Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54916 |
| ensemblid | ENSG00000070269.14 |
| hgncid | 20185 |
| symbol | TMEM260 |
| name | transmembrane protein 260 |
| refseq_nuc | NM_017799.4 |
| refseq_prot | NP_060269.3 |
| ensembl_nuc | ENST00000261556.11 |
| ensembl_prot | ENSP00000261556.6 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 56579798 |
| end | 56649515 |
| strand | + |
| ver | v1.2 |
| region | chr14:56579798-56649515 |
| region5000 | chr14:56574798-56654515 |
| regionname0 | TMEM260_chr14_56579798_56649515 |
| regionname5000 | TMEM260_chr14_56574798_56654515 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 707 | 233 | 60 | 33 | 108 | 8 | 24 | 88 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0002 | 1/1 | 707 | 88 | 14 | 15 | 47 | 1 | 9 | 35 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0003 | 0/0 | 707 | 24 | 6 | 8 | 1 | 3 | 6 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0004 | 0/0 | 707 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0005 | 0/0 | 707 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0006 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0007 | 0/0 | 707 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0008 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0009 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0010 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0011 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0012 | 0/0 | 707 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0013 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0014 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| a0015 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | MSPHG others(702): Show |
chr14 | 56574798 | 56654515 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2121 | 124 | 36 | 12 | 57 | 5 | 14 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0001c0002 | 0/0 | 2121 | 75 | 4 | 17 | 44 | 2 | 8 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0001c0004 | 0/0 | 2121 | 32 | 19 | 3 | 7 | 1 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0001c0011 | 0/0 | 2121 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0001c0020 | 0/0 | 2121 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0002c0003 | 0/0 | 2121 | 34 | 1 | 7 | 26 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0002c0005 | 1/1 | 2121 | 29 | 12 | 5 | 0 | 1 | 9 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0002c0006 | 0/0 | 2121 | 25 | 1 | 3 | 21 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0003c0007 | 0/0 | 2121 | 24 | 6 | 8 | 1 | 3 | 6 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0004c0008 | 0/0 | 2121 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0005c0009 | 0/0 | 2121 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0006c0010 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0007c0017 | 0/0 | 2121 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0008c0015 | 0/0 | 2121 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0009c0012 | 0/0 | 2121 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0010c0013 | 0/0 | 2121 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0011c0016 | 0/0 | 2121 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0012c0014 | 0/0 | 2121 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0013c0019 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0014c0018 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 | ||
| a0015c0021 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | ATGAG others(2116): Show |
chr14 | 56574798 | 56654515 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4259 | 42 | 13 | 2 | 21 | 0 | 6 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0002 | 0/0 | 4261 | 43 | 7 | 9 | 16 | 4 | 7 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4256): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0005 | 0/0 | 4259 | 10 | 0 | 1 | 7 | 1 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0006 | 0/0 | 4259 | 10 | 10 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0008 | 0/0 | 4259 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0009 | 0/0 | 4260 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4255): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0010 | 0/0 | 4261 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4256): Show |
chr14 | 56574798 | 56654515 |
| a0001c0001t0025 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | TACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0002t0001 | 0/0 | 4259 | 73 | 4 | 17 | 43 | 2 | 7 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0002t0019 | 0/0 | 4260 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4255): Show |
chr14 | 56574798 | 56654515 |
| a0001c0002t0023 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0004t0003 | 0/0 | 4258 | 9 | 0 | 0 | 7 | 1 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0001c0004t0004 | 0/0 | 4258 | 16 | 13 | 3 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0001c0004t0011 | 0/0 | 4257 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4252): Show |
chr14 | 56574798 | 56654515 |
| a0001c0004t0014 | 0/0 | 4258 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0001c0004t0015 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0001c0004t0016 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0001c0011t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0001c0020t0011 | 0/0 | 4257 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4252): Show |
chr14 | 56574798 | 56654515 |
| a0002c0003t0001 | 0/0 | 4259 | 24 | 1 | 4 | 19 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0003t0007 | 0/0 | 4259 | 7 | 0 | 3 | 4 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0003t0017 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0003t0020 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0003t0021 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0005t0001 | 1/0 | 4259 | 13 | 10 | 1 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0005t0002 | 0/1 | 4261 | 11 | 1 | 4 | 0 | 1 | 4 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4256): Show |
chr14 | 56574798 | 56654515 |
| a0002c0005t0012 | 0/0 | 4260 | 4 | 1 | 0 | 0 | 0 | 3 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4255): Show |
chr14 | 56574798 | 56654515 |
| a0002c0005t0013 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0002c0006t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0002c0006t0003 | 0/0 | 4258 | 24 | 0 | 3 | 21 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0003c0007t0001 | 0/0 | 4259 | 19 | 5 | 8 | 0 | 3 | 3 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0003c0007t0006 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0003c0007t0013 | 0/0 | 4258 | 3 | 0 | 0 | 1 | 0 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0003c0007t0022 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0004c0008t0004 | 0/0 | 4258 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0004c0008t0005 | 0/0 | 4259 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0004c0008t0006 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0004c0008t0018 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4253): Show |
chr14 | 56574798 | 56654515 |
| a0005c0009t0001 | 0/0 | 4259 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0006c0010t0001 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0007c0017t0007 | 0/0 | 4259 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0008c0015t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0009c0012t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0010c0013t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0011c0016t0001 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0012c0014t0024 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0013c0019t0001 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0014c0018t0001 | 0/0 | 4259 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4254): Show |
chr14 | 56574798 | 56654515 |
| a0015c0021t0002 | 0/0 | 4261 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | GACCC others(4256): Show |
chr14 | 56574798 | 56654515 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0010g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0001t0025g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0002 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0019g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0002t0023g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0011g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0014g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0015g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0004t0016g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0011t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0001c0020t0011g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0017g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0020g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0003t0021g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0019 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0002g0312 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0012g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0012g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0005t0013g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0002c0006t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0013g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0013g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0013g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0003c0007t0022g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0004c0008t0018g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0005c0009t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0005c0009t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0006c0010t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0007c0017t0007g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0008c0015t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0009c0012t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0010c0013t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0011c0016t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0012c0014t0024g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0013c0019t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0014c0018t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| a0015c0021t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00099 | hp2 | a0002 | c0005 | t0002 | g0016 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00140 | hp1 | a0003 | c0007 | t0001 | g0255 