g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.348+4177C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065174 | |||||||
| chr9:98065249 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.348+4252C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065249 | |||||||
| chr9:98065308 | C | CT | 16 | a0001c0001t0002g0199 a0001c0001t0002g0208 a0001c0001t0002g0226 others(13): Show |
16 | HG01192.hp2 HG01884.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+4332dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065308 | ||||||
| chr9:98065308 | C | CTT | 48 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(45): Show |
62 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.348+4331_348+4332d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065308 | ||||||
| chr9:98065308 | C | CTTT | 9 | a0001c0003t0001g0138 a0001c0003t0001g0139 a0001c0003t0001g0140 others(6): Show |
9 | HG01981.hp1 HG02273.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.348+4330_348+4332d others(5): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065308 | ||||||
| chr9:98065308 | CT | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0036 others(26): Show |
34 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.348+4332delT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065308 | ||||||
| chr9:98065366 | GCAAT | G | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+4374_348+4377d others(6): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065366 | ||||||
| chr9:98065385 | C | T | 2 | a0002c0002t0001g0075 a0002c0002t0001g0092 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.348+4388C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065385 | |||||||
| chr9:98065483 | A | AT | 65 | a0001c0001t0002g0032 a0001c0001t0002g0162 a0001c0001t0002g0164 others(62): Show |
89 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.348+4513dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATT | 21 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0210 others(18): Show |
22 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.348+4512_348+4513d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTT | 33 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0022 others(30): Show |
44 | HG01109.hp2 HG01192.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.348+4509_348+4513d others(7): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTT | 17 | a0001c0003t0001g0014 a0001c0003t0001g0025 a0001c0003t0001g0119 others(14): Show |
20 | HG00741.hp2 HG02056.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.348+4508_348+4513d others(8): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTTT | 6 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0143 others(3): Show |
6 | HG01256.hp2 HG01515.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+4507_348+4513d others(9): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTTT others(1): Show |
4 | a0001c0001t0002g0223 a0001c0004t0001g0021 a0001c0004t0002g0012 others(1): Show |
8 | HG00323.hp2 HG00423.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+4506_348+4513d others(10): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTTT others(2): Show |
3 | a0001c0001t0002g0160 a0001c0004t0001g0013 a0001c0004t0002g0020 |
6 | HG00099.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+4505_348+4513d others(11): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTTT others(3): Show |
4 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0101 others(1): Show |
4 | HG01358.hp1 HG02738.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+4504_348+4513d others(12): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTTT others(5): Show |
1 | a0001c0004t0002g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.348+4502_348+4513d others(14): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | A | ATTTTTTT others(6): Show |
1 | a0001c0004t0002g0098 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.348+4501_348+4513d others(15): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | ATTTTTTT others(3): Show |
A | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+4504_348+4513d others(12): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065483 | ATTTTTTT others(5): Show |
A | 4 | a0001c0003t0001g0110 a0002c0002t0001g0064 a0002c0002t0001g0094 others(1): Show |
4 | NA18747.hp1 NA19043.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+4502_348+4513d others(14): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065483 | ||||||
| chr9:98065528 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.348+4531G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065528 | |||||||
| chr9:98065548 | A | G | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+4551A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065548 | |||||||
| chr9:98065564 | C | T | 3 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 |
3 | HG02559.hp2 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.348+4567C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065564 | |||||||
| chr9:98065571 | T | C | 1 | a0001c0004t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.348+4574T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065571 | |||||||
| chr9:98065640 | C | CTT | 8 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+4654_348+4655d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98065640 | ||||||
| chr9:98065734 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+4737G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065734 | |||||||
| chr9:98065772 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.348+4775T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065772 | |||||||
| chr9:98065800 | C | A | 54 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(51): Show |
68 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.348+4803C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98065800 | |||||||
| chr9:98066074 | C | T | 11 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(8): Show |
16 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.348+5077C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066074 | |||||||
| chr9:98066121 | T | C | 6 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+5124T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066121 | |||||||
| chr9:98066138 | A | C | 2 | a0001c0003t0001g0116 a0001c0003t0001g0118 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.348+5141A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066138 | |||||||
| chr9:98066154 | T | C | 1 | a0001c0003t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.348+5157T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066154 | |||||||
| chr9:98066181 | A | G | 5 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0044 others(2): Show |
5 | HG01081.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+5184A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066181 | |||||||
| chr9:98066283 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5286G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066283 | |||||||
