Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 388512 |
| ensemblid | ENSG00000187912.12 |
| hgncid | 34520 |
| symbol | CLEC17A |
| name | C-type lectin domain containing 17A |
| refseq_nuc | NM_001204118.2 |
| refseq_prot | NP_001191047.1 |
| ensembl_nuc | ENST00000417570.6 |
| ensembl_prot | ENSP00000393719.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 14583084 |
| end | 14612035 |
| strand | + |
| ver | v1.2 |
| region | chr19:14583084-14612035 |
| region5000 | chr19:14578084-14617035 |
| regionname0 | CLEC17A_chr19_14583084_14612035 |
| regionname5000 | CLEC17A_chr19_14578084_14617035 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 378 | 323 | 69 | 67 | 139 | 18 | 28 | 97 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(373): Show |
chr19 | 14578084 | 14617035 |
| a0002 | 0/0 | 379 | 27 | 21 | 1 | 1 | 0 | 4 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(374): Show |
chr19 | 14578084 | 14617035 |
| a0003 | 0/0 | 378 | 8 | 0 | 1 | 2 | 0 | 5 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(373): Show |
chr19 | 14578084 | 14617035 |
| a0004 | 0/0 | 378 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(373): Show |
chr19 | 14578084 | 14617035 |
| a0005 | 0/0 | 353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(348): Show |
chr19 | 14578084 | 14617035 |
| a0006 | 0/0 | 378 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(373): Show |
chr19 | 14578084 | 14617035 |
| a0007 | 0/0 | 378 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(373): Show |
chr19 | 14578084 | 14617035 |
| a0008 | 0/0 | 378 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(373): Show |
chr19 | 14578084 | 14617035 |
| a0009 | 0/0 | 352 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | MHNLY others(347): Show |
chr19 | 14578084 | 14617035 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1134 | 323 | 69 | 67 | 139 | 18 | 28 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1129): Show |
chr19 | 14578084 | 14617035 | ||
| a0002c0002 | 0/0 | 1137 | 27 | 21 | 1 | 1 | 0 | 4 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1132): Show |
chr19 | 14578084 | 14617035 | ||
| a0003c0003 | 0/0 | 1134 | 8 | 0 | 1 | 2 | 0 | 5 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1129): Show |
chr19 | 14578084 | 14617035 | ||
| a0004c0009 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1129): Show |
chr19 | 14578084 | 14617035 | ||
| a0005c0004 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1054): Show |
chr19 | 14578084 | 14617035 | ||
| a0006c0007 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1129): Show |
chr19 | 14578084 | 14617035 | ||
| a0007c0005 | 0/0 | 1134 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1129): Show |
chr19 | 14578084 | 14617035 | ||
| a0008c0006 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1129): Show |
chr19 | 14578084 | 14617035 | ||
| a0009c0008 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | ATGCA others(1051): Show |
chr19 | 14578084 | 14617035 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3052 | 95 | 0 | 26 | 59 | 3 | 7 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0002 | 0/1 | 3051 | 55 | 11 | 16 | 12 | 6 | 9 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0003 | 0/0 | 3053 | 43 | 9 | 8 | 17 | 4 | 5 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0004 | 0/0 | 3052 | 49 | 10 | 10 | 26 | 1 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0005 | 0/0 | 3051 | 14 | 13 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0006 | 0/0 | 3052 | 15 | 7 | 2 | 4 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0007 | 0/0 | 3053 | 6 | 0 | 1 | 5 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0008 | 0/0 | 3052 | 6 | 4 | 1 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0009 | 0/0 | 3054 | 6 | 0 | 2 | 3 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3049): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0010 | 0/0 | 3053 | 5 | 3 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0011 | 0/0 | 3052 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0012 | 0/0 | 3054 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3049): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0013 | 0/0 | 3050 | 3 | 1 | 0 | 1 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3045): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0015 | 1/0 | 3053 | 2 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0016 | 0/0 | 3051 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0017 | 0/0 | 3051 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0018 | 0/0 | 3053 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0019 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0020 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0021 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0022 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3049): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0023 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0024 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0025 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0026 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0027 | 0/0 | 3053 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0001c0001t0028 | 0/0 | 3053 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0001 | 0/0 | 3055 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3050): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0002 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3049): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0003 | 0/0 | 3056 | 10 | 5 | 1 | 1 | 0 | 3 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3051): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0004 | 0/0 | 3055 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3050): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0005 | 0/0 | 3054 | 9 | 9 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3049): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0006 | 0/0 | 3055 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3050): Show |
chr19 | 14578084 | 14617035 |
| a0002c0002t0014 | 0/0 | 3054 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3049): Show |
chr19 | 14578084 | 14617035 |
| a0003c0003t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0003c0003t0002 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0003c0003t0003 | 0/0 | 3053 | 3 | 0 | 0 | 0 | 0 | 3 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0003c0003t0006 | 0/0 | 3052 | 3 | 0 | 1 | 1 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0004c0009t0002 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3046): Show |
chr19 | 14578084 | 14617035 |
| a0005c0004t0002 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(2971): Show |
chr19 | 14578084 | 14617035 |
| a0006c0007t0004 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0007c0005t0004 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3047): Show |
chr19 | 14578084 | 14617035 |
| a0008c0006t0007 | 0/0 | 3053 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(3048): Show |
chr19 | 14578084 | 14617035 |
| a0009c0008t0003 | 0/0 | 2975 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | AGACG others(2970): Show |
chr19 | 14578084 | 14617035 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0009g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0010g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0010g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0011g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0013g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0015g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0015g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0016g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0017g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0017g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0018g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0018g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0019g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0021g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0022g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0023g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0024g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0025g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0027g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0001c0001t0028g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0002c0002t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0003c0003t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0004c0009t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0005c0004t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0006c0007t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0007c0005t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0008c0006t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| a0009c0008t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0116 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0117 | EUR | GBR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0171 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0197 | EUR | FIN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0305 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | CHS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0259 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0144 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0134 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0321 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01243 | hp2 | a0003 | c0003 | t0006 | g0035 | AMR | PUR | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0236 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01361 | hp1 | a0001 | c0001 | t0021 | g0072 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0199 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0015 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0015 | EUR | IBS | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0082 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0110 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0080 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01943 | hp1 | a0004 | c0009 | t0002 | g0176 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0285 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0075 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02056 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02056 | hp2 | a0003 | c0003 | t0006 | g0060 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02080 | hp2 | a0001 | c0001 | t0009 | g0177 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02132 | hp2 | a0006 | c0007 | t0004 | g0166 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0093 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0266 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02155 | hp1 | a0001 | c0001 | t0025 | g0216 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | CDX | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02257 | hp2 | a0002 | c0002 | t0004 | g0032 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0150 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0068 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PEL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | KHV | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0081 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02615 | hp2 | a0002 | c0002 | t0003 | g0103 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02622 | hp1 | a0002 | c0002 | t0014 | g0086 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02647 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0255 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0069 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02723 | hp2 | a0002 | c0002 | t0005 | g0099 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02809 | hp2 | a0002 | c0002 | t0005 | g0095 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02886 | hp2 | a0002 | c0002 | t0014 | g0085 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02922 | hp2 | a0002 | c0002 | t0005 | g0098 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02965 | hp1 | a0002 | c0002 | t0005 | g0100 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02970 | hp2 | a0002 | c0002 | t0005 | g0101 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02976 | hp2 | a0002 | c0002 | t0005 | g0102 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0105 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03130 | hp1 | a0002 | c0002 | t0005 | g0097 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03130 | hp2 | a0007 | c0005 | t0004 | g0056 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03139 | hp2 | a0002 | c0002 | t0005 | g0096 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03195 | hp1 | a0002 | c0002 | t0005 | g0087 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0070 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0229 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03453 | hp1 | a0002 | c0002 | t0014 | g0090 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03486 | hp1 | a0002 | c0002 | t0003 | g0088 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03490 | hp1 | a0008 | c0006 | t0007 | g0329 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03491 | hp1 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03492 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | ESN | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0073 | AFR | GWD | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0079 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0283 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0084 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03942 | hp1 | a0003 | c0003 | t0006 | g0058 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0123 | SAS | BEB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0034 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0330 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG04204 | hp1 | a0001 | c0001 | t0015 | g0328 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | STU | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18747 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18747 | hp2 | a0001 | c0001 | t0023 | g0251 | EAS | CHB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0078 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18944 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18946 | hp1 | a0001 | c0001 | t0017 | g0316 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18951 | hp2 | a0001 | c0001 | t0013 | g0322 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18961 | hp1 | a0001 | c0001 | t0019 | g0222 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18963 | hp2 | a0001 | c0001 | t0028 | g0260 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18982 | hp1 | a0001 | c0001 | t0024 | g0297 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18983 | hp2 | a0001 | c0001 | t0018 | g0152 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18987 | hp1 | a0001 | c0001 | t0017 | g0111 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0052 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19060 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19063 | hp1 | a0009 | c0008 | t0003 | g0129 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19081 | hp1 | a0001 | c0001 | t0027 | g0279 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19240 | hp1 | a0001 | c0001 | t0026 | g0061 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0181 | AFR | YRI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ASW | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | ASW | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0146 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | TSI | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | GIH | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA20905 | hp2 | a0003 | c0003 | t0003 | g0033 | SAS | GIH | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02109 | hp2 | a0005 | c0004 | t0002 | g0094 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03471 | hp1 | a0002 | c0002 | t0006 | g0092 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | MSL | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | USA | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | USA | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0288 | EAS | JPT | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | LWK | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0125 | REF | REF | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0015 | g0244 | REF | REF | CLEC17A_chr19_14578084_14617035 | CLEC17A | chr19 | 14578084 | 14617035 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14583201 | C | T | 1 | a0004 | 1 | HG01943.hp1 | missense_variant&splice_region_variant | MODERATE | c.41C>T | p.Pro14Leu | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/14 | 118/3053 | 41/1137 | 14/378 | chr19 | 14583201 | |||
| chr19:14583363 | T | TGGA | 2 | a0002 a0005 |
28 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(25): Show |
disruptive_inframe_insertion | MODERATE | c.66_68dupGGA | p.Glu22dup | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/14 | 146/3053 | 69/1137 | 23/378 | INFO_REALIGN_3_PRIME | chr19 | 14583363 | ||
| chr19:14585083 | TCCTTTCA others(4254): Show |
T | 1 | a0005 | 1 | HG02109.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.121+1827_199+1830d others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 14585083 | ||||||
| chr19:14585489 | TGACTCAG others(4256): Show |
T | 1 | a0009 | 1 | NA19063.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.122-1613_200-2018d others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 14585489 | ||||||
| chr19:14592338 | A | G | 1 | a0003 | 8 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(5): Show |
missense_variant | MODERATE | c.257A>G | p.Lys86Arg | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/14 | 334/3053 | 257/1137 | 86/378 | chr19 | 14592338 | |||
| chr19:14594762 | T | C | 2 | a0002 a0005 |
28 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(25): Show |
missense_variant | MODERATE | c.365T>C | p.Leu122Pro | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/14 | 442/3053 | 365/1137 | 122/378 | chr19 | 14594762 | |||
| chr19:14597126 | T | C | 1 | a0007 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.611T>C | p.Met204Thr | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/14 | 688/3053 | 611/1137 | 204/378 | chr19 | 14597126 | |||
| chr19:14599761 | C | T | 1 | a0006 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.691C>T | p.Arg231Cys | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 11/14 | 768/3053 | 691/1137 | 231/378 | chr19 | 14599761 | |||
| chr19:14600072 | G | A | 1 | a0008 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.784G>A | p.Glu262Lys | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/14 | 861/3053 | 784/1137 | 262/378 | chr19 | 14600072 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14610207 | C | T | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 11 | chr19 | 14610207 | ||||||
| chr19:14610243 | A | G | 1 | a0001c0001t0016 | 2 | NA18747.hp1 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*47A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 47 | chr19 | 14610243 | ||||||
| chr19:14610447 | T | C | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0017 others(5): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*251T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 251 | chr19 | 14610447 | ||||||
| chr19:14610456 | G | A | 1 | a0001c0001t0023 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 260 | chr19 | 14610456 | ||||||
| chr19:14610774 | G | T | 1 | a0002c0002t0014 | 3 | HG02622.hp1 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 578 | chr19 | 14610774 | ||||||