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | GBR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00280 | hp1 | a0003 | c0007 | t0001 | g0270 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0054 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | FIN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00438 | hp1 | a0001 | c0002 | t0023 | g0102 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00609 | hp2 | a0002 | c0006 | t0003 | g0276 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00621 | hp2 | a0006 | c0010 | t0001 | g0093 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00642 | hp1 | a0002 | c0005 | t0002 | g0017 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | CHS | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00735 | hp1 | a0003 | c0007 | t0001 | g0254 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00738 | hp2 | a0002 | c0005 | t0002 | g0017 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01070 | hp1 | a0002 | c0006 | t0003 | g0021 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0090 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01071 | hp1 | a0002 | c0006 | t0003 | g0021 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01081 | hp2 | a0001 | c0004 | t0004 | g0188 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01099 | hp2 | a0007 | c0017 | t0007 | g0024 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01109 | hp1 | a0005 | c0009 | t0001 | g0159 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01109 | hp2 | a0003 | c0007 | t0001 | g0256 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01167 | hp2 | a0003 | c0007 | t0001 | g0258 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01175 | hp2 | a0003 | c0007 | t0001 | g0248 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01243 | hp1 | a0001 | c0004 | t0004 | g0185 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01243 | hp2 | a0001 | c0004 | t0004 | g0179 | AMR | PUR | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01255 | hp2 | a0003 | c0007 | t0001 | g0266 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0058 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01256 | hp2 | a0003 | c0007 | t0001 | g0257 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01261 | hp1 | a0003 | c0007 | t0001 | g0247 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0327 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01361 | hp2 | a0002 | c0005 | t0002 | g0218 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01433 | hp1 | a0001 | c0020 | t0011 | g0302 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01433 | hp2 | a0004 | c0008 | t0005 | g0249 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01496 | hp1 | a0002 | c0003 | t0007 | g0111 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01884 | hp1 | a0003 | c0007 | t0006 | g0250 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01884 | hp2 | a0002 | c0005 | t0001 | g0014 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0194 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01891 | hp2 | a0002 | c0005 | t0001 | g0015 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01934 | hp2 | a0002 | c0005 | t0002 | g0231 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01943 | hp2 | a0004 | c0008 | t0005 | g0251 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01978 | hp1 | a0003 | c0007 | t0001 | g0268 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01981 | hp2 | a0002 | c0005 | t0001 | g0019 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02015 | hp1 | a0002 | c0006 | t0003 | g0280 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02027 | hp1 | a0002 | c0003 | t0001 | g0107 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0315 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02055 | hp1 | a0002 | c0005 | t0002 | g0016 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02074 | hp1 | a0002 | c0003 | t0020 | g0097 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02080 | hp1 | a0002 | c0006 | t0003 | g0309 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02080 | hp2 | a0002 | c0003 | t0007 | g0035 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02135 | hp1 | a0002 | c0003 | t0017 | g0311 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0106 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02145 | hp1 | a0008 | c0015 | t0001 | g0055 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02145 | hp2 | a0001 | c0004 | t0004 | g0178 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02148 | hp1 | a0002 | c0003 | t0007 | g0025 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | CDX | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02257 | hp1 | a0002 | c0005 | t0001 | g0172 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0241 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02300 | hp2 | a0002 | c0006 | t0003 | g0285 | AMR | PEL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02451 | hp2 | a0003 | c0007 | t0001 | g0260 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0123 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02572 | hp1 | a0003 | c0007 | t0001 | g0253 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0192 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02622 | hp2 | a0001 | c0004 | t0004 | g0186 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02630 | hp1 | a0001 | c0004 | t0004 | g0187 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02698 | hp1 | a0003 | c0007 | t0001 | g0263 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02698 | hp2 | a0002 | c0005 | t0002 | g0154 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02717 | hp1 | a0003 | c0007 | t0001 | g0259 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02717 | hp2 | a0009 | c0012 | t0001 | g0119 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02738 | hp1 | a0001 | c0004 | t0016 | g0306 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0325 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02809 | hp1 | a0004 | c0008 | t0006 | g0113 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02818 | hp1 | a0001 | c0004 | t0004 | g0182 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02886 | hp2 | a0001 | c0004 | t0004 | g0184 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02895 | hp1 | a0002 | c0005 | t0001 | g0234 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02922 | hp2 | a0001 | c0004 | t0014 | g0020 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02965 | hp2 | a0001 | c0004 | t0004 | g0005 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02970 | hp2 | a0002 | c0005 | t0012 | g0134 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02976 | hp1 | a0002 | c0005 | t0001 | g0014 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03017 | hp1 | a0002 | c0005 | t0012 | g0133 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03041 | hp1 | a0001 | c0004 | t0014 | g0020 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03041 | hp2 | a0003 | c0007 | t0001 | g0262 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03130 | hp1 | a0001 | c0004 | t0004 | g0005 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03130 | hp2 | a0010 | c0013 | t0001 | g0167 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03139 | hp2 | a0003 | c0007 | t0001 | g0252 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03195 | hp1 | a0001 | c0004 | t0004 | g0181 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03195 | hp2 | a0004 | c0008 | t0004 | g0127 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03209 | hp1 | a0001 | c0004 | t0004 | g0183 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03209 | hp2 | a0005 | c0009 | t0001 | g0135 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0195 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03225 | hp2 | a0002 | c0005 | t0001 | g0272 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03239 | hp1 | a0001 | c0004 | t0003 | g0295 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03239 | hp2 | a0002 | c0005 | t0002 | g0156 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03453 | hp1 | a0004 | c0008 | t0004 | g0128 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03486 | hp1 | a0001 | c0011 | t0001 | g0313 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03486 | hp2 | a0004 | c0008 | t0004 | g0175 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03516 | hp2 | a0002 | c0005 | t0001 | g0166 | AFR | ESN | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03579 | hp1 | a0011 | c0016 | t0001 | g0099 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03579 | hp2 | a0002 | c0005 | t0001 | g0173 | AFR | MSL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03669 | hp1 | a0002 | c0005 | t0002 | g0213 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03688 | hp1 | a0002 | c0005 | t0001 | g0158 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03688 | hp2 | a0002 | c0005 | t0002 | g0165 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03704 | hp2 | a0012 | c0014 | t0024 | g0038 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03710 | hp1 | a0002 | c0005 | t0012 | g0131 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03831 | hp2 | a0003 | c0007 | t0013 | g0267 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03834 | hp2 | a0003 | c0007 | t0001 | g0018 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG03927 | hp2 | a0003 | c0007 | t0001 | g0018 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04184 | hp2 | a0003 | c0007 | t0013 | g0264 | SAS | BEB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04199 | hp1 | a0001 | c0002 | t0019 | g0032 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04199 | hp2 | a0002 | c0005 | t0013 | g0210 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04228 | hp1 | a0003 | c0007 | t0022 | g0265 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0196 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18612 | hp2 | a0002 | c0006 | t0003 | g0286 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18747 | hp2 | a0013 | c0019 | t0001 | g0050 | EAS | CHB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18906 | hp2 | a0001 | c0004 | t0004 | g0177 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18939 | hp1 | a0001 | c0004 | t0003 | g0294 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18942 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18943 | hp2 | a0001 | c0001 | t0008 | g0126 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18951 | hp2 | a0002 | c0003 | t0007 | g0043 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18963 | hp2 | a0001 | c0004 | t0003 | g0308 