| chr9:98066342 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5345C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066342 | |||||||
| chr9:98066343 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5346A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066343 | |||||||
| chr9:98066490 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5493A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066490 | |||||||
| chr9:98066584 | G | A | 155 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(152): Show |
200 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.348+5587G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066584 | |||||||
| chr9:98066590 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5593A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066590 | |||||||
| chr9:98066596 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5599T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066596 | |||||||
| chr9:98066653 | A | AT | 71 | a0001c0001t0002g0238 a0001c0003t0001g0110 a0001c0003t0001g0111 others(68): Show |
95 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.348+5671dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98066653 | ||||||
| chr9:98066802 | C | A | 1 | a0001c0001t0002g0208 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.348+5805C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066802 | |||||||
| chr9:98066876 | T | C | 156 | a0001c0001t0001g0100 a0001c0001t0002g0159 a0001c0001t0002g0160 others(153): Show |
201 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.348+5879T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066876 | |||||||
| chr9:98066902 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+5905T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066902 | |||||||
| chr9:98066968 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.348+5971T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98066968 | |||||||
| chr9:98067042 | A | G | 1 | a0001c0003t0001g0024 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.348+6045A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067042 | |||||||
| chr9:98067050 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.348+6053T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067050 | |||||||
| chr9:98067104 | T | C | 2 | a0001c0003t0001g0122 a0001c0014t0001g0132 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.348+6107T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067104 | |||||||
| chr9:98067200 | A | C | 1 | a0001c0001t0002g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.348+6203A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067200 | |||||||
| chr9:98067211 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+6214G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067211 | |||||||
| chr9:98067337 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+6340C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067337 | |||||||
| chr9:98067363 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+6366G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067363 | |||||||
| chr9:98067401 | C | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.348+6404C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067401 | |||||||
| chr9:98067590 | A | G | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+6593A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067590 | |||||||
| chr9:98067596 | T | C | 1 | a0001c0003t0001g0232 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.348+6599T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067596 | |||||||
| chr9:98067727 | T | C | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348+6730T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067727 | |||||||
| chr9:98067758 | C | T | 8 | a0002c0002t0001g0011 a0002c0002t0001g0060 a0002c0002t0001g0064 others(5): Show |
10 | HG00558.hp2 HG02083.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+6761C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067758 | |||||||
| chr9:98067786 | A | C | 1 | a0001c0001t0002g0192 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.348+6789A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067786 | |||||||
| chr9:98067834 | AC | A | 53 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(50): Show |
67 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(64): Show |
intron_variant | MODIFIER | c.348+6839delC | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98067834 | ||||||
| chr9:98067847 | A | G | 18 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(15): Show |
25 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.348+6850A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98067847 | |||||||
| chr9:98068018 | C | T | 1 | a0001c0003t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.348+7021C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068018 | |||||||
| chr9:98068110 | A | G | 156 | a0001c0001t0001g0100 a0001c0001t0002g0159 a0001c0001t0002g0160 others(153): Show |
201 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.348+7113A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068110 | |||||||
| chr9:98068157 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+7160T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068157 | |||||||
| chr9:98068175 | C | A | 6 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+7178C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068175 | |||||||
| chr9:98068211 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.348+7214T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068211 | |||||||
| chr9:98068347 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+7350T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068347 | |||||||
| chr9:98068386 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.348+7389T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068386 | |||||||
| chr9:98068407 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.348+7410A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068407 | |||||||
| chr9:98068456 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.348+7459T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068456 | |||||||
| chr9:98068605 | G | C | 1 | a0001c0003t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.348+7608G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068605 | |||||||
| chr9:98068650 | T | TA | 18 | a0001c0001t0002g0177 a0001c0003t0001g0005 a0001c0003t0001g0025 others(15): Show |
22 | HG00741.hp2 HG01192.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.348+7669dupA | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98068650 | ||||||
| chr9:98068650 | T | TAA | 8 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+7668_348+7669d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98068650 | ||||||
| chr9:98068719 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+7722A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068719 | |||||||
| chr9:98068828 | TA | T | 94 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0162 others(91): Show |