| chr19:14610844 | T | C | 1 | a0001c0001t0011 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*648T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 648 | chr19 | 14610844 | ||||||
| chr19:14610893 | G | A | 1 | a0001c0001t0011 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*697G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 697 | chr19 | 14610893 | ||||||
| chr19:14610909 | G | A | 1 | a0001c0001t0020 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 713 | chr19 | 14610909 | ||||||
| chr19:14610948 | C | T | 1 | a0002c0002t0014 | 3 | HG02622.hp1 HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*752C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 752 | chr19 | 14610948 | ||||||
| chr19:14610968 | T | C | 2 | a0001c0001t0010 a0001c0001t0012 |
9 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*772T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 772 | chr19 | 14610968 | ||||||
| chr19:14611000 | CT | C | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0013 others(10): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*818delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 818 | INFO_REALIGN_3_PRIME | chr19 | 14611000 | |||||
| chr19:14611014 | T | C | 2 | a0001c0001t0018 a0001c0001t0024 |
3 | NA18955.hp2 NA18982.hp1 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*818T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 818 | chr19 | 14611014 | ||||||
| chr19:14611015 | C | T | 1 | a0001c0001t0011 | 4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*819C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 819 | chr19 | 14611015 | ||||||
| chr19:14611051 | T | C | 1 | a0001c0001t0025 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*855T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 855 | chr19 | 14611051 | ||||||
| chr19:14611153 | C | T | 1 | a0001c0001t0028 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*957C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 957 | chr19 | 14611153 | ||||||
| chr19:14611185 | T | C | 1 | a0001c0001t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 989 | chr19 | 14611185 | ||||||
| chr19:14611371 | C | CT | 3 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0022 |
11 | HG01069.hp2 HG01169.hp1 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1199dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1200 | INFO_REALIGN_3_PRIME | chr19 | 14611371 | |||||
| chr19:14611371 | CT | C | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(19): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1199delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1199 | INFO_REALIGN_3_PRIME | chr19 | 14611371 | |||||
| chr19:14611371 | CTT | C | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(1): Show |
28 | HG00323.hp1 HG02109.hp1 HG02257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1198_*1199delTT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1198 | INFO_REALIGN_3_PRIME | chr19 | 14611371 | |||||
| chr19:14611380 | T | C | 1 | a0001c0001t0027 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1184T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1184 | chr19 | 14611380 | ||||||
| chr19:14611864 | C | T | 1 | a0001c0001t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1668C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1668 | chr19 | 14611864 | ||||||
| chr19:14611865 | G | A | 1 | a0001c0001t0021 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1669G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 14/14 | 1669 | chr19 | 14611865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14583214 | G | C | 1 | a0001c0001t0002g0029 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.43+11G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/13 | chr19 | 14583214 | |||||||
| chr19:14583233 | C | A | 1 | a0001c0001t0002g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.43+30C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/13 | chr19 | 14583233 | |||||||
| chr19:14583347 | C | A | 1 | a0001c0001t0003g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-10C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 1/13 | chr19 | 14583347 | |||||||
| chr19:14583478 | T | C | 1 | a0002c0002t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.121+44T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583478 | |||||||
| chr19:14583491 | G | A | 3 | a0003c0003t0002g0034 a0003c0003t0003g0033 a0003c0003t0006g0035 |
3 | HG01243.hp2 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.121+57G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583491 | |||||||
| chr19:14583580 | C | G | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+146C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583580 | |||||||
| chr19:14583600 | G | A | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+166G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583600 | |||||||
| chr19:14583605 | T | C | 80 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.121+171T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583605 | |||||||
| chr19:14583606 | G | A | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+172G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583606 | |||||||
| chr19:14583609 | T | A | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+175T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583609 | |||||||
| chr19:14583769 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.121+335G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583769 | |||||||
| chr19:14583834 | G | A | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+400G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583834 | |||||||
| chr19:14583883 | T | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+449T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583883 | |||||||
| chr19:14583898 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+464A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583898 | |||||||
| chr19:14583900 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+466C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583900 | |||||||
| chr19:14583969 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+535G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583969 | |||||||
| chr19:14583993 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+559G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583993 | |||||||
| chr19:14583995 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+561T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583995 | |||||||
| chr19:14583997 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+563A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14583997 | |||||||
| chr19:14584025 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+591A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584025 | |||||||
| chr19:14584039 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+605A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584039 | |||||||
| chr19:14584059 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+625T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584059 | |||||||
| chr19:14584068 | C | CA | 143 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0124 others(140): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.121+649dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14584068 | ||||||
| chr19:14584068 | C | CAA | 12 | a0001c0001t0001g0108 a0001c0001t0002g0107 a0001c0001t0003g0109 others(9): Show |
12 | HG01433.hp1 HG01934.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+648_121+649dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14584068 | ||||||
| chr19:14584083 | A | AAAAAAG | 49 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0066 others(46): Show |
54 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(51): Show |
intron_variant | MODIFIER | c.121+649_121+650ins others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584083 | |||||||
| chr19:14584083 | A | AAAAAG | 27 | a0001c0001t0004g0054 a0002c0002t0001g0089 a0002c0002t0002g0083 others(24): Show |
27 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.121+649_121+650ins others(5): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584083 | |||||||
| chr19:14584095 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+661G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584095 | |||||||
| chr19:14584100 | G | T | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+666G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584100 | |||||||
| chr19:14584156 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+722A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584156 | |||||||
| chr19:14584179 | G | T | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+745G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584179 | |||||||
| chr19:14584188 | C | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+754C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584188 | |||||||
| chr19:14584193 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+759C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584193 | |||||||
| chr19:14584197 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+763C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584197 | |||||||
| chr19:14584222 | C | T | 21 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(18): Show |
24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+788C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584222 | |||||||
| chr19:14584241 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.121+807G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584241 | |||||||
| chr19:14584243 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+809G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584243 | |||||||
| chr19:14584299 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+865G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584299 | |||||||
| chr19:14584304 | A | C | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+870A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584304 | |||||||
| chr19:14584305 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+871G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584305 | |||||||
| chr19:14584306 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+872T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584306 | |||||||
| chr19:14584318 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+884A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584318 | |||||||
| chr19:14584329 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+895T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584329 | |||||||
| chr19:14584355 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.121+921G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584355 | |||||||
| chr19:14584481 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0008g0236 |
2 | HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1047C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584481 | |||||||
| chr19:14584482 | G | C | 6 | a0001c0001t0002g0106 a0001c0001t0003g0116 a0001c0001t0003g0117 others(3): Show |
7 | HG00140.hp1 HG00140.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+1048G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584482 | |||||||
| chr19:14584484 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0008g0236 |
2 | HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1050A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584484 | |||||||
| chr19:14584512 | T | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0002g0009 others(6): Show |
10 | HG00642.hp2 HG01081.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+1078T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584512 | |||||||
| chr19:14584524 | G | A | 79 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0066 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.121+1090G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584524 | |||||||
| chr19:14584533 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.121+1099G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584533 | |||||||
| chr19:14584546 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+1112A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584546 | |||||||
| chr19:14584555 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+1121G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584555 | |||||||
| chr19:14584594 | A | G | 2 | a0001c0001t0001g0326 a0001c0001t0002g0036 |
2 | NA19087.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.121+1160A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584594 | |||||||
| chr19:14584876 | A | C | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.121+1442A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14584876 | |||||||
| chr19:14585033 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.121+1599C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585033 | |||||||
| chr19:14585083 | T | C | 3 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0003g0119 |
3 | HG00099.hp1 HG01081.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.121+1649T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585083 | |||||||
| chr19:14585091 | A | G | 1 | a0003c0003t0006g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.121+1657A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585091 | |||||||
| chr19:14585168 | G | T | 9 | a0002c0002t0003g0103 a0002c0002t0005g0095 a0002c0002t0005g0096 others(6): Show |
9 | HG02615.hp2 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+1734G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585168 | |||||||
| chr19:14585209 | A | T | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.121+1775A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585209 | |||||||
| chr19:14585244 | A | G | 1 | a0001c0001t0004g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.121+1810A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585244 | |||||||
| chr19:14585281 | T | C | 2 | a0001c0001t0026g0061 a0007c0005t0004g0056 |
2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121+1847T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585281 | |||||||
| chr19:14585370 | A | C | 5 | a0001c0001t0002g0036 a0001c0001t0002g0104 a0001c0001t0004g0053 others(2): Show |
6 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+1936A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585370 | |||||||
| chr19:14585416 | T | G | 1 | a0001c0001t0003g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.121+1982T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585416 | |||||||
| chr19:14585445 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0004g0323 |
3 | NA18955.hp1 NA19079.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.121+2011C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585445 | |||||||
| chr19:14585484 | C | T | 21 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(18): Show |
24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+2050C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585484 | |||||||
| chr19:14585621 | C | T | 18 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(15): Show |
21 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-1993C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585621 | |||||||
| chr19:14585721 | C | T | 17 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(14): Show |
19 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-1893C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585721 | |||||||
| chr19:14585778 | C | G | 1 | a0002c0002t0006g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122-1836C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14585778 | |||||||
| chr19:14586001 | T | C | 1 | a0002c0002t0005g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.122-1613T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586001 | |||||||
| chr19:14586042 | C | CT | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.122-1572_122-1571i others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586042 | |||||||
| chr19:14586122 | C | CT | 10 | a0001c0001t0001g0319 a0001c0001t0002g0018 a0001c0001t0002g0076 others(7): Show |
10 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-1475dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586122 | ||||||
| chr19:14586122 | CT | C | 42 | a0001c0001t0003g0238 a0001c0001t0003g0327 a0001c0001t0004g0202 others(39): Show |
43 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.122-1475delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586122 | ||||||
| chr19:14586189 | A | G | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-1425A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586189 | |||||||
| chr19:14586242 | C | T | 2 | a0001c0001t0004g0062 a0001c0001t0004g0065 |
2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.122-1372C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586242 | |||||||
| chr19:14586247 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.122-1367T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586247 | |||||||
| chr19:14586282 | G | A | 21 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(18): Show |
24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-1332G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586282 | |||||||
| chr19:14586341 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.122-1273C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586341 | |||||||
| chr19:14586406 | G | A | 9 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(6): Show |
9 | HG00544.hp2 HG00597.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-1208G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586406 | |||||||
| chr19:14586478 | A | G | 2 | a0001c0001t0002g0017 a0001c0001t0005g0220 |
3 | HG01070.hp1 HG01071.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.122-1136A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586478 | |||||||
| chr19:14586525 | C | G | 83 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(80): Show |
88 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(85): Show |
intron_variant | MODIFIER | c.122-1089C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586525 | |||||||
| chr19:14586578 | T | A | 35 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(32): Show |
36 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(33): Show |
intron_variant | MODIFIER | c.122-1036T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586578 | |||||||
| chr19:14586599 | A | AT | 79 | a0001c0001t0001g0290 a0001c0001t0002g0036 a0001c0001t0002g0048 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.122-1007dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586599 | ||||||
| chr19:14586632 | G | A | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-982G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586632 | |||||||
| chr19:14586671 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.122-943C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586671 | |||||||
| chr19:14586887 | C | CT | 30 | a0002c0002t0002g0083 a0002c0002t0003g0059 a0002c0002t0003g0079 others(27): Show |
31 | HG01243.hp2 HG01934.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.122-724dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586887 | ||||||
| chr19:14586889 | TTC | T | 38 | a0001c0001t0002g0036 a0001c0001t0002g0066 a0001c0001t0002g0067 others(35): Show |
41 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.122-723_122-722del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586889 | ||||||
| chr19:14586891 | C | CT | 8 | a0001c0001t0003g0207 a0001c0001t0004g0206 a0001c0001t0004g0217 others(5): Show |
8 | HG01891.hp1 HG02080.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-708dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586891 | ||||||
| chr19:14586891 | C | T | 31 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(28): Show |
