Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57799 |
| ensemblid | ENSG00000197562.10 |
| hgncid | 18285 |
| symbol | RAB40C |
| name | RAB40C, member RAS oncogene family |
| refseq_nuc | NM_021168.5 |
| refseq_prot | NP_066991.3 |
| ensembl_nuc | ENST00000248139.8 |
| ensembl_prot | ENSP00000248139.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 590066 |
| end | 629268 |
| strand | + |
| ver | v1.2 |
| region | chr16:590066-629268 |
| region5000 | chr16:585066-634268 |
| regionname0 | RAB40C_chr16_590066_629268 |
| regionname5000 | RAB40C_chr16_585066_634268 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 281 | 349 | 94 | 70 | 125 | 12 | 46 | 93 | RAB40C_chr16_585066_634268 | RAB40C | MGSQG others(276): Show |
chr16 | 585066 | 634268 |
| a0002 | 0/0 | 281 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | MGSQG others(276): Show |
chr16 | 585066 | 634268 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 843 | 346 | 92 | 70 | 124 | 12 | 46 | RAB40C_chr16_585066_634268 | RAB40C | ATGGG others(838): Show |
chr16 | 585066 | 634268 | ||
| a0001c0003 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | ATGGG others(838): Show |
chr16 | 585066 | 634268 | ||
| a0001c0004 | 0/0 | 843 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | ATGGG others(838): Show |
chr16 | 585066 | 634268 | ||
| a0001c0005 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | ATGGG others(838): Show |
chr16 | 585066 | 634268 | ||
| a0002c0002 | 0/0 | 843 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | ATGGG others(838): Show |
chr16 | 585066 | 634268 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2718 | 135 | 40 | 33 | 45 | 4 | 11 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0002 | 0/0 | 2718 | 105 | 3 | 25 | 56 | 3 | 18 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0003 | 0/0 | 2718 | 48 | 16 | 5 | 11 | 3 | 13 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0004 | 0/0 | 2715 | 10 | 8 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2710): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0005 | 0/0 | 2718 | 5 | 1 | 1 | 2 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0006 | 0/0 | 2718 | 5 | 4 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0007 | 0/0 | 2718 | 5 | 5 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0008 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2710): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0009 | 0/0 | 2718 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0010 | 0/0 | 2718 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0011 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0012 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2710): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0013 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2710): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0014 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0015 | 0/0 | 2718 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0016 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0017 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0018 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0019 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0020 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0021 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2710): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0022 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0025 | 0/0 | 2718 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0026 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0027 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0028 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0029 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0030 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0031 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0032 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0033 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2729): Show |
chr16 | 585066 | 634268 |
| a0001c0001t0034 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0003t0001 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0001c0004t0023 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2710): Show |
chr16 | 585066 | 634268 |
| a0001c0005t0001 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| a0002c0002t0024 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | GCGGC others(2713): Show |
chr16 | 585066 | 634268 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0009g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0009g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0011g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0012g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0013g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0014g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0015g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0015g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0016g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0018g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0019g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0020g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0021g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0022g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0025g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0026g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0027g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0028g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0029g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0030g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0031g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0032g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0033g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0001t0034g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0004t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0001c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| a0002c0002t0024g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0225 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0206 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00140 | hp2 | a0001 | c0001 | t0026 | g0007 | EUR | GBR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0281 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0305 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0226 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0207 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01255 | hp1 | a0001 | c0001 | t0015 | g0104 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01256 | hp1 | a0001 | c0001 | t0025 | g0004 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01496 | hp1 | a0001 | c0001 | t0015 | g0005 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01884 | hp2 | a0001 | c0001 | t0031 | g0156 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02083 | hp1 | a0001 | c0001 | t0017 | g0235 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02132 | hp2 | a0001 | c0001 | t0022 | g0012 | EAS | KHV | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CDX | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0325 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0321 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0193 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02622 | hp2 | a0001 | c0001 | t0033 | g0061 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0150 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0219 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02970 | hp2 | a0001 | c0001 | t0029 | g0183 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0151 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03041 | hp2 | a0001 | c0001 | t0013 | g0021 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0167 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0031 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03195 | hp2 | a0001 | c0004 | t0023 | g0038 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03579 | hp1 | a0001 | c0001 | t0028 | g0030 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03704 | hp1 | a0001 | c0001 | t0019 | g0292 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0322 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | BEB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | STU | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0153 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18954 | hp1 | a0001 | c0001 | t0011 | g0307 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18961 | hp2 | a0001 | c0001 | t0014 | g0116 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18963 | hp2 | a0001 | c0001 | t0016 | g0326 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18971 | hp2 | a0001 | c0001 | t0011 | g0295 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18973 | hp2 | a0001 | c0001 | t0032 | g0017 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18982 | hp2 | a0001 | c0001 | t0030 | g0199 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19000 | hp2 | a0001 | c0001 | t0018 | g0089 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19001 | hp2 | a0002 | c0002 | t0024 | g0229 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19002 | hp1 | a0001 | c0001 | t0014 | g0073 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19043 | hp2 | a0001 | c0001 | t0021 | g0180 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19084 | hp2 | a0001 | c0005 | t0001 | g0053 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ASW | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20805 | hp2 | a0001 | c0001 | t0027 | g0146 | EUR | TSI | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | GIH | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | GIH | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0327 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | USA | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0105 | REF | REF | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0121 | REF | REF | RAB40C_chr16_585066_634268 | RAB40C | chr16 | 585066 | 634268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:627519 | G | T | 1 | a0002 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.743G>T | p.Gly248Val | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 969/2718 | 743/846 | 248/281 | chr16 | 627519 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:590315 | G | T | 1 | a0001c0005 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.24G>T | p.Val8Val | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 250/2718 | 24/846 | 8/281 | chr16 | 590315 | |||
| chr16:617212 | C | T | 1 | a0001c0004 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.147C>T | p.Ile49Ile | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/6 | 373/2718 | 147/846 | 49/281 | chr16 | 617212 | |||
| chr16:627511 | C | T | 1 | a0001c0003 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.735C>T | p.Ser245Ser | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 961/2718 | 735/846 | 245/281 | chr16 | 627511 | |||
| chr16:627517 | C | G | 1 | a0002c0002 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.741C>G | p.Ala247Ala | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 967/2718 | 741/846 | 247/281 | chr16 | 627517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:590087 | T | A | 1 | a0001c0001t0005 | 5 | HG00738.hp1 HG02683.hp1 NA18982.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-205T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 205 | chr16 | 590087 | ||||||
| chr16:590131 | C | A | 1 | a0001c0001t0016 | 1 | NA18963.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 161 | chr16 | 590131 | ||||||
| chr16:590138 | G | A | 1 | a0001c0001t0017 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 154 | chr16 | 590138 | ||||||
| chr16:590186 | G | A | 1 | a0001c0001t0018 | 1 | NA19000.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 106 | chr16 | 590186 | ||||||
| chr16:590192 | A | G | 1 | a0001c0001t0034 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 100 | chr16 | 590192 | ||||||
| chr16:590245 | G | A | 1 | a0001c0001t0008 | 2 | HG02258.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-47G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 47 | chr16 | 590245 | ||||||
| chr16:590265 | C | CCGGCGCG others(9): Show |
1 | a0001c0001t0033 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18_-3dupGGCGCAGGC others(7): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/6 | 2 | INFO_REALIGN_3_PRIME | chr16 | 590265 | |||||
| chr16:627629 | T | C | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(12): Show |
134 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 7 | chr16 | 627629 | ||||||
| chr16:627740 | G | A | 1 | a0001c0001t0009 | 2 | HG02602.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*118G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 118 | chr16 | 627740 | ||||||
| chr16:627770 | C | G | 1 | a0001c0001t0013 | 2 | HG02970.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*148C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 148 | chr16 | 627770 | ||||||
| chr16:627770 | C | T | 3 | a0001c0001t0004 a0001c0001t0008 a0001c0004t0023 |
13 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*148C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 148 | chr16 | 627770 | ||||||
| chr16:627854 | G | T | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*232G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 232 | chr16 | 627854 | ||||||
| chr16:628020 | G | A | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(4): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*398G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 398 | chr16 | 628020 | ||||||
| chr16:628044 | A | G | 1 | a0001c0001t0022 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 422 | chr16 | 628044 | ||||||
| chr16:628116 | T | G | 1 | a0001c0001t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 494 | chr16 | 628116 | ||||||
| chr16:628174 | G | C | 1 | a0001c0001t0019 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 552 | chr16 | 628174 | ||||||
| chr16:628264 | C | G | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(3): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*642C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 642 | chr16 | 628264 | ||||||
| chr16:628304 | G | A | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(3): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*682G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 682 | chr16 | 628304 | ||||||
| chr16:628336 | CCTT | C | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(3): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*718delTTC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 716 | INFO_REALIGN_3_PRIME | chr16 | 628336 | |||||
| chr16:628430 | C | T | 1 | a0001c0001t0015 | 2 | HG01255.hp1 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*808C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 808 | chr16 | 628430 | ||||||
| chr16:628433 | T | C | 1 | a0001c0001t0021 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 811 | chr16 | 628433 | ||||||
| chr16:628443 | G | A | 1 | a0001c0001t0010 | 2 | HG02257.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 821 | chr16 | 628443 | ||||||
| chr16:628497 | T | C | 1 | a0002c0002t0024 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*875T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 875 | chr16 | 628497 | ||||||
| chr16:628531 | G | A | 1 | a0001c0001t0011 | 2 | NA18954.hp1 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*909G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 909 | chr16 | 628531 | ||||||
| chr16:628568 | T | C | 1 | a0001c0001t0014 | 2 | NA18961.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*946T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 946 | chr16 | 628568 | ||||||
| chr16:628592 | G | A | 1 | a0001c0001t0029 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*970G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 970 | chr16 | 628592 | ||||||
| chr16:628678 | G | A | 1 | a0001c0001t0032 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1056G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1056 | chr16 | 628678 | ||||||
| chr16:628821 | G | A | 1 | a0001c0001t0030 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1199 | chr16 | 628821 | ||||||
| chr16:628841 | C | G | 2 | a0001c0001t0010 a0001c0001t0020 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1219C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1219 | chr16 | 628841 | ||||||
| chr16:628843 | C | T | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(14): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1221C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1221 | chr16 | 628843 | ||||||
| chr16:628877 | C | T | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(3): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1255C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1255 | chr16 | 628877 | ||||||
| chr16:628879 | T | C | 3 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0031 |
7 | HG01884.hp2 HG01981.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1257T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1257 | chr16 | 628879 | ||||||
| chr16:628907 | A | C | 1 | a0001c0001t0027 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1285 | chr16 | 628907 | ||||||
| chr16:628907 | A | T | 1 | a0001c0001t0004 | 10 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1285A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1285 | chr16 | 628907 | ||||||
| chr16:628980 | G | A | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(3): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1358G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1358 | chr16 | 628980 | ||||||
| chr16:629147 | T | C | 1 | a0001c0001t0025 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1525T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1525 | chr16 | 629147 | ||||||
| chr16:629241 | G | T | 1 | a0001c0001t0026 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1619G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 6/6 | 1619 | chr16 | 629241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:590440 | C | T | 2 | a0001c0001t0002g0330 a0001c0001t0002g0331 |
2 | HG00639.hp1 HG00741.hp1 |
splice_region_variant&intron_variant | LOW | c.142+7C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590440 | |||||||
| chr16:590459 | T | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 |
4 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+26T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590459 | |||||||
| chr16:590590 | G | T | 1 | a0001c0001t0001g0329 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.142+157G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590590 | |||||||
| chr16:590923 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.142+490C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590923 | |||||||
| chr16:590949 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.142+516A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590949 | |||||||
| chr16:590968 | A | G | 1 | a0001c0001t0004g0327 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+535A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 590968 | |||||||
| chr16:591004 | A | AGGAAGGT others(210): Show |
3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0032g0017 |
3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+606_142+822dup others(217): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 591004 | ||||||
| chr16:591004 | A | T | 1 | a0001c0001t0016g0326 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+571A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591004 | |||||||
| chr16:591044 | A | G | 165 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(162): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.142+611A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591044 | |||||||
| chr16:591098 | G | A | 6 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+665G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591098 | |||||||
| chr16:591134 | T | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | NA18981.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.142+701T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591134 | |||||||
| chr16:591164 | G | T | 165 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(162): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.142+731G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591164 | |||||||
| chr16:591174 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142+741G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591174 | |||||||
| chr16:591193 | G | C | 1 | a0001c0001t0016g0326 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+760G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591193 | |||||||
| chr16:591209 | C | T | 13 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0004g0157 others(10): Show |
13 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+776C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591209 | |||||||
| chr16:591217 | TCA | T | 6 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+785_142+786del others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591217 | |||||||
| chr16:591258 | A | G | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+825A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591258 | |||||||
| chr16:591260 | G | A | 59 | a0001c0001t0001g0222 a0001c0001t0002g0178 a0001c0001t0003g0011 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.142+827G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591260 | |||||||
| chr16:591392 | C | T | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+959C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591392 | |||||||
| chr16:591445 | G | T | 105 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(102): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.142+1012G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591445 | |||||||
| chr16:591471 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+1038T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591471 | |||||||
| chr16:591486 | C | G | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+1053C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591486 | |||||||
| chr16:591486 | C | T | 24 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+1053C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591486 | |||||||
| chr16:591514 | G | A | 1 | a0001c0001t0013g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142+1081G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591514 | |||||||
| chr16:591544 | C | G | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+1111C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591544 | |||||||
| chr16:591582 | C | G | 3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0034g0151 |