123 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.348+7847delA | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98068828 | ||||||
| chr9:98068828 | TAA | T | 56 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(53): Show |
70 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(67): Show |
intron_variant | MODIFIER | c.348+7846_348+7847d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98068828 | ||||||
| chr9:98068966 | T | A | 1 | a0001c0003t0001g0022 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.349-7952T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98068966 | |||||||
| chr9:98069019 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-7899A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069019 | |||||||
| chr9:98069133 | G | A | 6 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-7785G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069133 | |||||||
| chr9:98069143 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.349-7775G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069143 | |||||||
| chr9:98069250 | CTCAGCAA others(24): Show |
C | 9 | a0001c0001t0002g0016 a0001c0001t0002g0027 a0001c0001t0002g0030 others(6): Show |
13 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-7666_349-7636d others(33): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98069250 | ||||||
| chr9:98069280 | C | CTT | 6 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-7628_349-7627d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98069280 | ||||||
| chr9:98069297 | G | A | 11 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(8): Show |
16 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.349-7621G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069297 | |||||||
| chr9:98069359 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.349-7559C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069359 | |||||||
| chr9:98069366 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-7552C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069366 | |||||||
| chr9:98069434 | C | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-7484C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069434 | |||||||
| chr9:98069518 | C | T | 1 | a0001c0003t0001g0129 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.349-7400C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069518 | |||||||
| chr9:98069658 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-7260C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069658 | |||||||
| chr9:98069727 | T | C | 8 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-7191T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069727 | |||||||
| chr9:98069747 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.349-7171G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069747 | |||||||
| chr9:98069837 | C | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-7081C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069837 | |||||||
| chr9:98069842 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-7076A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069842 | |||||||
| chr9:98069872 | T | G | 8 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-7046T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069872 | |||||||
| chr9:98069934 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.349-6984G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069934 | |||||||
| chr9:98069967 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-6951G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98069967 | |||||||
| chr9:98070158 | C | T | 5 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-6760C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070158 | |||||||
| chr9:98070222 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-6696G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070222 | |||||||
| chr9:98070265 | A | G | 57 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(54): Show |
71 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.349-6653A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070265 | |||||||
| chr9:98070266 | T | A | 6 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-6652T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070266 | |||||||
| chr9:98070274 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.349-6644T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070274 | |||||||
| chr9:98070414 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-6504A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070414 | |||||||
| chr9:98070579 | C | T | 1 | a0002c0002t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.349-6339C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070579 | |||||||
| chr9:98070624 | T | G | 1 | a0001c0001t0002g0197 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.349-6294T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070624 | |||||||
| chr9:98070664 | C | T | 2 | a0001c0003t0001g0111 a0001c0003t0001g0113 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.349-6254C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070664 | |||||||
| chr9:98070718 | T | C | 155 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(152): Show |
200 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.349-6200T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070718 | |||||||
| chr9:98070782 | A | G | 4 | a0001c0001t0002g0203 a0001c0001t0002g0208 a0001c0001t0002g0209 others(1): Show |
4 | HG02080.hp1 NA18952.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-6136A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070782 | |||||||
| chr9:98070807 | A | AT | 52 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(49): Show |
66 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(63): Show |
intron_variant | MODIFIER | c.349-6096dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98070807 | ||||||
| chr9:98070817 | T | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-6101T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98070817 | |||||||
| chr9:98071028 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.349-5890G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071028 | |||||||
| chr9:98071049 | A | G | 1 | a0001c0003t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.349-5869A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071049 | |||||||
| chr9:98071200 | T | C | 1 | a0001c0001t0002g0226 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.349-5718T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071200 | |||||||
| chr9:98071235 | C | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-5683C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071235 | |||||||
| chr9:98071261 | C | T | 65 | a0001c0003t0001g0120 a0002c0002t0001g0002 a0002c0002t0001g0007 others(62): Show |
89 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.349-5657C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071261 | |||||||
| chr9:98071348 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-5570T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071348 | |||||||