32 | HG01243.hp2 HG01934.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.122-723C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586891 | |||||||
| chr19:14586920 | A | G | 2 | a0001c0001t0008g0074 a0001c0001t0008g0075 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.122-694A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586920 | |||||||
| chr19:14586925 | GTCACTCA others(21): Show |
G | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-686_122-659del others(28): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14586925 | ||||||
| chr19:14586935 | C | T | 2 | a0001c0001t0004g0053 a0001c0001t0004g0054 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.122-679C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14586935 | |||||||
| chr19:14587034 | A | G | 79 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.122-580A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587034 | |||||||
| chr19:14587035 | G | C | 56 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(53): Show |
61 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(58): Show |
intron_variant | MODIFIER | c.122-579G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587035 | |||||||
| chr19:14587035 | G | T | 27 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(24): Show |
27 | HG01891.hp1 HG01934.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.122-579G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587035 | |||||||
| chr19:14587090 | C | T | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-524C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587090 | |||||||
| chr19:14587142 | C | T | 27 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(24): Show |
27 | HG01891.hp1 HG01934.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.122-472C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587142 | |||||||
| chr19:14587233 | A | ATG | 28 | a0001c0001t0001g0108 a0001c0001t0001g0161 a0001c0001t0001g0306 others(25): Show |
29 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.122-353_122-352dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | A | ATGTG | 26 | a0001c0001t0001g0256 a0001c0001t0002g0030 a0001c0001t0003g0063 others(23): Show |
28 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.122-355_122-352dup others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | A | ATGTGTG | 9 | a0001c0001t0002g0036 a0001c0001t0002g0071 a0001c0001t0004g0053 others(6): Show |
10 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-357_122-352dup others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | A | ATGTGTGT others(1): Show |
12 | a0001c0001t0012g0070 a0002c0002t0004g0093 a0002c0002t0005g0097 others(9): Show |
13 | HG01243.hp2 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-359_122-352dup others(8): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | A | ATGTGTGT others(3): Show |
13 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0079 others(10): Show |
13 | HG01891.hp1 HG02257.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-361_122-352dup others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | A | ATGTGTGT others(5): Show |
7 | a0002c0002t0003g0059 a0002c0002t0003g0080 a0002c0002t0003g0084 others(4): Show |
7 | HG01934.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-363_122-352dup others(12): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | A | ATGTGTGT others(7): Show |
1 | a0002c0002t0005g0099 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.122-365_122-352dup others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | ATG | A | 47 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(44): Show |
49 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.122-353_122-352del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587233 | ATGTGTG | A | 5 | a0001c0001t0003g0213 a0001c0001t0003g0230 a0001c0001t0004g0211 others(2): Show |
5 | HG02074.hp2 HG02080.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-357_122-352del others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587233 | ||||||
| chr19:14587253 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-355_122-346del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 14587253 | ||||||
| chr19:14587262 | T | TG | 4 | a0001c0001t0001g0148 a0001c0001t0001g0159 a0001c0001t0002g0182 others(1): Show |
4 | HG03516.hp2 NA18999.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-352_122-351ins others(1): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587262 | |||||||
| chr19:14587263 | T | G | 73 | a0001c0001t0002g0036 a0001c0001t0002g0066 a0001c0001t0002g0067 others(70): Show |
77 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(74): Show |
intron_variant | MODIFIER | c.122-351T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587263 | |||||||
| chr19:14587268 | T | TGTGTGTG others(4): Show |
1 | a0003c0003t0006g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.122-346_122-345ins others(11): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587268 | |||||||
| chr19:14587269 | T | G | 1 | a0002c0002t0006g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122-345T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587269 | |||||||
| chr19:14587419 | T | C | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-195T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587419 | |||||||
| chr19:14587593 | G | C | 2 | a0001c0001t0001g0028 a0001c0001t0004g0323 |
3 | NA18955.hp1 NA19079.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.122-21G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587593 | |||||||
| chr19:14587604 | C | A | 33 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(30): Show |
35 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.122-10C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 2/13 | chr19 | 14587604 | |||||||
| chr19:14587757 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.199+66T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587757 | |||||||
| chr19:14587775 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.199+84C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587775 | |||||||
| chr19:14587788 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.199+97C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587788 | |||||||
| chr19:14587837 | G | C | 79 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+146G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587837 | |||||||
| chr19:14587888 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.199+197A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587888 | |||||||
| chr19:14587934 | C | T | 1 | a0001c0001t0004g0203 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.199+243C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587934 | |||||||
| chr19:14587946 | A | T | 79 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+255A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14587946 | |||||||
| chr19:14588021 | T | A | 1 | a0001c0001t0004g0217 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.199+330T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588021 | |||||||
| chr19:14588114 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.199+423G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588114 | |||||||
| chr19:14588165 | C | T | 159 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(156): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.199+474C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588165 | |||||||
| chr19:14588171 | G | A | 79 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+480G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588171 | |||||||
| chr19:14588184 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0002g0030 a0001c0001t0002g0304 others(1): Show |
5 | HG00639.hp2 HG00741.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+493T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588184 | |||||||
| chr19:14588250 | G | A | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+559G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588250 | |||||||
| chr19:14588300 | C | A | 1 | a0001c0001t0017g0111 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.199+609C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588300 | |||||||
| chr19:14588325 | C | CA | 63 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0306 others(60): Show |
68 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(65): Show |
intron_variant | MODIFIER | c.199+650dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14588325 | ||||||
| chr19:14588325 | C | CAA | 6 | a0001c0001t0002g0051 a0001c0001t0002g0104 a0001c0001t0017g0111 others(3): Show |
6 | HG02056.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+649_199+650dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14588325 | ||||||
| chr19:14588336 | A | AC | 14 | a0001c0001t0003g0045 a0001c0001t0005g0038 a0001c0001t0005g0040 others(11): Show |
14 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.199+645_199+646ins others(1): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588336 | |||||||
| chr19:14588392 | A | C | 1 | a0001c0001t0002g0009 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.199+701A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588392 | |||||||
| chr19:14588393 | C | T | 1 | a0001c0001t0002g0009 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.199+702C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588393 | |||||||
| chr19:14588411 | G | T | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+720G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588411 | |||||||
| chr19:14588453 | T | G | 79 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+762T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588453 | |||||||
| chr19:14588464 | A | G | 79 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(76): Show |
84 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(81): Show |
intron_variant | MODIFIER | c.199+773A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588464 | |||||||
| chr19:14588484 | C | T | 21 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(18): Show |
24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.199+793C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588484 | |||||||
| chr19:14588505 | G | A | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+814G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588505 | |||||||
| chr19:14588590 | T | C | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.199+899T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588590 | |||||||
| chr19:14588615 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0003g0207 a0001c0001t0004g0206 others(2): Show |
5 | HG00673.hp1 NA18945.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+924C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588615 | |||||||
| chr19:14588640 | A | G | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+949A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588640 | |||||||
| chr19:14588646 | A | C | 1 | a0001c0001t0017g0111 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.199+955A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588646 | |||||||
| chr19:14588648 | C | T | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+957C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588648 | |||||||
| chr19:14588657 | A | G | 1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+966A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588657 | |||||||
| chr19:14588692 | G | A | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1001G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588692 | |||||||
| chr19:14588807 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.199+1116G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588807 | |||||||
| chr19:14588849 | A | C | 21 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(18): Show |
24 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.199+1158A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14588849 | |||||||
| chr19:14589025 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.199+1334C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589025 | |||||||
| chr19:14589133 | C | A | 11 | a0001c0001t0003g0045 a0001c0001t0005g0038 a0001c0001t0005g0040 others(8): Show |
11 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+1442C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589133 | |||||||
| chr19:14589137 | C | A | 4 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(1): Show |
4 | NA18951.hp2 NA18971.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1446C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589137 | |||||||
| chr19:14589266 | T | C | 82 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0002g0036 others(79): Show |
87 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(84): Show |
intron_variant | MODIFIER | c.199+1575T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589266 | |||||||
| chr19:14589344 | C | T | 80 | a0001c0001t0001g0270 a0001c0001t0002g0036 a0001c0001t0002g0048 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.199+1653C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589344 | |||||||
| chr19:14589429 | G | T | 1 | a0002c0002t0003g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.199+1738G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589429 | |||||||
| chr19:14589519 | C | G | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+1828C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589519 | |||||||
| chr19:14589522 | T | C | 6 | a0001c0001t0001g0271 a0001c0001t0003g0327 a0001c0001t0004g0274 others(3): Show |
6 | HG02165.hp1 HG03490.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+1831T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589522 | |||||||
| chr19:14589525 | G | A | 1 | a0007c0005t0004g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.199+1834G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589525 | |||||||
| chr19:14589542 | T | C | 80 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.199+1851T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589542 | |||||||
| chr19:14589560 | A | G | 1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199+1869A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589560 | |||||||
| chr19:14589598 | TCA | T | 328 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(325): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.199+1910_199+1911d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14589598 | ||||||
| chr19:14589633 | A | C | 44 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
48 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.199+1942A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589633 | |||||||
| chr19:14589708 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.199+2017T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14589708 | |||||||
| chr19:14590208 | A | G | 4 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(1): Show |
4 | NA18951.hp2 NA18971.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-2073A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590208 | |||||||
| chr19:14590281 | G | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0026 others(283): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.200-2000G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590281 | |||||||
| chr19:14590386 | CT | C | 8 | a0001c0001t0001g0239 a0003c0003t0001g0057 a0003c0003t0002g0034 others(5): Show |
9 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-1879delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590386 | ||||||
| chr19:14590386 | CTT | C | 43 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(40): Show |
47 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(44): Show |
intron_variant | MODIFIER | c.200-1880_200-1879d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590386 | ||||||
| chr19:14590401 | T | C | 1 | a0002c0002t0003g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.200-1880T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590401 | |||||||
| chr19:14590542 | C | T | 1 | a0001c0001t0003g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.200-1739C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590542 | |||||||
| chr19:14590547 | C | T | 1 | a0001c0001t0006g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.200-1734C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590547 | |||||||
| chr19:14590548 | C | T | 1 | a0001c0001t0004g0321 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.200-1733C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590548 | |||||||
| chr19:14590574 | A | G | 62 | a0001c0001t0002g0036 a0001c0001t0002g0066 a0001c0001t0002g0067 others(59): Show |
66 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(63): Show |
intron_variant | MODIFIER | c.200-1707A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590574 | |||||||
| chr19:14590697 | T | C | 80 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.200-1584T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590697 | |||||||
| chr19:14590717 | C | T | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0011g0078 |
3 | HG01884.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.200-1564C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590717 | |||||||
| chr19:14590862 | A | AT | 82 | a0001c0001t0001g0025 a0001c0001t0001g0223 a0001c0001t0001g0267 others(79): Show |
88 | HG01099.hp2 HG01109.hp1 HG01243.hp2 others(85): Show |
intron_variant | MODIFIER | c.200-1403dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590862 | ||||||
| chr19:14590862 | A | ATT | 8 | a0001c0001t0002g0076 a0001c0001t0002g0104 a0001c0001t0003g0227 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-1404_200-1403d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14590862 | ||||||
| chr19:14590923 | C | A | 1 | a0001c0001t0002g0120 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.200-1358C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590923 | |||||||
| chr19:14590956 | C | T | 1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.200-1325C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14590956 | |||||||
| chr19:14591005 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0008g0236 |
2 | HG01256.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.200-1276G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591005 | |||||||
| chr19:14591006 | C | A | 1 | a0001c0001t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.200-1275C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591006 | |||||||
| chr19:14591006 | C | T | 3 | a0001c0001t0002g0107 a0001c0001t0008g0236 a0001c0001t0010g0052 |
3 | HG01256.hp1 HG01433.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.200-1275C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591006 | |||||||
| chr19:14591119 | G | T | 1 | a0001c0001t0003g0022 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.200-1162G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591119 | |||||||
| chr19:14591121 | T | G | 1 | a0001c0001t0003g0022 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.200-1160T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591121 | |||||||
| chr19:14591189 | C | G | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.200-1092C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591189 | |||||||
| chr19:14591215 | C | T | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | NA18946.hp1 NA18989.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-1066C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591215 | |||||||
| chr19:14591304 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.200-977G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591304 | |||||||
| chr19:14591324 | T | G | 18 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(15): Show |
21 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.200-957T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591324 | |||||||