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18964 | hp1 | a0001 | c0004 | t0003 | g0293 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18965 | hp2 | a0002 | c0006 | t0003 | g0283 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18967 | hp1 | a0001 | c0001 | t0025 | g0320 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18970 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0069 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18979 | hp2 | a0002 | c0006 | t0003 | g0304 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18980 | hp2 | a0002 | c0006 | t0003 | g0290 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18982 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18984 | hp1 | a0001 | c0004 | t0003 | g0278 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0314 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18989 | hp2 | a0002 | c0006 | t0003 | g0284 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18993 | hp2 | a0001 | c0004 | t0003 | g0292 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18998 | hp2 | a0001 | c0004 | t0003 | g0307 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18999 | hp1 | a0014 | c0018 | t0001 | g0003 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19000 | hp1 | a0002 | c0006 | t0003 | g0279 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19000 | hp2 | a0002 | c0003 | t0007 | g0003 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19002 | hp1 | a0002 | c0006 | t0003 | g0281 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19003 | hp1 | a0002 | c0006 | t0003 | g0287 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19005 | hp2 | a0002 | c0006 | t0003 | g0297 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19007 | hp1 | a0002 | c0006 | t0003 | g0296 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19009 | hp1 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19030 | hp1 | a0001 | c0004 | t0011 | g0300 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19030 | hp2 | a0001 | c0004 | t0004 | g0176 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19043 | hp1 | a0002 | c0005 | t0001 | g0168 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19043 | hp2 | a0001 | c0004 | t0015 | g0303 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19056 | hp2 | a0002 | c0006 | t0003 | g0282 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19058 | hp1 | a0002 | c0006 | t0003 | g0291 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19064 | hp1 | a0003 | c0007 | t0013 | g0246 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19065 | hp1 | a0002 | c0006 | t0003 | g0022 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19070 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19077 | hp1 | a0002 | c0006 | t0003 | g0305 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19078 | hp1 | a0002 | c0003 | t0007 | g0039 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19079 | hp1 | a0002 | c0003 | t0021 | g0045 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19081 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19082 | hp1 | a0002 | c0006 | t0003 | g0277 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19085 | hp1 | a0002 | c0006 | t0003 | g0022 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19086 | hp2 | a0002 | c0006 | t0003 | g0288 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19087 | hp1 | a0001 | c0004 | t0003 | g0298 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19087 | hp2 | a0015 | c0021 | t0002 | g0006 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19089 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19091 | hp1 | a0002 | c0006 | t0003 | g0289 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19240 | hp1 | a0004 | c0008 | t0018 | g0118 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ASW | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20129 | hp2 | a0001 | c0004 | t0011 | g0299 | AFR | ASW | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20752 | hp1 | a0001 | c0004 | t0003 | g0310 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0326 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20805 | hp2 | a0003 | c0007 | t0001 | g0261 | EUR | TSI | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20905 | hp1 | a0002 | c0005 | t0012 | g0132 | SAS | GIH | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | GIH | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG01123 | hp2 | a0002 | c0003 | t0007 | g0023 | AMR | CLM | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02109 | hp2 | a0001 | c0004 | t0004 | g0180 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02486 | hp1 | a0001 | c0004 | t0004 | g0005 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG02559 | hp2 | a0001 | c0004 | t0011 | g0301 | AFR | ACB | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0191 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| HG06807 | hp2 | a0002 | c0005 | t0001 | g0015 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0091 | AFR | USA | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| NA21309 | hp2 | a0002 | c0006 | t0001 | g0269 | AFR | LWK | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| homoSapiens | chm13v2 | a0002 | c0005 | t0002 | g0312 | REF | REF | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| homoSapiens | grch38p0 | a0002 | c0005 | t0001 | g0019 | REF | REF | TMEM260_chr14_56574798_56654515 | TMEM260 | chr14 | 56574798 | 56654515 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:56580018 | C | T | 1 | a0015 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.104C>T | p.Ala35Val | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 221/4259 | 104/2124 | 35/707 | chr14 | 56580018 | |||
| chr14:56580050 | C | A | 1 | a0006 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.136C>A | p.Pro46Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 253/4259 | 136/2124 | 46/707 | chr14 | 56580050 | |||
| chr14:56585852 | A | G | 1 | a0010 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.284A>G | p.Asn95Ser | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/16 | 401/4259 | 284/2124 | 95/707 | chr14 | 56585852 | |||
| chr14:56609137 | G | T | 1 | a0005 | 2 | HG01109.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.668G>T | p.Ser223Ile | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/16 | 785/4259 | 668/2124 | 223/707 | chr14 | 56609137 | |||
| chr14:56609202 | G | T | 2 | a0003 a0004 |
31 | HG00140.hp1 HG00280.hp1 HG00735.hp1 others(28): Show |
missense_variant | MODERATE | c.733G>T | p.Ala245Ser | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/16 | 850/4259 | 733/2124 | 245/707 | chr14 | 56609202 | |||
| chr14:56616015 | G | A | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.929G>A | p.Cys310Tyr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/16 | 1046/4259 | 929/2124 | 310/707 | chr14 | 56616015 | |||
| chr14:56625394 | G | A | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1411G>A | p.Glu471Lys | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/16 | 1528/4259 | 1411/2124 | 471/707 | chr14 | 56625394 | |||
| chr14:56632995 | A | C | 1 | a0013 | 1 | NA18747.hp2 | missense_variant&splice_region_variant | MODERATE | c.1548A>C | p.Gln516His | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/16 | 1665/4259 | 1548/2124 | 516/707 | chr14 | 56632995 | |||
| chr14:56633102 | T | C | 1 | a0011 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1655T>C | p.Ile552Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/16 | 1772/4259 | 1655/2124 | 552/707 | chr14 | 56633102 | |||
| chr14:56633141 | G | A | 9 | a0001 a0004 a0005 others(6): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
missense_variant | MODERATE | c.1694G>A | p.Ser565Asn | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/16 | 1811/4259 | 1694/2124 | 565/707 | chr14 | 56633141 | |||
| chr14:56634924 | G | T | 1 | a0014 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.1750G>T | p.Val584Leu | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/16 | 1867/4259 | 1750/2124 | 584/707 | chr14 | 56634924 | |||
| chr14:56636584 | G | A | 1 | a0009 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1855G>A | p.Ala619Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/16 | 1972/4259 | 1855/2124 | 619/707 | chr14 | 56636584 | |||
| chr14:56647339 | A | G | 1 | a0007 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1966A>G | p.Arg656Gly | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 2083/4259 | 1966/2124 | 656/707 | chr14 | 56647339 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:56580070 | C | T | 1 | a0001c0020 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.156C>T | p.Asp52Asp | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 273/4259 | 156/2124 | 52/707 | chr14 | 56580070 | |||
| chr14:56585793 | G | T | 9 | a0001c0002 a0002c0003 a0006c0010 others(6): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
synonymous_variant | LOW | c.225G>T | p.Thr75Thr | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/16 | 342/4259 | 225/2124 | 75/707 | chr14 | 56585793 | |||
| chr14:56585829 | T | C | 1 | a0001c0011 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.261T>C | p.Phe87Phe | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/16 | 378/4259 | 261/2124 | 87/707 | chr14 | 56585829 | |||
| chr14:56605620 | C | T | 3 | a0001c0004 a0001c0020 a0002c0006 |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
synonymous_variant | LOW | c.573C>T | p.His191His | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/16 | 690/4259 | 573/2124 | 191/707 | chr14 | 56605620 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:56579798 | G | T | 1 | a0001c0001t0025 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 117 | chr14 | 56579798 | ||||||
| chr14:56579846 | C | G | 1 | a0001c0001t0010 | 5 | HG02074.hp2 NA18942.hp2 NA18982.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 69 | chr14 | 56579846 | ||||||
| chr14:56579888 | T | A | 8 | a0001c0004t0003 a0001c0004t0011 a0001c0004t0014 others(5): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-27T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/16 | 27 | chr14 | 56579888 | ||||||
| chr14:56647567 | C | CA | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(2): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*72dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 73 | INFO_REALIGN_3_PRIME | chr14 | 56647567 | |||||
| chr14:56647604 | C | T | 1 | a0012c0014t0024 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 107 | chr14 | 56647604 | ||||||
