Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 126129 |
| ensemblid | ENSG00000169169.15 |
| hgncid | 18540 |
| symbol | CPT1C |
| name | carnitine palmitoyltransferase 1C |
| refseq_nuc | NM_001199753.2 |
| refseq_prot | NP_001186682.1 |
| ensembl_nuc | ENST00000598293.6 |
| ensembl_prot | ENSP00000473028.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 49691116 |
| end | 49713731 |
| strand | + |
| ver | v1.2 |
| region | chr19:49691116-49713731 |
| region5000 | chr19:49686116-49718731 |
| regionname0 | CPT1C_chr19_49691116_49713731 |
| regionname5000 | CPT1C_chr19_49686116_49718731 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 803 | 331 | 82 | 64 | 124 | 14 | 45 | 80 | CPT1C_chr19_49686116_49718731 | CPT1C | MAEAH others(798): Show |
chr19 | 49686116 | 49718731 |
| a0002 | 0/0 | 328 | 16 | 2 | 7 | 6 | 0 | 1 | 4 | CPT1C_chr19_49686116_49718731 | CPT1C | MAEAH others(323): Show |
chr19 | 49686116 | 49718731 |
| a0003 | 0/0 | 803 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | MAEAH others(798): Show |
chr19 | 49686116 | 49718731 |
| a0004 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | MAEAH others(323): Show |
chr19 | 49686116 | 49718731 |
| a0005 | 0/0 | 803 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | MAEAH others(798): Show |
chr19 | 49686116 | 49718731 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2409 | 308 | 80 | 50 | 122 | 12 | 42 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0001c0002 | 0/0 | 2409 | 13 | 1 | 10 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0001c0004 | 0/0 | 2409 | 4 | 1 | 0 | 0 | 2 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0001c0006 | 0/0 | 2409 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0001c0008 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0001c0009 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0001c0012 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0002c0003 | 0/0 | 2410 | 13 | 2 | 4 | 6 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2405): Show |
chr19 | 49686116 | 49718731 | ||
| a0002c0005 | 0/0 | 2410 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2405): Show |
chr19 | 49686116 | 49718731 | ||
| a0003c0010 | 0/0 | 2409 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 | ||
| a0004c0007 | 0/0 | 2410 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2405): Show |
chr19 | 49686116 | 49718731 | ||
| a0005c0011 | 0/0 | 2409 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | ATGGC others(2404): Show |
chr19 | 49686116 | 49718731 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2846 | 195 | 40 | 31 | 89 | 10 | 24 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0001t0002 | 0/1 | 2846 | 67 | 17 | 18 | 22 | 2 | 7 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0001t0003 | 0/0 | 2846 | 38 | 19 | 1 | 10 | 0 | 8 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0001t0004 | 0/0 | 2846 | 3 | 0 | 0 | 0 | 0 | 3 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0001t0005 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0001t0006 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0001t0007 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0002t0002 | 0/0 | 2846 | 13 | 1 | 10 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0004t0002 | 0/0 | 2846 | 4 | 1 | 0 | 0 | 2 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0006t0001 | 0/0 | 2846 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0008t0001 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0009t0001 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0001c0012t0001 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0002c0003t0001 | 0/0 | 2847 | 6 | 0 | 4 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2842): Show |
chr19 | 49686116 | 49718731 |
| a0002c0003t0002 | 0/0 | 2847 | 4 | 1 | 0 | 3 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2842): Show |
chr19 | 49686116 | 49718731 |
| a0002c0003t0003 | 0/0 | 2847 | 2 | 1 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2842): Show |
chr19 | 49686116 | 49718731 |
| a0002c0003t0004 | 0/0 | 2847 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2842): Show |
chr19 | 49686116 | 49718731 |
| a0002c0005t0002 | 0/0 | 2847 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2842): Show |
chr19 | 49686116 | 49718731 |
| a0003c0010t0001 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| a0004c0007t0002 | 0/0 | 2847 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2842): Show |
chr19 | 49686116 | 49718731 |
| a0005c0011t0001 | 0/0 | 2846 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | GAATA others(2841): Show |
chr19 | 49686116 | 49718731 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0006t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0006t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0006t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0008t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0009t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0001c0012t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0003t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0005t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0005t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0002c0005t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0003c0010t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0004c0007t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| a0005c0011t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | FIN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0106 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0275 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00735 | hp2 | a0002 | c0005 | t0002 | g0195 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0221 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01081 | hp2 | a0003 | c0010 | t0001 | g0285 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0264 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01106 | hp1 | a0002 | c0005 | t0002 | g0014 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01175 | hp1 | a0001 | c0006 | t0001 | g0005 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0139 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01346 | hp1 | a0001 | c0008 | t0001 | g0016 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01496 | hp1 | a0002 | c0005 | t0002 | g0200 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01516 | hp2 | a0001 | c0004 | t0002 | g0202 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | IBS | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0142 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01975 | hp1 | a0001 | c0006 | t0001 | g0151 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02071 | hp2 | a0001 | c0012 | t0001 | g0240 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CDX | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02293 | hp2 | a0001 | c0006 | t0001 | g0148 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02622 | hp2 | a0002 | c0003 | t0003 | g0071 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0223 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02738 | hp2 | a0001 | c0004 | t0002 | g0189 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02976 | hp2 | a0001 | c0004 | t0002 | g0193 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03209 | hp2 | a0005 | c0011 | t0001 | g0124 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03927 | hp2 | a0002 | c0003 | t0004 | g0307 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0305 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | STU | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0232 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19005 | hp1 | a0001 | c0001 | t0007 | g0099 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19062 | hp1 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19062 | hp2 | a0002 | c0003 | t0002 | g0093 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19066 | hp1 | a0001 | c0009 | t0001 | g0002 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19082 | hp1 | a0002 | c0003 | t0003 | g0053 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | YRI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ASW | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ASW | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0203 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02109 | hp1 | a0002 | c0003 | t0002 | g0209 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02109 | hp2 | a0004 | c0007 | t0002 | g0207 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0029 | REF | REF | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0276 | REF | REF | CPT1C_chr19_49686116_49718731 | CPT1C | chr19 | 49686116 | 49718731 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49704737 | T | C | 1 | a0004 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.721T>C | p.Tyr241His | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/20 | 1029/2846 | 721/2412 | 241/803 | chr19 | 49704737 | |||
| chr19:49705086 | A | AC | 2 | a0002 a0004 |
17 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(14): Show |
frameshift_variant | HIGH | c.853dupC | p.Arg285fs | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 9/20 | 1162/2846 | 854/2412 | 285/803 | INFO_REALIGN_3_PRIME | chr19 | 49705086 | ||
| chr19:49708796 | C | T | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1523C>T | p.Thr508Ile | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/20 | 1831/2846 | 1523/2412 | 508/803 | chr19 | 49708796 | |||
| chr19:49712808 | A | G | 1 | a0003 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.2092A>G | p.Asn698Asp | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 18/20 | 2400/2846 | 2092/2412 | 698/803 | chr19 | 49712808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49701586 | G | A | 4 | a0001c0002 a0001c0004 a0002c0005 others(1): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
synonymous_variant | LOW | c.645G>A | p.Ser215Ser | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/20 | 953/2846 | 645/2412 | 215/803 | chr19 | 49701586 | |||
| chr19:49705030 | G | A | 1 | a0001c0008 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.795G>A | p.Thr265Thr | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 9/20 | 1103/2846 | 795/2412 | 265/803 | chr19 | 49705030 | |||
| chr19:49705961 | C | T | 1 | a0001c0012 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.1017C>T | p.Gly339Gly | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 11/20 | 1325/2846 | 1017/2412 | 339/803 | chr19 | 49705961 | |||
| chr19:49706285 | G | A | 1 | a0001c0009 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.1215G>A | p.Leu405Leu | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/20 | 1523/2846 | 1215/2412 | 405/803 | chr19 | 49706285 | |||
| chr19:49706396 | C | T | 4 | a0001c0002 a0001c0004 a0002c0005 others(1): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
synonymous_variant | LOW | c.1326C>T | p.Ala442Ala | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/20 | 1634/2846 | 1326/2412 | 442/803 | chr19 | 49706396 | |||
| chr19:49708767 | C | T | 1 | a0001c0004 | 4 | HG01516.hp2 HG02738.hp2 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.1494C>T | p.Asp498Asp | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/20 | 1802/2846 | 1494/2412 | 498/803 | chr19 | 49708767 | |||
| chr19:49708797 | A | G | 1 | a0001c0006 | 3 | HG01175.hp1 HG01975.hp1 HG02293.hp2 |
synonymous_variant | LOW | c.1524A>G | p.Thr508Thr | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/20 | 1832/2846 | 1524/2412 | 508/803 | chr19 | 49708797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49691142 | G | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(8): Show |
136 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(133): Show |
5_prime_UTR_variant | MODIFIER | c.-282G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 1111 | chr19 | 49691142 | ||||||
| chr19:49691268 | T | A | 1 | a0001c0001t0007 | 1 | NA19005.hp1 | 5_prime_UTR_variant | MODIFIER | c.-156T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 985 | chr19 | 49691268 | ||||||
| chr19:49691269 | C | T | 1 | a0001c0001t0007 | 1 | NA19005.hp1 | 5_prime_UTR_variant | MODIFIER | c.-155C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 984 | chr19 | 49691269 | ||||||
| chr19:49691286 | G | C | 3 | a0001c0001t0003 a0001c0001t0005 a0002c0003t0003 |
42 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/20 | 967 | chr19 | 49691286 | ||||||
| chr19:49713634 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(1): Show |
8 | HG02451.hp1 HG02630.hp2 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*29A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 20/20 | 29 | chr19 | 49713634 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:49691376 | GGGCCT | G | 16 | a0001c0001t0001g0039 a0001c0001t0002g0023 a0001c0001t0002g0024 others(13): Show |
16 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.-84+39_-84+43delCC others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 49691376 | ||||||
| chr19:49691461 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-84+121A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | chr19 | 49691461 | |||||||
| chr19:49691521 | G | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG01070.hp1 HG01433.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84+181G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | chr19 | 49691521 | |||||||
| chr19:49691588 | C | A | 96 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(93): Show |
103 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.-83-233C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 1/19 | chr19 | 49691588 | |||||||
| chr19:49691973 | GGAGGAGG others(66): Show |
G | 7 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
9 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+166_-14-112del others(73): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr19 | 49691973 | ||||||
| chr19:49691982 | G | A | 32 | a0001c0001t0002g0010 a0001c0001t0002g0086 a0001c0001t0002g0087 others(29): Show |
33 | HG00423.hp2 HG00621.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15+93G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49691982 | |||||||
| chr19:49692022 | G | A | 8 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0121 others(5): Show |
8 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+133G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692022 | |||||||
| chr19:49692055 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
9 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+166G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692055 | |||||||
| chr19:49692098 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-14-141G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692098 | |||||||
| chr19:49692130 | T | TGGGGCCT others(33): Show |
3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG00609.hp1 NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-14-92_-14-53dupGG others(38): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr19 | 49692130 | ||||||
| chr19:49692198 | G | A | 38 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(35): Show |
42 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14-41G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692198 | |||||||
| chr19:49692227 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-12T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 2/19 | chr19 | 49692227 | |||||||
| chr19:49692484 | C | T | 19 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(16): Show |
19 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.141+91C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692484 | |||||||
| chr19:49692513 | T | C | 197 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0041 others(194): Show |
208 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.141+120T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692513 | |||||||
| chr19:49692514 | T | G | 197 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0041 others(194): Show |
208 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.141+121T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692514 | |||||||
| chr19:49692612 | C | T | 2 | a0001c0001t0002g0208 a0002c0003t0002g0209 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.141+219C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692612 | |||||||