| chr9:98071393 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-5525T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071393 | |||||||
| chr9:98071398 | T | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-5520T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071398 | |||||||
| chr9:98071427 | C | A | 6 | a0001c0003t0001g0121 a0001c0003t0001g0125 a0001c0003t0001g0126 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-5491C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071427 | |||||||
| chr9:98071590 | AGGACATC others(17): Show |
A | 1 | a0002c0002t0001g0051 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.349-5310_349-5287d others(26): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98071590 | ||||||
| chr9:98071643 | T | C | 90 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(87): Show |
111 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.349-5275T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071643 | |||||||
| chr9:98071680 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-5238C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071680 | |||||||
| chr9:98071699 | A | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-5219A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071699 | |||||||
| chr9:98071879 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG00597.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.349-5039A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071879 | |||||||
| chr9:98071931 | G | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0206 |
2 | NA18985.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.349-4987G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98071931 | |||||||
| chr9:98072012 | C | T | 153 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(150): Show |
198 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.349-4906C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072012 | |||||||
| chr9:98072030 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.349-4888C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072030 | |||||||
| chr9:98072036 | C | G | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-4882C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072036 | |||||||
| chr9:98072165 | G | A | 1 | a0001c0003t0001g0133 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.349-4753G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072165 | |||||||
| chr9:98072226 | A | C | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-4692A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072226 | |||||||
| chr9:98072284 | G | A | 1 | a0001c0003t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349-4634G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072284 | |||||||
| chr9:98072312 | C | T | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-4606C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072312 | |||||||
| chr9:98072343 | G | T | 1 | a0001c0001t0002g0202 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.349-4575G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072343 | |||||||
| chr9:98072356 | T | A | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-4562T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072356 | |||||||
| chr9:98072413 | A | AT | 15 | a0001c0001t0001g0100 a0001c0001t0002g0107 a0001c0001t0002g0108 others(12): Show |
15 | HG00741.hp1 HG01081.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.349-4489dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98072413 | ||||||
| chr9:98072413 | A | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-4505A>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072413 | |||||||
| chr9:98072413 | AT | A | 5 | a0001c0001t0002g0170 a0001c0003t0001g0025 a0001c0003t0001g0110 others(2): Show |
6 | HG02523.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-4489delT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98072413 | ||||||
| chr9:98072560 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-4358G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072560 | |||||||
| chr9:98072600 | A | G | 10 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.349-4318A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072600 | |||||||
| chr9:98072720 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.349-4198T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072720 | |||||||
| chr9:98072796 | G | A | 7 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(4): Show |
7 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-4122G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072796 | |||||||
| chr9:98072881 | A | G | 66 | a0001c0001t0002g0175 a0001c0003t0001g0120 a0002c0002t0001g0002 others(63): Show |
90 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.349-4037A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98072881 | |||||||
| chr9:98073072 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3846T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073072 | |||||||
| chr9:98073080 | A | G | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3838A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073080 | |||||||
| chr9:98073104 | C | G | 2 | a0001c0003t0001g0111 a0001c0003t0001g0113 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.349-3814C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073104 | |||||||
| chr9:98073136 | C | T | 1 | a0001c0003t0001g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.349-3782C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073136 | |||||||
| chr9:98073204 | T | C | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3714T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073204 | |||||||
| chr9:98073271 | C | CT | 32 | a0001c0001t0002g0027 a0001c0001t0002g0029 a0001c0001t0002g0030 others(29): Show |
39 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.349-3616dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | C | CTT | 24 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0107 others(21): Show |
29 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.349-3617_349-3616d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | C | CTTT | 11 | a0001c0001t0002g0015 a0001c0001t0002g0036 a0001c0001t0002g0162 others(8): Show |
13 | HG01358.hp2 HG02056.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-3618_349-3616d others(5): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CT | C | 34 | a0001c0001t0002g0028 a0001c0003t0001g0120 a0001c0004t0001g0044 others(31): Show |
51 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.349-3616delT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CTT | C | 7 | a0001c0003t0001g0112 a0001c0003t0001g0124 a0001c0003t0001g0144 others(4): Show |
7 | HG00438.hp2 HG01891.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-3617_349-3616d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CTTT | C | 19 | a0001c0003t0001g0038 a0001c0003t0001g0119 a0001c0003t0001g0129 others(16): Show |