3 | HG02280.hp2 HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.142+1149C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591582 | |||||||
| chr16:591587 | C | G | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+1154C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591587 | |||||||
| chr16:591596 | C | CT | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0007g0152 others(3): Show |
6 | HG02622.hp1 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+1177dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 591596 | ||||||
| chr16:591596 | CT | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG00140.hp1 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1177delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 591596 | ||||||
| chr16:591702 | C | G | 2 | a0001c0001t0003g0204 a0001c0001t0003g0205 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142+1269C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591702 | |||||||
| chr16:591744 | A | T | 3 | a0001c0001t0006g0166 a0001c0001t0006g0167 a0001c0001t0006g0168 |
3 | HG01981.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.142+1311A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591744 | |||||||
| chr16:591899 | C | T | 2 | a0001c0001t0003g0204 a0001c0001t0003g0205 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142+1466C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591899 | |||||||
| chr16:591926 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.142+1493G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591926 | |||||||
| chr16:591927 | C | T | 1 | a0001c0001t0027g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.142+1494C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 591927 | |||||||
| chr16:592062 | G | C | 2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | NA18997.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.142+1629G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592062 | |||||||
| chr16:592222 | C | T | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+1789C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592222 | |||||||
| chr16:592249 | T | C | 200 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(197): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.142+1816T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592249 | |||||||
| chr16:592610 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(221): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.142+2177T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592610 | |||||||
| chr16:592761 | G | A | 1 | a0001c0001t0033g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142+2328G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592761 | |||||||
| chr16:592829 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.142+2396C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592829 | |||||||
| chr16:592845 | C | G | 3 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0016g0326 |
3 | HG02083.hp2 NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.142+2412C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592845 | |||||||
| chr16:592910 | T | A | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+2477T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 592910 | |||||||
| chr16:593027 | C | T | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+2594C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593027 | |||||||
| chr16:593064 | G | A | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.142+2631G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593064 | |||||||
| chr16:593090 | G | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+2657G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593090 | |||||||
| chr16:593098 | C | T | 51 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0179 others(48): Show |
52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.142+2665C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593098 | |||||||
| chr16:593151 | G | A | 18 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0004g0157 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+2718G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593151 | |||||||
| chr16:593156 | CAGCACAA | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0032g0017 |
3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+2724_142+2730d others(9): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593156 | |||||||
| chr16:593236 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.142+2803G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593236 | |||||||
| chr16:593264 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.142+2831A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593264 | |||||||
| chr16:593318 | G | T | 2 | a0001c0001t0009g0321 a0001c0001t0009g0322 |
2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.142+2885G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593318 | |||||||
| chr16:593338 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.142+2905G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593338 | |||||||
| chr16:593402 | G | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+2969G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593402 | |||||||
| chr16:593760 | G | T | 2 | a0001c0001t0005g0227 a0001c0001t0005g0228 |
2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.142+3327G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593760 | |||||||
| chr16:593873 | A | G | 6 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+3440A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593873 | |||||||
| chr16:593894 | G | A | 4 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0227 others(1): Show |
4 | HG00738.hp1 NA18982.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+3461G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 593894 | |||||||
| chr16:594048 | C | T | 105 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(102): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.142+3615C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594048 | |||||||
| chr16:594088 | G | C | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+3655G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594088 | |||||||
| chr16:594135 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.142+3702C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594135 | |||||||
| chr16:594180 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.142+3747C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594180 | |||||||
| chr16:594288 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0032g0017 |
3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+3855G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594288 | |||||||
| chr16:594344 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.142+3911G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594344 | |||||||
| chr16:594393 | G | A | 29 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0179 others(26): Show |
30 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.142+3960G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594393 | |||||||
| chr16:594438 | G | A | 6 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+4005G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594438 | |||||||
| chr16:594494 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.142+4061C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594494 | |||||||
| chr16:594502 | C | T | 1 | a0001c0001t0002g0320 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.142+4069C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594502 | |||||||
| chr16:594612 | C | G | 2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+4179C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594612 | |||||||
| chr16:594818 | C | CT | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0147 others(9): Show |
12 | HG00673.hp2 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+4405dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 594818 | ||||||
| chr16:594818 | CT | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
9 | HG01070.hp2 HG02897.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+4405delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 594818 | ||||||
| chr16:594824 | T | TC | 55 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.142+4391_142+4392i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594824 | |||||||
| chr16:594825 | T | C | 2 | a0001c0001t0003g0185 a0001c0001t0005g0227 |
2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.142+4392T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594825 | |||||||
| chr16:594842 | C | G | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+4409C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594842 | |||||||
| chr16:594860 | C | T | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.142+4427C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594860 | |||||||
| chr16:594907 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.142+4474C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 594907 | |||||||
| chr16:595071 | G | A | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | HG00733.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.142+4638G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595071 | |||||||
| chr16:595148 | T | A | 1 | a0001c0001t0003g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.142+4715T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595148 | |||||||
| chr16:595201 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0003g0179 a0001c0001t0003g0184 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+4768C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595201 | |||||||
| chr16:595243 | G | C | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+4810G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595243 | |||||||
| chr16:595371 | G | A | 1 | a0001c0001t0017g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.142+4938G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595371 | |||||||
| chr16:595382 | G | C | 1 | a0001c0001t0003g0209 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.142+4949G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595382 | |||||||
| chr16:595473 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142+5040G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595473 | |||||||
| chr16:595603 | C | CT | 59 | a0001c0001t0001g0143 a0001c0001t0001g0222 a0001c0001t0001g0329 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.142+5187dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 595603 | ||||||
| chr16:595603 | CT | C | 14 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0040 others(11): Show |
14 | HG00323.hp2 HG00738.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.142+5187delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 595603 | ||||||
| chr16:595606 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+5173T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595606 | |||||||
| chr16:595671 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0143 |
3 | HG02080.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.142+5238C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595671 | |||||||
| chr16:595852 | C | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0003g0200 others(4): Show |
7 | HG01993.hp2 HG02148.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+5419C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595852 | |||||||
| chr16:595968 | C | T | 188 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(185): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.142+5535C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595968 | |||||||
| chr16:595969 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0032g0017 |
3 | HG01993.hp2 HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.142+5536A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595969 | |||||||
| chr16:595997 | G | A | 21 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(18): Show |
21 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.142+5564G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 595997 | |||||||
| chr16:596233 | C | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+5800C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596233 | |||||||
| chr16:596246 | G | A | 53 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(50): Show |
54 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.142+5813G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596246 | |||||||
| chr16:596251 | G | A | 1 | a0001c0001t0021g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+5818G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596251 | |||||||
| chr16:596257 | A | G | 16 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(13): Show |
16 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.142+5824A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596257 | |||||||
| chr16:596336 | G | A | 1 | a0001c0001t0021g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+5903G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596336 | |||||||
| chr16:596388 | G | A | 23 | a0001c0001t0001g0072 a0001c0001t0001g0158 a0001c0001t0001g0163 others(20): Show |
23 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.142+5955G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596388 | |||||||
| chr16:596421 | A | G | 128 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0002g0012 others(125): Show |
130 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.142+5988A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596421 | |||||||
| chr16:596452 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.142+6019C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596452 | |||||||
| chr16:596473 | C | T | 1 | a0001c0001t0007g0154 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142+6040C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596473 | |||||||
| chr16:596520 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+6087C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596520 | |||||||
| chr16:596520 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.142+6087C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596520 | |||||||
| chr16:596521 | G | A | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+6088G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596521 | |||||||
| chr16:596547 | G | A | 6 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+6114G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596547 | |||||||
| chr16:596571 | A | G | 106 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(103): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.142+6138A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596571 | |||||||
| chr16:596606 | T | G | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+6173T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596606 | |||||||
| chr16:596639 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(12): Show |
17 | HG00639.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.142+6206C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596639 | |||||||
| chr16:596865 | C | G | 80 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(77): Show |
81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.142+6432C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 596865 | |||||||
| chr16:597006 | G | A | 103 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(100): Show |
105 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.142+6573G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597006 | |||||||
| chr16:597094 | A | G | 24 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+6661A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597094 | |||||||
| chr16:597231 | G | A | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+6798G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597231 | |||||||
| chr16:597335 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.142+6902G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597335 | |||||||
| chr16:597346 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.142+6913A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597346 | |||||||
| chr16:597383 | G | A | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+6950G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597383 | |||||||
| chr16:597438 | A | G | 1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.142+7005A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597438 | |||||||
| chr16:597506 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.142+7073C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597506 | |||||||
| chr16:597519 | C | A | 6 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+7086C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597519 | |||||||
| chr16:597752 | G | C | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+7319G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597752 | |||||||
| chr16:597793 | C | G | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+7360C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597793 | |||||||
| chr16:597820 | G | T | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+7387G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597820 | |||||||
| chr16:597834 | C | T | 1 | a0002c0002t0024g0229 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.142+7401C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597834 | |||||||
| chr16:597875 | C | T | 2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+7442C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597875 | |||||||
| chr16:597937 | C | CA | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(117): Show |
122 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.142+7531dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | ||||||
| chr16:597937 | C | CAA | 50 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0019 others(47): Show |
51 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.142+7530_142+7531d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | ||||||
| chr16:597937 | C | CAAA | 8 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(5): Show |
8 | HG00438.hp2 HG01361.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+7529_142+7531d others(5): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | ||||||
| chr16:597937 | CA | C | 21 | a0001c0001t0001g0124 a0001c0001t0001g0222 a0001c0001t0003g0011 others(18): Show |
22 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+7531delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 597937 | ||||||
| chr16:597969 | G | A | 1 | a0001c0001t0016g0326 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+7536G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597969 | |||||||
| chr16:597975 | A | G | 1 | a0001c0001t0016g0326 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.142+7542A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 597975 | |||||||
| chr16:598014 | A | G | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+7581A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598014 | |||||||
| chr16:598072 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+7639C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598072 | |||||||
| chr16:598203 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
15 | HG00408.hp1 HG00544.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.142+7770C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598203 | |||||||
| chr16:598376 | CA | C | 190 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0136 others(187): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.142+7958delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 598376 | ||||||
| chr16:598384 | A | G | 1 | a0001c0001t0003g0173 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+7951A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598384 | |||||||
| chr16:598402 | A | G | 4 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0004g0181 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+7969A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598402 | |||||||
| chr16:598515 | T | C | 59 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.142+8082T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598515 | |||||||
| chr16:598542 | A | C | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.142+8109A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598542 | |||||||
| chr16:598547 | G | A | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.142+8114G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598547 | |||||||
| chr16:598561 | C | CA | 20 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(17): Show |
20 | HG01109.hp2 HG01175.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.142+8147dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 598561 | ||||||
| chr16:598561 | CA | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0122 others(2): Show |
6 | HG01106.hp1 HG01168.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+8147delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 598561 | ||||||
| chr16:598575 | A | G | 55 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.142+8142A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598575 | |||||||
| chr16:598577 | A | G | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.142+8144A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598577 | |||||||
| chr16:598605 | G | C | 1 | a0001c0001t0002g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.142+8172G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598605 | |||||||
| chr16:598826 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.142+8393G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598826 | |||||||
| chr16:598856 | G | A | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+8423G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598856 | |||||||
| chr16:598873 | G | A | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+8440G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 598873 | |||||||
| chr16:599132 | C | T | 1 | a0001c0001t0002g0330 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.142+8699C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599132 | |||||||
| chr16:599173 | G | T | 1 | a0001c0001t0002g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.142+8740G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599173 | |||||||
| chr16:599255 | G | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+8822G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599255 | |||||||
| chr16:599264 | C | T | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+8831C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599264 | |||||||
| chr16:599270 | G | A | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.142+8837G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599270 | |||||||
| chr16:599272 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.142+8839G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599272 | |||||||