| chr19:49692657 | C | T | 2 | a0001c0002t0002g0206 a0004c0007t0002g0207 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.141+264C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692657 | |||||||
| chr19:49692743 | C | CTGAGACA others(3): Show |
1 | a0001c0001t0001g0314 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141+352_141+361dup others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49692743 | ||||||
| chr19:49692908 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+515A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49692908 | |||||||
| chr19:49693169 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.141+776C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693169 | |||||||
| chr19:49693173 | C | G | 1 | a0001c0001t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.141+780C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693173 | |||||||
| chr19:49693194 | C | T | 37 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(34): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+801C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693194 | |||||||
| chr19:49693555 | A | G | 13 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(10): Show |
13 | HG01109.hp1 HG01261.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+1162A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693555 | |||||||
| chr19:49693599 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.141+1206T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693599 | |||||||
| chr19:49693661 | C | T | 16 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(13): Show |
16 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+1268C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693661 | |||||||
| chr19:49693733 | G | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0168 others(7): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+1340G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693733 | |||||||
| chr19:49693735 | A | G | 150 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(147): Show |
160 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.141+1342A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693735 | |||||||
| chr19:49693777 | G | T | 1 | a0001c0001t0003g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.141+1384G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693777 | |||||||
| chr19:49693966 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.141+1573G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49693966 | |||||||
| chr19:49694079 | T | A | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0210 others(3): Show |
6 | HG02015.hp1 HG02071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+1686T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694079 | |||||||
| chr19:49694080 | AAAATAAA others(4): Show |
A | 14 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(11): Show |
14 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.141+1695_141+1705d others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694080 | ||||||
| chr19:49694080 | AAAATAAA others(8): Show |
A | 1 | a0001c0001t0002g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.141+1695_141+1709d others(17): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694080 | ||||||
| chr19:49694084 | TAAA | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+1695_141+1697d others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694084 | ||||||
| chr19:49694087 | A | AAAAT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0230 others(3): Show |
6 | HG02071.hp2 HG02165.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+1729_141+1732d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | ||||||
| chr19:49694087 | A | AT | 3 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0002t0002g0204 |
3 | HG01358.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141+1694_141+1695i others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694087 | |||||||
| chr19:49694087 | AAAAT | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG02080.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+1729_141+1732d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | ||||||
| chr19:49694087 | AAAATAAA others(1): Show |
A | 35 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0214 others(32): Show |
39 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.141+1725_141+1732d others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | ||||||
| chr19:49694087 | AAAATAAA others(9): Show |
A | 78 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(75): Show |
83 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.141+1717_141+1732d others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694087 | ||||||
| chr19:49694089 | A | T | 1 | a0001c0001t0001g0314 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141+1696A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694089 | |||||||
| chr19:49694091 | T | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0287 a0001c0001t0001g0288 others(2): Show |
5 | HG01496.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1698T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694091 | |||||||
| chr19:49694107 | T | A | 1 | a0001c0001t0003g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141+1714T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694107 | |||||||
| chr19:49694149 | A | G | 145 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(142): Show |
155 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.141+1756A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694149 | |||||||
| chr19:49694162 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.141+1769G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694162 | |||||||
| chr19:49694338 | A | AG | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0003g0055 others(2): Show |
5 | HG02080.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+1950dupG | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694338 | ||||||
| chr19:49694351 | C | G | 1 | a0001c0001t0001g0314 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.141+1958C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694351 | |||||||
| chr19:49694360 | G | C | 2 | a0001c0001t0003g0056 a0001c0001t0003g0085 |
2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.141+1967G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694360 | |||||||
| chr19:49694415 | A | T | 2 | a0001c0002t0002g0206 a0004c0007t0002g0207 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.141+2022A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694415 | |||||||
| chr19:49694575 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(33): Show |
37 | HG00558.hp2 HG00609.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.141+2182G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694575 | |||||||
| chr19:49694628 | C | CA | 8 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0001t0001g0219 others(5): Show |
8 | HG00438.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.141+2253dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694628 | ||||||
| chr19:49694628 | CA | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0129 a0001c0001t0001g0310 others(12): Show |
17 | HG00735.hp1 HG01071.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+2253delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49694628 | ||||||
| chr19:49694646 | A | G | 12 | a0001c0001t0002g0023 a0001c0001t0002g0027 a0001c0001t0002g0028 others(9): Show |
12 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+2253A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694646 | |||||||
| chr19:49694788 | C | T | 37 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0003g0004 others(34): Show |
41 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+2395C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694788 | |||||||
| chr19:49694865 | G | A | 1 | a0002c0003t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.142-2461G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694865 | |||||||
| chr19:49694923 | G | A | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-2403G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49694923 | |||||||
| chr19:49695089 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142-2237C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695089 | |||||||
| chr19:49695090 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-2236G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695090 | |||||||
| chr19:49695144 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.142-2182A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695144 | |||||||
| chr19:49695249 | T | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.142-2077T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695249 | |||||||
| chr19:49695278 | A | AT | 49 | a0001c0001t0001g0167 a0001c0001t0001g0187 a0001c0001t0001g0213 others(46): Show |
52 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.142-2026dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695278 | ||||||
| chr19:49695278 | AT | A | 36 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(33): Show |
36 | HG00099.hp2 HG01070.hp1 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.142-2026delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695278 | ||||||
| chr19:49695446 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.142-1880G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695446 | |||||||
| chr19:49695553 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-1773G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695553 | |||||||
| chr19:49695584 | C | CT | 14 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0220 others(11): Show |
14 | HG00438.hp1 HG01168.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-1721dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695584 | ||||||
| chr19:49695584 | CT | C | 104 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0041 others(101): Show |
110 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.142-1721delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695584 | ||||||
| chr19:49695584 | CTT | C | 75 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0001g0167 others(72): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.142-1722_142-1721d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695584 | ||||||
| chr19:49695651 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0229 a0001c0001t0001g0294 |
4 | HG02074.hp1 HG02129.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1675C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695651 | |||||||
| chr19:49695709 | A | AACACTAG others(10): Show |
1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.142-1616_142-1615i others(19): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695709 | ||||||
| chr19:49695728 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.142-1598C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695728 | |||||||
| chr19:49695772 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.142-1554G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695772 | |||||||
| chr19:49695880 | C | CT | 42 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0026 others(39): Show |
46 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.142-1438dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49695880 | ||||||
| chr19:49695897 | G | A | 10 | a0001c0001t0002g0024 a0001c0001t0002g0028 a0001c0001t0002g0030 others(7): Show |
10 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1429G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49695897 | |||||||
| chr19:49696283 | G | C | 42 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0003g0004 others(39): Show |
46 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-1043G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696283 | |||||||
| chr19:49696307 | A | AT | 4 | a0001c0001t0002g0012 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
5 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-1018dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696307 | ||||||
| chr19:49696320 | T | C | 19 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(16): Show |
19 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-1006T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696320 | |||||||
| chr19:49696344 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.142-982G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696344 | |||||||
| chr19:49696359 | G | A | 153 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(150): Show |
163 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.142-967G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696359 | |||||||
| chr19:49696451 | CTTTTCT | C | 39 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0003g0004 others(36): Show |
43 | HG01243.hp2 HG01891.hp2 HG02083.hp1 others(40): Show |
intron_variant | MODIFIER | c.142-870_142-865del others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696451 | ||||||
| chr19:49696456 | C | CT | 11 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0144 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-852dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696456 | ||||||
| chr19:49696456 | CT | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(53): Show |
57 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.142-852delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696456 | ||||||
| chr19:49696456 | CTT | C | 62 | a0001c0001t0001g0167 a0001c0001t0001g0304 a0001c0001t0002g0003 others(59): Show |
65 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.142-853_142-852del others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696456 | ||||||
| chr19:49696461 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.142-865T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696461 | |||||||
| chr19:49696462 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.142-864T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696462 | |||||||
| chr19:49696564 | G | A | 16 | a0001c0001t0001g0167 a0001c0001t0002g0088 a0001c0001t0002g0090 others(13): Show |
16 | HG00621.hp2 HG02129.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.142-762G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696564 | |||||||
| chr19:49696628 | T | C | 22 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0002t0002g0013 others(19): Show |
23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-698T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696628 | |||||||
| chr19:49696636 | CT | C | 130 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(127): Show |
139 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.142-677delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 49696636 | ||||||
| chr19:49696702 | G | C | 22 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0002t0002g0013 others(19): Show |
23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-624G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696702 | |||||||
| chr19:49696851 | T | C | 22 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0002t0002g0013 others(19): Show |
23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.142-475T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49696851 | |||||||
| chr19:49697219 | C | T | 1 | a0001c0002t0002g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.142-107C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 3/19 | chr19 | 49697219 | |||||||
| chr19:49697500 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.281+35A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697500 | |||||||
| chr19:49697691 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0310 |
3 | HG02040.hp1 HG02132.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.281+226C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697691 | |||||||
| chr19:49697774 | ATGGTGGC others(19): Show |
A | 1 | a0001c0001t0001g0233 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.281+310_281+335del others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697774 | |||||||
| chr19:49697835 | A | G | 22 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0002t0002g0013 others(19): Show |
23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+370A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697835 | |||||||