19 | HG00741.hp2 HG01192.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.349-3618_349-3616d others(5): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CTTTT | C | 45 | a0001c0001t0002g0180 a0001c0003t0001g0003 a0001c0003t0001g0005 others(42): Show |
58 | HG01109.hp2 HG01255.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.349-3619_349-3616d others(6): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0001g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.349-3626_349-3616d others(13): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0188 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.349-3630_349-3616d others(17): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073271 | CTTTTTTT others(9): Show |
C | 13 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(10): Show |
20 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.349-3631_349-3616d others(18): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073271 | ||||||
| chr9:98073272 | T | C | 1 | a0001c0001t0002g0004 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.349-3646T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073272 | |||||||
| chr9:98073349 | C | A | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3569C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073349 | |||||||
| chr9:98073408 | C | T | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3510C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073408 | |||||||
| chr9:98073420 | G | T | 1 | a0001c0001t0002g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.349-3498G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073420 | |||||||
| chr9:98073505 | A | G | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3413A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073505 | |||||||
| chr9:98073519 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-3399G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073519 | |||||||
| chr9:98073590 | C | CT | 13 | a0001c0003t0001g0109 a0001c0003t0001g0110 a0001c0003t0001g0111 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.349-3315dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073590 | ||||||
| chr9:98073625 | C | A | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3293C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073625 | |||||||
| chr9:98073640 | A | G | 1 | a0001c0003t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-3278A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073640 | |||||||
| chr9:98073674 | C | T | 1 | a0001c0003t0001g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.349-3244C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073674 | |||||||
| chr9:98073811 | ATTTTT | A | 62 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(59): Show |
76 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-3105_349-3101d others(7): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98073811 | ||||||
| chr9:98073836 | G | A | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-3082G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073836 | |||||||
| chr9:98073849 | C | T | 2 | a0001c0003t0001g0218 a0003c0005t0001g0035 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349-3069C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073849 | |||||||
| chr9:98073991 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-2927G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98073991 | |||||||
| chr9:98074041 | C | T | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-2877C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074041 | |||||||
| chr9:98074051 | G | T | 1 | a0001c0001t0002g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.349-2867G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074051 | |||||||
| chr9:98074069 | G | A | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-2849G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074069 | |||||||
| chr9:98074118 | G | T | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-2800G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074118 | |||||||
| chr9:98074295 | C | G | 2 | a0001c0001t0002g0165 a0001c0001t0002g0204 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.349-2623C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074295 | |||||||
| chr9:98074326 | A | C | 1 | a0001c0003t0001g0215 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349-2592A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074326 | |||||||
| chr9:98074344 | G | C | 1 | a0001c0003t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349-2574G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074344 | |||||||
| chr9:98074398 | G | A | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-2520G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074398 | |||||||
| chr9:98074457 | A | G | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-2461A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074457 | |||||||
| chr9:98074588 | G | C | 1 | a0001c0003t0001g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.349-2330G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074588 | |||||||
| chr9:98074607 | C | T | 65 | a0001c0003t0001g0120 a0002c0002t0001g0002 a0002c0002t0001g0007 others(62): Show |
89 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.349-2311C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074607 | |||||||
| chr9:98074698 | C | T | 4 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0044 others(1): Show |
4 | HG01081.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2220C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074698 | |||||||
| chr9:98074756 | G | C | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-2162G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074756 | |||||||
| chr9:98074844 | G | T | 2 | a0001c0003t0001g0219 a0001c0003t0001g0220 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.349-2074G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98074844 | |||||||
| chr9:98075150 | TA | T | 66 | a0001c0001t0002g0184 a0001c0001t0002g0191 a0001c0001t0002g0201 others(63): Show |
90 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.349-1753delA | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98075150 | ||||||
| chr9:98075340 | C | CAG | 155 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(152): Show |
200 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.349-1575_349-1574d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98075340 | ||||||
| chr9:98075395 | G | T | 1 | a0005c0011t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.349-1523G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075395 | |||||||
| chr9:98075414 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-1504G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075414 | |||||||
| chr9:98075415 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349-1503G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075415 | |||||||
| chr9:98075514 | G | T | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-1404G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075514 | |||||||