| chr14:56647667 | G | A | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0025 others(8): Show |
81 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*170G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 170 | chr14 | 56647667 | ||||||
| chr14:56647816 | C | G | 3 | a0001c0001t0006 a0003c0007t0006 a0004c0008t0006 |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 319 | chr14 | 56647816 | ||||||
| chr14:56647854 | T | C | 5 | a0001c0004t0011 a0001c0004t0014 a0001c0004t0015 others(2): Show |
8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*357T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 357 | chr14 | 56647854 | ||||||
| chr14:56647922 | G | GA | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0002t0019 others(2): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*435dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 436 | INFO_REALIGN_3_PRIME | chr14 | 56647922 | |||||
| chr14:56647922 | GA | G | 15 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0025 others(12): Show |
84 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*435delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 435 | INFO_REALIGN_3_PRIME | chr14 | 56647922 | |||||
| chr14:56648029 | T | A | 1 | a0004c0008t0018 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 532 | chr14 | 56648029 | ||||||
| chr14:56648268 | T | TG | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0025 others(1): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*778dupG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 779 | INFO_REALIGN_3_PRIME | chr14 | 56648268 | |||||
| chr14:56648482 | C | G | 1 | a0001c0004t0016 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*985C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 985 | chr14 | 56648482 | ||||||
| chr14:56648688 | G | C | 1 | a0002c0003t0020 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1191 | chr14 | 56648688 | ||||||
| chr14:56648904 | C | G | 5 | a0001c0002t0023 a0001c0004t0003 a0002c0005t0013 others(2): Show |
38 | HG00438.hp1 HG00609.hp2 HG01070.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1407C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1407 | chr14 | 56648904 | ||||||
| chr14:56648935 | T | G | 1 | a0002c0003t0021 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1438T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1438 | chr14 | 56648935 | ||||||
| chr14:56648962 | G | T | 1 | a0003c0007t0022 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1465G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1465 | chr14 | 56648962 | ||||||
| chr14:56649373 | T | TG | 1 | a0002c0005t0012 | 4 | HG02970.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1878dupG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1879 | INFO_REALIGN_3_PRIME | chr14 | 56649373 | |||||
| chr14:56649421 | T | C | 3 | a0001c0001t0005 a0001c0001t0025 a0004c0008t0005 |
13 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1924T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1924 | chr14 | 56649421 | ||||||
| chr14:56649474 | TA | T | 3 | a0001c0004t0011 a0001c0004t0015 a0001c0020t0011 |
5 | HG01433.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1987delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 16/16 | 1987 | INFO_REALIGN_3_PRIME | chr14 | 56649474 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:56580111 | C | A | 97 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(94): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.160+37C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580111 | |||||||
| chr14:56580148 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+74C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580148 | |||||||
| chr14:56580195 | C | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+121C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580195 | |||||||
| chr14:56580311 | G | A | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+237G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580311 | |||||||
| chr14:56580425 | A | G | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+351A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580425 | |||||||
| chr14:56580532 | A | G | 1 | a0002c0003t0007g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.160+458A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580532 | |||||||
| chr14:56580546 | A | G | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+472A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580546 | |||||||
| chr14:56580562 | G | C | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.160+488G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580562 | |||||||
| chr14:56580632 | C | G | 40 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(37): Show |
43 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+558C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580632 | |||||||
| chr14:56580755 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+681C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580755 | |||||||
| chr14:56580764 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+690T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580764 | |||||||
| chr14:56580822 | T | C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.160+748T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580822 | |||||||
| chr14:56580928 | C | T | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.160+854C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580928 | |||||||
| chr14:56580937 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160+863C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56580937 | |||||||
| chr14:56581024 | A | G | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+950A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581024 | |||||||
| chr14:56581213 | A | G | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+1139A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581213 | |||||||
| chr14:56581326 | G | A | 290 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(287): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.160+1252G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581326 | |||||||
| chr14:56581489 | G | C | 1 | a0001c0001t0006g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+1415G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581489 | |||||||
| chr14:56581802 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.160+1728C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581802 | |||||||
| chr14:56581811 | C | T | 58 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(55): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.160+1737C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581811 | |||||||
| chr14:56581817 | T | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.160+1743T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581817 | |||||||
| chr14:56581819 | A | G | 57 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(54): Show |
62 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+1745A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581819 | |||||||
| chr14:56581964 | G | A | 3 | a0002c0003t0007g0023 a0002c0003t0007g0025 a0007c0017t0007g0024 |
3 | HG01099.hp2 HG01123.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.160+1890G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56581964 | |||||||
| chr14:56582093 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.160+2019C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582093 | |||||||
| chr14:56582255 | C | A | 2 | a0001c0001t0002g0275 a0001c0004t0014g0020 |
3 | HG02559.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.160+2181C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582255 | |||||||
| chr14:56582279 | C | G | 121 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(118): Show |
136 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.160+2205C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582279 | |||||||
| chr14:56582396 | A | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.160+2322A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582396 | |||||||
| chr14:56582523 | C | T | 2 | a0002c0005t0001g0172 a0002c0005t0001g0173 |
2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.160+2449C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582523 | |||||||
| chr14:56582614 | C | T | 2 | a0001c0002t0001g0108 a0002c0003t0001g0109 |
2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.161-2387C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582614 | |||||||
| chr14:56582777 | C | G | 52 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(49): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.161-2224C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582777 | |||||||
| chr14:56582935 | TTTATC | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(95): Show |
113 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.161-2063_161-2059d others(7): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56582935 | ||||||
| chr14:56582947 | G | A | 3 | a0001c0001t0008g0314 a0001c0001t0008g0315 a0001c0001t0008g0316 |
3 | HG02040.hp2 NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.161-2054G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56582947 | |||||||
| chr14:56583145 | A | T | 2 | a0001c0001t0002g0275 a0001c0004t0014g0020 |
3 | HG02559.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.161-1856A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583145 | |||||||
| chr14:56583208 | C | G | 1 | a0001c0002t0001g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-1793C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583208 | |||||||
| chr14:56583248 | T | G | 101 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(98): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.161-1753T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583248 | |||||||
| chr14:56583253 | G | C | 1 | a0001c0001t0006g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.161-1748G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583253 | |||||||
| chr14:56583490 | G | A | 6 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(3): Show |
6 | HG02523.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-1511G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583490 | |||||||
| chr14:56583503 | A | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-1498A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583503 | |||||||
| chr14:56583894 | A | G | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-1107A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583894 | |||||||