| chr19:49697998 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02965.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.281+533G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49697998 | |||||||
| chr19:49698049 | C | CA | 25 | a0001c0001t0001g0015 a0001c0001t0001g0117 a0001c0001t0001g0126 others(22): Show |
26 | HG00280.hp1 HG00423.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.281+606dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49698049 | ||||||
| chr19:49698049 | CA | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0150 a0001c0001t0001g0162 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+606delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49698049 | ||||||
| chr19:49698089 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.281+624G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698089 | |||||||
| chr19:49698118 | A | C | 1 | a0001c0001t0003g0009 | 2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.281+653A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698118 | |||||||
| chr19:49698181 | A | G | 4 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0084 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+716A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698181 | |||||||
| chr19:49698501 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.281+1036A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698501 | |||||||
| chr19:49698588 | G | A | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.281+1123G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698588 | |||||||
| chr19:49698603 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.281+1138C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698603 | |||||||
| chr19:49698649 | C | A | 13 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0027 others(10): Show |
13 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.281+1184C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698649 | |||||||
| chr19:49698662 | C | CA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0128 others(44): Show |
48 | HG00558.hp2 HG00609.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.281+1212dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49698662 | ||||||
| chr19:49698670 | A | G | 22 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0002t0002g0013 others(19): Show |
23 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+1205A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698670 | |||||||
| chr19:49698824 | G | A | 12 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0027 others(9): Show |
12 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.281+1359G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698824 | |||||||
| chr19:49698893 | A | G | 1 | a0001c0002t0002g0204 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281+1428A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698893 | |||||||
| chr19:49698898 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+1433C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49698898 | |||||||
| chr19:49699180 | T | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0237 a0001c0001t0001g0246 |
3 | HG02027.hp1 HG02056.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.282-1504T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699180 | |||||||
| chr19:49699199 | A | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0168 others(7): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-1485A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699199 | |||||||
| chr19:49699368 | T | C | 4 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0084 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-1316T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699368 | |||||||
| chr19:49699447 | C | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282-1237C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699447 | |||||||
| chr19:49699451 | T | C | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.282-1233T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699451 | |||||||
| chr19:49699457 | T | TA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(35): Show |
42 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.282-1193dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | T | TAA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0144 others(30): Show |
34 | HG00558.hp2 HG00621.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.282-1194_282-1193d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | T | TAAA | 20 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(17): Show |
20 | HG00438.hp2 HG01175.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.282-1195_282-1193d others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | T | TAAAA | 13 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG00609.hp2 HG01258.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.282-1196_282-1193d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | T | TAAAAA | 8 | a0001c0001t0002g0035 a0001c0001t0002g0096 a0001c0002t0002g0190 others(5): Show |
8 | HG00741.hp1 HG01192.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-1197_282-1193d others(7): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | T | TAAAAAA | 6 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0002t0002g0013 others(3): Show |
7 | HG00735.hp2 HG01069.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-1198_282-1193d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | T | TAAAAAAA others(11): Show |
1 | a0004c0007t0002g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.282-1210_282-1193d others(20): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TA | T | 57 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(54): Show |
63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.282-1193delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAA | T | 32 | a0001c0001t0001g0164 a0001c0001t0001g0180 a0001c0001t0001g0181 others(29): Show |
36 | HG01243.hp2 HG01346.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.282-1194_282-1193d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAAA | T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0176 a0001c0001t0002g0012 others(7): Show |
11 | HG00735.hp1 HG02083.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.282-1195_282-1193d others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAAAAAA | T | 13 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
13 | HG01070.hp1 HG01433.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.282-1198_282-1193d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.282-1203_282-1193d others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0034 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.282-1207_282-1193d others(17): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0001g0227 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.282-1211_282-1193d others(21): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699457 | TAAAAAAA others(13): Show |
T | 2 | a0001c0001t0002g0208 a0002c0003t0002g0209 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.282-1212_282-1193d others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699457 | ||||||
| chr19:49699470 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.282-1214A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699470 | |||||||
| chr19:49699760 | G | A | 10 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0168 others(7): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-924G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699760 | |||||||
| chr19:49699780 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.282-904C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699780 | |||||||
| chr19:49699796 | T | C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-888T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699796 | |||||||
| chr19:49699914 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-770A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699914 | |||||||
| chr19:49699932 | C | CGA | 3 | a0001c0004t0002g0189 a0001c0004t0002g0202 a0001c0004t0002g0203 |
3 | HG01516.hp2 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.282-751_282-750dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49699932 | ||||||
| chr19:49699966 | T | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0295 |
2 | HG02135.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.282-718T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699966 | |||||||
| chr19:49699976 | G | C | 42 | a0001c0001t0001g0228 a0001c0001t0001g0239 a0001c0001t0002g0025 others(39): Show |
46 | HG00099.hp2 HG00280.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.282-708G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699976 | |||||||
| chr19:49699985 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282-699C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49699985 | |||||||
| chr19:49700024 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
5 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-660G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700024 | |||||||
| chr19:49700165 | T | G | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.282-519T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700165 | |||||||
| chr19:49700244 | C | T | 1 | a0002c0003t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.282-440C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700244 | |||||||
| chr19:49700257 | C | CAA | 24 | a0001c0001t0001g0304 a0001c0001t0002g0003 a0001c0001t0002g0010 others(21): Show |
27 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.282-424_282-423dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700257 | ||||||
| chr19:49700257 | C | CAAA | 12 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0087 others(9): Show |
12 | HG00423.hp2 HG00738.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-425_282-423dup others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700257 | ||||||
| chr19:49700262 | C | A | 39 | a0001c0001t0001g0167 a0001c0001t0001g0304 a0001c0001t0002g0003 others(36): Show |
42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.282-422C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700262 | |||||||
| chr19:49700262 | C | CA | 71 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0127 others(68): Show |
76 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.282-411dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | ||||||
| chr19:49700262 | C | CAA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(37): Show |
41 | HG00558.hp2 HG00609.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-412_282-411dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | ||||||
| chr19:49700262 | CA | C | 17 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(14): Show |
17 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.282-411delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | ||||||
| chr19:49700262 | CAAA | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-413_282-411del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 49700262 | ||||||
| chr19:49700267 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.282-417A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700267 | |||||||
| chr19:49700296 | T | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-388T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700296 | |||||||
| chr19:49700328 | G | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-356G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700328 | |||||||
| chr19:49700334 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.282-350G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700334 | |||||||
| chr19:49700334 | G | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 others(1): Show |
5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-350G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700334 | |||||||
| chr19:49700427 | G | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-257G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700427 | |||||||
| chr19:49700660 | C | A | 1 | a0001c0001t0001g0302 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.282-24C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700660 | |||||||
| chr19:49700679 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01169.hp2 | splice_region_variant&intron_variant | LOW | c.282-5C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 4/19 | chr19 | 49700679 | |||||||
| chr19:49700869 | A | G | 15 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0123 others(12): Show |
16 | HG00735.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.453+14A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49700869 | |||||||
| chr19:49700944 | G | A | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.453+89G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49700944 | |||||||
| chr19:49700955 | T | TCTCTCTC others(84): Show |
19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.453+109_453+199dup others(91): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49700955 | ||||||
| chr19:49700955 | T | TCTCTCTC others(107): Show |
1 | a0001c0002t0002g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.453+139_453+140ins others(114): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49700955 | ||||||
| chr19:49700992 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.453+137T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49700992 | |||||||
| chr19:49701008 | CCTGGGTC others(15): Show |
C | 2 | a0001c0001t0001g0188 a0001c0001t0003g0059 |
2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.453+178_453+199del others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701008 | ||||||
| chr19:49701024 | C | CCT | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+176_453+177dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701024 | ||||||
| chr19:49701034 | G | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+179G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701034 | |||||||
| chr19:49701040 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+185T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701040 | |||||||
| chr19:49701046 | CCTCT | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+198_453+201del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701046 | ||||||
| chr19:49701052 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+197T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701052 | |||||||
| chr19:49701058 | T | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(47): Show |
52 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.453+203T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701058 | |||||||
| chr19:49701064 | C | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(47): Show |
52 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.453+209C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701064 | |||||||
| chr19:49701065 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+210G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701065 | |||||||
| chr19:49701066 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+211T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701066 | |||||||
| chr19:49701070 | C | CGACT | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+215_453+216ins others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701070 | |||||||
| chr19:49701072 | C | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+217C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701072 | |||||||
| chr19:49701085 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+230A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701085 | |||||||
| chr19:49701091 | G | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-226G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701091 | |||||||
| chr19:49701092 | A | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.454-225A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701092 | |||||||
| chr19:49701110 | C | CCCCCCTC others(17): Show |
81 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(78): Show |
86 | HG00280.hp2 HG00423.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.454-194_454-171dup others(24): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701110 | ||||||