| chr9:98075517 | TGGTCCGT others(1): Show |
T | 5 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0103 others(2): Show |
5 | HG01081.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1387_349-1380d others(10): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98075517 | ||||||
| chr9:98075531 | G | C | 1 | a0001c0001t0002g0231 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.349-1387G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075531 | |||||||
| chr9:98075720 | A | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-1198A>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075720 | |||||||
| chr9:98075789 | C | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-1129C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075789 | |||||||
| chr9:98075804 | T | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0191 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.349-1114T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075804 | |||||||
| chr9:98075844 | T | C | 13 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(10): Show |
20 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.349-1074T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075844 | |||||||
| chr9:98075904 | G | C | 2 | a0001c0003t0001g0125 a0001c0003t0001g0154 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.349-1014G>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075904 | |||||||
| chr9:98075983 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.349-935G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98075983 | |||||||
| chr9:98076069 | T | A | 1 | a0002c0002t0001g0056 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.349-849T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076069 | |||||||
| chr9:98076147 | T | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-771T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076147 | |||||||
| chr9:98076165 | A | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG02523.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.349-753A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076165 | |||||||
| chr9:98076380 | C | CT | 11 | a0001c0001t0001g0100 a0002c0002t0001g0009 a0002c0002t0001g0018 others(8): Show |
14 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-526dupT | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr9 | 98076380 | ||||||
| chr9:98076397 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-521T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076397 | |||||||
| chr9:98076406 | G | A | 1 | a0001c0004t0001g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349-512G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076406 | |||||||
| chr9:98076524 | G | A | 1 | a0002c0002t0001g0074 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.349-394G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076524 | |||||||
| chr9:98076557 | T | G | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-361T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076557 | |||||||
| chr9:98076617 | T | C | 9 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-301T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076617 | |||||||
| chr9:98076627 | G | T | 1 | a0001c0003t0001g0154 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.349-291G>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076627 | |||||||
| chr9:98076802 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.349-116C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076802 | |||||||
| chr9:98076848 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-70T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076848 | |||||||
| chr9:98076853 | T | C | 3 | a0001c0003t0001g0109 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG02818.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.349-65T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076853 | |||||||
| chr9:98076861 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.349-57A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 2/5 | chr9 | 98076861 | |||||||
| chr9:98077073 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.448+56A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077073 | |||||||
| chr9:98077159 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.448+142C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077159 | |||||||
| chr9:98077343 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.448+326T>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077343 | |||||||
| chr9:98077401 | GGTCT | G | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.448+389_448+392del others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr9 | 98077401 | ||||||
| chr9:98077486 | A | C | 1 | a0001c0003t0001g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.448+469A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077486 | |||||||
| chr9:98077528 | A | G | 1 | a0001c0001t0002g0163 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.448+511A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077528 | |||||||
| chr9:98077611 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.449-582G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077611 | |||||||
| chr9:98077884 | A | T | 1 | a0001c0001t0002g0162 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.449-309A>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077884 | |||||||
| chr9:98077924 | C | T | 1 | a0001c0003t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.449-269C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077924 | |||||||
| chr9:98077930 | G | A | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-263G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077930 | |||||||
| chr9:98077993 | C | T | 1 | a0001c0003t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.449-200C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98077993 | |||||||
| chr9:98078008 | C | A | 7 | a0001c0003t0001g0216 a0001c0003t0001g0217 a0001c0003t0001g0218 others(4): Show |
7 | HG01243.hp1 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-185C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98078008 | |||||||
| chr9:98078061 | G | A | 3 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0103 |
3 | HG01081.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.449-132G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 3/5 | chr9 | 98078061 | |||||||
| chr9:98078379 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.603+32G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98078379 | |||||||
| chr9:98078831 | A | AG | 5 | a0001c0003t0001g0232 a0001c0004t0001g0043 a0001c0004t0001g0044 others(2): Show |
5 | HG01081.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+489dupG | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 98078831 | ||||||
| chr9:98078836 | G | GA | 78 | a0001c0001t0001g0100 a0001c0001t0002g0037 a0001c0001t0002g0159 others(75): Show |
99 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.603+507dupA | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 98078836 | ||||||