| chr19:14591443 | C | T | 1 | a0002c0002t0003g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.200-838C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591443 | |||||||
| chr19:14591454 | C | CT | 7 | a0003c0003t0001g0057 a0003c0003t0002g0034 a0003c0003t0003g0004 others(4): Show |
8 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-819dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591454 | ||||||
| chr19:14591556 | C | CT | 34 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(31): Show |
36 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.200-710dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591556 | ||||||
| chr19:14591556 | C | CTT | 73 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0066 others(70): Show |
78 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(75): Show |
intron_variant | MODIFIER | c.200-711_200-710dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591556 | ||||||
| chr19:14591556 | C | CTTT | 9 | a0001c0001t0002g0051 a0001c0001t0003g0327 a0001c0001t0008g0074 others(6): Show |
9 | HG02055.hp2 HG02559.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-712_200-710dup others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591556 | ||||||
| chr19:14591751 | G | A | 28 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(25): Show |
28 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.200-530G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591751 | |||||||
| chr19:14591777 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.200-504C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591777 | |||||||
| chr19:14591807 | C | T | 80 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.200-474C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591807 | |||||||
| chr19:14591898 | A | ATG | 22 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0267 others(19): Show |
22 | HG02055.hp1 HG02071.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.200-347_200-346dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTG | 48 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(45): Show |
54 | HG01069.hp2 HG01081.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.200-349_200-346dup others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTG | 7 | a0001c0001t0001g0133 a0001c0001t0003g0003 a0001c0001t0003g0132 others(4): Show |
8 | HG02145.hp2 HG03098.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-351_200-346dup others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(1): Show |
8 | a0001c0001t0002g0076 a0001c0001t0003g0063 a0001c0001t0004g0062 others(5): Show |
8 | HG01109.hp1 HG02615.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-353_200-346dup others(8): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(3): Show |
6 | a0001c0001t0003g0131 a0001c0001t0004g0077 a0002c0002t0001g0089 others(3): Show |
6 | HG02257.hp2 HG02738.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-355_200-346dup others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(5): Show |
7 | a0001c0001t0010g0052 a0001c0001t0026g0061 a0002c0002t0003g0103 others(4): Show |
8 | HG02109.hp2 HG02615.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.200-357_200-346dup others(12): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(7): Show |
10 | a0002c0002t0003g0079 a0002c0002t0003g0105 a0002c0002t0005g0098 others(7): Show |
10 | HG01243.hp2 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-359_200-346dup others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(9): Show |
10 | a0002c0002t0002g0083 a0002c0002t0003g0059 a0002c0002t0003g0081 others(7): Show |
10 | HG01891.hp1 HG02056.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-361_200-346dup others(16): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(11): Show |
2 | a0002c0002t0003g0080 a0002c0002t0005g0096 |
2 | HG01934.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.200-363_200-346dup others(18): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | A | ATGTGTGT others(15): Show |
1 | a0002c0002t0005g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.200-367_200-346dup others(22): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | ATG | A | 9 | a0001c0001t0001g0192 a0001c0001t0001g0223 a0001c0001t0001g0277 others(6): Show |
10 | HG00621.hp1 HG00735.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-347_200-346del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | ATGTG | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0278 a0001c0001t0004g0266 |
3 | HG01515.hp2 HG02027.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.200-349_200-346del others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 |
3 | HG00140.hp1 HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.200-355_200-346del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591898 | ATGTGTGT others(11): Show |
A | 1 | a0002c0002t0004g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.200-363_200-346del others(18): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 14591898 | ||||||
| chr19:14591940 | G | T | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.200-341G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591940 | |||||||
| chr19:14591949 | A | G | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.200-332A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/13 | chr19 | 14591949 | |||||||
| chr19:14592483 | C | A | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+125C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592483 | |||||||
| chr19:14592487 | A | C | 84 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(81): Show |
89 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(86): Show |
intron_variant | MODIFIER | c.277+129A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592487 | |||||||
| chr19:14592565 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | HG00642.hp2 HG01175.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.277+207G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592565 | |||||||
| chr19:14592607 | A | G | 80 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.277+249A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592607 | |||||||
| chr19:14592674 | C | CT | 15 | a0001c0001t0002g0071 a0001c0001t0003g0063 a0001c0001t0004g0062 others(12): Show |
18 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.277+325dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14592674 | ||||||
| chr19:14592679 | TTTTTGAG others(6): Show |
T | 1 | a0001c0001t0004g0153 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.277+325_277+337del others(13): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14592679 | ||||||
| chr19:14592698 | C | T | 4 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+340C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592698 | |||||||
| chr19:14592808 | G | T | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | NA18946.hp1 NA18989.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+450G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592808 | |||||||
| chr19:14592856 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.277+498G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592856 | |||||||
| chr19:14592929 | G | T | 5 | a0001c0001t0003g0045 a0001c0001t0005g0038 a0001c0001t0005g0046 others(2): Show |
5 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+571G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14592929 | |||||||
| chr19:14593076 | A | G | 1 | a0001c0001t0004g0323 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.277+718A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593076 | |||||||
| chr19:14593215 | G | T | 1 | a0002c0002t0003g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.277+857G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593215 | |||||||
| chr19:14593290 | C | T | 4 | a0001c0001t0001g0277 a0001c0001t0004g0190 a0001c0001t0006g0228 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+932C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593290 | |||||||
| chr19:14593330 | TACCAAAA others(7): Show |
T | 2 | a0001c0001t0003g0003 a0001c0001t0004g0003 |
3 | HG02145.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.277+974_277+987del others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593330 | ||||||
| chr19:14593333 | C | CA | 30 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0268 others(27): Show |
30 | HG00597.hp1 HG01361.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.277+996dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593333 | ||||||
| chr19:14593333 | C | CAA | 51 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0071 others(48): Show |
55 | HG01243.hp2 HG01361.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.277+995_277+996dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593333 | ||||||
| chr19:14593333 | CA | C | 78 | a0001c0001t0001g0108 a0001c0001t0001g0122 a0001c0001t0001g0124 others(75): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.277+996delA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593333 | ||||||
| chr19:14593372 | C | T | 8 | a0001c0001t0002g0128 a0001c0001t0002g0189 a0001c0001t0003g0010 others(5): Show |
10 | HG00099.hp2 HG01069.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+1014C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593372 | |||||||
| chr19:14593415 | G | A | 36 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(33): Show |
37 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.277+1057G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593415 | |||||||
| chr19:14593474 | C | G | 22 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.278-1043C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593474 | |||||||
| chr19:14593709 | C | G | 80 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(77): Show |
85 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(82): Show |
intron_variant | MODIFIER | c.278-808C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593709 | |||||||
| chr19:14593767 | T | C | 2 | a0001c0001t0002g0155 a0001c0001t0020g0154 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.278-750T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593767 | |||||||
| chr19:14593893 | C | T | 1 | a0001c0001t0004g0321 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278-624C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593893 | |||||||
| chr19:14593918 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
5 | HG00597.hp1 NA18612.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-599C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593918 | |||||||
| chr19:14593959 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0195 |
2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.278-558C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593959 | |||||||
| chr19:14593964 | A | AAAACAAA others(1): Show |
33 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(30): Show |
35 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.278-529_278-522dup others(8): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 14593964 | ||||||
| chr19:14593983 | AC | A | 12 | a0001c0001t0003g0045 a0001c0001t0005g0038 a0001c0001t0005g0040 others(9): Show |
12 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.278-533delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593983 | |||||||
| chr19:14593984 | C | A | 1 | a0001c0001t0005g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278-533C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593984 | |||||||
| chr19:14593987 | AC | A | 5 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(2): Show |
6 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-529delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593987 | |||||||
| chr19:14593988 | C | A | 13 | a0001c0001t0003g0045 a0001c0001t0005g0038 a0001c0001t0005g0040 others(10): Show |
13 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-529C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593988 | |||||||
| chr19:14593991 | AC | A | 26 | a0001c0001t0002g0036 a0001c0001t0002g0066 a0001c0001t0002g0067 others(23): Show |
29 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.278-525delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593991 | |||||||
| chr19:14593992 | C | A | 18 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(15): Show |
19 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.278-525C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14593992 | |||||||
| chr19:14594007 | G | T | 1 | a0001c0001t0018g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.278-510G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594007 | |||||||
| chr19:14594208 | C | T | 9 | a0001c0001t0002g0071 a0001c0001t0010g0006 a0001c0001t0011g0007 others(6): Show |
12 | HG01361.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.278-309C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594208 | |||||||
| chr19:14594247 | A | C | 1 | a0001c0001t0028g0260 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.278-270A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594247 | |||||||
| chr19:14594365 | T | C | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-152T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594365 | |||||||
| chr19:14594504 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.278-13T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 4/13 | chr19 | 14594504 | |||||||
| chr19:14594551 | T | C | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | HG00544.hp2 HG01993.hp1 NA18983.hp1 |
splice_donor_variant&intron_variant | HIGH | c.310+2T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 5/13 | chr19 | 14594551 | |||||||
| chr19:14594687 | G | A | 36 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(33): Show |
37 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.361+5G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 6/13 | chr19 | 14594687 | |||||||
| chr19:14594697 | T | C | 84 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(81): Show |
89 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(86): Show |
intron_variant | MODIFIER | c.361+15T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 6/13 | chr19 | 14594697 | |||||||
| chr19:14594935 | G | A | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.403+135G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/13 | chr19 | 14594935 | |||||||
| chr19:14595011 | A | G | 33 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0001c0001t0001g0210 others(30): Show |
35 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.403+211A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/13 | chr19 | 14595011 | |||||||
| chr19:14595136 | T | G | 1 | a0001c0001t0011g0069 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.404-138T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 7/13 | chr19 | 14595136 | |||||||
| chr19:14595356 | A | G | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+41A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595356 | |||||||
| chr19:14595466 | C | T | 36 | a0002c0002t0001g0089 a0002c0002t0002g0083 a0002c0002t0003g0059 others(33): Show |
37 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.445+151C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595466 | |||||||
| chr19:14595468 | C | CTGCTCTA others(51): Show |
1 | a0001c0001t0002g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.445+156_445+213dup others(58): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595468 | ||||||
| chr19:14595526 | T | C | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+211T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595526 | |||||||
| chr19:14595556 | T | G | 3 | a0001c0001t0001g0136 a0001c0001t0003g0135 a0001c0001t0009g0134 |
3 | HG01109.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.445+241T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595556 | |||||||
| chr19:14595576 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.445+261T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595576 | |||||||
| chr19:14595672 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0020g0154 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.445+357G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595672 | |||||||
| chr19:14595672 | GGTAGTGA others(20): Show |
G | 1 | a0002c0002t0003g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.445+359_445+385del others(27): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595672 | ||||||
| chr19:14595684 | G | A | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+369G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595684 | |||||||
| chr19:14595811 | G | A | 1 | a0003c0003t0006g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445+496G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595811 | |||||||
| chr19:14595815 | G | T | 23 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(20): Show |
24 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.445+500G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595815 | |||||||
| chr19:14595877 | G | A | 1 | a0001c0001t0026g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445+562G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595877 | |||||||
| chr19:14595889 | A | G | 2 | a0001c0001t0004g0151 a0001c0001t0013g0150 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445+574A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14595889 | |||||||
| chr19:14595973 | A | ATGTTGTT others(2152): Show |
1 | a0003c0003t0006g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2159): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2404): Show |
1 | a0003c0003t0001g0057 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2411): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2068): Show |
1 | a0003c0003t0006g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2075): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2071): Show |
2 | a0003c0003t0002g0034 a0003c0003t0003g0033 |
2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2078): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1981): Show |
1 | a0003c0003t0003g0004 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1988): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1315): Show |
1 | a0003c0003t0006g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1322): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0002g0314 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1256): Show |
1 | a0001c0001t0002g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1263): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1456): Show |
1 | a0001c0001t0005g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1463): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1282): Show |
3 | a0001c0001t0004g0020 a0001c0001t0004g0197 a0001c0001t0004g0198 |
4 | HG00323.hp2 HG03710.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1289): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1240): Show |
1 | a0001c0001t0004g0021 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1247): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2236): Show |
1 | a0001c0001t0004g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2243): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1489): Show |
1 | a0001c0001t0003g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1496): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1318): Show |
1 | a0001c0001t0002g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1325): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1576): Show |
3 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0143 |
5 | HG01168.hp1 HG01516.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1583): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1696): Show |
1 | a0001c0001t0009g0144 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1703): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1381): Show |