| chr19:49701110 | C | CCCCCCTC others(155): Show |
10 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0002g0023 others(7): Show |
10 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.454-171_454-170ins others(162): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701110 | ||||||
| chr19:49701110 | C | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(28): Show |
32 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.454-207C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701110 | |||||||
| chr19:49701126 | G | GGTCTCTG others(38): Show |
20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-162_454-161ins others(45): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr19 | 49701126 | ||||||
| chr19:49701181 | T | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-136T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701181 | |||||||
| chr19:49701200 | G | A | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.454-117G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 5/19 | chr19 | 49701200 | |||||||
| chr19:49701730 | C | A | 1 | a0001c0001t0003g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.693+96C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701730 | |||||||
| chr19:49701771 | C | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+137C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701771 | |||||||
| chr19:49701817 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.693+183A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701817 | |||||||
| chr19:49701829 | AT | A | 17 | a0001c0001t0001g0176 a0001c0001t0001g0310 a0001c0001t0002g0011 others(14): Show |
18 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+196delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701829 | |||||||
| chr19:49701859 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+225A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701859 | |||||||
| chr19:49701860 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+226A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701860 | |||||||
| chr19:49701865 | ATAG | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+233_693+235del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701865 | ||||||
| chr19:49701870 | G | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+236G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701870 | |||||||
| chr19:49701877 | T | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0304 a0001c0001t0002g0003 others(34): Show |
40 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.693+243T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701877 | |||||||
| chr19:49701879 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+245A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701879 | |||||||
| chr19:49701880 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+246A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701880 | |||||||
| chr19:49701886 | ATATT | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0304 a0001c0001t0002g0003 others(34): Show |
40 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.693+260_693+263del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701886 | ||||||
| chr19:49701899 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+265A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701899 | |||||||
| chr19:49701901 | T | C | 2 | a0001c0002t0002g0206 a0004c0007t0002g0207 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.693+267T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701901 | |||||||
| chr19:49701902 | A | AT | 22 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(19): Show |
23 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.693+269dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701902 | ||||||
| chr19:49701902 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+268A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701902 | |||||||
| chr19:49701912 | A | ATATATAT others(312): Show |
1 | a0001c0002t0002g0199 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.693+281_693+282ins others(319): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701912 | ||||||
| chr19:49701912 | A | ATATATAT others(312): Show |
16 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(13): Show |
17 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.693+281_693+282ins others(319): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701912 | ||||||
| chr19:49701916 | T | A | 3 | a0001c0002t0002g0206 a0001c0004t0002g0193 a0004c0007t0002g0207 |
3 | HG02109.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+282T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701916 | |||||||
| chr19:49701920 | A | G | 3 | a0001c0002t0002g0206 a0001c0004t0002g0193 a0004c0007t0002g0207 |
3 | HG02109.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+286A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701920 | |||||||
| chr19:49701923 | C | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+289C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701923 | |||||||
| chr19:49701925 | A | T | 3 | a0001c0002t0002g0206 a0001c0004t0002g0193 a0004c0007t0002g0207 |
3 | HG02109.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+291A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701925 | |||||||
| chr19:49701930 | T | A | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+296T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701930 | |||||||
| chr19:49701930 | T | TTATTTAT others(263): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+296_693+297ins others(270): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701930 | |||||||
| chr19:49701930 | T | TTATTTAT others(306): Show |
2 | a0001c0002t0002g0206 a0004c0007t0002g0207 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.693+296_693+297ins others(313): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701930 | |||||||
| chr19:49701931 | A | T | 58 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(55): Show |
61 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.693+297A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701931 | |||||||
| chr19:49701936 | T | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+302T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701936 | |||||||
| chr19:49701936 | T | TTATA | 86 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(83): Show |
91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.693+303_693+306dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701936 | ||||||
| chr19:49701938 | A | T | 18 | a0001c0001t0003g0072 a0001c0002t0002g0013 a0001c0002t0002g0014 others(15): Show |
19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+304A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701938 | |||||||
| chr19:49701941 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+307A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701941 | |||||||
| chr19:49701944 | T | A | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+310T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701944 | |||||||
| chr19:49701953 | A | AATATAAA others(4): Show |
10 | a0001c0001t0001g0310 a0001c0001t0002g0023 a0001c0001t0002g0027 others(7): Show |
10 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+324_693+325ins others(11): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701953 | ||||||
| chr19:49701953 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.693+325_693+326ins others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701953 | ||||||
| chr19:49701953 | A | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+319A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701953 | |||||||
| chr19:49701954 | A | ATATATAA others(4): Show |
83 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(80): Show |
88 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.693+325_693+326ins others(11): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701954 | ||||||
| chr19:49701954 | A | ATATATAA others(43): Show |
1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.693+325_693+326ins others(50): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701954 | ||||||
| chr19:49701954 | A | ATATATAA others(43): Show |
6 | a0001c0001t0002g0011 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+325_693+326ins others(50): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701954 | ||||||
| chr19:49701956 | A | T | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+322A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701956 | |||||||
| chr19:49701958 | AT | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+327delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701958 | ||||||
| chr19:49701961 | T | A | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+327T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701961 | |||||||
| chr19:49701966 | A | T | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+332A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701966 | |||||||
| chr19:49701969 | A | AAT | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+336_693+337dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49701969 | ||||||
| chr19:49701969 | A | T | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+335A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701969 | |||||||
| chr19:49701972 | T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+338T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701972 | |||||||
| chr19:49701977 | A | T | 137 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0041 others(134): Show |
144 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.693+343A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701977 | |||||||
| chr19:49701981 | A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+347A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701981 | |||||||
| chr19:49701982 | A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+348A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701982 | |||||||
| chr19:49701989 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+355A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701989 | |||||||
| chr19:49701992 | A | T | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+358A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701992 | |||||||
| chr19:49701993 | T | TATATA | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+359_693+360ins others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701993 | |||||||
| chr19:49701998 | A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+364A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701998 | |||||||
| chr19:49701999 | A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+365A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49701999 | |||||||
| chr19:49702001 | A | G | 19 | a0001c0001t0001g0228 a0001c0001t0001g0239 a0001c0001t0002g0025 others(16): Show |
21 | HG00099.hp2 HG00280.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.693+367A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702001 | |||||||
| chr19:49702003 | A | T | 18 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(15): Show |
19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+369A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702003 | |||||||
| chr19:49702004 | T | TATATA | 18 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(15): Show |
19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+370_693+371ins others(5): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702004 | |||||||
| chr19:49702004 | T | TTAAATAT others(64): Show |
1 | a0001c0001t0001g0042 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(71): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | ||||||
| chr19:49702004 | T | TTAAATAT others(42): Show |
1 | a0001c0001t0002g0031 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(49): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | ||||||
| chr19:49702004 | T | TTAAATAT others(69): Show |
1 | a0001c0001t0002g0027 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | ||||||
| chr19:49702004 | T | TTAAATAT others(123): Show |
1 | a0001c0001t0002g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(130): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702004 | ||||||
| chr19:49702007 | A | AATATATT others(97): Show |
1 | a0001c0001t0001g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.693+383_693+384ins others(104): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(15): Show |
5 | a0001c0001t0001g0188 a0001c0001t0002g0036 a0001c0001t0002g0038 others(2): Show |
5 | HG00438.hp2 HG00544.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(40): Show |
5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG01099.hp1 HG01361.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(47): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(44): Show |
147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(51): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(69): Show |
7 | a0001c0001t0001g0133 a0001c0001t0001g0230 a0001c0001t0001g0242 others(4): Show |
7 | HG01256.hp1 HG02040.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(94): Show |
5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0231 others(2): Show |
5 | HG01099.hp2 HG01109.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(101): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(94): Show |
4 | a0001c0001t0002g0011 a0001c0001t0002g0170 a0001c0001t0002g0171 others(1): Show |
5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(101): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(316): Show |
2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.693+391_693+392ins others(323): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(69): Show |
7 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0003g0004 others(4): Show |
9 | HG02622.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | AATATATT others(127): Show |
1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(134): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702007 | ||||||
| chr19:49702007 | A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+373A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702007 | |||||||
| chr19:49702009 | T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+375T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702009 | |||||||
| chr19:49702013 | T | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+379T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702013 | |||||||
| chr19:49702014 | T | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+380T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702014 | |||||||
| chr19:49702018 | T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+384T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702018 | |||||||
| chr19:49702021 | TAAA | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+388_693+390del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702021 | |||||||
| chr19:49702023 | AATT | A | 49 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0001g0162 others(46): Show |
52 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.693+392_693+394del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702023 | ||||||
| chr19:49702024 | A | ATAAATAT others(94): Show |
1 | a0001c0001t0005g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(101): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702024 | ||||||
| chr19:49702024 | A | T | 1 | a0002c0003t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.693+390A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702024 | |||||||
| chr19:49702025 | T | TAAATATA others(63): Show |
1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(70): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(90): Show |
1 | a0005c0011t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(97): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(119): Show |
5 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0126 others(2): Show |
5 | HG02145.hp1 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(126): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(41): Show |
1 | a0001c0001t0001g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(48): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(68): Show |
1 | a0001c0001t0001g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(75): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(124): Show |