| chr16:599308 | C | G | 1 | a0001c0001t0003g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142+8875C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599308 | |||||||
| chr16:599320 | C | T | 2 | a0001c0001t0006g0028 a0001c0001t0028g0030 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.142+8887C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599320 | |||||||
| chr16:599454 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+9021C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599454 | |||||||
| chr16:599524 | G | A | 3 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 |
3 | HG02280.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.142+9091G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599524 | |||||||
| chr16:599555 | TGTCAGCG others(35): Show |
T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+9151_142+9192d others(44): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599555 | ||||||
| chr16:599588 | C | T | 21 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0003g0155 others(18): Show |
21 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.142+9155C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599588 | |||||||
| chr16:599612 | A | AGCAAGGT others(34): Show |
1 | a0001c0001t0007g0154 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.142+9192_142+9193i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599612 | ||||||
| chr16:599618 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.142+9185G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599618 | |||||||
| chr16:599626 | A | C | 1 | a0001c0001t0002g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+9193A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599626 | |||||||
| chr16:599638 | T | C | 195 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(192): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.142+9205T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599638 | |||||||
| chr16:599640 | A | G | 2 | a0001c0001t0002g0306 a0001c0001t0007g0154 |
2 | HG01993.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.142+9207A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599640 | |||||||
| chr16:599653 | C | CGCAAGGT others(33): Show |
1 | a0001c0001t0002g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+9220_142+9221i others(42): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599653 | |||||||
| chr16:599654 | A | AGCAAGGT others(34): Show |
3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0314 |
3 | NA18981.hp2 NA19054.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.142+9238_142+9239i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599654 | ||||||
| chr16:599654 | A | AGCAAGGT others(75): Show |
104 | a0001c0001t0001g0020 a0001c0001t0001g0124 a0001c0001t0002g0012 others(101): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.142+9238_142+9239i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599654 | ||||||
| chr16:599654 | A | AGCAAGGT others(75): Show |
1 | a0001c0001t0002g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.142+9238_142+9239i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599654 | ||||||
| chr16:599654 | A | C | 1 | a0001c0001t0002g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+9221A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599654 | |||||||
| chr16:599668 | C | CCCTCGTG others(34): Show |
1 | a0001c0001t0002g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.142+9238_142+9239i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599668 | ||||||
| chr16:599672 | T | C | 111 | a0001c0001t0001g0020 a0001c0001t0001g0124 a0001c0001t0002g0012 others(108): Show |
113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.142+9239T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599672 | |||||||
| chr16:599672 | T | TGTGGCAT others(34): Show |
41 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(38): Show |
47 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.142+9275_142+9276i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(75): Show |
86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
91 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.142+9275_142+9276i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(116): Show |
1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.142+9275_142+9276i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(157): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0142 |
2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142+9275_142+9276i others(166): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(75): Show |
1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.142+9275_142+9276i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(75): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0021g0180 |
4 | HG01167.hp2 HG01169.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+9549_142+9630d others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(34): Show |
14 | a0001c0001t0006g0028 a0001c0001t0007g0034 a0001c0001t0007g0152 others(11): Show |
14 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.142+9261_142+9262i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(117): Show |
1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+9261_142+9262i others(126): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(75): Show |
2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+9261_142+9262i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | T | TGTGGCAT others(116): Show |
1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+9261_142+9262i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599672 | TGTGGCAT others(34): Show |
T | 63 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+9590_142+9630d others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599672 | ||||||
| chr16:599695 | C | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+9262C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599695 | |||||||
| chr16:599696 | G | A | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+9263G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599696 | |||||||
| chr16:599709 | C | A | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+9276C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599709 | |||||||
| chr16:599736 | C | T | 63 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+9303C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599736 | |||||||
| chr16:599750 | C | A | 63 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+9317C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599750 | |||||||
| chr16:599823 | G | GGTTTTGT others(75): Show |
2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+9471_142+9472i others(84): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599823 | ||||||
| chr16:599952 | G | T | 24 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.142+9519G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 599952 | |||||||
| chr16:599983 | G | GCAAGGTT others(34): Show |
3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+9590_142+9591i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 599983 | ||||||
| chr16:600001 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.142+9568G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600001 | |||||||
| chr16:600024 | G | GCAAGGTT others(34): Show |
1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+9630_142+9631i others(43): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 600024 | ||||||
| chr16:600064 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+9631T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600064 | |||||||
| chr16:600069 | A | G | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+9636A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600069 | |||||||
| chr16:600440 | T | TTA | 52 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.142+10008_142+1000 others(6): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 600440 | ||||||
| chr16:600479 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142+10046A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600479 | |||||||
| chr16:600554 | C | G | 3 | a0001c0001t0006g0028 a0001c0001t0007g0034 a0001c0001t0028g0030 |
3 | HG03225.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142+10121C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600554 | |||||||
| chr16:600562 | C | G | 2 | a0001c0001t0002g0246 a0001c0001t0002g0247 |
2 | NA18981.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.142+10129C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600562 | |||||||
| chr16:600579 | C | T | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142+10146C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600579 | |||||||
| chr16:600683 | C | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+10250C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600683 | |||||||
| chr16:600708 | C | T | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+10275C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600708 | |||||||
| chr16:600783 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142+10350C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600783 | |||||||
| chr16:600788 | G | A | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.142+10355G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 600788 | |||||||
| chr16:601065 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02486.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+10632C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601065 | |||||||
| chr16:601113 | T | C | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+10680T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601113 | |||||||
| chr16:601115 | G | T | 192 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.142+10682G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601115 | |||||||
| chr16:601137 | C | G | 1 | a0001c0001t0007g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142+10704C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601137 | |||||||
| chr16:601193 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.142+10760A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601193 | |||||||
| chr16:601221 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.142+10788G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601221 | |||||||
| chr16:601279 | G | C | 192 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.142+10846G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601279 | |||||||
| chr16:601438 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+11005G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601438 | |||||||
| chr16:601495 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.142+11062G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601495 | |||||||
| chr16:601515 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.142+11082C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601515 | |||||||
| chr16:601517 | C | T | 108 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+11084C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601517 | |||||||
| chr16:601538 | G | A | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+11105G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601538 | |||||||
| chr16:601738 | A | G | 8 | a0001c0001t0003g0185 a0001c0001t0003g0197 a0001c0001t0003g0198 others(5): Show |
8 | NA18963.hp1 NA18967.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+11305A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601738 | |||||||
| chr16:601785 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.142+11352G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601785 | |||||||
| chr16:601815 | T | TA | 81 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0040 others(78): Show |
81 | HG00621.hp1 HG00621.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.142+11412dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601815 | T | TAA | 14 | a0001c0001t0002g0108 a0001c0001t0002g0275 a0001c0001t0002g0279 others(11): Show |
14 | HG00280.hp1 HG00673.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+11411_142+1141 others(6): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601815 | T | TAAAAAAA others(18): Show |
1 | a0001c0001t0002g0306 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142+11388_142+1141 others(29): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601815 | T | TAAAAAAA others(20): Show |
2 | a0001c0001t0002g0277 a0001c0001t0002g0278 |
2 | HG01255.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.142+11386_142+1141 others(31): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601815 | T | TAAAAAAA others(23): Show |
2 | a0001c0001t0002g0253 a0001c0001t0002g0331 |
2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.142+11383_142+1141 others(34): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601815 | T | TAAAAAAA others(25): Show |
1 | a0001c0001t0002g0330 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.142+11412_142+1141 others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601815 | TA | T | 87 | a0001c0001t0001g0022 a0001c0001t0001g0163 a0001c0001t0002g0012 others(84): Show |
89 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.142+11412delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 601815 | ||||||
| chr16:601850 | G | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+11417G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601850 | |||||||
| chr16:601909 | C | T | 1 | a0001c0001t0002g0304 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.142+11476C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601909 | |||||||
| chr16:601954 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0135 |
2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142+11521C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601954 | |||||||
| chr16:601960 | T | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+11527T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 601960 | |||||||
| chr16:602045 | C | G | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+11612C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602045 | |||||||
| chr16:602195 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0113 |
2 | HG00621.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.142+11762T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602195 | |||||||
| chr16:602214 | G | A | 3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0021g0180 |
3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.142+11781G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602214 | |||||||
| chr16:602218 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.142+11785T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602218 | |||||||
| chr16:602228 | C | T | 3 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0016g0326 |
3 | HG02083.hp2 NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.142+11795C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602228 | |||||||
| chr16:602248 | G | GT | 112 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0002g0012 others(109): Show |
114 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.142+11828dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 602248 | ||||||
| chr16:602268 | G | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+11835G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602268 | |||||||
| chr16:602572 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+12139G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602572 | |||||||
| chr16:602618 | A | G | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+12185A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602618 | |||||||
| chr16:602623 | A | G | 195 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(192): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.142+12190A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602623 | |||||||
| chr16:602638 | G | C | 2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+12205G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602638 | |||||||
| chr16:602639 | G | C | 2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.142+12206G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602639 | |||||||
| chr16:602941 | G | A | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+12508G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602941 | |||||||
| chr16:602999 | A | G | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142+12566A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 602999 | |||||||
| chr16:603051 | A | G | 108 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.142+12618A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603051 | |||||||
| chr16:603095 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+12662T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603095 | |||||||
| chr16:603110 | ATGTTCTG others(17): Show |
A | 1 | a0001c0001t0002g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.142+12681_142+1270 others(28): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 603110 | ||||||
| chr16:603265 | T | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+12832T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603265 | |||||||
| chr16:603298 | A | AT | 6 | a0001c0001t0003g0206 a0001c0001t0003g0211 a0001c0001t0003g0216 others(3): Show |
6 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+12868dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 603298 | ||||||
| chr16:603739 | T | C | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+13306T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603739 | |||||||
| chr16:603768 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.142+13335C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603768 | |||||||
| chr16:603773 | T | TCAGCCCC | 109 | a0001c0001t0001g0003 a0001c0001t0002g0012 a0001c0001t0002g0013 others(106): Show |
112 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.142+13352_142+1335 others(11): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 603773 | ||||||
| chr16:603925 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-13283C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 603925 | |||||||
| chr16:604042 | G | A | 1 | a0001c0001t0002g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-13166G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604042 | |||||||
| chr16:604061 | C | CT | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-13133dupT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 604061 | ||||||
| chr16:604200 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0163 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.143-13008A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604200 | |||||||
| chr16:604216 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.143-12992G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604216 | |||||||
| chr16:604224 | G | A | 192 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.143-12984G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604224 | |||||||
| chr16:604238 | AT | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.143-12959delT | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 604238 | ||||||
| chr16:604249 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.143-12959T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604249 | |||||||
| chr16:604269 | T | C | 2 | a0001c0001t0010g0032 a0001c0001t0010g0035 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.143-12939T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604269 | |||||||
| chr16:604280 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0047 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.143-12928C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604280 | |||||||
| chr16:604297 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.143-12911G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604297 | |||||||
| chr16:604319 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.143-12889C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604319 | |||||||
| chr16:604332 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.143-12876A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604332 | |||||||
| chr16:604349 | G | A | 14 | a0001c0001t0003g0185 a0001c0001t0003g0187 a0001c0001t0003g0192 others(11): Show |
14 | HG01433.hp2 HG02129.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-12859G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604349 | |||||||
| chr16:604425 | C | A | 1 | a0001c0001t0002g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.143-12783C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604425 | |||||||
| chr16:604447 | T | C | 1 | a0001c0001t0008g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-12761T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604447 | |||||||
| chr16:604449 | T | C | 1 | a0001c0001t0008g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-12759T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604449 | |||||||
| chr16:604459 | T | A | 2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.143-12749T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604459 | |||||||
| chr16:604491 | CCTT | C | 24 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.143-12714_143-1271 others(7): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 604491 | ||||||
| chr16:604665 | C | T | 1 | a0001c0001t0020g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.143-12543C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604665 | |||||||
| chr16:604698 | C | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-12510C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604698 | |||||||
| chr16:604917 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.143-12291G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 604917 | |||||||
| chr16:605090 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.143-12118C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605090 | |||||||
| chr16:605173 | C | T | 3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0021g0180 |
3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.143-12035C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605173 | |||||||
| chr16:605184 | C | T | 23 | a0001c0001t0001g0071 a0001c0001t0003g0185 a0001c0001t0003g0186 others(20): Show |
23 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-12024C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605184 | |||||||
| chr16:605262 | T | G | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-11946T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605262 | |||||||
| chr16:605266 | A | C | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.143-11942A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605266 | |||||||
| chr16:605338 | G | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0083 a0001c0001t0001g0102 others(2): Show |
5 | HG01167.hp1 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-11870G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605338 | |||||||