| chr14:56583903 | G | A | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-1098G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56583903 | |||||||
| chr14:56583906 | C | CGTCA | 42 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(39): Show |
45 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.161-1094_161-1091d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583906 | ||||||
| chr14:56583990 | T | TTG | 18 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(15): Show |
19 | HG00140.hp1 HG00609.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-975_161-974dup others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | ||||||
| chr14:56583990 | T | TTGTG | 11 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(8): Show |
11 | HG00621.hp1 HG01358.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-977_161-974dup others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | ||||||
| chr14:56583990 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0008g0314 a0001c0001t0008g0315 a0001c0001t0008g0316 |
3 | HG02040.hp2 NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.161-981_161-974dup others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | ||||||
| chr14:56583990 | TTG | T | 104 | a0001c0001t0001g0120 a0001c0001t0001g0151 a0001c0001t0001g0152 others(101): Show |
123 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.161-975_161-974del others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | ||||||
| chr14:56583990 | TTGTG | T | 121 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(118): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.161-977_161-974del others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | ||||||
| chr14:56583990 | TTGTGTGT others(11): Show |
T | 1 | a0001c0002t0001g0080 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.161-991_161-974del others(18): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 56583990 | ||||||
| chr14:56584084 | A | G | 15 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(12): Show |
17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-917A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584084 | |||||||
| chr14:56584179 | G | C | 15 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(12): Show |
17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-822G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584179 | |||||||
| chr14:56584382 | T | C | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-619T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584382 | |||||||
| chr14:56584441 | G | A | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.161-560G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584441 | |||||||
| chr14:56584473 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161-528C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584473 | |||||||
| chr14:56584630 | G | A | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-371G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584630 | |||||||
| chr14:56584630 | G | T | 2 | a0002c0003t0001g0106 a0002c0003t0001g0107 |
2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.161-371G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584630 | |||||||
| chr14:56584672 | A | G | 1 | a0001c0001t0009g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161-329A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584672 | |||||||
| chr14:56584729 | C | T | 1 | a0003c0007t0001g0270 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-272C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584729 | |||||||
| chr14:56584773 | C | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-228C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584773 | |||||||
| chr14:56584775 | A | G | 2 | a0001c0002t0001g0104 a0001c0002t0001g0105 |
2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.161-226A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584775 | |||||||
| chr14:56584791 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.161-210C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584791 | |||||||
| chr14:56584812 | T | C | 4 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(1): Show |
4 | NA18959.hp1 NA18967.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-189T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584812 | |||||||
| chr14:56584879 | G | T | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.161-122G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584879 | |||||||
| chr14:56584971 | A | G | 1 | a0001c0002t0001g0103 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.161-30A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 1/15 | chr14 | 56584971 | |||||||
| chr14:56585174 | ATTTAC | A | 7 | a0001c0004t0004g0176 a0001c0004t0004g0177 a0001c0004t0004g0178 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+147_192+151del others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 56585174 | ||||||
| chr14:56585246 | CTTA | C | 3 | a0002c0006t0003g0276 a0002c0006t0003g0277 a0003c0007t0001g0270 |
3 | HG00280.hp1 HG00609.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.192+219_192+221del others(3): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 56585246 | ||||||
| chr14:56585537 | C | T | 2 | a0001c0001t0002g0239 a0002c0005t0002g0017 |
3 | HG00642.hp1 HG00738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.193-224C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | chr14 | 56585537 | |||||||
| chr14:56585564 | G | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(109): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.193-197G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 2/15 | chr14 | 56585564 | |||||||
| chr14:56586069 | C | T | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+157C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586069 | |||||||
| chr14:56586179 | G | A | 302 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.344+267G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586179 | |||||||
| chr14:56586204 | A | T | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+292A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586204 | |||||||
| chr14:56586272 | C | T | 1 | a0001c0002t0023g0102 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.344+360C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586272 | |||||||
| chr14:56586297 | G | A | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.344+385G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586297 | |||||||
| chr14:56586304 | C | T | 108 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(105): Show |
123 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.344+392C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586304 | |||||||
| chr14:56586305 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.344+393C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586305 | |||||||
| chr14:56586377 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.344+465A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586377 | |||||||
| chr14:56586415 | G | A | 2 | a0004c0008t0004g0127 a0004c0008t0004g0128 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.344+503G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586415 | |||||||
| chr14:56586461 | T | C | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+549T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586461 | |||||||
| chr14:56586515 | A | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+603A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586515 | |||||||
| chr14:56586635 | G | A | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+723G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586635 | |||||||
| chr14:56586675 | A | T | 8 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0002g0236 others(5): Show |
8 | HG01358.hp1 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+763A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586675 | |||||||
| chr14:56586936 | T | G | 5 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(2): Show |
5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1024T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56586936 | |||||||
| chr14:56587035 | G | C | 5 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(2): Show |
5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1123G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587035 | |||||||
| chr14:56587147 | T | C | 127 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(124): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.344+1235T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587147 | |||||||
| chr14:56587266 | T | G | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+1354T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587266 | |||||||
| chr14:56587386 | T | C | 102 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(99): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.344+1474T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587386 | |||||||
| chr14:56587529 | G | A | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+1617G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587529 | |||||||
| chr14:56587741 | T | C | 5 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(2): Show |
5 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+1829T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587741 | |||||||
| chr14:56587744 | G | A | 1 | a0003c0007t0013g0246 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.344+1832G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587744 | |||||||
| chr14:56587775 | T | G | 1 | a0001c0002t0001g0031 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.344+1863T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56587775 | |||||||
| chr14:56588103 | C | T | 52 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(49): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.344+2191C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588103 | |||||||
| chr14:56588566 | A | G | 1 | a0001c0004t0003g0310 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.344+2654A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588566 | |||||||
| chr14:56588568 | CT | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
60 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.344+2659delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56588568 | ||||||
| chr14:56588576 | A | G | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+2664A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588576 | |||||||
| chr14:56588710 | G | GTATT | 302 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.344+2802_344+2805d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56588710 | ||||||