4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(1): Show |
4 | HG01070.hp1 HG01433.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(131): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(93): Show |
1 | a0001c0001t0002g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(100): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(68): Show |
4 | a0001c0001t0002g0012 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
5 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(75): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(39): Show |
1 | a0001c0001t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.693+391_693+392ins others(46): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(66): Show |
1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.693+391_693+392ins others(73): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(19): Show |
32 | a0001c0001t0001g0017 a0001c0001t0001g0121 a0001c0001t0001g0122 others(29): Show |
33 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(48): Show |
6 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0103 others(3): Show |
6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+391_693+392ins others(55): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702025 | T | TAAATATA others(19): Show |
3 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0079 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.693+391_693+392ins others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702025 | |||||||
| chr19:49702026 | T | A | 62 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0041 others(59): Show |
64 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.693+392T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702026 | |||||||
| chr19:49702026 | T | TATAA | 8 | a0001c0001t0001g0188 a0001c0001t0002g0011 a0001c0001t0002g0168 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+396_693+399dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702026 | ||||||
| chr19:49702030 | A | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+396A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702030 | |||||||
| chr19:49702032 | T | TAA | 7 | a0001c0001t0001g0042 a0001c0001t0002g0027 a0001c0001t0002g0031 others(4): Show |
7 | HG00438.hp2 HG00544.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+399_693+400ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702032 | ||||||
| chr19:49702034 | T | A | 20 | a0001c0001t0001g0274 a0001c0002t0002g0013 a0001c0002t0002g0014 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+400T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702034 | |||||||
| chr19:49702035 | A | G | 6 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0103 others(3): Show |
6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+401A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702035 | |||||||
| chr19:49702035 | A | T | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+401A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702035 | |||||||
| chr19:49702039 | T | TTATTTAT others(43): Show |
3 | a0001c0001t0001g0259 a0002c0003t0001g0232 a0002c0003t0001g0275 |
3 | HG00544.hp2 HG01109.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.693+424_693+425ins others(50): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702039 | ||||||
| chr19:49702043 | T | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+409T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702043 | |||||||
| chr19:49702048 | AATT | A | 3 | a0001c0001t0005g0082 a0001c0001t0006g0108 a0001c0001t0006g0109 |
3 | HG02451.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+417_693+419del others(3): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702048 | ||||||
| chr19:49702049 | AT | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+417delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702049 | ||||||
| chr19:49702050 | T | TATTTATA others(6): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+416_693+417ins others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702050 | |||||||
| chr19:49702051 | T | TATAA | 58 | a0001c0001t0001g0042 a0001c0001t0001g0118 a0001c0001t0001g0120 others(55): Show |
63 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+421_693+424dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702051 | ||||||
| chr19:49702051 | T | TATAAATA others(55): Show |
2 | a0001c0001t0003g0080 a0001c0001t0003g0081 |
2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.693+424_693+425ins others(62): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702051 | ||||||
| chr19:49702051 | T | TATAAATA others(26): Show |
1 | a0001c0001t0003g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.693+424_693+425ins others(33): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702051 | ||||||
| chr19:49702057 | T | TAA | 6 | a0001c0001t0002g0023 a0001c0001t0002g0027 a0001c0001t0002g0030 others(3): Show |
6 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+424_693+425ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702057 | ||||||
| chr19:49702057 | T | TAAATATA others(76): Show |
1 | a0001c0001t0001g0310 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.693+424_693+425ins others(83): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702057 | ||||||
| chr19:49702060 | A | G | 3 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0007g0099 |
3 | HG02809.hp2 NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.693+426A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702060 | |||||||
| chr19:49702060 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+426A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702060 | |||||||
| chr19:49702068 | T | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+434T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702068 | |||||||
| chr19:49702074 | A | T | 1 | a0001c0001t0005g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.693+440A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702074 | |||||||
| chr19:49702075 | T | G | 6 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0103 others(3): Show |
6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+441T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702075 | |||||||
| chr19:49702075 | T | TATTTATA | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+441_693+442ins others(7): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702075 | |||||||
| chr19:49702075 | T | TATTTATA others(6): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+441_693+442ins others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702075 | |||||||
| chr19:49702076 | T | TATAA | 9 | a0001c0001t0001g0304 a0001c0001t0002g0011 a0001c0001t0002g0168 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+446_693+449dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | ||||||
| chr19:49702076 | T | TATAAATA others(55): Show |
1 | a0002c0003t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.693+449_693+450ins others(62): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | ||||||
| chr19:49702076 | T | TATAAATA others(59): Show |
1 | a0001c0001t0001g0236 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.693+449_693+450ins others(66): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | ||||||
| chr19:49702076 | T | TATAAATA others(30): Show |
3 | a0001c0001t0005g0082 a0001c0001t0006g0108 a0001c0001t0006g0109 |
3 | HG02451.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+449_693+450ins others(37): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | ||||||
| chr19:49702076 | T | TATAAATA others(63): Show |
9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(6): Show |
9 | HG01070.hp1 HG01433.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(70): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702076 | ||||||
| chr19:49702080 | A | AATAAATA others(1): Show |
6 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0103 others(3): Show |
6 | HG02683.hp1 NA18951.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | ||||||
| chr19:49702080 | A | AATAAATA others(30): Show |
1 | a0001c0001t0002g0208 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.693+449_693+450ins others(37): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | ||||||
| chr19:49702080 | A | AATAAATA others(201): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.693+449_693+450ins others(208): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | ||||||
| chr19:49702080 | A | AATAAATA others(175): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.693+449_693+450ins others(182): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | ||||||
| chr19:49702080 | A | AATAAATA others(55): Show |
29 | a0001c0001t0001g0167 a0001c0001t0002g0003 a0001c0001t0002g0010 others(26): Show |
32 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(62): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702080 | ||||||
| chr19:49702082 | T | TAA | 8 | a0001c0001t0001g0310 a0001c0001t0002g0023 a0001c0001t0002g0027 others(5): Show |
8 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+449_693+450ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702082 | ||||||
| chr19:49702084 | T | A | 1 | a0001c0001t0004g0305 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.693+450T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702084 | |||||||
| chr19:49702085 | A | ATATTTAT others(76): Show |
1 | a0001c0001t0001g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.693+458_693+459ins others(83): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702085 | ||||||
| chr19:49702085 | A | ATATTTAT others(22): Show |
1 | a0002c0003t0004g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.693+475_693+503dup others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702085 | ||||||
| chr19:49702085 | A | T | 41 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(38): Show |
44 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.693+451A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702085 | |||||||
| chr19:49702085 | ATATT | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(23): Show |
27 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+459_693+462del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702085 | ||||||
| chr19:49702089 | T | A | 20 | a0001c0001t0004g0305 a0001c0002t0002g0013 a0001c0002t0002g0014 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+455T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702089 | |||||||
| chr19:49702093 | T | A | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+459T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702093 | |||||||
| chr19:49702098 | A | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(16): Show |
20 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+464A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702098 | |||||||
| chr19:49702099 | A | G | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.693+465A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702099 | |||||||
| chr19:49702099 | A | T | 1 | a0001c0001t0003g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.693+465A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702099 | |||||||
| chr19:49702100 | T | G | 3 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0007g0099 |
3 | HG02809.hp2 NA18967.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.693+466T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | |||||||
| chr19:49702100 | T | TAAATATA others(72): Show |
1 | a0001c0002t0002g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.693+466_693+467ins others(79): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | |||||||
| chr19:49702100 | T | TAAATATA others(82): Show |
15 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0194 others(12): Show |
16 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+466_693+467ins others(89): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | |||||||
| chr19:49702100 | T | TAAATATA others(96): Show |
2 | a0001c0002t0002g0206 a0004c0007t0002g0207 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.693+466_693+467ins others(103): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | |||||||
| chr19:49702100 | T | TAAATATT others(4): Show |
1 | a0002c0005t0002g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.693+466_693+467ins others(11): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702100 | |||||||
| chr19:49702101 | T | TATAA | 51 | a0001c0001t0001g0042 a0001c0001t0001g0117 a0001c0001t0001g0118 others(48): Show |
55 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.693+471_693+474dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702101 | T | TATAAATA others(30): Show |
2 | a0001c0001t0002g0095 a0001c0001t0007g0099 |
2 | HG02809.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.693+474_693+475ins others(37): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702101 | T | TATAAATA others(62): Show |
1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+474_693+475ins others(69): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702101 | T | TATAAATA others(92): Show |
1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.693+474_693+475ins others(99): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702101 | T | TATAAATA others(92): Show |
1 | a0005c0011t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.693+474_693+475ins others(99): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702101 | T | TATAAATA others(134): Show |
1 | a0001c0001t0002g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.693+474_693+475ins others(141): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702101 | T | TATAAATA others(84): Show |
1 | a0001c0001t0001g0304 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.693+474_693+475ins others(91): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702101 | ||||||
| chr19:49702109 | T | A | 31 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(28): Show |
32 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.693+475T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702109 | |||||||
| chr19:49702110 | ATATT | A | 15 | a0001c0001t0001g0138 a0001c0001t0001g0241 a0001c0001t0001g0242 others(12): Show |
15 | HG00544.hp2 HG00609.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.693+488_693+491del others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702110 | ||||||
| chr19:49702114 | T | A | 51 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(48): Show |
53 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.693+480T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702114 | |||||||
| chr19:49702114 | T | TTATTTAT others(99): Show |
1 | a0001c0001t0002g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.693+487_693+488ins others(106): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | ||||||
| chr19:49702114 | T | TTATTTAT others(155): Show |
1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.693+487_693+488ins others(162): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | ||||||
| chr19:49702114 | T | TTATTTAT others(22): Show |
1 | a0001c0001t0003g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.693+522_693+550dup others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | ||||||
| chr19:49702114 | T | TTATTTAT others(51): Show |
2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.693+522_693+523ins others(58): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702114 | ||||||
| chr19:49702117 | T | TAA | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0194 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+483_693+484ins others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702117 | |||||||
| chr19:49702118 | T | A | 18 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(15): Show |
19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+484T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702118 | |||||||
| chr19:49702118 | T | TTATAAAT others(31): Show |
1 | a0001c0001t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.693+487_693+488ins others(38): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702118 | ||||||
| chr19:49702122 | T | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+488T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702122 | |||||||
| chr19:49702128 | A | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0118 a0001c0001t0001g0120 others(6): Show |