| chr16:605396 | A | G | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-11812A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605396 | |||||||
| chr16:605417 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0093 a0001c0001t0001g0097 others(6): Show |
10 | HG01106.hp1 HG01243.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-11791G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605417 | |||||||
| chr16:605425 | A | C | 1 | a0001c0001t0002g0255 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.143-11783A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605425 | |||||||
| chr16:605430 | G | A | 20 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0003g0155 others(17): Show |
20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.143-11778G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605430 | |||||||
| chr16:605452 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-11756C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605452 | |||||||
| chr16:605615 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.143-11593C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605615 | |||||||
| chr16:605646 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0182 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.143-11562C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605646 | |||||||
| chr16:605652 | G | A | 27 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(24): Show |
27 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.143-11556G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605652 | |||||||
| chr16:605686 | T | C | 30 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0179 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-11522T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605686 | |||||||
| chr16:605734 | C | G | 1 | a0001c0001t0002g0303 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.143-11474C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605734 | |||||||
| chr16:605763 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.143-11445C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605763 | |||||||
| chr16:605781 | G | A | 1 | a0001c0001t0003g0216 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.143-11427G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605781 | |||||||
| chr16:605809 | G | A | 9 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0239 others(6): Show |
9 | HG00639.hp1 HG00741.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-11399G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605809 | |||||||
| chr16:605985 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-11223C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 605985 | |||||||
| chr16:606033 | T | C | 194 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(191): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.143-11175T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606033 | |||||||
| chr16:606065 | T | A | 1 | a0001c0001t0002g0255 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.143-11143T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606065 | |||||||
| chr16:606105 | T | C | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-11103T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606105 | |||||||
| chr16:606236 | A | ACAGTCCT others(59): Show |
3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0021g0180 |
3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.143-10907_143-1090 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606236 | ||||||
| chr16:606302 | A | ACAGTCCT others(59): Show |
13 | a0001c0001t0001g0060 a0001c0001t0001g0112 a0001c0001t0002g0232 others(10): Show |
13 | HG01081.hp2 HG02132.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-10801_143-1073 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606302 | ||||||
| chr16:606302 | A | G | 9 | a0001c0001t0001g0046 a0001c0001t0002g0302 a0001c0001t0003g0191 others(6): Show |
9 | HG00408.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-10906A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606302 | |||||||
| chr16:606331 | G | GGTTTCCC others(59): Show |
1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-10812_143-1081 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606331 | ||||||
| chr16:606368 | G | GCAGTCCT others(59): Show |
51 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0179 others(48): Show |
52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-10775_143-1077 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606368 | ||||||
| chr16:606434 | G | A | 56 | a0001c0001t0001g0046 a0001c0001t0001g0222 a0001c0001t0003g0011 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-10774G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606434 | |||||||
| chr16:606434 | G | GCAGTCCT others(59): Show |
260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.143-10736_143-1073 others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606434 | ||||||
| chr16:606434 | G | GCAGTCCT others(125): Show |
1 | a0001c0001t0002g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.143-10736_143-1073 others(136): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 606434 | ||||||
| chr16:606484 | A | G | 2 | a0001c0001t0003g0213 a0001c0001t0003g0224 |
2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-10724A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606484 | |||||||
| chr16:606487 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.143-10721T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606487 | |||||||
| chr16:606539 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.143-10669G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606539 | |||||||
| chr16:606624 | A | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0240 |
2 | HG01943.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.143-10584A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606624 | |||||||
| chr16:606625 | T | C | 1 | a0001c0001t0010g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-10583T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606625 | |||||||
| chr16:606703 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.143-10505G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606703 | |||||||
| chr16:606818 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.143-10390G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606818 | |||||||
| chr16:606842 | G | T | 59 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-10366G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606842 | |||||||
| chr16:606862 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-10346G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606862 | |||||||
| chr16:606879 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143-10329G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606879 | |||||||
| chr16:606985 | G | A | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.143-10223G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606985 | |||||||
| chr16:606997 | C | G | 59 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-10211C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 606997 | |||||||
| chr16:607073 | G | C | 59 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-10135G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607073 | |||||||
| chr16:607087 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-10121C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607087 | |||||||
| chr16:607446 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-9762T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607446 | |||||||
| chr16:607459 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.143-9749C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607459 | |||||||
| chr16:607466 | A | G | 60 | a0001c0001t0001g0120 a0001c0001t0001g0222 a0001c0001t0003g0011 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.143-9742A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607466 | |||||||
| chr16:607501 | C | CA | 10 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0097 others(7): Show |
10 | HG00741.hp1 HG01169.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.143-9692dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 607501 | ||||||
| chr16:607501 | C | CAA | 54 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.143-9693_143-9692d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 607501 | ||||||
| chr16:607501 | CA | C | 28 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0119 others(25): Show |
28 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.143-9692delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 607501 | ||||||
| chr16:607517 | C | A | 54 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.143-9691C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607517 | |||||||
| chr16:607517 | C | G | 5 | a0001c0001t0003g0179 a0001c0001t0003g0184 a0001c0001t0003g0213 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-9691C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607517 | |||||||
| chr16:607531 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02486.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-9677C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607531 | |||||||
| chr16:607532 | G | A | 1 | a0001c0001t0010g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143-9676G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607532 | |||||||
| chr16:607552 | G | C | 197 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(194): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.143-9656G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607552 | |||||||
| chr16:607575 | G | A | 1 | a0001c0001t0010g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-9633G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607575 | |||||||
| chr16:607646 | G | C | 1 | a0001c0001t0002g0256 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9562G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607646 | |||||||
| chr16:607651 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9557C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607651 | |||||||
| chr16:607653 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9555C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607653 | |||||||
| chr16:607658 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-9550G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607658 | |||||||
| chr16:607745 | C | T | 1 | a0001c0001t0010g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-9463C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607745 | |||||||
| chr16:607746 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.143-9462G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607746 | |||||||
| chr16:607954 | C | G | 1 | a0001c0001t0010g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143-9254C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607954 | |||||||
| chr16:607972 | G | C | 1 | a0001c0001t0002g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.143-9236G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607972 | |||||||
| chr16:607988 | C | T | 2 | a0001c0001t0003g0179 a0001c0001t0003g0189 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.143-9220C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 607988 | |||||||
| chr16:608038 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-9170C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608038 | |||||||
| chr16:608201 | G | C | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-9007G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608201 | |||||||
| chr16:608252 | C | T | 1 | a0001c0001t0012g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-8956C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608252 | |||||||
| chr16:608271 | G | T | 39 | a0001c0001t0001g0062 a0001c0001t0002g0290 a0001c0001t0003g0011 others(36): Show |
40 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.143-8937G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608271 | |||||||
| chr16:608326 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-8882C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608326 | |||||||
| chr16:608330 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.143-8878C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 608330 | |||||||
| chr16:609022 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.143-8186T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609022 | |||||||
| chr16:609057 | G | C | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-8151G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609057 | |||||||
| chr16:609172 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0046 |
2 | HG00408.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.143-8036C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609172 | |||||||
| chr16:609339 | GGGGGACA others(8): Show |
G | 2 | a0001c0001t0001g0134 a0001c0001t0010g0032 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.143-7854_143-7840d others(17): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 609339 | ||||||
| chr16:609403 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0135 |
2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.143-7805C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609403 | |||||||
| chr16:609469 | C | T | 55 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.143-7739C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609469 | |||||||
| chr16:609543 | A | G | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-7665A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609543 | |||||||
| chr16:609576 | G | A | 2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-7632G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609576 | |||||||
| chr16:609739 | G | A | 1 | a0001c0001t0029g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.143-7469G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609739 | |||||||
| chr16:609852 | G | A | 21 | a0001c0001t0003g0155 a0001c0001t0004g0157 a0001c0001t0004g0159 others(18): Show |
21 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-7356G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609852 | |||||||
| chr16:609873 | G | C | 1 | a0001c0001t0010g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143-7335G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609873 | |||||||
| chr16:609874 | G | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-7334G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 609874 | |||||||
| chr16:610020 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-7188C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610020 | |||||||
| chr16:610060 | A | G | 2 | a0001c0001t0003g0211 a0001c0001t0003g0226 |
2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.143-7148A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610060 | |||||||
| chr16:610086 | G | C | 1 | a0001c0001t0005g0208 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143-7122G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610086 | |||||||
| chr16:610285 | T | G | 1 | a0001c0001t0002g0242 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.143-6923T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610285 | |||||||
| chr16:610303 | G | A | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-6905G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610303 | |||||||
| chr16:610325 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0054 |
2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.143-6883G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610325 | |||||||
| chr16:610362 | AC | A | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-6844delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 610362 | ||||||
| chr16:610491 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.143-6717G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610491 | |||||||
| chr16:610493 | C | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-6715C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610493 | |||||||
| chr16:610997 | C | T | 1 | a0001c0001t0008g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-6211C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610997 | |||||||
| chr16:610998 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0050 |
2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.143-6210G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 610998 | |||||||
| chr16:611059 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.143-6149C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611059 | |||||||
| chr16:611080 | C | T | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-6128C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611080 | |||||||
| chr16:611109 | C | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-6099C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611109 | |||||||
| chr16:611137 | G | A | 4 | a0001c0001t0006g0028 a0001c0001t0007g0034 a0001c0001t0028g0030 others(1): Show |
4 | HG01884.hp2 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-6071G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611137 | |||||||
| chr16:611142 | T | C | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-6066T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611142 | |||||||
| chr16:611335 | T | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0041 others(202): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.143-5873T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611335 | |||||||
| chr16:611361 | G | C | 2 | a0001c0001t0008g0037 a0001c0004t0023g0038 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-5847G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611361 | |||||||
| chr16:611395 | T | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-5813T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611395 | |||||||
| chr16:611439 | A | G | 195 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(192): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.143-5769A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611439 | |||||||
| chr16:611451 | A | G | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-5757A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611451 | |||||||
| chr16:611572 | G | A | 3 | a0001c0001t0003g0187 a0001c0001t0003g0195 a0001c0001t0003g0196 |
3 | NA18940.hp1 NA18974.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.143-5636G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611572 | |||||||
| chr16:611595 | CGGGACAG others(509): Show |
C | 2 | a0001c0001t0003g0213 a0001c0001t0003g0224 |
2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-5543_143-5028d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611595 | ||||||
| chr16:611595 | CGGGACAG others(543): Show |
C | 1 | a0001c0001t0003g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.143-5543_143-4994d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611595 | ||||||
| chr16:611628 | CAGGGACA others(441): Show |
C | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-5543_143-5096d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611628 | ||||||
| chr16:611662 | CAGAGACA others(407): Show |
C | 24 | a0001c0001t0003g0155 a0001c0001t0004g0157 a0001c0001t0004g0159 others(21): Show |
24 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-5543_143-5130d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611662 | ||||||
| chr16:611665 | A | G | 166 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0222 others(163): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.143-5543A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611665 | |||||||
| chr16:611665 | AGACAGCC others(27): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.143-5486_143-5453d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611665 | ||||||
| chr16:611730 | CAGGGACA others(957): Show |
C | 1 | a0001c0001t0005g0207 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143-5452_143-4489d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611730 | ||||||
| chr16:611746 | GGCCTGTA others(62): Show |
G | 50 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(47): Show |
51 | HG00280.hp1 HG00673.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.143-5452_143-5384d others(71): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611746 | ||||||
| chr16:611756 | T | A | 113 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0014 others(110): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.143-5452T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611756 | |||||||
| chr16:611764 | CAGGGACA others(923): Show |
C | 51 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(48): Show |
52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-5408_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611764 | ||||||
| chr16:611780 | GGCCTGTA others(28): Show |
G | 1 | a0001c0001t0002g0014 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.143-5408_143-5374d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611780 | ||||||
| chr16:611780 | GGCCTGTA others(236): Show |
G | 15 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(12): Show |
15 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-5408_143-5166d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611780 | ||||||
| chr16:611798 | CA | C | 35 | a0001c0001t0002g0014 a0001c0001t0002g0230 a0001c0001t0002g0231 others(32): Show |
35 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.143-5408delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611798 | ||||||
| chr16:611798 | CAAGGGAC others(889): Show |
C | 2 | a0001c0001t0003g0179 a0001c0001t0007g0325 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.143-5408_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611798 | ||||||
| chr16:611799 | AAGGGACA others(63): Show |
A | 8 | a0001c0001t0002g0249 a0001c0001t0002g0256 a0001c0001t0002g0263 others(5): Show |
8 | HG00408.hp2 HG00639.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-5408_143-5339d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611799 | |||||||
| chr16:611799 | AAGGGACA others(98): Show |
A | 1 | a0001c0001t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.143-5408_143-5304d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611799 | |||||||
| chr16:611813 | T | C | 34 | a0001c0001t0002g0014 a0001c0001t0002g0231 a0001c0001t0002g0234 others(31): Show |
34 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.143-5395T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611813 | |||||||
| chr16:611815 | C | G | 34 | a0001c0001t0002g0014 a0001c0001t0002g0231 a0001c0001t0002g0234 others(31): Show |
34 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.143-5393C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611815 | |||||||
| chr16:611867 | CACGGGAC others(202): Show |
C | 3 | a0001c0001t0002g0242 a0001c0001t0002g0305 a0001c0001t0032g0017 |
3 | HG00280.hp2 HG01361.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.143-5339_143-5131d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611867 | ||||||