1 | a0001c0001t0012g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1388): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2674): Show |
1 | a0002c0002t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2681): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1720): Show |
1 | a0001c0001t0003g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1727): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0004g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1873): Show |
1 | a0001c0001t0022g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1880): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0003g0063 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2023): Show |
1 | a0001c0001t0008g0075 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2030): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1384): Show |
2 | a0001c0001t0002g0071 a0001c0001t0012g0005 |
3 | HG02258.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1391): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1279): Show |
3 | a0001c0001t0004g0065 a0001c0001t0005g0064 a0001c0001t0008g0074 |
3 | HG01109.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1279): Show |
3 | a0001c0001t0010g0006 a0001c0001t0011g0069 a0001c0001t0021g0072 |
4 | HG01361.hp1 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1483): Show |
1 | a0001c0001t0011g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1490): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1486): Show |
2 | a0001c0001t0011g0007 a0001c0001t0012g0073 |
3 | HG03540.hp2 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1273): Show |
2 | a0001c0001t0004g0013 a0001c0001t0004g0147 |
3 | NA19064.hp2 NA19079.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1273): Show |
1 | a0001c0001t0004g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1276): Show |
1 | a0001c0001t0001g0163 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1276): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0164 a0001c0001t0007g0014 |
3 | NA18945.hp2 NA18964.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1570): Show |
1 | a0001c0001t0001g0165 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1577): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1354): Show |
1 | a0001c0001t0004g0199 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1361): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1525): Show |
1 | a0001c0001t0004g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1532): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1441): Show |
1 | a0001c0001t0001g0200 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1448): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1234): Show |
1 | a0001c0001t0004g0201 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1241): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1273): Show |
1 | a0001c0001t0004g0202 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1780): Show |
1 | a0001c0001t0004g0203 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1787): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1234): Show |
18 | a0001c0001t0001g0205 a0001c0001t0001g0210 a0001c0001t0003g0196 others(15): Show |
18 | HG00673.hp1 HG01358.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1241): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1402): Show |
1 | a0001c0001t0004g0214 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1409): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1237): Show |
1 | a0001c0001t0003g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1244): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1522): Show |
1 | a0001c0001t0004g0215 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1529): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2371): Show |
1 | a0001c0001t0001g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2378): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1192): Show |
1 | a0001c0001t0025g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1199): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1231): Show |
1 | a0001c0001t0001g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1238): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1447): Show |
1 | a0001c0001t0004g0226 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1454): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1237): Show |
1 | a0001c0001t0004g0217 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1244): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2134): Show |
1 | a0001c0001t0004g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2141): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2092): Show |
1 | a0001c0001t0003g0241 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2099): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1804): Show |
2 | a0001c0001t0003g0003 a0001c0001t0004g0003 |
3 | HG02145.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1811): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0002g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1804): Show |
1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1811): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2059): Show |
2 | a0001c0001t0004g0053 a0001c0001t0004g0054 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2066): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2065): Show |
1 | a0001c0001t0004g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2072): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2608): Show |
1 | a0001c0001t0026g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2615): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0002g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2071): Show |
1 | a0001c0001t0002g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2078): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0010g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2194): Show |
1 | a0001c0001t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2201): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2071): Show |
2 | a0001c0001t0003g0016 a0001c0001t0003g0291 |
3 | HG02129.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2078): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2572): Show |
1 | a0001c0001t0007g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2579): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1774): Show |
1 | a0007c0005t0004g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1781): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1690): Show |
1 | a0001c0001t0002g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1697): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1144): Show |
1 | a0001c0001t0003g0119 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1151): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1219): Show |
1 | a0001c0001t0001g0122 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1226): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2608): Show |
1 | a0001c0001t0013g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2615): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1282): Show |
2 | a0001c0001t0001g0192 a0001c0001t0002g0019 |
3 | HG00735.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1289): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1360): Show |
3 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0170 |
3 | HG00099.hp1 HG00642.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1367): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1408): Show |
1 | a0001c0001t0013g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1415): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
2 | a0001c0001t0003g0193 a0001c0001t0009g0194 |
2 | HG00621.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1492): Show |
1 | a0001c0001t0002g0017 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1499): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
2 | a0001c0001t0002g0018 a0001c0001t0002g0191 |
3 | HG03704.hp2 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1408): Show |
1 | a0001c0001t0001g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1415): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1324): Show |
1 | a0001c0001t0002g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1331): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1246): Show |
2 | a0001c0001t0003g0131 a0001c0001t0003g0219 |
2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1253): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1069): Show |
1 | a0001c0001t0001g0148 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1076): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1120): Show |
1 | a0001c0001t0001g0246 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1127): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1852): Show |
1 | a0001c0001t0008g0039 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1859): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2533): Show |
1 | a0005c0004t0002g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2540): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2662): Show |
1 | a0002c0002t0003g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2669): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2779): Show |
1 | a0002c0002t0003g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2786): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2656): Show |
1 | a0002c0002t0003g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2663): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2578): Show |
1 | a0002c0002t0003g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2585): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2509): Show |
3 | a0002c0002t0004g0032 a0002c0002t0004g0093 a0002c0002t0005g0087 |
3 | HG02145.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2516): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2638): Show |
1 | a0002c0002t0003g0091 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2645): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2596): Show |
1 | a0002c0002t0003g0082 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2603): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2656): Show |
1 | a0002c0002t0002g0083 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2663): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2491): Show |
1 | a0002c0002t0006g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2498): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(3124): Show |
1 | a0002c0002t0003g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(3131): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(3019): Show |
1 | a0002c0002t0003g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(3026): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2713): Show |
1 | a0002c0002t0005g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2720): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2968): Show |
5 | a0002c0002t0005g0095 a0002c0002t0005g0096 a0002c0002t0005g0098 others(2): Show |
5 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(2975): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2779): Show |
2 | a0002c0002t0005g0101 a0002c0002t0005g0102 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2786): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2659): Show |
1 | a0002c0002t0001g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2666): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(709): Show |
1 | a0001c0001t0003g0045 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(716): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2149): Show |
1 | a0001c0001t0005g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2156): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1897): Show |
5 | a0001c0001t0005g0041 a0001c0001t0005g0044 a0001c0001t0005g0049 others(2): Show |
5 | HG02559.hp2 HG02630.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1904): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2368): Show |
1 | a0001c0001t0005g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2375): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(751): Show |
4 | a0001c0001t0005g0038 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02109.hp1 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(758): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2827): Show |
1 | a0002c0002t0014g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2834): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2491): Show |
2 | a0002c0002t0014g0085 a0002c0002t0014g0086 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2498): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1849): Show |
1 | a0001c0001t0008g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1856): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2368): Show |
1 | a0001c0001t0003g0022 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(2375): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1666): Show |
1 | a0001c0001t0001g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1673): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1591): Show |
1 | a0001c0001t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1598): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1327): Show |
1 | a0001c0001t0006g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1334): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
4 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(1): Show |
4 | NA18951.hp2 NA18971.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0007g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1276): Show |
1 | a0001c0001t0008g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1591): Show |
1 | a0001c0001t0006g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1598): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1717): Show |
4 | a0001c0001t0001g0136 a0001c0001t0003g0135 a0001c0001t0003g0149 others(1): Show |
4 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1724): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1891): Show |
1 | a0001c0001t0003g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1898): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1273): Show |
1 | a0001c0001t0003g0174 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1280): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1363): Show |
1 | a0001c0001t0001g0292 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1370): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1693): Show |
1 | a0001c0001t0003g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1700): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1282): Show |
1 | a0001c0001t0001g0326 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1289): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2215): Show |
1 | a0001c0001t0002g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2222): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2176): Show |
1 | a0004c0009t0002g0176 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2183): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1618): Show |
1 | a0001c0001t0002g0294 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1625): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1525): Show |
2 | a0001c0001t0001g0295 a0001c0001t0001g0315 |
2 | NA18963.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1532): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1279): Show |
1 | a0001c0001t0003g0296 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2359): Show |
1 | a0001c0001t0004g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2366): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1450): Show |
1 | a0001c0001t0024g0297 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1457): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1468): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0298 |
3 | NA18990.hp2 NA19056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1475): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1450): Show |
1 | a0001c0001t0009g0177 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1457): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1423): Show |
1 | a0001c0001t0003g0299 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1430): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0301 a0001c0001t0001g0317 others(6): Show |
12 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0002g0302 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1492): Show |
1 | a0001c0001t0001g0303 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1499): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0001g0027 | 2 | HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1948): Show |
1 | a0001c0001t0002g0304 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1955): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2278): Show |
1 | a0001c0001t0006g0305 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2285): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1771): Show |
1 | a0001c0001t0004g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1778): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2401): Show |
1 | a0001c0001t0001g0237 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2408): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1864): Show |
1 | a0001c0001t0001g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1871): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1693): Show |
1 | a0001c0001t0003g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1700): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1696): Show |
1 | a0001c0001t0003g0248 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1703): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
11 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0250 others(8): Show |
13 | HG02027.hp2 NA18747.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1360): Show |
1 | a0001c0001t0001g0308 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1367): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1738): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0252 a0001c0001t0001g0253 |
4 | HG01257.hp2 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1745): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1822): Show |
1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1829): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1447): Show |
1 | a0001c0001t0002g0179 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1454): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2287): Show |
1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2294): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1492): Show |
1 | a0001c0001t0006g0255 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1499): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1402): Show |
1 | a0001c0001t0001g0309 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1409): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0001g0310 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1876): Show |
1 | a0001c0001t0001g0256 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1883): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1564): Show |
1 | a0001c0001t0001g0311 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1571): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1447): Show |
1 | a0001c0001t0004g0153 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1454): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1531): Show |
1 | a0001c0001t0001g0262 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1538): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1696): Show |
1 | a0001c0001t0001g0312 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1703): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2053): Show |