10 | HG00735.hp1 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+494A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702128 | |||||||
| chr19:49702129 | T | TA | 18 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(15): Show |
19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+495_693+496ins others(1): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702129 | |||||||
| chr19:49702129 | T | TATATCTA others(110): Show |
1 | a0002c0005t0002g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.693+495_693+496ins others(117): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702129 | |||||||
| chr19:49702129 | T | TATATCTA others(124): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+495_693+496ins others(131): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702129 | |||||||
| chr19:49702134 | A | AATATATA others(14): Show |
2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.693+503_693+504ins others(21): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702134 | ||||||
| chr19:49702134 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+500A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702134 | |||||||
| chr19:49702136 | T | A | 1 | a0001c0002t0002g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.693+502T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702136 | |||||||
| chr19:49702138 | A | AAT | 18 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0194 others(15): Show |
19 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.693+511_693+512dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702138 | ||||||
| chr19:49702138 | A | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(30): Show |
34 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.693+504A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702138 | |||||||
| chr19:49702143 | A | ATATT | 61 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(58): Show |
64 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.693+517_693+520dup others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | ||||||
| chr19:49702143 | A | ATATTTAT others(113): Show |
1 | a0001c0001t0003g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693+550_693+551ins others(120): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | ||||||
| chr19:49702143 | A | ATATTTAT others(142): Show |
1 | a0001c0001t0003g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.693+550_693+551ins others(149): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | ||||||
| chr19:49702143 | A | ATATTTAT others(22): Show |
1 | a0001c0001t0001g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.693+537_693+538ins others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | ||||||
| chr19:49702143 | A | ATATTTAT others(59): Show |
5 | a0001c0001t0001g0130 a0001c0001t0002g0012 a0001c0001t0002g0173 others(2): Show |
6 | HG00735.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+520_693+521ins others(66): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | ||||||
| chr19:49702143 | A | ATATTTAT others(88): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0118 a0001c0001t0001g0120 others(1): Show |
4 | HG01255.hp1 HG01884.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+520_693+521ins others(95): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702143 | ||||||
| chr19:49702143 | A | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(30): Show |
34 | HG00558.hp2 HG00609.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.693+509A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702143 | |||||||
| chr19:49702163 | A | AATAAATA others(51): Show |
1 | a0001c0001t0002g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.693+550_693+551ins others(58): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702163 | ||||||
| chr19:49702163 | A | AATAAATA others(22): Show |
5 | a0001c0001t0001g0310 a0001c0001t0002g0023 a0001c0001t0002g0027 others(2): Show |
5 | HG00544.hp1 HG00642.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+550_693+551ins others(29): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702163 | ||||||
| chr19:49702163 | A | G | 4 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0208 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+529A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702163 | |||||||
| chr19:49702163 | A | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+529A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702163 | |||||||
| chr19:49702171 | T | A | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.693+537T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702171 | |||||||
| chr19:49702180 | T | TTA | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+553_693+554dup others(2): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702180 | ||||||
| chr19:49702299 | T | A | 1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+665T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702299 | |||||||
| chr19:49702307 | C | G | 1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+673C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702307 | |||||||
| chr19:49702308 | A | C | 1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+674A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702308 | |||||||
| chr19:49702309 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+675A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702309 | |||||||
| chr19:49702310 | A | T | 1 | a0001c0001t0002g0096 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693+676A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702310 | |||||||
| chr19:49702347 | A | G | 21 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(18): Show |
22 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.693+713A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702347 | |||||||
| chr19:49702399 | C | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+765C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702399 | |||||||
| chr19:49702414 | TCAAGACC others(8): Show |
T | 1 | a0001c0001t0001g0317 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.693+784_693+798del others(15): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702414 | ||||||
| chr19:49702491 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+857A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702491 | |||||||
| chr19:49702512 | C | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+878C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702512 | |||||||
| chr19:49702513 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.693+879G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702513 | |||||||
| chr19:49702525 | C | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+891C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702525 | |||||||
| chr19:49702608 | A | C | 1 | a0001c0001t0002g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.693+974A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702608 | |||||||
| chr19:49702630 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+996A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702630 | |||||||
| chr19:49702638 | G | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1004G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702638 | |||||||
| chr19:49702638 | G | GA | 7 | a0001c0001t0001g0217 a0001c0001t0002g0011 a0001c0001t0002g0168 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+1015dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702638 | ||||||
| chr19:49702641 | A | AAC | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1008_693+1009i others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49702641 | ||||||
| chr19:49702643 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1009A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702643 | |||||||
| chr19:49702824 | G | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1190G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702824 | |||||||
| chr19:49702833 | G | A | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0084 |
3 | HG02572.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.693+1199G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702833 | |||||||
| chr19:49702921 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.693+1287C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702921 | |||||||
| chr19:49702936 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1302A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702936 | |||||||
| chr19:49702974 | G | A | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.693+1340G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49702974 | |||||||
| chr19:49703055 | G | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1421G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703055 | |||||||
| chr19:49703070 | T | TAC | 8 | a0001c0001t0001g0217 a0001c0001t0001g0228 a0001c0001t0002g0175 others(5): Show |
8 | HG00099.hp2 HG01099.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+1465_693+1466d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | ||||||
| chr19:49703070 | TAC | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(153): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.693+1465_693+1466d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | ||||||
| chr19:49703070 | TACAC | T | 122 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(119): Show |
129 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.693+1463_693+1466d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | ||||||
| chr19:49703070 | TACACAC | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG01070.hp1 HG01433.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+1461_693+1466d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703070 | ||||||
| chr19:49703121 | T | TTCCC | 18 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0176 others(15): Show |
20 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.693+1503_693+1506d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703121 | ||||||
| chr19:49703121 | TTCCC | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.693+1503_693+1506d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703121 | ||||||
| chr19:49703237 | TCTCA | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-1469_694-1466d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703237 | ||||||
| chr19:49703248 | C | T | 33 | a0001c0001t0001g0167 a0001c0001t0002g0003 a0001c0001t0002g0045 others(30): Show |
35 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.694-1462C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703248 | |||||||
| chr19:49703326 | C | T | 1 | a0002c0003t0001g0264 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.694-1384C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703326 | |||||||
| chr19:49703345 | A | T | 1 | a0002c0003t0001g0264 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.694-1365A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703345 | |||||||
| chr19:49703350 | C | CTT | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-1346_694-1345d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703350 | ||||||
| chr19:49703369 | T | G | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-1341T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703369 | |||||||
| chr19:49703372 | T | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(1): Show |
4 | HG00280.hp2 HG01169.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-1338T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703372 | |||||||
| chr19:49703390 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694-1320T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703390 | |||||||
| chr19:49703391 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694-1319G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703391 | |||||||
| chr19:49703392 | G | A | 33 | a0001c0001t0001g0167 a0001c0001t0002g0003 a0001c0001t0002g0045 others(30): Show |
35 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.694-1318G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703392 | |||||||
| chr19:49703491 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
71 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.694-1219A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703491 | |||||||
| chr19:49703496 | C | T | 1 | a0002c0003t0002g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.694-1214C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703496 | |||||||
| chr19:49703500 | C | CTCTT | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-1194_694-1191d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703500 | ||||||
| chr19:49703563 | T | TCCTC | 16 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0246 others(13): Show |
18 | HG00597.hp2 HG02027.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-1115_694-1112d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | T | TCCTCCCT others(1): Show |
7 | a0001c0001t0001g0231 a0001c0001t0002g0033 a0001c0001t0002g0035 others(4): Show |
8 | HG00280.hp2 HG02056.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1119_694-1112d others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | T | TCCTCCCT others(5): Show |
11 | a0001c0001t0001g0134 a0001c0001t0001g0145 a0001c0001t0001g0146 others(8): Show |
11 | HG01169.hp2 HG01891.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.694-1123_694-1112d others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | T | TCCTCCCT others(9): Show |
14 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0144 others(11): Show |
15 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.694-1127_694-1112d others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | T | TCCTCCCT others(13): Show |
4 | a0001c0001t0001g0121 a0001c0001t0002g0032 a0001c0001t0003g0060 others(1): Show |
4 | HG03669.hp2 HG04204.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-1131_694-1112d others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | T | TCCTCCCT others(17): Show |
6 | a0001c0001t0001g0228 a0001c0001t0001g0239 a0001c0001t0003g0056 others(3): Show |
6 | HG00099.hp2 HG00280.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-1135_694-1112d others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | T | TCCTCCCT others(21): Show |
1 | a0001c0001t0003g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.694-1139_694-1112d others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | TCCTC | T | 21 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0176 others(18): Show |
23 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.694-1115_694-1112d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | TCCTCCCT others(1): Show |
T | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-1119_694-1112d others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703563 | TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.694-1123_694-1112d others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703563 | ||||||
| chr19:49703568 | C | T | 35 | a0001c0001t0001g0167 a0001c0001t0002g0088 a0001c0001t0002g0090 others(32): Show |
36 | HG00621.hp2 HG00735.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.694-1142C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703568 | |||||||
| chr19:49703587 | C | CCTTCCCT others(13): Show |
1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694-1122_694-1121i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | ||||||
| chr19:49703587 | C | CCTTCCCT others(17): Show |
3 | a0001c0002t0002g0198 a0001c0002t0002g0206 a0004c0007t0002g0207 |
3 | HG01192.hp2 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.694-1122_694-1121i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | ||||||
| chr19:49703587 | C | CCTTCCCT others(21): Show |
4 | a0001c0002t0002g0196 a0001c0002t0002g0204 a0001c0004t0002g0202 others(1): Show |
4 | HG01074.hp2 HG01106.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-1122_694-1121i others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | ||||||
| chr19:49703587 | C | CCTTCCCT others(25): Show |
8 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(5): Show |
9 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.694-1122_694-1121i others(34): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | ||||||
| chr19:49703587 | C | CCTTCCCT others(29): Show |
2 | a0001c0002t0002g0197 a0002c0005t0002g0200 |