| chr16:611868 | AC | A | 82 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(79): Show |
84 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.143-5339delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611868 | |||||||
| chr16:611902 | CACGGGAC others(167): Show |
C | 18 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(15): Show |
18 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.143-5304_143-5131d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611902 | ||||||
| chr16:611903 | AC | A | 72 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(69): Show |
74 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.143-5304delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611903 | |||||||
| chr16:611904 | CGGGACAG others(27): Show |
C | 1 | a0001c0001t0027g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-5269_143-5236d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611904 | ||||||
| chr16:611905 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.143-5303G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611905 | |||||||
| chr16:611906 | G | A | 1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-5302G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611906 | |||||||
| chr16:611927 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.143-5281G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611927 | |||||||
| chr16:611937 | CAGGGACA others(28): Show |
C | 1 | a0001c0001t0002g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.143-5222_143-5188d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611937 | ||||||
| chr16:611963 | A | T | 12 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0237 others(9): Show |
13 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.143-5245A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611963 | |||||||
| chr16:611971 | CA | C | 70 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(67): Show |
72 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.143-5235delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611971 | ||||||
| chr16:611971 | CAAGGGAC others(98): Show |
C | 1 | a0001c0001t0011g0295 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.143-5235_143-5131d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611971 | ||||||
| chr16:611972 | A | AGGGACAG others(26): Show |
1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-5236_143-5235i others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611972 | |||||||
| chr16:611988 | GGCCTGTA others(28): Show |
G | 41 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(38): Show |
41 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.143-5200_143-5166d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 611988 | ||||||
| chr16:611997 | A | G | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-5211A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611997 | |||||||
| chr16:611998 | A | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0311 |
2 | HG03654.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.143-5210A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 611998 | |||||||
| chr16:612006 | CA | C | 18 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0237 others(15): Show |
19 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.143-5200delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612006 | ||||||
| chr16:612006 | CAAGGGAC others(63): Show |
C | 12 | a0001c0001t0002g0013 a0001c0001t0002g0177 a0001c0001t0002g0178 others(9): Show |
12 | HG01943.hp1 HG02683.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.143-5200_143-5131d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612006 | ||||||
| chr16:612021 | T | C | 7 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(4): Show |
7 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-5187T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612021 | |||||||
| chr16:612023 | T | C | 13 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0237 others(10): Show |
14 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-5185T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612023 | |||||||
| chr16:612023 | T | G | 6 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5185T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612023 | |||||||
| chr16:612023 | TGCCTGTA others(96): Show |
G | 1 | a0001c0001t0002g0287 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.143-5185_143-5083d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612023 | |||||||
| chr16:612024 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.143-5184G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612024 | |||||||
| chr16:612033 | A | T | 6 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5175A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612033 | |||||||
| chr16:612066 | C | A | 75 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(72): Show |
76 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.143-5142C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612066 | |||||||
| chr16:612067 | A | T | 41 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(38): Show |
41 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.143-5141A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612067 | |||||||
| chr16:612075 | CA | C | 62 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0018 others(59): Show |
62 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.143-5131delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612075 | ||||||
| chr16:612076 | A | AAGGGACA others(27): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0117 |
3 | HG00099.hp1 HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.143-4868_143-4835d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612076 | ||||||
| chr16:612076 | AAGGGACA others(27): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0088 others(2): Show |
5 | HG01243.hp2 HG02080.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4868_143-4835d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612076 | ||||||
| chr16:612076 | AAGGGACA others(61): Show |
A | 2 | a0001c0001t0001g0043 a0001c0005t0001g0053 |
2 | NA18943.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.143-4902_143-4835d others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612076 | ||||||
| chr16:612077 | A | C | 13 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0237 others(10): Show |
14 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-5131A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612077 | |||||||
| chr16:612090 | C | T | 6 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5118C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612090 | |||||||
| chr16:612092 | G | C | 6 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5116G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612092 | |||||||
| chr16:612100 | G | A | 2 | a0001c0001t0002g0253 a0001c0001t0002g0306 |
2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.143-5108G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612100 | |||||||
| chr16:612102 | A | T | 11 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0232 others(8): Show |
11 | HG01943.hp1 HG02683.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-5106A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612102 | |||||||
| chr16:612111 | A | AC | 13 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0237 others(10): Show |
14 | HG00738.hp2 HG01261.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.143-5097_143-5096i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612111 | |||||||
| chr16:612122 | C | T | 1 | a0001c0001t0002g0298 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.143-5086C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612122 | |||||||
| chr16:612124 | C | T | 42 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(39): Show |
43 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.143-5084C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612124 | |||||||
| chr16:612126 | G | C | 42 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(39): Show |
43 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.143-5082G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612126 | |||||||
| chr16:612136 | A | T | 19 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(16): Show |
19 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-5072A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612136 | |||||||
| chr16:612145 | A | AC | 6 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-5063_143-5062i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612145 | |||||||
| chr16:612158 | C | T | 11 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0232 others(8): Show |
11 | HG01943.hp1 HG02683.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-5050C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612158 | |||||||
| chr16:612160 | G | C | 11 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0232 others(8): Show |
11 | HG01943.hp1 HG02683.hp2 HG04199.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-5048G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612160 | |||||||
| chr16:612170 | A | T | 2 | a0001c0001t0002g0242 a0001c0001t0002g0305 |
2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.143-5038A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612170 | |||||||
| chr16:612178 | C | CA | 8 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0248 others(5): Show |
9 | HG00738.hp2 HG01978.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-5029dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612178 | ||||||
| chr16:612179 | A | AC | 51 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(48): Show |
52 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.143-5029_143-5028i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612179 | |||||||
| chr16:612179 | AGGGACAG others(26): Show |
A | 3 | a0001c0001t0002g0237 a0001c0001t0002g0255 a0001c0001t0002g0298 |
3 | HG01261.hp1 NA18966.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.143-5028_143-4996d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612179 | |||||||
| chr16:612179 | AGGGACAG others(60): Show |
A | 2 | a0001c0001t0002g0309 a0001c0001t0002g0313 |
2 | NA18974.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.143-5028_143-4962d others(69): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612179 | |||||||
| chr16:612192 | C | T | 26 | a0001c0001t0002g0014 a0001c0001t0002g0231 a0001c0001t0002g0234 others(23): Show |
27 | HG00438.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.143-5016C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612192 | |||||||
| chr16:612194 | G | C | 19 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(16): Show |
19 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-5014G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612194 | |||||||
| chr16:612194 | G | GGCCTGTA others(28): Show |
1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-4995_143-4994i others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612194 | ||||||
| chr16:612194 | G | T | 7 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0248 others(4): Show |
8 | HG00738.hp2 HG01978.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-5014G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612194 | |||||||
| chr16:612203 | A | C | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-5005A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612203 | |||||||
| chr16:612204 | A | T | 16 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(13): Show |
16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-5004A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612204 | |||||||
| chr16:612213 | A | AC | 54 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(51): Show |
55 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.143-4995_143-4994i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612213 | |||||||
| chr16:612226 | C | T | 5 | a0001c0001t0002g0237 a0001c0001t0002g0242 a0001c0001t0002g0255 others(2): Show |
5 | HG00280.hp2 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4982C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612226 | |||||||
| chr16:612228 | G | C | 2 | a0001c0001t0002g0242 a0001c0001t0002g0305 |
2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.143-4980G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612228 | |||||||
| chr16:612228 | G | T | 3 | a0001c0001t0002g0237 a0001c0001t0002g0255 a0001c0001t0002g0298 |
3 | HG01261.hp1 NA18966.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.143-4980G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612228 | |||||||
| chr16:612237 | A | C | 8 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0248 others(5): Show |
9 | HG00738.hp2 HG01978.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-4971A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612237 | |||||||
| chr16:612246 | C | CA | 15 | a0001c0001t0002g0014 a0001c0001t0002g0234 a0001c0001t0002g0248 others(12): Show |
16 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4961dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612246 | ||||||
| chr16:612247 | A | AC | 32 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0231 others(29): Show |
32 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.143-4961_143-4960i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612247 | |||||||
| chr16:612247 | AGGGACAG others(94): Show |
A | 2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-4960_143-4860d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612247 | |||||||
| chr16:612260 | C | T | 24 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(21): Show |
24 | HG00544.hp1 HG00639.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-4948C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612260 | |||||||
| chr16:612262 | G | C | 16 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(13): Show |
16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4946G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612262 | |||||||
| chr16:612262 | G | T | 8 | a0001c0001t0002g0249 a0001c0001t0002g0263 a0001c0001t0002g0278 others(5): Show |
8 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-4946G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612262 | |||||||
| chr16:612271 | A | C | 3 | a0001c0001t0002g0237 a0001c0001t0002g0255 a0001c0001t0002g0298 |
3 | HG01261.hp1 NA18966.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.143-4937A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612271 | |||||||
| chr16:612272 | ATCAAGAG others(95): Show |
A | 2 | a0001c0001t0002g0249 a0001c0001t0002g0278 |
2 | NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.143-4892_143-4791d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612272 | ||||||
| chr16:612280 | C | CA | 23 | a0001c0001t0002g0013 a0001c0001t0002g0176 a0001c0001t0002g0233 others(20): Show |
24 | HG00280.hp1 HG00408.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-4927dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612280 | ||||||
| chr16:612281 | A | AC | 21 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(18): Show |
21 | HG00280.hp2 HG00438.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4927_143-4926i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612281 | |||||||
| chr16:612281 | AGGGACAG others(26): Show |
A | 21 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0175 others(18): Show |
21 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-4926_143-4894d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612281 | |||||||
| chr16:612281 | AGGGACAG others(60): Show |
A | 1 | a0001c0001t0008g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.143-4926_143-4860d others(69): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612281 | |||||||
| chr16:612284 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4924G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612284 | |||||||
| chr16:612294 | C | T | 20 | a0001c0001t0002g0013 a0001c0001t0002g0176 a0001c0001t0002g0233 others(17): Show |
21 | HG00280.hp1 HG00408.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-4914C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612294 | |||||||
| chr16:612296 | G | T | 20 | a0001c0001t0002g0013 a0001c0001t0002g0176 a0001c0001t0002g0233 others(17): Show |
21 | HG00280.hp1 HG00408.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-4912G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612296 | |||||||
| chr16:612296 | GGCCTGTA others(130): Show |
G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0250 a0001c0001t0002g0300 |
4 | HG02300.hp2 HG04115.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-4858_143-4722d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612296 | ||||||
| chr16:612305 | A | C | 6 | a0001c0001t0002g0263 a0001c0001t0002g0299 a0001c0001t0002g0309 others(3): Show |
6 | HG00639.hp1 HG01081.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-4903A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612305 | |||||||
| chr16:612306 | ATCAAGAG others(61): Show |
A | 16 | a0001c0001t0002g0013 a0001c0001t0002g0176 a0001c0001t0002g0233 others(13): Show |
17 | HG00280.hp1 HG01070.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.143-4858_143-4791d others(70): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612306 | ||||||
| chr16:612314 | C | CA | 16 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0232 others(13): Show |
16 | HG00639.hp1 HG01081.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-4893dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612314 | ||||||
| chr16:612315 | A | AC | 16 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(13): Show |
16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4893_143-4892i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612315 | |||||||
| chr16:612315 | AGGGACAG others(26): Show |
A | 4 | a0001c0001t0002g0242 a0001c0001t0002g0258 a0001c0001t0002g0268 others(1): Show |
4 | HG00280.hp2 HG01071.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-4892_143-4860d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612315 | |||||||
| chr16:612315 | AGGGACAG others(129): Show |
A | 1 | a0001c0001t0008g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4892_143-4757d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612315 | |||||||
| chr16:612328 | C | T | 31 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0175 others(28): Show |
31 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-4880C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612328 | |||||||
| chr16:612330 | G | T | 30 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0175 others(27): Show |
30 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-4878G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612330 | |||||||
| chr16:612330 | GGCCTGTA others(96): Show |
T | 1 | a0001c0001t0002g0232 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.143-4878_143-4775d others(110): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612330 | |||||||
| chr16:612339 | A | C | 4 | a0001c0001t0002g0256 a0001c0001t0002g0274 a0001c0001t0002g0285 others(1): Show |
4 | HG00408.hp2 HG02027.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-4869A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612339 | |||||||
| chr16:612340 | ATCAAGAG others(27): Show |
A | 25 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0240 others(22): Show |
25 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.143-4834_143-4801d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612340 | ||||||
| chr16:612348 | C | CA | 23 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(20): Show |
23 | HG00438.hp2 HG00733.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-4859dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612348 | ||||||
| chr16:612349 | A | AC | 16 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(13): Show |
16 | HG00544.hp1 HG01256.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-4859_143-4858i others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612349 | |||||||
| chr16:612349 | A | C | 5 | a0001c0001t0002g0242 a0001c0001t0002g0305 a0001c0001t0008g0036 others(2): Show |
5 | HG00280.hp2 HG01361.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-4859A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612349 | |||||||
| chr16:612349 | AGGGACAG others(26): Show |
A | 1 | a0001c0001t0002g0256 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.143-4858_143-4826d others(35): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612349 | |||||||
| chr16:612362 | C | T | 21 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(18): Show |
21 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4846C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612362 | |||||||
| chr16:612364 | G | T | 21 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0238 others(18): Show |
21 | HG00438.hp2 HG00733.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4844G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612364 | |||||||
| chr16:612373 | A | C | 5 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0002g0178 others(2): Show |
5 | NA18966.hp2 NA18981.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4835A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612373 | |||||||
| chr16:612374 | T | A | 64 | a0001c0001t0002g0012 a0001c0001t0002g0175 a0001c0001t0002g0177 others(61): Show |
64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.143-4834T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612374 | |||||||
| chr16:612374 | TTCAAGAG others(407): Show |
T | 28 | a0001c0001t0002g0230 a0001c0001t0003g0155 a0001c0001t0004g0157 others(25): Show |
28 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.143-4651_143-4238d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612374 | ||||||
| chr16:612382 | C | CA | 5 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0002g0178 others(2): Show |
5 | NA18966.hp2 NA18981.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4825dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612382 | ||||||
| chr16:612383 | AGGGACAG others(97): Show |
A | 1 | a0001c0001t0002g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143-4790_143-4687d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612383 | ||||||
| chr16:612392 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.143-4816C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612392 | |||||||
| chr16:612398 | GGCCTGTA others(28): Show |
G | 3 | a0001c0001t0002g0274 a0001c0001t0002g0297 a0001c0001t0002g0299 |
3 | HG01081.hp2 HG02027.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.143-4790_143-4756d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612398 | ||||||
| chr16:612398 | GGCCTGTA others(236): Show |
G | 2 | a0001c0001t0002g0275 a0001c0001t0034g0151 |