1 | a0009c0008t0003g0129 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2060): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2977): Show |
1 | a0001c0001t0028g0260 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(2984): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1033): Show |
6 | a0001c0001t0004g0190 a0001c0001t0006g0110 a0001c0001t0006g0114 others(3): Show |
6 | HG01884.hp2 HG01934.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1040): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1117): Show |
1 | a0001c0001t0006g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1124): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1324): Show |
2 | a0001c0001t0001g0124 a0001c0001t0002g0120 |
2 | HG02293.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1331): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1276): Show |
3 | a0001c0001t0003g0221 a0001c0001t0003g0227 a0001c0001t0005g0220 |
3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1283): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1993): Show |
1 | a0001c0001t0001g0271 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2000): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1654): Show |
8 | a0001c0001t0001g0025 a0001c0001t0001g0239 a0001c0001t0001g0267 others(5): Show |
9 | HG02135.hp2 HG02165.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+668_445+669ins others(1661): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1819): Show |
1 | a0001c0001t0001g0276 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1826): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1279): Show |
1 | a0001c0001t0002g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1286): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1663): Show |
3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0004g0266 |
3 | HG01515.hp2 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1670): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1237): Show |
1 | a0001c0001t0004g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1244): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1549): Show |
3 | a0001c0001t0002g0139 a0001c0001t0003g0132 a0001c0001t0009g0140 |
3 | HG03704.hp1 HG04228.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1556): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0002g0029 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1894): Show |
1 | a0001c0001t0001g0126 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1901): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1333): Show |
1 | a0001c0001t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1340): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1120): Show |
1 | a0001c0001t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1127): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1324): Show |
1 | a0001c0001t0001g0258 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1331): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1540): Show |
1 | a0001c0001t0002g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1547): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1534): Show |
1 | a0001c0001t0001g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1541): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
1 | a0001c0001t0007g0259 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1411): Show |
1 | a0001c0001t0003g0184 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1418): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1653): Show |
1 | a0001c0001t0027g0279 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1660): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1666): Show |
1 | a0001c0001t0001g0141 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1673): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1408): Show |
1 | a0001c0001t0004g0321 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1415): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1363): Show |
1 | a0001c0001t0001g0313 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1370): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1531): Show |
1 | a0001c0001t0007g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1538): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1263): Show |
1 | a0001c0001t0002g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1270): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
1 | a0001c0001t0001g0142 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1321): Show |
2 | a0001c0001t0001g0186 a0001c0001t0002g0185 |
2 | HG00408.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1328): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1474): Show |
1 | a0001c0001t0019g0222 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1481): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1042): Show |
1 | a0001c0001t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1049): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1939): Show |
1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1946): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1735): Show |
2 | a0001c0001t0004g0008 a0001c0001t0004g0115 |
3 | HG01123.hp2 HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1742): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1813): Show |
2 | a0001c0001t0002g0155 a0001c0001t0020g0154 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.445+668_445+669ins others(1820): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1444): Show |
1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1451): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1873): Show |
1 | a0001c0001t0015g0328 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1880): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1291): Show |
1 | a0001c0001t0009g0330 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1298): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1510): Show |
1 | a0001c0001t0003g0327 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1517): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1405): Show |
1 | a0008c0006t0007g0329 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1412): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1399): Show |
1 | a0001c0001t0003g0116 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(1406): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0003g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(1486): Show |
1 | a0001c0001t0003g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.445+668_445+669ins others(1493): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14595973 | A | ATGTTGTT others(2404): Show |
1 | a0002c0002t0003g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.445+668_445+669ins others(2411): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 14595973 | ||||||
| chr19:14596095 | G | C | 1 | a0001c0001t0006g0037 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.445+780G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596095 | |||||||
| chr19:14596218 | T | C | 74 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(71): Show |
78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.446-658T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596218 | |||||||
| chr19:14596326 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.446-550C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596326 | |||||||
| chr19:14596355 | T | C | 25 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(22): Show |
26 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.446-521T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596355 | |||||||
| chr19:14596443 | C | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(93): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.446-433C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596443 | |||||||
| chr19:14596488 | G | C | 28 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(25): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.446-388G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596488 | |||||||
| chr19:14596625 | C | A | 3 | a0002c0002t0004g0032 a0002c0002t0004g0093 a0002c0002t0005g0087 |
3 | HG02145.hp1 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.446-251C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596625 | |||||||
| chr19:14596752 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.446-124C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596752 | |||||||
| chr19:14596765 | A | G | 134 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(131): Show |
140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.446-111A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596765 | |||||||
| chr19:14596799 | G | C | 2 | a0001c0001t0003g0241 a0001c0001t0004g0240 |
2 | HG02071.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.446-77G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 8/13 | chr19 | 14596799 | |||||||
| chr19:14597091 | C | G | 2 | a0002c0002t0003g0080 a0002c0002t0003g0084 |
2 | HG01934.hp2 HG03834.hp2 |
splice_region_variant&intron_variant | LOW | c.584-8C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 9/13 | chr19 | 14597091 | |||||||
| chr19:14597203 | C | G | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+42C>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597203 | |||||||
| chr19:14597316 | G | T | 1 | a0001c0001t0002g0314 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.646+155G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597316 | |||||||
| chr19:14597332 | T | C | 157 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.646+171T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597332 | |||||||
| chr19:14597453 | C | T | 1 | a0001c0001t0023g0251 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.646+292C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597453 | |||||||
| chr19:14597708 | C | T | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+547C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597708 | |||||||
| chr19:14597744 | C | T | 5 | a0001c0001t0004g0053 a0001c0001t0004g0054 a0002c0002t0004g0032 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.646+583C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597744 | |||||||
| chr19:14597761 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.646+600G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597761 | |||||||
| chr19:14597774 | A | T | 1 | a0001c0001t0022g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646+613A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597774 | |||||||
| chr19:14597774 | AT | A | 19 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(16): Show |
20 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.646+623delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14597774 | ||||||
| chr19:14597819 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.646+658G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597819 | |||||||
| chr19:14597842 | A | G | 52 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(49): Show |
55 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.646+681A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597842 | |||||||
| chr19:14597853 | C | A | 17 | a0001c0001t0002g0071 a0001c0001t0002g0104 a0001c0001t0003g0063 others(14): Show |
20 | HG01109.hp1 HG01361.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.646+692C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597853 | |||||||
| chr19:14597960 | G | A | 31 | a0001c0001t0006g0283 a0002c0002t0001g0089 a0002c0002t0002g0083 others(28): Show |
32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.646+799G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597960 | |||||||
| chr19:14597996 | A | C | 1 | a0001c0001t0004g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.646+835A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14597996 | |||||||
| chr19:14598000 | A | G | 1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.646+839A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598000 | |||||||
| chr19:14598024 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.646+863A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598024 | |||||||
| chr19:14598036 | A | G | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.646+875A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598036 | |||||||
| chr19:14598152 | GC | G | 54 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(51): Show |
58 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.646+992delC | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598152 | |||||||
| chr19:14598173 | A | G | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+1012A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598173 | |||||||
| chr19:14598286 | C | T | 9 | a0001c0001t0002g0071 a0001c0001t0010g0006 a0001c0001t0011g0007 others(6): Show |
12 | HG01361.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.646+1125C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598286 | |||||||
| chr19:14598295 | G | GTTCT | 5 | a0001c0001t0003g0213 a0001c0001t0003g0230 a0001c0001t0004g0211 others(2): Show |
5 | HG02074.hp2 HG02080.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.646+1143_646+1146d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598295 | ||||||
| chr19:14598304 | T | TTC | 50 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(47): Show |
53 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.646+1164_646+1165d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | ||||||
| chr19:14598304 | T | TTCTC | 49 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(46): Show |
53 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.646+1162_646+1165d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | ||||||
| chr19:14598304 | T | TTCTTTCT others(5): Show |
1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.646+1146_646+1147i others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | ||||||
| chr19:14598304 | TTC | T | 54 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0051 others(51): Show |
57 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(54): Show |
intron_variant | MODIFIER | c.646+1164_646+1165d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598304 | ||||||
| chr19:14598327 | A | T | 1 | a0001c0001t0025g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1166A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598327 | |||||||
| chr19:14598330 | A | C | 1 | a0001c0001t0025g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1169A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598330 | |||||||
| chr19:14598331 | T | A | 1 | a0001c0001t0025g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1170T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598331 | |||||||
| chr19:14598332 | C | CTCTT | 22 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.646+1189_646+1192d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598332 | ||||||
| chr19:14598332 | CTCTT | C | 35 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 others(32): Show |
37 | HG01123.hp2 HG01243.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.646+1189_646+1192d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598332 | ||||||
| chr19:14598334 | C | A | 1 | a0001c0001t0025g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1173C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598334 | |||||||
| chr19:14598336 | T | C | 1 | a0001c0001t0025g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.646+1175T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598336 | |||||||
| chr19:14598396 | CTCCT | C | 54 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(51): Show |
58 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.646+1253_646+1256d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14598396 | ||||||
| chr19:14598537 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.647-1180G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598537 | |||||||
| chr19:14598586 | G | T | 1 | a0001c0001t0001g0268 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.647-1131G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598586 | |||||||
| chr19:14598682 | C | A | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647-1035C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598682 | |||||||
| chr19:14598694 | C | T | 1 | a0001c0001t0022g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.647-1023C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598694 | |||||||
| chr19:14598735 | A | G | 2 | a0001c0001t0002g0155 a0001c0001t0020g0154 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.647-982A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598735 | |||||||
| chr19:14598766 | C | T | 12 | a0001c0001t0002g0071 a0001c0001t0003g0063 a0001c0001t0004g0062 others(9): Show |
15 | HG01109.hp1 HG01361.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.647-951C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598766 | |||||||
| chr19:14598804 | T | A | 4 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.647-913T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598804 | |||||||
| chr19:14598811 | A | T | 163 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(160): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.647-906A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14598811 | |||||||
| chr19:14599003 | C | T | 30 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(27): Show |
30 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.647-714C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599003 | |||||||
| chr19:14599034 | T | C | 6 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0197 others(3): Show |
8 | HG00323.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.647-683T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599034 | |||||||
| chr19:14599077 | T | A | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647-640T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599077 | |||||||
| chr19:14599079 | C | CT | 36 | a0001c0001t0001g0267 a0001c0001t0001g0270 a0001c0001t0001g0275 others(33): Show |
40 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.647-612dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599079 | C | CTTT | 28 | a0001c0001t0001g0126 a0001c0001t0001g0141 a0001c0001t0001g0142 others(25): Show |
28 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.647-614_647-612dup others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599079 | C | CTTTT | 52 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0137 others(49): Show |
56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.647-615_647-612dup others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599079 | C | CTTTTT | 15 | a0001c0001t0001g0133 a0001c0001t0001g0210 a0001c0001t0003g0031 others(12): Show |
15 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.647-616_647-612dup others(5): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599079 | CT | C | 33 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0272 others(30): Show |
34 | HG01243.hp2 HG01515.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.647-612delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599079 | CTTT | C | 20 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(17): Show |
21 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.647-614_647-612del others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599079 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.647-624_647-612del others(13): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 14599079 | ||||||
| chr19:14599181 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.647-536G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599181 | |||||||
| chr19:14599224 | A | T | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.647-493A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599224 | |||||||