2 | HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.694-1122_694-1121i others(38): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | ||||||
| chr19:49703587 | C | CCTTCCCT others(33): Show |
2 | a0001c0002t0002g0194 a0002c0005t0002g0195 |
2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.694-1122_694-1121i others(42): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703587 | ||||||
| chr19:49703591 | C | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-1119C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703591 | |||||||
| chr19:49703595 | C | CCCTCCCT others(17): Show |
3 | a0001c0001t0001g0136 a0001c0001t0001g0143 a0001c0001t0002g0172 |
3 | HG03453.hp2 NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(13): Show |
6 | a0001c0001t0001g0140 a0001c0001t0001g0155 a0001c0001t0001g0159 others(3): Show |
7 | HG00558.hp2 HG00735.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(21): Show |
1 | a0001c0001t0002g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.694-1112_694-1111i others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(9): Show |
16 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0132 others(13): Show |
18 | HG00609.hp2 HG01175.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(13): Show |
1 | a0001c0001t0002g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(17): Show |
6 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(3): Show |
8 | HG00642.hp1 HG01168.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(5): Show |
4 | a0001c0001t0001g0158 a0001c0001t0002g0173 a0001c0001t0002g0174 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(13): Show |
1 | a0001c0001t0002g0047 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(17): Show |
7 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0104 others(4): Show |
7 | HG00423.hp2 HG02055.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(21): Show |
1 | a0001c0001t0002g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.694-1112_694-1111i others(30): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(1): Show |
7 | a0001c0001t0001g0141 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(10): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(13): Show |
9 | a0001c0001t0001g0167 a0001c0001t0002g0088 a0001c0001t0002g0090 others(6): Show |
9 | HG02129.hp1 HG02135.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.694-1112_694-1111i others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTCCCT others(17): Show |
1 | a0001c0001t0002g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.694-1112_694-1111i others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTT | 3 | a0001c0001t0001g0162 a0001c0001t0001g0210 a0001c0001t0001g0317 |
3 | HG00609.hp1 HG02015.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.694-1093_694-1090d others(6): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTTCCT others(13): Show |
4 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0103 others(1): Show |
4 | HG02683.hp1 NA18951.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1109_694-1090d others(22): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | CCCTTCCT others(17): Show |
2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | NA18952.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.694-1113_694-1090d others(26): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr19 | 49703595 | ||||||
| chr19:49703595 | C | T | 37 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0176 others(34): Show |
40 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.694-1115C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703595 | |||||||
| chr19:49703599 | T | C | 2 | a0001c0001t0003g0008 a0001c0001t0003g0065 |
3 | HG03491.hp1 HG03492.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.694-1111T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703599 | |||||||
| chr19:49703787 | T | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-923T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703787 | |||||||
| chr19:49703793 | T | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-917T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703793 | |||||||
| chr19:49703908 | G | C | 229 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0040 others(226): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.694-802G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703908 | |||||||
| chr19:49703948 | A | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-762A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703948 | |||||||
| chr19:49703949 | C | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-761C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703949 | |||||||
| chr19:49703958 | C | T | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-752C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703958 | |||||||
| chr19:49703960 | A | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-750A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703960 | |||||||
| chr19:49703963 | G | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-747G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703963 | |||||||
| chr19:49703967 | G | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-743G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703967 | |||||||
| chr19:49703969 | G | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-741G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703969 | |||||||
| chr19:49703971 | C | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-739C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703971 | |||||||
| chr19:49703972 | A | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-738A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703972 | |||||||
| chr19:49703974 | A | T | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-736A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703974 | |||||||
| chr19:49703976 | G | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-734G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703976 | |||||||
| chr19:49703979 | C | A | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-731C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703979 | |||||||
| chr19:49703980 | C | A | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-730C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703980 | |||||||
| chr19:49703983 | T | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-727T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703983 | |||||||
| chr19:49703984 | T | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-726T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703984 | |||||||
| chr19:49703986 | T | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-724T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703986 | |||||||
| chr19:49703987 | T | A | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-723T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703987 | |||||||
| chr19:49703988 | T | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-722T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703988 | |||||||
| chr19:49703992 | T | A | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-718T>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703992 | |||||||
| chr19:49703996 | A | T | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-714A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703996 | |||||||
| chr19:49703997 | C | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-713C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703997 | |||||||
| chr19:49703999 | A | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-711A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49703999 | |||||||
| chr19:49704001 | A | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-709A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704001 | |||||||
| chr19:49704006 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.694-704C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704006 | |||||||
| chr19:49704007 | A | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-703A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704007 | |||||||
| chr19:49704008 | A | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-702A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704008 | |||||||
| chr19:49704009 | A | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-701A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704009 | |||||||
| chr19:49704024 | C | G | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-686C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704024 | |||||||
| chr19:49704025 | A | T | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-685A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704025 | |||||||
| chr19:49704026 | G | A | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-684G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704026 | |||||||
| chr19:49704028 | T | C | 1 | a0002c0003t0003g0053 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.694-682T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704028 | |||||||
| chr19:49704149 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.694-561T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704149 | |||||||
| chr19:49704253 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.694-457C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704253 | |||||||
| chr19:49704266 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694-444G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704266 | |||||||
| chr19:49704296 | C | T | 2 | a0001c0002t0002g0199 a0002c0005t0002g0200 |
2 | HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.694-414C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704296 | |||||||
| chr19:49704301 | A | G | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
26 | HG00735.hp1 HG01070.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-409A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704301 | |||||||
| chr19:49704328 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG01261.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-382C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704328 | |||||||
| chr19:49704329 | G | A | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-381G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704329 | |||||||
| chr19:49704406 | A | G | 2 | a0001c0002t0002g0190 a0001c0002t0002g0196 |
2 | HG01074.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.694-304A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704406 | |||||||
| chr19:49704460 | C | A | 2 | a0001c0001t0002g0112 a0002c0003t0002g0106 |
2 | HG00423.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.694-250C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704460 | |||||||
| chr19:49704462 | T | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-248T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704462 | |||||||
| chr19:49704512 | G | A | 2 | a0001c0001t0002g0112 a0002c0003t0002g0106 |
2 | HG00423.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.694-198G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704512 | |||||||
| chr19:49704517 | A | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.694-193A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704517 | |||||||
| chr19:49704583 | G | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-127G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 7/19 | chr19 | 49704583 | |||||||
| chr19:49704902 | AT | A | 39 | a0001c0001t0001g0167 a0001c0001t0001g0304 a0001c0001t0002g0003 others(36): Show |
42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.772-104delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704902 | |||||||
| chr19:49704923 | G | T | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.772-84G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704923 | |||||||
| chr19:49704931 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.772-76C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704931 | |||||||
| chr19:49704956 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.772-51G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704956 | |||||||
| chr19:49704997 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.772-10T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 8/19 | chr19 | 49704997 | |||||||
| chr19:49705370 | C | T | 14 | a0001c0001t0001g0228 a0001c0001t0001g0239 a0001c0001t0003g0008 others(11): Show |
16 | HG00099.hp2 HG00280.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.964+72C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705370 | |||||||
| chr19:49705453 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0268 a0001c0001t0001g0279 others(3): Show |
8 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.964+155A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705453 | |||||||
| chr19:49705492 | G | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0304 a0001c0001t0002g0003 others(34): Show |
40 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.964+194G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705492 | |||||||
| chr19:49705658 | C | G | 1 | a0001c0002t0002g0204 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.965-251C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705658 | |||||||
| chr19:49705685 | C | G | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.965-224C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705685 | |||||||
| chr19:49705685 | C | T | 5 | a0001c0001t0002g0088 a0001c0001t0002g0090 a0001c0001t0002g0091 others(2): Show |
5 | HG02129.hp1 NA18942.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-224C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705685 | |||||||
| chr19:49705686 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.965-223G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705686 | |||||||
| chr19:49705701 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.965-208A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705701 | |||||||
| chr19:49705750 | C | T | 1 | a0001c0001t0005g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.965-159C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705750 | |||||||
| chr19:49705838 | T | G | 48 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0176 others(45): Show |
52 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.965-71T>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705838 | |||||||
| chr19:49705881 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0302 |
2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.965-28C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 10/19 | chr19 | 49705881 | |||||||
| chr19:49706177 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1161-54G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 11/19 | chr19 | 49706177 | |||||||
| chr19:49706472 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1343+59C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706472 | |||||||
| chr19:49706476 | G | A | 1 | a0001c0001t0005g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1343+63G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706476 | |||||||
| chr19:49706482 | T | C | 20 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1343+69T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706482 | |||||||
| chr19:49706608 | A | G | 1 | a0001c0004t0002g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1343+195A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706608 | |||||||
| chr19:49706688 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+275C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706688 | |||||||
| chr19:49706690 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+277C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706690 | |||||||
| chr19:49706691 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+278A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706691 | |||||||
| chr19:49706692 | G | C | 1 | a0001c0001t0001g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+279G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706692 | |||||||
| chr19:49706695 | A | C | 1 | a0001c0001t0001g0257 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1343+282A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706695 | |||||||