2 | HG01978.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.143-4790_143-4548d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612398 | ||||||
| chr16:612405 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0115 others(1): Show |
4 | HG00099.hp1 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-4803A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612405 | |||||||
| chr16:612407 | A | C | 64 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(61): Show |
65 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.143-4801A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612407 | |||||||
| chr16:612416 | CA | C | 11 | a0001c0001t0002g0175 a0001c0001t0002g0177 a0001c0001t0002g0178 others(8): Show |
11 | HG00408.hp2 HG00738.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-4790delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612416 | ||||||
| chr16:612417 | AAGGGACA others(63): Show |
A | 5 | a0001c0001t0002g0263 a0001c0001t0002g0285 a0001c0001t0002g0298 others(2): Show |
5 | HG00639.hp1 HG02273.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-4790_143-4721d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612417 | |||||||
| chr16:612418 | A | C | 1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-4790A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612418 | |||||||
| chr16:612431 | T | C | 76 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(73): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.143-4777T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612431 | |||||||
| chr16:612433 | C | G | 76 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(73): Show |
77 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.143-4775C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612433 | |||||||
| chr16:612433 | C | T | 21 | a0001c0001t0002g0012 a0001c0001t0002g0239 a0001c0001t0002g0241 others(18): Show |
21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4775C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612433 | |||||||
| chr16:612461 | C | T | 2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-4747C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612461 | |||||||
| chr16:612465 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4743C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612465 | |||||||
| chr16:612467 | G | T | 1 | a0001c0001t0008g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4741G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612467 | |||||||
| chr16:612476 | A | C | 22 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(19): Show |
22 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.143-4732A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612476 | |||||||
| chr16:612485 | CACGGGAC others(202): Show |
C | 3 | a0001c0001t0002g0237 a0001c0001t0002g0248 a0001c0001t0002g0255 |
3 | HG01261.hp1 NA19001.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.143-4721_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612485 | ||||||
| chr16:612485 | CACGGGAC others(236): Show |
C | 1 | a0001c0001t0002g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.143-4721_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612485 | ||||||
| chr16:612486 | AC | A | 78 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0018 others(75): Show |
80 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.143-4721delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612486 | |||||||
| chr16:612487 | C | A | 23 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(20): Show |
23 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.143-4721C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612487 | |||||||
| chr16:612496 | C | CGCCTTTG others(27): Show |
1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-4709_143-4708i others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612496 | ||||||
| chr16:612496 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-4712C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612496 | |||||||
| chr16:612511 | A | C | 2 | a0001c0001t0008g0037 a0001c0004t0023g0038 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-4697A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612511 | |||||||
| chr16:612520 | CACGGGAC others(167): Show |
C | 1 | a0001c0001t0002g0313 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.143-4686_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612520 | ||||||
| chr16:612521 | AC | A | 104 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(101): Show |
106 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.143-4686delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612521 | |||||||
| chr16:612522 | C | A | 2 | a0001c0001t0008g0037 a0001c0004t0023g0038 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-4686C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612522 | |||||||
| chr16:612555 | CACGGGAC others(132): Show |
C | 1 | a0001c0001t0002g0299 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.143-4651_143-4513d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612555 | ||||||
| chr16:612556 | AC | A | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-4651delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612556 | |||||||
| chr16:612590 | CAGGGACA others(97): Show |
C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0175 a0001c0001t0002g0177 others(7): Show |
11 | HG00408.hp2 HG00639.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-4582_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612590 | ||||||
| chr16:612590 | CAGGGACA others(131): Show |
C | 1 | a0001c0001t0002g0298 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.143-4582_143-4445d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612590 | ||||||
| chr16:612624 | CA | C | 21 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(18): Show |
21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4582delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612624 | ||||||
| chr16:612624 | CAAGGGAC others(63): Show |
C | 68 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(65): Show |
69 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.143-4582_143-4513d others(72): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612624 | ||||||
| chr16:612624 | CAAGGGAC others(97): Show |
C | 5 | a0001c0001t0002g0250 a0001c0001t0002g0273 a0001c0001t0002g0274 others(2): Show |
5 | HG02027.hp1 HG02300.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-4582_143-4479d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612624 | ||||||
| chr16:612639 | T | C | 21 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(18): Show |
21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4569T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612639 | |||||||
| chr16:612641 | T | G | 21 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(18): Show |
21 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-4567T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612641 | |||||||
| chr16:612659 | CAGGGACA others(407): Show |
C | 3 | a0001c0001t0003g0213 a0001c0001t0003g0215 a0001c0001t0003g0224 |
3 | HG03688.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-4539_143-4126d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612659 | ||||||
| chr16:612669 | T | C | 34 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0051 others(31): Show |
34 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.143-4539T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612669 | |||||||
| chr16:612684 | C | A | 23 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(20): Show |
23 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.143-4524C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612684 | |||||||
| chr16:612693 | CA | C | 23 | a0001c0001t0002g0012 a0001c0001t0002g0232 a0001c0001t0002g0239 others(20): Show |
23 | HG00280.hp2 HG00544.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.143-4513delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612693 | ||||||
| chr16:612694 | AAGGGACA others(27): Show |
A | 1 | a0001c0001t0027g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-4410_143-4377d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 612694 | ||||||
| chr16:612720 | A | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4488A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612720 | |||||||
| chr16:612754 | A | T | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.143-4454A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612754 | |||||||
| chr16:612773 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0294 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.143-4435G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612773 | |||||||
| chr16:612776 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4432C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612776 | |||||||
| chr16:612778 | G | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4430G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612778 | |||||||
| chr16:612788 | A | T | 165 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(162): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.143-4420A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612788 | |||||||
| chr16:612832 | A | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4376A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612832 | |||||||
| chr16:612841 | C | T | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.143-4367C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612841 | |||||||
| chr16:612845 | T | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4363T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612845 | |||||||
| chr16:612847 | C | G | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4361C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612847 | |||||||
| chr16:612936 | C | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4272C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612936 | |||||||
| chr16:612946 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.143-4262G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612946 | |||||||
| chr16:612949 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4259C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612949 | |||||||
| chr16:612951 | G | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4257G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612951 | |||||||
| chr16:612976 | A | T | 1 | a0001c0001t0007g0153 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.143-4232A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612976 | |||||||
| chr16:612980 | G | A | 107 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.143-4228G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612980 | |||||||
| chr16:612994 | A | C | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4214A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612994 | |||||||
| chr16:612994 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.143-4214A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 612994 | |||||||
| chr16:613004 | AAGGGACA others(27): Show |
A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-4190_143-4157d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 613004 | ||||||
| chr16:613063 | CATCAAGA others(28): Show |
C | 55 | a0001c0001t0001g0070 a0001c0001t0001g0222 a0001c0001t0003g0011 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.143-4099_143-4065d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 613063 | ||||||
| chr16:613098 | A | C | 3 | a0001c0001t0003g0213 a0001c0001t0003g0215 a0001c0001t0003g0224 |
3 | HG03688.hp1 HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-4110A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613098 | |||||||
| chr16:613127 | CTGTAGAA others(160): Show |
C | 2 | a0001c0001t0013g0021 a0001c0001t0013g0033 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.143-4050_143-3884d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 613127 | ||||||
| chr16:613136 | CAA | C | 3 | a0001c0001t0006g0166 a0001c0001t0006g0167 a0001c0001t0006g0168 |
3 | HG01981.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.143-4071_143-4070d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613136 | |||||||
| chr16:613193 | A | G | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-4015A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613193 | |||||||
| chr16:613218 | G | T | 24 | a0001c0001t0003g0155 a0001c0001t0004g0157 a0001c0001t0004g0159 others(21): Show |
24 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-3990G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613218 | |||||||
| chr16:613294 | T | G | 2 | a0001c0001t0003g0213 a0001c0001t0003g0224 |
2 | HG03927.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.143-3914T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613294 | |||||||
| chr16:613319 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.143-3889C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613319 | |||||||
| chr16:613389 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.143-3819G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613389 | |||||||
| chr16:613395 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-3813G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613395 | |||||||
| chr16:613430 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0002g0303 |
2 | HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.143-3778C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613430 | |||||||
| chr16:613431 | G | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-3777G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613431 | |||||||
| chr16:613546 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.143-3662G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613546 | |||||||
| chr16:613687 | G | A | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-3521G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613687 | |||||||
| chr16:613841 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.143-3367T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613841 | |||||||
| chr16:613880 | G | A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-3328G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 613880 | |||||||
| chr16:614013 | A | AGATGGTG others(24): Show |
1 | a0001c0001t0005g0207 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143-3181_143-3151d others(33): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614013 | ||||||
| chr16:614037 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.143-3171C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614037 | |||||||
| chr16:614105 | C | T | 4 | a0001c0001t0002g0251 a0001c0001t0007g0152 a0001c0001t0007g0153 others(1): Show |
4 | HG02622.hp1 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-3103C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614105 | |||||||
| chr16:614160 | A | ATCCCGAT others(54): Show |
1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-3031_143-3030i others(63): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614160 | ||||||
| chr16:614176 | GC | G | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-3030delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614176 | ||||||
| chr16:614179 | G | T | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-3029G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614179 | |||||||
| chr16:614186 | A | G | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-3022A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614186 | |||||||
| chr16:614189 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-3019G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614189 | |||||||
| chr16:614196 | T | G | 193 | a0001c0001t0001g0003 a0001c0001t0001g0222 a0001c0001t0002g0012 others(190): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.143-3012T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614196 | |||||||
| chr16:614207 | G | GC | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-3000dupC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614207 | ||||||
| chr16:614216 | G | A | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2992G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614216 | |||||||
| chr16:614217 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.143-2991C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614217 | |||||||
| chr16:614219 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2989G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614219 | |||||||
| chr16:614219 | G | T | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2989G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614219 | |||||||
| chr16:614221 | A | G | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2987A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614221 | |||||||
| chr16:614225 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2983C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614225 | |||||||
| chr16:614240 | T | A | 1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2968T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614240 | |||||||
| chr16:614245 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2963C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614245 | |||||||
| chr16:614246 | T | TACCACAT others(81): Show |
1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2959_143-2958i others(90): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614246 | ||||||
| chr16:614246 | T | TACCACAT others(81): Show |
23 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(20): Show |
23 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-2959_143-2958i others(90): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614246 | ||||||
| chr16:614246 | T | TACCACAT others(81): Show |
32 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(29): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.143-2959_143-2958i others(90): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614246 | ||||||
| chr16:614278 | A | G | 1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2930A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614278 | |||||||
| chr16:614281 | A | G | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2927A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614281 | |||||||
| chr16:614299 | G | GC | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2908dupC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614299 | ||||||
| chr16:614308 | G | A | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2900G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614308 | |||||||
| chr16:614341 | G | A | 57 | a0001c0001t0001g0222 a0001c0001t0002g0269 a0001c0001t0003g0011 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-2867G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614341 | |||||||
| chr16:614351 | G | A | 1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-2857G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614351 | |||||||
| chr16:614405 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.143-2803C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614405 | |||||||
| chr16:614428 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2780C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614428 | |||||||
| chr16:614429 | C | T | 2 | a0001c0001t0002g0252 a0001c0001t0032g0017 |
2 | HG03669.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.143-2779C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614429 | |||||||
| chr16:614492 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2716C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614492 | |||||||
| chr16:614493 | ATCCCGAT others(24): Show |
A | 1 | a0001c0001t0001g0117 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.143-2696_143-2666d others(33): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614493 | ||||||
| chr16:614497 | C | T | 1 | a0001c0005t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.143-2711C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614497 | |||||||
| chr16:614551 | G | A | 56 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.143-2657G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614551 | |||||||
| chr16:614555 | C | T | 5 | a0001c0001t0008g0036 a0001c0001t0008g0037 a0001c0001t0013g0021 others(2): Show |
5 | HG02258.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-2653C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614555 | |||||||
| chr16:614556 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2652G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614556 | |||||||
| chr16:614580 | G | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2628G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614580 | |||||||
| chr16:614582 | A | G | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2626A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614582 | |||||||
| chr16:614587 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2621G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614587 | |||||||
| chr16:614611 | A | ACATCCCA others(116): Show |
2 | a0001c0001t0005g0227 a0001c0001t0005g0228 |
2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.143-2591_143-2590i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | ||||||
| chr16:614611 | A | ACATCCCA others(116): Show |
52 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.143-2591_143-2590i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | ||||||
| chr16:614611 | A | ACATCCCA others(116): Show |
1 | a0001c0001t0003g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.143-2591_143-2590i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | ||||||
| chr16:614611 | A | ACATCCCG others(116): Show |
1 | a0001c0001t0005g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.143-2475_143-2474i others(125): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 614611 | ||||||
| chr16:614611 | A | G | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-2597A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614611 | |||||||
| chr16:614647 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.143-2561C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614647 | |||||||
| chr16:614797 | G | A | 1 | a0001c0001t0006g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.143-2411G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614797 | |||||||
| chr16:614802 | G | A | 108 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-2406G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614802 | |||||||
| chr16:614825 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143-2383C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614825 | |||||||
| chr16:614915 | A | G | 1 | a0001c0001t0009g0322 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143-2293A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 614915 | |||||||
| chr16:615185 | C | T | 2 | a0001c0001t0009g0321 a0001c0001t0009g0322 |
2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.143-2023C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615185 | |||||||