| chr19:14599246 | C | A | 1 | a0001c0001t0001g0298 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.647-471C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599246 | |||||||
| chr19:14599250 | A | G | 147 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(144): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.647-467A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599250 | |||||||
| chr19:14599307 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.647-410T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599307 | |||||||
| chr19:14599316 | G | A | 65 | a0001c0001t0001g0108 a0001c0001t0001g0122 a0001c0001t0001g0124 others(62): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.647-401G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599316 | |||||||
| chr19:14599366 | G | A | 4 | a0001c0001t0003g0327 a0001c0001t0009g0330 a0001c0001t0015g0328 others(1): Show |
4 | HG03490.hp1 HG03710.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-351G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599366 | |||||||
| chr19:14599453 | C | T | 31 | a0001c0001t0006g0283 a0002c0002t0001g0089 a0002c0002t0002g0083 others(28): Show |
32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.647-264C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599453 | |||||||
| chr19:14599595 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.647-122C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 10/13 | chr19 | 14599595 | |||||||
| chr19:14599932 | G | T | 1 | a0001c0001t0002g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.743-99G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 11/13 | chr19 | 14599932 | |||||||
| chr19:14600243 | T | C | 3 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 |
4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+61T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600243 | |||||||
| chr19:14600471 | T | C | 2 | a0001c0001t0003g0174 a0001c0001t0004g0013 |
3 | NA19000.hp2 NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.894+289T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600471 | |||||||
| chr19:14600483 | G | T | 3 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 |
4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+301G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600483 | |||||||
| chr19:14600563 | G | A | 53 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(50): Show |
55 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(52): Show |
intron_variant | MODIFIER | c.894+381G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600563 | |||||||
| chr19:14600580 | T | A | 31 | a0001c0001t0006g0283 a0002c0002t0001g0089 a0002c0002t0002g0083 others(28): Show |
32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+398T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600580 | |||||||
| chr19:14600587 | C | CT | 22 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+417dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600587 | ||||||
| chr19:14600587 | CTTTTTTT others(314): Show |
C | 1 | a0001c0001t0003g0174 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.894+431_894+751del | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600587 | ||||||
| chr19:14600669 | C | A | 1 | a0001c0001t0004g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+487C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600669 | |||||||
| chr19:14600675 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+493G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600675 | |||||||
| chr19:14600743 | G | A | 1 | a0001c0001t0004g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+561G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600743 | |||||||
| chr19:14600795 | C | T | 1 | a0001c0001t0010g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.894+613C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600795 | |||||||
| chr19:14600831 | T | C | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+649T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600831 | |||||||
| chr19:14600836 | G | T | 1 | a0002c0002t0014g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.894+654G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600836 | |||||||
| chr19:14600874 | C | T | 1 | a0001c0001t0006g0283 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.894+692C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600874 | |||||||
| chr19:14600880 | C | T | 3 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 |
4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+698C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600880 | |||||||
| chr19:14600884 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.894+702C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600884 | |||||||
| chr19:14600888 | CTTCTTTT others(3): Show |
C | 1 | a0001c0001t0004g0208 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.894+709_894+718del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600888 | ||||||
| chr19:14600891 | C | CT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0192 others(20): Show |
23 | HG00544.hp1 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+738dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600891 | CT | C | 58 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0163 others(55): Show |
62 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.894+738delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600891 | CTT | C | 18 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0002g0071 others(15): Show |
20 | HG01109.hp1 HG01123.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.894+737_894+738del others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600891 | CTTT | C | 31 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(28): Show |
32 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+736_894+738del others(3): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600891 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894+729_894+738del others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600891 | CTTTTTTT others(4): Show |
C | 30 | a0001c0001t0006g0283 a0002c0002t0001g0089 a0002c0002t0002g0083 others(27): Show |
31 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.894+728_894+738del others(11): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600891 | CTTTTTTT others(5): Show |
C | 22 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(19): Show |
23 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.894+727_894+738del others(12): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14600891 | ||||||
| chr19:14600942 | A | T | 34 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(31): Show |
34 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.894+760A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14600942 | |||||||
| chr19:14601040 | T | A | 29 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.894+858T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601040 | |||||||
| chr19:14601083 | A | G | 144 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(141): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.894+901A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601083 | |||||||
| chr19:14601379 | A | C | 31 | a0001c0001t0006g0283 a0002c0002t0001g0089 a0002c0002t0002g0083 others(28): Show |
32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+1197A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601379 | |||||||
| chr19:14601426 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.894+1244A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601426 | |||||||
| chr19:14601561 | C | T | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894+1379C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601561 | |||||||
| chr19:14601627 | C | T | 31 | a0001c0001t0006g0283 a0002c0002t0001g0089 a0002c0002t0002g0083 others(28): Show |
32 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.894+1445C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601627 | |||||||
| chr19:14601648 | T | G | 12 | a0001c0001t0002g0071 a0001c0001t0003g0063 a0001c0001t0004g0062 others(9): Show |
15 | HG01109.hp1 HG01361.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.894+1466T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601648 | |||||||
| chr19:14601893 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.894+1711C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601893 | |||||||
| chr19:14601917 | C | T | 32 | a0001c0001t0006g0283 a0001c0001t0008g0236 a0002c0002t0001g0089 others(29): Show |
33 | HG01243.hp2 HG01256.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.894+1735C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601917 | |||||||
| chr19:14601918 | G | A | 29 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.894+1736G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601918 | |||||||
| chr19:14601943 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.894+1761C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14601943 | |||||||
| chr19:14602013 | C | T | 1 | a0001c0001t0004g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+1831C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602013 | |||||||
| chr19:14602014 | G | C | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894+1832G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602014 | |||||||
| chr19:14602083 | C | T | 2 | a0001c0001t0004g0151 a0001c0001t0022g0068 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.894+1901C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602083 | |||||||
| chr19:14602129 | G | C | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG00438.hp1 NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.894+1947G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602129 | |||||||
| chr19:14602182 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.894+2000T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602182 | |||||||
| chr19:14602279 | G | A | 31 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.894+2097G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602279 | |||||||
| chr19:14602350 | C | T | 2 | a0001c0001t0003g0193 a0001c0001t0005g0218 |
2 | HG00621.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.894+2168C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602350 | |||||||
| chr19:14602390 | A | C | 1 | a0001c0001t0006g0283 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.894+2208A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602390 | |||||||
| chr19:14602397 | A | C | 163 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(160): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.894+2215A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602397 | |||||||
| chr19:14602438 | G | A | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.894+2256G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602438 | |||||||
| chr19:14602458 | A | G | 2 | a0001c0001t0002g0175 a0004c0009t0002g0176 |
2 | HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.894+2276A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602458 | |||||||
| chr19:14602539 | C | T | 1 | a0001c0001t0004g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.894+2357C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602539 | |||||||
| chr19:14602540 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+2358G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602540 | |||||||
| chr19:14602681 | G | A | 240 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0001g0122 others(237): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.894+2499G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602681 | |||||||
| chr19:14602710 | T | C | 7 | a0001c0001t0006g0283 a0003c0003t0001g0057 a0003c0003t0002g0034 others(4): Show |
8 | HG01243.hp2 HG02056.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+2528T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602710 | |||||||
| chr19:14602847 | C | T | 3 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 |
4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+2665C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602847 | |||||||
| chr19:14602902 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.894+2720A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14602902 | |||||||
| chr19:14603183 | A | C | 1 | a0001c0001t0005g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.894+3001A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603183 | |||||||
| chr19:14603194 | T | C | 3 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 |
4 | HG01123.hp2 HG01891.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+3012T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603194 | |||||||
| chr19:14603305 | G | T | 22 | a0001c0001t0001g0256 a0001c0001t0002g0048 a0001c0001t0002g0051 others(19): Show |
23 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.894+3123G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603305 | |||||||
| chr19:14603394 | A | C | 1 | a0001c0001t0004g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.894+3212A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603394 | |||||||
| chr19:14603561 | G | T | 4 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0003g0003 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+3379G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603561 | |||||||
| chr19:14603607 | G | C | 5 | a0001c0001t0001g0136 a0001c0001t0003g0135 a0001c0001t0003g0149 others(2): Show |
5 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-3386G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603607 | |||||||
| chr19:14603634 | AT | A | 13 | a0001c0001t0002g0071 a0001c0001t0003g0063 a0001c0001t0004g0062 others(10): Show |
16 | HG01109.hp1 HG01361.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.895-3348delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14603634 | ||||||
| chr19:14603638 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.895-3355T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603638 | |||||||
| chr19:14603672 | G | T | 31 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0136 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.895-3321G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603672 | |||||||
| chr19:14603764 | A | G | 145 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(142): Show |
151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.895-3229A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603764 | |||||||
| chr19:14603895 | T | C | 1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.895-3098T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603895 | |||||||
| chr19:14603976 | C | T | 1 | a0001c0001t0009g0140 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.895-3017C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603976 | |||||||
| chr19:14603977 | A | G | 7 | a0002c0002t0005g0095 a0002c0002t0005g0096 a0002c0002t0005g0097 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-3016A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603977 | |||||||
| chr19:14603999 | C | A | 92 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(89): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.895-2994C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14603999 | |||||||
| chr19:14604158 | C | T | 1 | a0001c0001t0008g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.895-2835C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604158 | |||||||
| chr19:14604259 | C | T | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.895-2734C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604259 | |||||||
| chr19:14604295 | A | T | 3 | a0001c0001t0002g0076 a0001c0001t0004g0077 a0001c0001t0026g0061 |
3 | HG02976.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.895-2698A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604295 | |||||||
| chr19:14604334 | A | C | 92 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0133 others(89): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.895-2659A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604334 | |||||||
| chr19:14604475 | T | C | 1 | a0001c0001t0002g0127 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.895-2518T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604475 | |||||||
| chr19:14604677 | C | T | 4 | a0001c0001t0002g0036 a0001c0001t0004g0008 a0001c0001t0004g0115 others(1): Show |
5 | HG01123.hp2 HG01891.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.895-2316C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604677 | |||||||
| chr19:14604772 | A | T | 3 | a0001c0001t0001g0148 a0001c0001t0002g0018 a0001c0001t0003g0327 |
4 | HG03704.hp2 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-2221A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604772 | |||||||
| chr19:14604787 | T | A | 1 | a0001c0001t0006g0305 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.895-2206T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14604787 | |||||||
| chr19:14605055 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0051 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.895-1938G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605055 | |||||||
| chr19:14605102 | A | AT | 25 | a0001c0001t0005g0218 a0002c0002t0001g0089 a0002c0002t0002g0083 others(22): Show |
25 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.895-1880dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14605102 | ||||||
| chr19:14605222 | C | T | 1 | a0002c0002t0003g0079 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.895-1771C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605222 | |||||||
| chr19:14605246 | A | C | 108 | a0001c0001t0001g0014 a0001c0001t0001g0137 a0001c0001t0001g0141 others(105): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.895-1747A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605246 | |||||||
| chr19:14605270 | A | T | 1 | a0001c0001t0009g0140 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.895-1723A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605270 | |||||||
| chr19:14605297 | C | T | 1 | a0007c0005t0004g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.895-1696C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605297 | |||||||
| chr19:14605343 | G | T | 3 | a0001c0001t0002g0130 a0001c0001t0002g0189 a0001c0001t0003g0293 |
3 | HG00099.hp2 HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.895-1650G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605343 | |||||||
| chr19:14605386 | G | A | 1 | a0001c0001t0015g0328 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.895-1607G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605386 | |||||||
| chr19:14605387 | C | T | 1 | a0001c0001t0004g0321 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.895-1606C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605387 | |||||||
| chr19:14605396 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.895-1597A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605396 | |||||||
| chr19:14605430 | G | A | 63 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(60): Show |
68 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.895-1563G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605430 | |||||||
| chr19:14605601 | C | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(72): Show |
83 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.895-1392C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605601 | |||||||
| chr19:14605678 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.895-1315T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605678 | |||||||
| chr19:14605689 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.895-1304C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605689 | |||||||
| chr19:14605896 | G | A | 3 | a0001c0001t0008g0039 a0001c0001t0008g0074 a0001c0001t0008g0075 |
3 | HG02055.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.895-1097G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605896 | |||||||