| chr14:56588780 | A | G | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+2868A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588780 | |||||||
| chr14:56588918 | G | A | 1 | a0001c0002t0019g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.344+3006G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56588918 | |||||||
| chr14:56589134 | T | C | 5 | a0002c0003t0001g0033 a0002c0003t0001g0034 a0002c0003t0001g0189 others(2): Show |
5 | HG02135.hp1 NA18956.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+3222T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589134 | |||||||
| chr14:56589209 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+3297C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589209 | |||||||
| chr14:56589254 | C | T | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344+3342C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589254 | |||||||
| chr14:56589277 | C | T | 1 | a0001c0004t0004g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.344+3365C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589277 | |||||||
| chr14:56589284 | G | A | 2 | a0003c0007t0001g0247 a0003c0007t0001g0248 |
2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.344+3372G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589284 | |||||||
| chr14:56589315 | G | A | 6 | a0001c0004t0004g0176 a0001c0004t0004g0177 a0001c0004t0004g0178 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+3403G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589315 | |||||||
| chr14:56589316 | C | G | 7 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0166 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.344+3404C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589316 | |||||||
| chr14:56589368 | C | T | 102 | a0001c0001t0002g0232 a0001c0002t0001g0001 a0001c0002t0001g0002 others(99): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.344+3456C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589368 | |||||||
| chr14:56589656 | C | T | 101 | a0001c0001t0002g0232 a0001c0002t0001g0001 a0001c0002t0001g0002 others(98): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.344+3744C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589656 | |||||||
| chr14:56589887 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.344+3975A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56589887 | |||||||
| chr14:56590072 | C | T | 58 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
66 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.344+4160C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590072 | |||||||
| chr14:56590109 | G | A | 1 | a0009c0012t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.344+4197G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590109 | |||||||
| chr14:56590243 | G | A | 1 | a0001c0004t0004g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+4331G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590243 | |||||||
| chr14:56590277 | A | T | 1 | a0001c0001t0009g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.344+4365A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590277 | |||||||
| chr14:56590312 | C | T | 1 | a0001c0001t0006g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.344+4400C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590312 | |||||||
| chr14:56590317 | C | G | 1 | a0002c0005t0002g0231 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.344+4405C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56590317 | |||||||
| chr14:56591407 | C | A | 15 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(12): Show |
17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.344+5495C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591407 | |||||||
| chr14:56591435 | G | C | 1 | a0001c0002t0001g0031 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.344+5523G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591435 | |||||||
| chr14:56591527 | G | A | 15 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(12): Show |
17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.344+5615G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591527 | |||||||
| chr14:56591628 | T | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+5716T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591628 | |||||||
| chr14:56591796 | T | C | 4 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0166 others(1): Show |
6 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+5884T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591796 | |||||||
| chr14:56591829 | C | T | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.344+5917C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56591829 | |||||||
| chr14:56592230 | G | A | 54 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(51): Show |
59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.344+6318G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592230 | |||||||
| chr14:56592356 | A | T | 1 | a0001c0004t0004g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.344+6444A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592356 | |||||||
| chr14:56592370 | C | G | 1 | a0002c0006t0003g0309 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.344+6458C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592370 | |||||||
| chr14:56592662 | T | G | 19 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(16): Show |
19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.344+6750T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592662 | |||||||
| chr14:56592854 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18999.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.344+6942T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592854 | |||||||
| chr14:56592943 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.344+7031G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56592943 | |||||||
| chr14:56593071 | A | G | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.344+7159A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593071 | |||||||
| chr14:56593280 | T | TA | 15 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(12): Show |
17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.344+7369dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593280 | ||||||
| chr14:56593422 | G | A | 173 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(170): Show |
193 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.344+7510G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593422 | |||||||
| chr14:56593491 | A | G | 1 | a0001c0001t0005g0327 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.344+7579A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593491 | |||||||
| chr14:56593529 | C | T | 2 | a0001c0004t0003g0307 a0001c0004t0003g0308 |
2 | NA18963.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.344+7617C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593529 | |||||||
| chr14:56593566 | G | A | 1 | a0001c0002t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.344+7654G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593566 | |||||||
| chr14:56593593 | G | A | 5 | a0001c0001t0009g0191 a0001c0001t0009g0192 a0001c0001t0009g0193 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+7681G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593593 | |||||||
| chr14:56593659 | G | A | 1 | a0004c0008t0004g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.344+7747G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593659 | |||||||
| chr14:56593677 | C | CT | 60 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(57): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.344+7793dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTT | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
53 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.344+7792_344+7793d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0120 a0001c0001t0001g0130 others(4): Show |
8 | HG02258.hp2 HG02683.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+7791_344+7793d others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0317 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.344+7782_344+7793d others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0005g0318 a0001c0001t0005g0319 |
2 | NA19078.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.344+7780_344+7793d others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0008g0315 a0001c0001t0025g0320 |
2 | HG02040.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.344+7779_344+7793d others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0008g0316 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.344+7775_344+7793d others(21): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0005g0327 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.344+7774_344+7793d others(22): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0005g0325 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.344+7769_344+7793d others(27): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0005g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.344+7793_344+7794i others(31): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | CT | C | 85 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0321 others(82): Show |
100 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.344+7793delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | CTTTTTTT others(4): Show |
C | 3 | a0001c0004t0016g0306 a0002c0006t0003g0022 a0002c0006t0003g0305 |
4 | HG02738.hp1 NA19065.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+7783_344+7793d others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | CTTTTTTT others(5): Show |
C | 51 | a0001c0001t0002g0275 a0001c0004t0003g0292 a0001c0004t0003g0293 others(48): Show |
55 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.344+7782_344+7793d others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593677 | CTTTTTTT others(6): Show |
C | 2 | a0001c0004t0003g0278 a0004c0008t0005g0249 |
2 | HG01433.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.344+7781_344+7793d others(15): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56593677 | ||||||
| chr14:56593711 | T | G | 118 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(115): Show |
133 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.344+7799T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593711 | |||||||
| chr14:56593756 | C | T | 2 | a0004c0008t0004g0127 a0004c0008t0004g0128 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.344+7844C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593756 | |||||||