| chr16:615266 | A | G | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-1942A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615266 | |||||||
| chr16:615305 | C | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.143-1903C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615305 | |||||||
| chr16:615323 | A | G | 57 | a0001c0001t0001g0222 a0001c0001t0002g0293 a0001c0001t0003g0011 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-1885A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615323 | |||||||
| chr16:615405 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.143-1803C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615405 | |||||||
| chr16:615439 | C | T | 1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143-1769C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615439 | |||||||
| chr16:615606 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.143-1602G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615606 | |||||||
| chr16:615625 | G | A | 21 | a0001c0001t0003g0155 a0001c0001t0004g0157 a0001c0001t0004g0159 others(18): Show |
21 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.143-1583G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615625 | |||||||
| chr16:615732 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(38): Show |
47 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.143-1476C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615732 | |||||||
| chr16:615777 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.143-1431C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615777 | |||||||
| chr16:615811 | A | C | 108 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.143-1397A>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615811 | |||||||
| chr16:615860 | G | T | 1 | a0001c0001t0005g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.143-1348G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615860 | |||||||
| chr16:615877 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-1331G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615877 | |||||||
| chr16:615886 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0063 others(13): Show |
16 | HG00140.hp2 HG00733.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-1322C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615886 | |||||||
| chr16:615891 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.143-1317G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615891 | |||||||
| chr16:615957 | A | G | 1 | a0001c0001t0031g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-1251A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 615957 | |||||||
| chr16:616028 | C | T | 1 | a0001c0001t0007g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.143-1180C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616028 | |||||||
| chr16:616149 | A | G | 192 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.143-1059A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616149 | |||||||
| chr16:616151 | C | G | 57 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(54): Show |
58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.143-1057C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616151 | |||||||
| chr16:616255 | C | CA | 11 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0078 others(8): Show |
11 | HG01891.hp1 HG02083.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-938dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616255 | ||||||
| chr16:616273 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143-935C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616273 | |||||||
| chr16:616320 | C | T | 11 | a0001c0001t0003g0155 a0001c0001t0006g0028 a0001c0001t0007g0034 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-888C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616320 | |||||||
| chr16:616333 | T | TTTTA | 97 | a0001c0001t0001g0048 a0001c0001t0002g0012 a0001c0001t0002g0013 others(94): Show |
99 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.143-844_143-841dup others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | ||||||
| chr16:616333 | T | TTTTATTT others(1): Show |
124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
136 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.143-848_143-841dup others(8): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | ||||||
| chr16:616333 | T | TTTTATTT others(5): Show |
22 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0001g0091 others(19): Show |
22 | HG00099.hp2 HG01074.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.143-852_143-841dup others(12): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | ||||||
| chr16:616333 | T | TTTTATTT others(9): Show |
29 | a0001c0001t0003g0011 a0001c0001t0003g0169 a0001c0001t0003g0171 others(26): Show |
30 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-856_143-841dup others(16): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | ||||||
| chr16:616333 | T | TTTTATTT others(13): Show |
11 | a0001c0001t0003g0170 a0001c0001t0003g0172 a0001c0001t0003g0174 others(8): Show |
11 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-860_143-841dup others(20): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 616333 | ||||||
| chr16:616382 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0041 others(202): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.143-826A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616382 | |||||||
| chr16:616393 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-815C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616393 | |||||||
| chr16:616474 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-734G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616474 | |||||||
| chr16:616482 | G | C | 37 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(34): Show |
38 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.143-726G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616482 | |||||||
| chr16:616517 | T | G | 191 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(188): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.143-691T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616517 | |||||||
| chr16:616528 | C | T | 19 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(16): Show |
20 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.143-680C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616528 | |||||||
| chr16:616584 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.143-624C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616584 | |||||||
| chr16:616686 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143-522G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616686 | |||||||
| chr16:616709 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.143-499C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 616709 | |||||||
| chr16:617108 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.143-100G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617108 | |||||||
| chr16:617110 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.143-98G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617110 | |||||||
| chr16:617158 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.143-50G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617158 | |||||||
| chr16:617177 | C | T | 5 | a0001c0001t0002g0260 a0001c0001t0002g0275 a0001c0001t0002g0279 others(2): Show |
5 | HG00280.hp1 HG01074.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-31C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617177 | |||||||
| chr16:617203 | C | T | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.143-5C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 1/5 | chr16 | 617203 | |||||||
| chr16:617311 | A | G | 24 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(21): Show |
24 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.203+43A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617311 | |||||||
| chr16:617345 | C | T | 1 | a0001c0001t0010g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.203+77C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617345 | |||||||
| chr16:617396 | C | G | 24 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(21): Show |
24 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.203+128C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617396 | |||||||
| chr16:617440 | GTCTGGGA others(44): Show |
G | 1 | a0001c0001t0003g0197 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.203+173_203+223del others(51): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617440 | |||||||
| chr16:617457 | C | A | 1 | a0001c0001t0003g0212 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.203+189C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617457 | |||||||
| chr16:617467 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.203+199G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617467 | |||||||
| chr16:617490 | A | G | 60 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.203+222A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617490 | |||||||
| chr16:617513 | A | G | 59 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.203+245A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617513 | |||||||
| chr16:617554 | A | G | 17 | a0001c0001t0003g0155 a0001c0001t0004g0157 a0001c0001t0004g0159 others(14): Show |
17 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.203+286A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617554 | |||||||
| chr16:617583 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.203+315C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617583 | |||||||
| chr16:617628 | AG | A | 115 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(112): Show |
117 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.203+362delG | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 617628 | ||||||
| chr16:617791 | T | A | 33 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.204-409T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617791 | |||||||
| chr16:617799 | C | T | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.204-401C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 617799 | |||||||
| chr16:617849 | GA | G | 24 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(21): Show |
24 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.204-339delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr16 | 617849 | ||||||
| chr16:618034 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.204-166G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618034 | |||||||
| chr16:618099 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0003g0190 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.204-101C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618099 | |||||||
| chr16:618165 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204-35A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618165 | |||||||
| chr16:618173 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.204-27G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618173 | |||||||
| chr16:618185 | C | T | 1 | a0001c0001t0010g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.204-15C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 2/5 | chr16 | 618185 | |||||||
| chr16:618274 | C | T | 2 | a0001c0001t0011g0295 a0001c0001t0011g0307 |
2 | NA18954.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.264+14C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618274 | |||||||
| chr16:618297 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.264+37G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618297 | |||||||
| chr16:618443 | A | G | 196 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(193): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.264+183A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618443 | |||||||
| chr16:618451 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.264+191A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618451 | |||||||
| chr16:618540 | G | GGGTGTAC others(603): Show |
1 | a0001c0001t0001g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.264+347_264+956dup others(610): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618540 | ||||||
| chr16:618540 | GGGTGTAC others(728): Show |
G | 1 | a0001c0001t0001g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264+397_264+1131de others(1): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618540 | ||||||
| chr16:618563 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.264+303T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618563 | |||||||
| chr16:618606 | G | A | 1 | a0001c0001t0012g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.264+346G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618606 | |||||||
| chr16:618672 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.264+412C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618672 | |||||||
| chr16:618685 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.264+425G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618685 | |||||||
| chr16:618711 | CAG | C | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+452_264+453del others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618711 | |||||||
| chr16:618718 | A | T | 1 | a0001c0001t0003g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.264+458A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618718 | |||||||
| chr16:618722 | G | GTA | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+463_264+464ins others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618722 | ||||||
| chr16:618751 | A | G | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+491A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618751 | |||||||
| chr16:618752 | C | G | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+492C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618752 | |||||||
| chr16:618843 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.264+583A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618843 | |||||||
| chr16:618854 | T | C | 1 | a0001c0001t0003g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.264+594T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618854 | |||||||
| chr16:618885 | A | T | 3 | a0001c0001t0002g0263 a0001c0001t0002g0270 a0001c0001t0002g0318 |
3 | HG01261.hp2 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.264+625A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618885 | |||||||
| chr16:618902 | T | G | 27 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(24): Show |
27 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.264+642T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618902 | |||||||
| chr16:618907 | T | TGTG | 195 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(192): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.264+648_264+650dup others(3): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 618907 | ||||||
| chr16:618930 | G | T | 7 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+670G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618930 | |||||||
| chr16:618971 | G | A | 3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0021g0180 |
3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.264+711G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618971 | |||||||
| chr16:618975 | T | G | 27 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(24): Show |
27 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.264+715T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 618975 | |||||||
| chr16:619073 | C | CGGCCATG others(116): Show |
1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+852_264+853ins others(123): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619073 | ||||||
| chr16:619074 | G | A | 2 | a0001c0001t0010g0032 a0001c0001t0010g0035 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+814G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619074 | |||||||
| chr16:619153 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.264+893T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619153 | |||||||
| chr16:619259 | AGT | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | NA18940.hp1 NA18979.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+1007_264+1008d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619259 | ||||||
| chr16:619268 | G | GCAGGTGT others(360): Show |
1 | a0001c0001t0003g0195 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.264+1061_264+1062i others(369): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619268 | ||||||
| chr16:619274 | GTGGTGTA others(118): Show |
G | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+1020_264+1144d others(2): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 619274 | ||||||
| chr16:619283 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0025 others(6): Show |
9 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+1023T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619283 | |||||||
| chr16:619342 | C | G | 1 | a0001c0001t0003g0195 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.264+1082C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619342 | |||||||
| chr16:619416 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+1156C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619416 | |||||||
| chr16:619480 | G | T | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+1220G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619480 | |||||||
| chr16:619708 | T | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0025 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.264+1448T>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619708 | |||||||
| chr16:619784 | C | A | 5 | a0001c0001t0007g0325 a0001c0001t0010g0032 a0001c0001t0010g0035 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+1524C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619784 | |||||||
| chr16:619857 | G | T | 55 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.264+1597G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619857 | |||||||
| chr16:619865 | A | G | 5 | a0001c0001t0001g0222 a0001c0001t0003g0210 a0001c0001t0003g0213 others(2): Show |
5 | HG01074.hp2 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1605A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619865 | |||||||
| chr16:619872 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0124 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.264+1612G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619872 | |||||||
| chr16:619961 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.264+1701C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619961 | |||||||
| chr16:619995 | G | A | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+1735G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 619995 | |||||||
| chr16:620097 | A | G | 1 | a0001c0001t0002g0302 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.264+1837A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620097 | |||||||
| chr16:620117 | T | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0041 others(206): Show |
213 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.264+1857T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620117 | |||||||
| chr16:620122 | C | T | 2 | a0001c0001t0003g0179 a0001c0001t0003g0184 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.264+1862C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620122 | |||||||
| chr16:620133 | G | T | 1 | a0001c0001t0002g0284 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.264+1873G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620133 | |||||||
| chr16:620168 | A | G | 196 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(193): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.264+1908A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620168 | |||||||
| chr16:620336 | TGAGCCGA others(28): Show |
T | 4 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 others(1): Show |
4 | HG02257.hp2 HG03139.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+2079_264+2113d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620336 | ||||||
| chr16:620341 | C | T | 1 | a0001c0001t0013g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264+2081C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620341 | |||||||
| chr16:620371 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+2111C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620371 | |||||||
| chr16:620391 | C | CA | 6 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG00621.hp2 HG02083.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+2140dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620391 | ||||||
| chr16:620470 | C | A | 7 | a0001c0001t0004g0157 a0001c0001t0004g0159 a0001c0001t0004g0160 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+2210C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620470 | |||||||
| chr16:620522 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+2262C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620522 | |||||||
| chr16:620596 | AGGCTCCA others(27): Show |
A | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.264+2345_264+2378d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620596 | ||||||
| chr16:620605 | T | C | 200 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(197): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.264+2345T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620605 | |||||||
| chr16:620626 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.264+2366C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620626 | |||||||
| chr16:620664 | CGGGCTCC others(27): Show |
C | 2 | a0001c0001t0002g0066 a0001c0001t0018g0089 |
2 | NA18988.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.264+2434_264+2467d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620664 | ||||||
| chr16:620692 | CCCCGATG others(29): Show |
C | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+2435_264+2470d others(38): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620692 | ||||||
| chr16:620693 | C | CCCGACGG others(28): Show |
1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.264+2437_264+2438i others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620693 | ||||||
| chr16:620698 | T | C | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.264+2438T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620698 | |||||||
| chr16:620698 | T | TGGGCTCC others(28): Show |
1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+2534_264+2568d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620698 | ||||||
| chr16:620698 | TGGGCTCC others(28): Show |
T | 71 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0155 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.264+2534_264+2568d others(37): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620698 | ||||||
| chr16:620710 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0002g0254 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.264+2450C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620710 | |||||||