| chr19:14605903 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.895-1090T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14605903 | |||||||
| chr19:14606097 | T | C | 233 | a0001c0001t0001g0014 a0001c0001t0001g0141 a0001c0001t0001g0145 others(230): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.895-896T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606097 | |||||||
| chr19:14606169 | C | CA | 22 | a0001c0001t0003g0045 a0001c0001t0005g0038 a0001c0001t0005g0040 others(19): Show |
22 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.895-816dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606169 | ||||||
| chr19:14606232 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.895-761C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606232 | |||||||
| chr19:14606374 | C | CA | 38 | a0001c0001t0001g0239 a0001c0001t0001g0306 a0001c0001t0001g0326 others(35): Show |
39 | HG00408.hp1 HG01109.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.895-600dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606374 | ||||||
| chr19:14606374 | C | CAA | 40 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(37): Show |
44 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.895-601_895-600dup others(2): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606374 | ||||||
| chr19:14606374 | CA | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(27): Show |
35 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.895-600delA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606374 | ||||||
| chr19:14606403 | A | G | 70 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(67): Show |
74 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.895-590A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606403 | |||||||
| chr19:14606487 | T | C | 53 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(50): Show |
57 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.895-506T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606487 | |||||||
| chr19:14606540 | C | T | 3 | a0001c0001t0004g0162 a0001c0001t0009g0177 a0001c0001t0009g0330 |
3 | HG00558.hp1 HG02080.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.895-453C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606540 | |||||||
| chr19:14606541 | G | A | 43 | a0001c0001t0001g0312 a0001c0001t0002g0066 a0001c0001t0002g0067 others(40): Show |
50 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.895-452G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606541 | |||||||
| chr19:14606595 | G | A | 43 | a0001c0001t0001g0312 a0001c0001t0002g0066 a0001c0001t0002g0067 others(40): Show |
50 | HG00597.hp2 HG01069.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.895-398G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606595 | |||||||
| chr19:14606679 | C | CA | 18 | a0001c0001t0001g0122 a0001c0001t0001g0256 a0001c0001t0001g0290 others(15): Show |
18 | HG00408.hp1 HG00642.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.895-296dupA | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 14606679 | ||||||
| chr19:14606712 | C | T | 53 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(50): Show |
57 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.895-281C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606712 | |||||||
| chr19:14606778 | G | A | 328 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(325): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.895-215G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606778 | |||||||
| chr19:14606953 | T | C | 1 | a0001c0001t0010g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.895-40T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606953 | |||||||
| chr19:14606979 | A | G | 128 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(125): Show |
140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.895-14A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 12/13 | chr19 | 14606979 | |||||||
| chr19:14607209 | C | CT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0256 a0001c0001t0004g0151 others(4): Show |
9 | HG01175.hp2 HG01943.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1004+120dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607209 | ||||||
| chr19:14607209 | C | CTT | 26 | a0001c0001t0003g0045 a0001c0001t0004g0077 a0001c0001t0005g0038 others(23): Show |
26 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1004+119_1004+120d others(4): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607209 | ||||||
| chr19:14607359 | A | G | 1 | a0001c0001t0008g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1004+257A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607359 | |||||||
| chr19:14607360 | T | C | 3 | a0001c0001t0003g0241 a0001c0001t0008g0043 a0005c0004t0002g0094 |
3 | HG02109.hp2 HG03540.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1004+258T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607360 | |||||||
| chr19:14607367 | C | A | 1 | a0001c0001t0008g0039 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1004+265C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607367 | |||||||
| chr19:14607370 | A | AT | 72 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0001g0145 others(69): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1004+274dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607370 | ||||||
| chr19:14607394 | G | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1004+292G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607394 | |||||||
| chr19:14607403 | C | T | 1 | a0008c0006t0007g0329 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1004+301C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607403 | |||||||
| chr19:14607416 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1004+314G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607416 | |||||||
| chr19:14607418 | T | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0272 |
2 | NA18964.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1004+316T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607418 | |||||||
| chr19:14607419 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0002g0182 |
2 | HG00438.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1004+317G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607419 | |||||||
| chr19:14607424 | T | C | 164 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0122 others(161): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1004+322T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607424 | |||||||
| chr19:14607425 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(14): Show |
19 | HG00558.hp1 HG00673.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1004+323G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607425 | |||||||
| chr19:14607436 | C | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(25): Show |
31 | HG00558.hp1 HG00673.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1004+334C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607436 | |||||||
| chr19:14607439 | G | A | 4 | a0001c0001t0010g0006 a0001c0001t0012g0005 a0001c0001t0012g0070 others(1): Show |
6 | HG02258.hp2 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004+337G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607439 | |||||||
| chr19:14607445 | T | C | 27 | a0001c0001t0001g0014 a0001c0001t0001g0163 a0001c0001t0001g0164 others(24): Show |
30 | HG00323.hp2 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1004+343T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607445 | |||||||
| chr19:14607446 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1004+344G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607446 | |||||||
| chr19:14607450 | G | A | 1 | a0001c0001t0003g0010 | 2 | HG01516.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1004+348G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607450 | |||||||
| chr19:14607454 | T | C | 10 | a0001c0001t0003g0010 a0001c0001t0003g0045 a0001c0001t0004g0053 others(7): Show |
11 | HG01516.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1004+352T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607454 | |||||||
| chr19:14607482 | C | T | 3 | a0001c0001t0008g0039 a0001c0001t0008g0074 a0001c0001t0008g0075 |
3 | HG02055.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1004+380C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607482 | |||||||
| chr19:14607483 | G | A | 4 | a0001c0001t0006g0037 a0001c0001t0022g0068 a0002c0002t0003g0091 others(1): Show |
4 | HG02280.hp1 HG02897.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+381G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607483 | |||||||
| chr19:14607487 | G | A | 1 | a0001c0001t0004g0242 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1004+385G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607487 | |||||||
| chr19:14607493 | G | A | 3 | a0001c0001t0006g0037 a0001c0001t0022g0068 a0002c0002t0006g0092 |
3 | HG02280.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1004+391G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607493 | |||||||
| chr19:14607499 | G | A | 1 | a0001c0001t0004g0249 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1004+397G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607499 | |||||||
| chr19:14607541 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0004g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1004+447_1004+458d others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607541 | ||||||
| chr19:14607546 | TTTTA | T | 5 | a0001c0001t0004g0077 a0001c0001t0005g0040 a0001c0001t0005g0041 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1004+447_1004+450d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607546 | ||||||
| chr19:14607549 | T | A | 21 | a0001c0001t0002g0036 a0001c0001t0002g0076 a0001c0001t0003g0045 others(18): Show |
22 | HG01123.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004+447T>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607549 | |||||||
| chr19:14607550 | A | ATTAT | 33 | a0001c0001t0001g0270 a0001c0001t0002g0019 a0001c0001t0002g0066 others(30): Show |
37 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1004+486_1004+489d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | ||||||
| chr19:14607550 | A | ATTATTTA others(1): Show |
4 | a0001c0001t0001g0163 a0001c0001t0002g0012 a0001c0001t0004g0062 others(1): Show |
4 | HG01346.hp1 HG02886.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+482_1004+489d others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | ||||||
| chr19:14607550 | A | T | 21 | a0001c0001t0002g0036 a0001c0001t0002g0076 a0001c0001t0003g0045 others(18): Show |
22 | HG01123.hp2 HG01891.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1004+448A>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607550 | |||||||
| chr19:14607550 | ATTAT | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(90): Show |
103 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1004+486_1004+489d others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | ||||||
| chr19:14607550 | ATTATTTA others(1): Show |
A | 6 | a0001c0001t0001g0223 a0001c0001t0006g0037 a0001c0001t0011g0007 others(3): Show |
7 | HG01099.hp2 HG02723.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1004+482_1004+489d others(10): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | ||||||
| chr19:14607550 | ATTATTTA others(13): Show |
A | 1 | a0001c0001t0015g0328 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1004+470_1004+489d others(22): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14607550 | ||||||
| chr19:14607676 | G | A | 1 | a0001c0001t0015g0328 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1004+574G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607676 | |||||||
| chr19:14607791 | G | T | 1 | a0001c0001t0024g0297 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1004+689G>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607791 | |||||||
| chr19:14607901 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(181): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1004+799C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607901 | |||||||
| chr19:14607964 | A | C | 1 | a0001c0001t0021g0072 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1004+862A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14607964 | |||||||
| chr19:14608014 | T | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(268): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1004+912T>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608014 | |||||||
| chr19:14608056 | G | C | 3 | a0001c0001t0011g0007 a0001c0001t0011g0069 a0001c0001t0011g0078 |
4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+954G>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608056 | |||||||
| chr19:14608066 | TTTA | T | 3 | a0002c0002t0014g0085 a0002c0002t0014g0086 a0002c0002t0014g0090 |
3 | HG02622.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1004+965_1004+967d others(5): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608066 | |||||||
| chr19:14608160 | C | T | 3 | a0001c0001t0011g0007 a0001c0001t0011g0069 a0001c0001t0011g0078 |
4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+1058C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608160 | |||||||
| chr19:14608205 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1004+1103C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608205 | |||||||
| chr19:14608250 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1004+1148T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608250 | |||||||
| chr19:14608270 | C | T | 3 | a0001c0001t0011g0007 a0001c0001t0011g0069 a0001c0001t0011g0078 |
4 | HG02723.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004+1168C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608270 | |||||||
| chr19:14608380 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0076 |
2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1004+1278C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608380 | |||||||
| chr19:14608442 | C | A | 81 | a0001c0001t0002g0036 a0001c0001t0002g0076 a0001c0001t0003g0003 others(78): Show |
87 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1004+1340C>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608442 | |||||||
| chr19:14608628 | A | AT | 74 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0235 others(71): Show |
82 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1005-1413dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | ||||||
| chr19:14608628 | A | ATT | 6 | a0001c0001t0003g0135 a0001c0001t0004g0077 a0001c0001t0004g0242 others(3): Show |
7 | HG01168.hp2 HG02080.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1005-1414_1005-141 others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | ||||||
| chr19:14608628 | AT | A | 18 | a0001c0001t0001g0164 a0001c0001t0001g0195 a0001c0001t0001g0239 others(15): Show |
19 | HG00639.hp1 HG01256.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.1005-1413delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | ||||||
| chr19:14608628 | ATTTTT | A | 18 | a0001c0001t0006g0110 a0001c0001t0006g0114 a0001c0001t0006g0138 others(15): Show |
18 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1005-1417_1005-141 others(9): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608628 | ||||||
| chr19:14608658 | G | A | 1 | a0001c0001t0003g0022 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1005-1406G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608658 | |||||||
| chr19:14608703 | G | GACCCAAT others(5): Show |
1 | a0001c0001t0001g0309 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1005-1360_1005-134 others(16): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608703 | ||||||
| chr19:14608747 | CCT | C | 4 | a0001c0001t0008g0043 a0002c0002t0014g0085 a0002c0002t0014g0086 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-1315_1005-131 others(6): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608747 | ||||||
| chr19:14608800 | A | AT | 91 | a0001c0001t0001g0108 a0001c0001t0001g0273 a0001c0001t0002g0012 others(88): Show |
99 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1005-1247dupT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608800 | ||||||
| chr19:14608800 | AT | A | 8 | a0001c0001t0001g0164 a0001c0001t0001g0269 a0001c0001t0001g0277 others(5): Show |
8 | HG01167.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005-1247delT | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 14608800 | ||||||
| chr19:14608937 | T | C | 4 | a0001c0001t0008g0043 a0002c0002t0014g0085 a0002c0002t0014g0086 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-1127T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608937 | |||||||
| chr19:14608945 | G | A | 46 | a0001c0001t0003g0174 a0001c0001t0003g0207 a0001c0001t0003g0293 others(43): Show |
50 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1005-1119G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14608945 | |||||||
| chr19:14609019 | C | T | 2 | a0001c0001t0006g0037 a0002c0002t0006g0092 |
2 | HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1005-1045C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609019 | |||||||
| chr19:14609042 | T | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(270): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.1005-1022T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609042 | |||||||
| chr19:14609046 | C | T | 2 | a0001c0001t0006g0305 a0003c0003t0006g0035 |
2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1005-1018C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609046 | |||||||
| chr19:14609047 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1005-1017G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609047 | |||||||
| chr19:14609087 | A | C | 1 | a0001c0001t0007g0225 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1005-977A>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609087 | |||||||
| chr19:14609104 | A | G | 4 | a0001c0001t0008g0043 a0002c0002t0014g0085 a0002c0002t0014g0086 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005-960A>G | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609104 | |||||||
| chr19:14609138 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1005-926C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609138 | |||||||
| chr19:14609214 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(96): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1005-850C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609214 | |||||||
| chr19:14609235 | C | T | 9 | a0001c0001t0006g0138 a0001c0001t0006g0167 a0001c0001t0006g0255 others(6): Show |
9 | HG00639.hp2 HG01243.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005-829C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609235 | |||||||
| chr19:14609440 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1005-624T>C | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609440 | |||||||
| chr19:14609522 | ACAGAAAC others(5): Show |
A | 1 | a0001c0001t0001g0309 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1005-541_1005-530d others(14): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609522 | |||||||
| chr19:14609565 | C | T | 1 | a0001c0001t0008g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1005-499C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609565 | |||||||
| chr19:14609612 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1005-452C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609612 | |||||||
| chr19:14609666 | C | T | 6 | a0001c0001t0010g0006 a0001c0001t0010g0015 a0001c0001t0010g0052 others(3): Show |
9 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1005-398C>T | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609666 | |||||||
| chr19:14609933 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1005-131G>A | CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 13/13 | chr19 | 14609933 |