| chr19:49706749 | C | T | 17 | a0001c0002t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0190 others(14): Show |
18 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1343+336C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706749 | |||||||
| chr19:49706909 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1343+496C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49706909 | |||||||
| chr19:49707049 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1344-469C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707049 | |||||||
| chr19:49707084 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1344-434G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707084 | |||||||
| chr19:49707216 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1344-302C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707216 | |||||||
| chr19:49707240 | G | A | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344-278G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707240 | |||||||
| chr19:49707241 | C | A | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344-277C>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707241 | |||||||
| chr19:49707244 | C | T | 3 | a0001c0001t0003g0062 a0001c0001t0003g0067 a0001c0001t0003g0078 |
3 | HG02970.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1344-274C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707244 | |||||||
| chr19:49707285 | C | G | 6 | a0001c0001t0001g0162 a0001c0001t0002g0012 a0001c0001t0002g0035 others(3): Show |
7 | HG00735.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344-233C>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707285 | |||||||
| chr19:49707331 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1344-187C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707331 | |||||||
| chr19:49707355 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0269 a0001c0001t0001g0306 |
3 | HG01106.hp2 HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1344-163G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707355 | |||||||
| chr19:49707387 | G | C | 3 | a0001c0001t0003g0062 a0001c0001t0003g0067 a0001c0001t0003g0078 |
3 | HG02970.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1344-131G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 12/19 | chr19 | 49707387 | |||||||
| chr19:49707724 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1449+101C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49707724 | |||||||
| chr19:49707895 | C | T | 1 | a0001c0001t0003g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1449+272C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49707895 | |||||||
| chr19:49707929 | G | A | 1 | a0001c0002t0002g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1449+306G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49707929 | |||||||
| chr19:49708002 | C | CA | 20 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0001g0131 others(17): Show |
22 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1449+404dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | ||||||
| chr19:49708002 | CA | C | 30 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(27): Show |
31 | HG00558.hp1 HG00621.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1449+404delA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | ||||||
| chr19:49708002 | CAA | C | 7 | a0001c0001t0001g0041 a0001c0001t0002g0087 a0001c0002t0002g0206 others(4): Show |
7 | HG01070.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1449+403_1449+404d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | ||||||
| chr19:49708002 | CAAAAA | C | 26 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0176 others(23): Show |
29 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1449+400_1449+404d others(7): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr19 | 49708002 | ||||||
| chr19:49708022 | A | G | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+399A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708022 | |||||||
| chr19:49708227 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0127 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1450-496G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708227 | |||||||
| chr19:49708291 | C | T | 1 | a0001c0001t0005g0057 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1450-432C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708291 | |||||||
| chr19:49708310 | A | C | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450-413A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708310 | |||||||
| chr19:49708338 | A | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0239 |
2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.1450-385A>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708338 | |||||||
| chr19:49708584 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(26): Show |
30 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1450-139G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708584 | |||||||
| chr19:49708662 | G | A | 3 | a0001c0004t0002g0189 a0001c0004t0002g0202 a0001c0004t0002g0203 |
3 | HG01516.hp2 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1450-61G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708662 | |||||||
| chr19:49708715 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.1450-8G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 13/19 | chr19 | 49708715 | |||||||
| chr19:49708945 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1566+106A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49708945 | |||||||
| chr19:49708995 | C | T | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+156C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49708995 | |||||||
| chr19:49709031 | C | T | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1566+192C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709031 | |||||||
| chr19:49709366 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG01070.hp1 HG01255.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1566+527G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709366 | |||||||
| chr19:49709386 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1566+547C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709386 | |||||||
| chr19:49709555 | A | AT | 16 | a0001c0001t0001g0186 a0001c0001t0001g0214 a0001c0001t0001g0257 others(13): Show |
17 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1566+733dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709555 | ||||||
| chr19:49709555 | AT | A | 39 | a0001c0001t0001g0167 a0001c0001t0001g0226 a0001c0001t0001g0304 others(36): Show |
42 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1566+733delT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709555 | ||||||
| chr19:49709767 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1567-553G>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709767 | |||||||
| chr19:49709855 | A | AT | 10 | a0001c0001t0001g0133 a0001c0001t0001g0141 a0001c0001t0001g0166 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1567-455dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709855 | ||||||
| chr19:49709855 | A | ATT | 19 | a0001c0001t0001g0125 a0001c0001t0001g0129 a0001c0001t0001g0176 others(16): Show |
21 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567-456_1567-455d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 49709855 | ||||||
| chr19:49709910 | G | A | 6 | a0001c0002t0002g0206 a0001c0004t0002g0189 a0001c0004t0002g0193 others(3): Show |
6 | HG01516.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-410G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709910 | |||||||
| chr19:49709976 | A | G | 2 | a0001c0001t0004g0222 a0001c0001t0004g0223 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1567-344A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49709976 | |||||||
| chr19:49710075 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1567-245C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710075 | |||||||
| chr19:49710084 | G | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1567-236G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710084 | |||||||
| chr19:49710139 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0079 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1567-181C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710139 | |||||||
| chr19:49710241 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1567-79C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 14/19 | chr19 | 49710241 | |||||||
| chr19:49710921 | G | A | 7 | a0001c0001t0005g0057 a0001c0002t0002g0206 a0001c0004t0002g0189 others(4): Show |
7 | HG01516.hp2 HG02109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1866+64G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49710921 | |||||||
| chr19:49711151 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1866+294T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711151 | |||||||
| chr19:49711167 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1866+310T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711167 | |||||||
| chr19:49711210 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0002g0208 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1866+353C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711210 | |||||||
| chr19:49711260 | A | AT | 99 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0125 others(96): Show |
105 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1866+421dupT | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr19 | 49711260 | ||||||
| chr19:49711260 | A | ATT | 43 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(40): Show |
44 | HG00423.hp2 HG00642.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1866+420_1866+421d others(4): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr19 | 49711260 | ||||||
| chr19:49711296 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1866+439G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711296 | |||||||
| chr19:49711298 | G | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0003g0052 |
3 | HG02615.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1866+441G>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711298 | |||||||
| chr19:49711359 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1867-450G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711359 | |||||||
| chr19:49711396 | T | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0040 a0001c0001t0001g0041 others(129): Show |
140 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.1867-413T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711396 | |||||||
| chr19:49711424 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1867-385A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711424 | |||||||
| chr19:49711567 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(38): Show |
42 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.1867-242A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711567 | |||||||
| chr19:49711580 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1867-229G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711580 | |||||||
| chr19:49711611 | G | A | 43 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0304 others(40): Show |
47 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1867-198G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711611 | |||||||
| chr19:49711644 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(27): Show |
31 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1867-165A>G | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 16/19 | chr19 | 49711644 | |||||||
| chr19:49712010 | G | A | 5 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0305 others(2): Show |
5 | HG02630.hp2 HG02735.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019+49G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712010 | |||||||
| chr19:49712081 | G | A | 37 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(34): Show |
38 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.2019+120G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712081 | |||||||
| chr19:49712110 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2019+149A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712110 | |||||||
| chr19:49712117 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2019+156C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712117 | |||||||
| chr19:49712203 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(35): Show |
39 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.2019+242T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712203 | |||||||
| chr19:49712343 | C | CA | 11 | a0001c0001t0001g0178 a0001c0001t0001g0183 a0001c0001t0001g0184 others(8): Show |
11 | HG00621.hp2 HG01261.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.2020-377dupA | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0005g0082 a0001c0001t0006g0108 |
2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2020-387_2020-377d others(13): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0006g0109 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2019+387_2020-377d others(14): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0145 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2019+386_2020-377d others(15): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(7): Show |
18 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0137 others(15): Show |
19 | HG01175.hp1 HG01975.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.2019+385_2020-377d others(16): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0150 others(3): Show |
6 | HG02015.hp1 HG02080.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2019+384_2020-377d others(17): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0133 a0001c0001t0001g0141 a0001c0001t0001g0153 others(1): Show |
4 | HG00558.hp2 HG00609.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019+383_2020-377d others(18): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712343 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2020-377_2020-376i others(19): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712343 | ||||||
| chr19:49712385 | G | A | 1 | a0001c0006t0001g0151 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2020-351G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712385 | |||||||
| chr19:49712446 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2020-290A>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712446 | |||||||
| chr19:49712483 | G | A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0045 a0001c0001t0002g0046 others(11): Show |
16 | HG00423.hp2 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.2020-253G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712483 | |||||||
| chr19:49712510 | G | A | 1 | a0002c0003t0001g0232 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2020-226G>A | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712510 | |||||||
| chr19:49712545 | CGTGGGT | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0133 others(34): Show |
38 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.2020-183_2020-178d others(8): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 49712545 | ||||||
| chr19:49712700 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0229 a0001c0001t0001g0294 others(1): Show |
5 | HG02056.hp1 HG02074.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.2020-36C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 17/19 | chr19 | 49712700 | |||||||
| chr19:49713130 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2226+66C>T | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | chr19 | 49713130 | |||||||
| chr19:49713185 | A | AGGAGTCC others(67): Show |
1 | a0001c0001t0001g0250 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2226+156_2227-127d others(76): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr19 | 49713185 | ||||||
| chr19:49713185 | AGGAGTCC others(30): Show |
A | 2 | a0001c0002t0002g0198 a0002c0003t0001g0142 |
2 | HG01192.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.2227-163_2227-127d others(39): Show |
CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr19 | 49713185 | ||||||
| chr19:49713314 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2227-106T>C | CPT1C | ENSG00000169169.15 | transcript | ENST00000598293.6 | protein_coding | 19/19 | chr19 | 49713314 |