| chr16:620712 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.264+2452G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620712 | |||||||
| chr16:620724 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0048 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+2464C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620724 | |||||||
| chr16:620727 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.264+2467C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620727 | |||||||
| chr16:620730 | C | T | 1 | a0001c0001t0006g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.264+2470C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620730 | |||||||
| chr16:620733 | C | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+2473C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620733 | |||||||
| chr16:620765 | C | T | 16 | a0001c0001t0004g0157 a0001c0001t0004g0159 a0001c0001t0004g0160 others(13): Show |
16 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.264+2505C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620765 | |||||||
| chr16:620794 | C | A | 5 | a0001c0001t0003g0173 a0001c0001t0003g0197 a0001c0001t0003g0201 others(2): Show |
5 | HG03098.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+2534C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620794 | |||||||
| chr16:620795 | CCCGCCGA others(27): Show |
C | 5 | a0001c0001t0003g0173 a0001c0001t0003g0197 a0001c0001t0003g0201 others(2): Show |
5 | HG03098.hp1 HG03471.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+2538_264+2571d others(36): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 620795 | ||||||
| chr16:620853 | A | G | 3 | a0001c0001t0006g0028 a0001c0001t0007g0034 a0001c0001t0028g0030 |
3 | HG03225.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.264+2593A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620853 | |||||||
| chr16:620895 | G | C | 1 | a0001c0001t0002g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.264+2635G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620895 | |||||||
| chr16:620934 | T | A | 1 | a0001c0001t0002g0315 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264+2674T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620934 | |||||||
| chr16:620964 | G | T | 22 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0187 others(19): Show |
22 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+2704G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620964 | |||||||
| chr16:620998 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0002g0294 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.264+2738C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 620998 | |||||||
| chr16:621209 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+2949G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621209 | |||||||
| chr16:621211 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0003g0190 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.264+2951C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621211 | |||||||
| chr16:621233 | C | G | 1 | a0001c0001t0002g0267 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.264+2973C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621233 | |||||||
| chr16:621245 | G | A | 58 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.264+2985G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621245 | |||||||
| chr16:621257 | GTC | G | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+3002_264+3003d others(4): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 621257 | ||||||
| chr16:621415 | TA | T | 4 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 others(1): Show |
4 | HG02257.hp2 HG03139.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+3156delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621415 | |||||||
| chr16:621451 | G | A | 3 | a0001c0001t0012g0149 a0001c0001t0012g0150 a0001c0001t0021g0180 |
3 | HG02280.hp2 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.264+3191G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621451 | |||||||
| chr16:621453 | G | T | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.264+3193G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621453 | |||||||
| chr16:621502 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.264+3242C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621502 | |||||||
| chr16:621527 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.264+3267C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621527 | |||||||
| chr16:621556 | C | T | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.264+3296C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621556 | |||||||
| chr16:621653 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.264+3393C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621653 | |||||||
| chr16:621682 | A | G | 202 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(199): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.264+3422A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621682 | |||||||
| chr16:621906 | G | A | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.265-3526G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621906 | |||||||
| chr16:621914 | G | C | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-3518G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621914 | |||||||
| chr16:621919 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0106 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.265-3513G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621919 | |||||||
| chr16:621939 | G | A | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-3493G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621939 | |||||||
| chr16:621987 | A | G | 9 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0251 others(6): Show |
9 | HG01081.hp2 NA18945.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-3445A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 621987 | |||||||
| chr16:622040 | G | A | 125 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(122): Show |
127 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.265-3392G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622040 | |||||||
| chr16:622243 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-3189C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622243 | |||||||
| chr16:622244 | G | A | 2 | a0001c0001t0010g0032 a0001c0001t0010g0035 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.265-3188G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622244 | |||||||
| chr16:622284 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0288 |
2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.265-3148G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622284 | |||||||
| chr16:622328 | A | G | 1 | a0001c0001t0002g0257 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.265-3104A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622328 | |||||||
| chr16:622361 | C | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0048 others(28): Show |
32 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.265-3071C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622361 | |||||||
| chr16:622406 | ACGT | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0048 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.265-3024_265-3022d others(5): Show |
RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 622406 | ||||||
| chr16:622412 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.265-3020G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622412 | |||||||
| chr16:622469 | G | A | 13 | a0001c0001t0003g0185 a0001c0001t0003g0186 a0001c0001t0003g0191 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.265-2963G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622469 | |||||||
| chr16:622478 | T | C | 2 | a0001c0001t0002g0257 a0001c0001t0002g0287 |
2 | NA19007.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.265-2954T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622478 | |||||||
| chr16:622484 | C | G | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-2948C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622484 | |||||||
| chr16:622506 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.265-2926C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622506 | |||||||
| chr16:622507 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.265-2925G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622507 | |||||||
| chr16:622548 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.265-2884G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622548 | |||||||
| chr16:622598 | C | T | 1 | a0001c0001t0034g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-2834C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622598 | |||||||
| chr16:622627 | G | C | 48 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0169 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.265-2805G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622627 | |||||||
| chr16:622661 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.265-2771G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622661 | |||||||
| chr16:622662 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.265-2770C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622662 | |||||||
| chr16:622799 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0041 others(197): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.265-2633T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622799 | |||||||
| chr16:622919 | C | T | 1 | a0001c0001t0002g0249 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.265-2513C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622919 | |||||||
| chr16:622972 | G | A | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.265-2460G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622972 | |||||||
| chr16:622991 | C | T | 3 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0016g0326 |
3 | HG02083.hp2 NA18612.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.265-2441C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 622991 | |||||||
| chr16:623044 | G | A | 2 | a0001c0001t0002g0305 a0001c0001t0002g0320 |
2 | HG00280.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.265-2388G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623044 | |||||||
| chr16:623060 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.265-2372C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623060 | |||||||
| chr16:623158 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.265-2274G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623158 | |||||||
| chr16:623167 | A | G | 3 | a0001c0001t0007g0152 a0001c0001t0007g0153 a0001c0001t0007g0154 |
3 | HG02622.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.265-2265A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623167 | |||||||
| chr16:623200 | C | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0122 a0001c0001t0001g0145 |
4 | HG01106.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-2232C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623200 | |||||||
| chr16:623277 | C | T | 112 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(109): Show |
114 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.265-2155C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623277 | |||||||
| chr16:623371 | C | T | 1 | a0001c0001t0012g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.265-2061C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623371 | |||||||
| chr16:623376 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.265-2056G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623376 | |||||||
| chr16:623383 | C | G | 2 | a0001c0001t0002g0288 a0001c0001t0032g0017 |
2 | HG03490.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.265-2049C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623383 | |||||||
| chr16:623398 | C | T | 13 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(10): Show |
13 | HG01884.hp1 HG02280.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.265-2034C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623398 | |||||||
| chr16:623430 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0041 others(93): Show |
98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.265-2002G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623430 | |||||||
| chr16:623454 | C | T | 37 | a0001c0001t0002g0019 a0001c0001t0002g0239 a0001c0001t0002g0249 others(34): Show |
37 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.265-1978C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623454 | |||||||
| chr16:623465 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-1967C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623465 | |||||||
| chr16:623515 | A | G | 1 | a0001c0001t0003g0197 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.265-1917A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623515 | |||||||
| chr16:623537 | C | T | 1 | a0001c0001t0029g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.265-1895C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623537 | |||||||
| chr16:623577 | C | A | 24 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.265-1855C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623577 | |||||||
| chr16:623584 | C | T | 1 | a0001c0001t0004g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.265-1848C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623584 | |||||||
| chr16:623596 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.265-1836G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623596 | |||||||
| chr16:623636 | C | CA | 14 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0065 others(11): Show |
14 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-1780dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 623636 | ||||||
| chr16:623636 | CA | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0163 a0001c0001t0002g0018 others(3): Show |
6 | HG01993.hp1 HG01993.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-1780delA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 623636 | ||||||
| chr16:623793 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.265-1639A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623793 | |||||||
| chr16:623948 | A | T | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.265-1484A>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 623948 | |||||||
| chr16:624006 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.265-1426C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624006 | |||||||
| chr16:624024 | T | C | 111 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(108): Show |
113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-1408T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624024 | |||||||
| chr16:624029 | C | T | 111 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(108): Show |
113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-1403C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624029 | |||||||
| chr16:624060 | G | C | 2 | a0001c0001t0002g0176 a0001c0001t0002g0247 |
2 | NA18981.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.265-1372G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624060 | |||||||
| chr16:624090 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | NA18988.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.265-1342C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624090 | |||||||
| chr16:624205 | C | A | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.265-1227C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624205 | |||||||
| chr16:624424 | G | A | 201 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(198): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.265-1008G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624424 | |||||||
| chr16:624565 | T | TA | 3 | a0001c0001t0001g0119 a0001c0001t0002g0330 a0002c0002t0024g0229 |
3 | HG00741.hp1 NA18957.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.265-862dupA | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 624565 | ||||||
| chr16:624571 | C | T | 1 | a0001c0001t0032g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.265-861C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624571 | |||||||
| chr16:624601 | C | T | 24 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0206 others(21): Show |
25 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.265-831C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624601 | |||||||
| chr16:624737 | G | A | 111 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(108): Show |
113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-695G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624737 | |||||||
| chr16:624770 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.265-662G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 624770 | |||||||
| chr16:625067 | C | A | 16 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0239 others(13): Show |
16 | HG00639.hp1 HG00741.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.265-365C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625067 | |||||||
| chr16:625087 | AC | A | 132 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(129): Show |
134 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.265-344delC | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625087 | |||||||
| chr16:625101 | C | T | 8 | a0001c0001t0003g0155 a0001c0001t0006g0028 a0001c0001t0006g0166 others(5): Show |
8 | HG01884.hp2 HG01981.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.265-331C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625101 | |||||||
| chr16:625215 | G | A | 133 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(130): Show |
135 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.265-217G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625215 | |||||||
| chr16:625281 | G | C | 18 | a0001c0001t0004g0157 a0001c0001t0004g0159 a0001c0001t0004g0160 others(15): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.265-151G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625281 | |||||||
| chr16:625310 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.265-122C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 3/5 | chr16 | 625310 | |||||||
| chr16:625617 | C | A | 18 | a0001c0001t0004g0157 a0001c0001t0004g0159 a0001c0001t0004g0160 others(15): Show |
18 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+108C>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625617 | |||||||
| chr16:625680 | T | C | 201 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(198): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.342+171T>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625680 | |||||||
| chr16:625709 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0124 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.343-190C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625709 | |||||||
| chr16:625712 | C | T | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.343-187C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625712 | |||||||
| chr16:625776 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.343-123G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625776 | |||||||
| chr16:625863 | C | T | 1 | a0001c0001t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.343-36C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625863 | |||||||
| chr16:625874 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG02257.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.343-25C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 4/5 | chr16 | 625874 | |||||||
| chr16:626155 | C | T | 1 | a0001c0004t0023g0038 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.565+34C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626155 | |||||||
| chr16:626180 | A | G | 1 | a0001c0001t0007g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.565+59A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626180 | |||||||
| chr16:626184 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565+63A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626184 | |||||||
| chr16:626216 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.565+95G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626216 | |||||||
| chr16:626239 | G | A | 2 | a0001c0001t0010g0035 a0001c0001t0020g0031 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.565+118G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626239 | |||||||
| chr16:626257 | C | G | 1 | a0002c0002t0024g0229 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.565+136C>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626257 | |||||||
| chr16:626261 | G | C | 65 | a0001c0001t0001g0222 a0001c0001t0003g0011 a0001c0001t0003g0155 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.565+140G>C | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626261 | |||||||
| chr16:626325 | G | A | 3 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 |
3 | HG02280.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.565+204G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626325 | |||||||
| chr16:626492 | G | A | 31 | a0001c0001t0001g0087 a0001c0001t0001g0097 a0001c0001t0003g0171 others(28): Show |
31 | HG01433.hp2 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.565+371G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626492 | |||||||
| chr16:626686 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.565+565C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626686 | |||||||
| chr16:626735 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.566-607C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626735 | |||||||
| chr16:626795 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.566-547G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626795 | |||||||
| chr16:626898 | A | G | 1 | a0001c0001t0029g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.566-444A>G | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626898 | |||||||
| chr16:626989 | C | T | 75 | a0001c0001t0001g0098 a0001c0001t0002g0320 a0001c0001t0003g0011 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.566-353C>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 626989 | |||||||
| chr16:627000 | T | A | 3 | a0001c0001t0010g0032 a0001c0001t0010g0035 a0001c0001t0020g0031 |
3 | HG02257.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.566-342T>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 627000 | |||||||
| chr16:627020 | G | T | 131 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(128): Show |
133 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.566-322G>T | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 627020 | |||||||
| chr16:627191 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.566-151G>A | RAB40C | ENSG00000197562.10 | transcript | ENST00000248139.8 | protein_coding | 5/5 | chr16 | 627191 |