| chr14:56593983 | G | A | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.344+8071G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56593983 | |||||||
| chr14:56594016 | G | A | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+8104G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594016 | |||||||
| chr14:56594050 | A | T | 1 | a0001c0002t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.344+8138A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594050 | |||||||
| chr14:56594099 | A | G | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.344+8187A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594099 | |||||||
| chr14:56594165 | T | G | 303 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.344+8253T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594165 | |||||||
| chr14:56594171 | T | C | 303 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.344+8259T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594171 | |||||||
| chr14:56594172 | T | C | 1 | a0003c0007t0013g0264 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.344+8260T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594172 | |||||||
| chr14:56594218 | A | G | 1 | a0002c0006t0003g0304 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.344+8306A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594218 | |||||||
| chr14:56594231 | T | C | 55 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(52): Show |
60 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.344+8319T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594231 | |||||||
| chr14:56594237 | C | G | 101 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(98): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.344+8325C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594237 | |||||||
| chr14:56594240 | G | GTTAAAAT others(10): Show |
1 | a0001c0002t0001g0029 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.344+8334_344+8350d others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56594240 | ||||||
| chr14:56594316 | A | G | 3 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0098 |
3 | HG00639.hp1 HG00738.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.344+8404A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594316 | |||||||
| chr14:56594455 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.344+8543T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594455 | |||||||
| chr14:56594464 | A | G | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.344+8552A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594464 | |||||||
| chr14:56594550 | T | C | 1 | a0001c0001t0009g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.344+8638T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594550 | |||||||
| chr14:56594577 | G | A | 1 | a0002c0003t0007g0035 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.344+8665G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594577 | |||||||
| chr14:56594737 | C | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG03491.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.344+8825C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594737 | |||||||
| chr14:56594820 | T | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(22): Show |
29 | HG00438.hp2 HG00609.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.344+8908T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56594820 | |||||||
| chr14:56595202 | A | G | 1 | a0002c0005t0012g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.345-8613A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595202 | |||||||
| chr14:56595207 | T | C | 1 | a0003c0007t0006g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.345-8608T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595207 | |||||||
| chr14:56595210 | T | C | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-8605T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595210 | |||||||
| chr14:56595280 | G | A | 294 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(291): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.345-8535G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595280 | |||||||
| chr14:56595304 | A | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 |
6 | NA18951.hp1 NA18956.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-8511A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595304 | |||||||
| chr14:56595336 | A | G | 1 | a0003c0007t0001g0270 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.345-8479A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595336 | |||||||
| chr14:56595449 | G | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-8366G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595449 | |||||||
| chr14:56595457 | A | T | 1 | a0001c0004t0004g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.345-8358A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595457 | |||||||
| chr14:56595489 | C | A | 1 | a0001c0004t0004g0181 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.345-8326C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595489 | |||||||
| chr14:56595566 | A | G | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-8249A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595566 | |||||||
| chr14:56595624 | C | T | 7 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0166 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-8191C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595624 | |||||||
| chr14:56595625 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.345-8190A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595625 | |||||||
| chr14:56595717 | A | C | 59 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(56): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.345-8098A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595717 | |||||||
| chr14:56595966 | A | G | 2 | a0001c0001t0002g0275 a0001c0004t0014g0020 |
3 | HG02559.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.345-7849A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56595966 | |||||||
| chr14:56596013 | A | C | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.345-7802A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596013 | |||||||
| chr14:56596190 | T | C | 127 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(124): Show |
142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.345-7625T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596190 | |||||||
| chr14:56596269 | G | A | 6 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-7546G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596269 | |||||||
| chr14:56596381 | A | AGAGT | 14 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0137 others(11): Show |
15 | HG00639.hp2 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGAGTGT | 27 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
30 | HG00438.hp2 HG00609.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGAGTGTG others(1): Show |
9 | a0001c0001t0002g0121 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
10 | HG00099.hp2 HG00140.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(10): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGAGTGTG others(3): Show |
4 | a0001c0001t0002g0198 a0001c0001t0002g0223 a0001c0001t0002g0239 others(1): Show |
4 | HG01123.hp1 HG02683.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGAGTGTG others(5): Show |
34 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0122 others(31): Show |
39 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGAGTGTG others(7): Show |
8 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(5): Show |
8 | HG01071.hp2 HG01358.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-7433_345-7432i others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGT | 75 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(72): Show |
86 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.345-7409_345-7408d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGTGT | 24 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0001g0064 others(21): Show |
25 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.345-7411_345-7408d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGTGTGT | 7 | a0001c0002t0001g0079 a0002c0003t0001g0106 a0002c0006t0003g0021 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-7413_345-7408d others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGTGTGTG others(1): Show |
21 | a0001c0002t0001g0080 a0001c0004t0003g0278 a0001c0004t0003g0292 others(18): Show |
22 | HG00609.hp2 HG03239.hp1 HG03453.hp1 others(19): Show |
intron_variant | MODIFIER | c.345-7415_345-7408d others(10): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGTGTGTG others(3): Show |
4 | a0001c0004t0011g0299 a0001c0004t0014g0020 a0001c0004t0016g0306 others(1): Show |
5 | HG02738.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-7417_345-7408d others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGTGTGTG others(5): Show |
3 | a0001c0004t0011g0300 a0001c0004t0011g0301 a0001c0020t0011g0302 |
3 | HG01433.hp1 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.345-7419_345-7408d others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | A | AGTGTGTG others(7): Show |
1 | a0001c0004t0015g0303 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345-7421_345-7408d others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | AGT | A | 3 | a0002c0005t0012g0132 a0002c0005t0012g0133 a0003c0007t0001g0253 |
3 | HG02572.hp1 HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.345-7409_345-7408d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596381 | AGTGT | A | 3 | a0002c0005t0012g0134 a0003c0007t0001g0252 a0003c0007t0022g0265 |
3 | HG02970.hp2 HG03139.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.345-7411_345-7408d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596381 | ||||||
| chr14:56596383 | T | A | 20 | a0001c0001t0001g0120 a0001c0001t0006g0241 a0001c0001t0006g0242 others(17): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-7432T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596383 | |||||||
| chr14:56596383 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.345-7432T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596383 | |||||||
| chr14:56596385 | T | A | 2 | a0002c0005t0012g0132 a0002c0005t0012g0133 |
2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.345-7430T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596385 | |||||||
| chr14:56596387 | T | A | 1 | a0002c0005t0012g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.345-7428T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596387 | |||||||