| chr9:98078836 | G | GAA | 70 | a0001c0001t0002g0175 a0001c0003t0001g0115 a0001c0003t0001g0120 others(67): Show |
94 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.603+506_603+507dup others(2): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 98078836 | ||||||
| chr9:98078837 | A | G | 1 | a0003c0005t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.603+490A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98078837 | |||||||
| chr9:98079106 | A | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.603+759A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079106 | |||||||
| chr9:98079122 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.603+775G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079122 | |||||||
| chr9:98079236 | C | T | 2 | a0001c0003t0001g0127 a0005c0011t0001g0040 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.603+889C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079236 | |||||||
| chr9:98079336 | TTCTA | T | 3 | a0002c0002t0001g0067 a0003c0005t0001g0034 a0003c0005t0001g0035 |
3 | HG01106.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.603+1000_603+1003d others(6): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 98079336 | ||||||
| chr9:98079411 | G | A | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.603+1064G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079411 | |||||||
| chr9:98079472 | C | CTT | 157 | a0001c0001t0001g0100 a0001c0001t0002g0159 a0001c0001t0002g0160 others(154): Show |
202 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.603+1126_603+1127d others(4): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr9 | 98079472 | ||||||
| chr9:98079622 | C | T | 2 | a0001c0003t0001g0155 a0001c0003t0001g0156 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.604-1194C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079622 | |||||||
| chr9:98079670 | T | G | 1 | a0001c0003t0001g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.604-1146T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079670 | |||||||
| chr9:98079685 | C | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.604-1131C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079685 | |||||||
| chr9:98079686 | G | A | 1 | a0002c0002t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604-1130G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079686 | |||||||
| chr9:98079723 | C | T | 54 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(51): Show |
68 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.604-1093C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079723 | |||||||
| chr9:98079744 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.604-1072G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079744 | |||||||
| chr9:98079768 | T | C | 1 | a0001c0003t0001g0235 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.604-1048T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079768 | |||||||
| chr9:98079930 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.604-886G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079930 | |||||||
| chr9:98079993 | C | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.604-823C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98079993 | |||||||
| chr9:98080032 | G | A | 4 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-784G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98080032 | |||||||
| chr9:98080087 | A | G | 2 | a0001c0003t0001g0232 a0001c0004t0001g0043 |
2 | HG01081.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.604-729A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98080087 | |||||||
| chr9:98080182 | C | T | 1 | a0001c0001t0002g0176 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.604-634C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98080182 | |||||||
| chr9:98080295 | C | T | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.604-521C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98080295 | |||||||
| chr9:98080357 | G | A | 1 | a0002c0002t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.604-459G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98080357 | |||||||
| chr9:98080565 | T | G | 1 | a0001c0001t0002g0192 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.604-251T>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 4/5 | chr9 | 98080565 | |||||||
| chr9:98081086 | T | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.870+4T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081086 | |||||||
| chr9:98081089 | C | G | 7 | a0001c0003t0001g0110 a0001c0003t0001g0111 a0001c0003t0001g0113 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.870+7C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081089 | |||||||
| chr9:98081135 | A | G | 156 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0175 others(153): Show |
201 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.870+53A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081135 | |||||||
| chr9:98081140 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.870+58G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081140 | |||||||
| chr9:98081195 | C | G | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.870+113C>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081195 | |||||||
| chr9:98081197 | G | A | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.870+115G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081197 | |||||||
| chr9:98081378 | C | A | 54 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(51): Show |
68 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.870+296C>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081378 | |||||||
| chr9:98081755 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.870+673G>A | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081755 | |||||||
| chr9:98081916 | T | C | 17 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0223 others(14): Show |
24 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.870+834T>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98081916 | |||||||
| chr9:98081986 | CAT | C | 3 | a0001c0003t0001g0123 a0001c0003t0001g0142 a0006c0012t0001g0135 |
3 | NA18939.hp2 NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.871-858_871-857del others(2): Show |
NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr9 | 98081986 | ||||||
| chr9:98082023 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.871-823C>T | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98082023 | |||||||
| chr9:98082626 | A | C | 2 | a0003c0005t0001g0034 a0003c0005t0001g0035 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.871-220A>C | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98082626 | |||||||
| chr9:98082725 | A | G | 61 | a0001c0003t0001g0003 a0001c0003t0001g0005 a0001c0003t0001g0014 others(58): Show |
75 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(72): Show |
intron_variant | MODIFIER | c.871-121A>G | NANS | ENSG00000095380.11 | transcript | ENST00000210444.6 | protein_coding | 5/5 | chr9 | 98082725 |