| chr14:56596396 | G | A | 2 | a0004c0008t0005g0249 a0004c0008t0005g0251 |
2 | HG01433.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.345-7419G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596396 | |||||||
| chr14:56596402 | G | A | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-7413G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596402 | |||||||
| chr14:56596404 | G | A | 3 | a0002c0005t0012g0131 a0002c0005t0012g0132 a0002c0005t0012g0133 |
3 | HG03017.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.345-7411G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596404 | |||||||
| chr14:56596406 | G | A | 12 | a0001c0001t0001g0120 a0002c0005t0001g0014 a0002c0005t0001g0015 others(9): Show |
14 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-7409G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596406 | |||||||
| chr14:56596406 | G | GTGTGTA | 3 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0002c0003t0001g0069 |
3 | NA18943.hp2 NA18979.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.345-7408_345-7407i others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | ||||||
| chr14:56596406 | G | GTGTGTGT others(5): Show |
4 | a0001c0001t0005g0321 a0001c0001t0005g0322 a0001c0001t0005g0323 others(1): Show |
4 | HG00621.hp1 NA18945.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-7408_345-7407i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | ||||||
| chr14:56596406 | G | GTGTGTGT others(5): Show |
9 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(6): Show |
9 | HG01358.hp2 HG02040.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-7408_345-7407i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | ||||||
| chr14:56596406 | G | GTGTGTGT others(21): Show |
1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.345-7408_345-7407i others(30): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | ||||||
| chr14:56596406 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0025g0320 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.345-7408_345-7407i others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596406 | ||||||
| chr14:56596408 | A | G | 183 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(180): Show |
206 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.345-7407A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596408 | |||||||
| chr14:56596410 | A | G | 74 | a0001c0001t0001g0155 a0001c0002t0001g0002 a0001c0002t0001g0026 others(71): Show |
84 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.345-7405A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596410 | |||||||
| chr14:56596412 | A | G | 12 | a0001c0004t0003g0278 a0001c0004t0003g0298 a0001c0004t0003g0308 others(9): Show |
14 | HG01433.hp1 HG02015.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.345-7403A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596412 | |||||||
| chr14:56596414 | A | G | 1 | a0001c0004t0003g0308 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.345-7401A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596414 | |||||||
| chr14:56596422 | A | G | 1 | a0002c0006t0003g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.345-7393A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596422 | |||||||
| chr14:56596423 | T | C | 9 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(6): Show |
9 | HG01071.hp2 HG02896.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-7392T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596423 | |||||||
| chr14:56596423 | T | TAC | 42 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0199 others(39): Show |
48 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.345-7391_345-7390i others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596423 | ||||||
| chr14:56596423 | TATAC | T | 8 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(5): Show |
8 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-7386_345-7383d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596423 | ||||||
| chr14:56596425 | T | C | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.345-7390T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596425 | |||||||
| chr14:56596425 | T | TACAC | 12 | a0001c0001t0002g0198 a0001c0001t0002g0223 a0001c0001t0002g0239 others(9): Show |
12 | HG01123.hp1 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-7387_345-7386i others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596425 | ||||||
| chr14:56596425 | T | TATAC | 7 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-7389_345-7388i others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596425 | ||||||
| chr14:56596425 | TAC | T | 6 | a0001c0002t0001g0084 a0002c0003t0001g0189 a0002c0003t0001g0190 others(3): Show |
6 | HG02135.hp1 HG03540.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-7388_345-7387d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596425 | ||||||
| chr14:56596427 | C | T | 149 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(146): Show |
169 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.345-7388C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596427 | |||||||
| chr14:56596429 | T | C | 121 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(118): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.345-7386T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596429 | |||||||
| chr14:56596541 | T | C | 183 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(180): Show |
203 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.345-7274T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596541 | |||||||
| chr14:56596560 | A | G | 59 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(56): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.345-7255A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596560 | |||||||
| chr14:56596569 | C | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-7246C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596569 | |||||||
| chr14:56596618 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0160 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.345-7197C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596618 | |||||||
| chr14:56596695 | G | A | 2 | a0001c0001t0008g0125 a0001c0004t0004g0181 |
2 | HG03195.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.345-7120G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596695 | |||||||
| chr14:56596767 | C | CA | 107 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.345-7033dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596767 | ||||||
| chr14:56596782 | A | AAT | 10 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG00438.hp2 HG02258.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-7033_345-7032i others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596782 | |||||||
| chr14:56596782 | A | G | 2 | a0002c0006t0003g0282 a0002c0006t0003g0283 |
2 | NA18965.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.345-7033A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596782 | |||||||
| chr14:56596782 | A | T | 1 | a0001c0004t0003g0307 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.345-7033A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596782 | |||||||
| chr14:56596783 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.345-7032T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596783 | |||||||
| chr14:56596784 | T | A | 11 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG00438.hp2 HG02258.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-7031T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596784 | |||||||
| chr14:56596784 | T | TA | 16 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(13): Show |
16 | HG00621.hp1 HG02040.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.345-7020dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596784 | ||||||
| chr14:56596784 | T | TAA | 14 | a0001c0002t0001g0008 a0001c0002t0001g0040 a0001c0002t0001g0046 others(11): Show |
15 | HG01993.hp2 HG03017.hp2 HG03195.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-7021_345-7020d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596784 | ||||||
| chr14:56596784 | T | TAAA | 83 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(80): Show |
97 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.345-7022_345-7020d others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596784 | ||||||
| chr14:56596785 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.345-7030A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596785 | |||||||
| chr14:56596794 | A | AAAAAAAA others(3): Show |
3 | a0001c0004t0004g0179 a0001c0004t0004g0182 a0001c0004t0004g0183 |
3 | HG01243.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.345-7020_345-7019i others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | ||||||
| chr14:56596794 | A | AAAAAATA others(3): Show |
8 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0180 others(5): Show |
10 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-7020_345-7019i others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | ||||||
| chr14:56596794 | A | AAAAAATA others(5): Show |
1 | a0001c0004t0004g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.345-7020_345-7019i others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | ||||||
| chr14:56596794 | A | AAAAATAT others(4): Show |
1 | a0001c0004t0004g0181 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.345-7020_345-7019i others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | ||||||
| chr14:56596794 | A | AAAAATAT others(6): Show |
1 | a0004c0008t0004g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.345-7020_345-7019i others(15): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | ||||||
| chr14:56596794 | A | AAAATATA others(7): Show |
1 | a0001c0004t0004g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.345-7020_345-7019i others(16): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56596794 | ||||||
| chr14:56596794 | A | AT | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
55 | HG00639.hp2 HG01109.hp1 HG01496.hp2 others(52): Show |
intron_variant | MODIFIER | c.345-7021_345-7020i others(3): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596794 | |||||||
| chr14:56596794 | A | T | 59 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(56): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.345-7021A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596794 | |||||||
| chr14:56596795 | A | AAAATG | 37 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(34): Show |
40 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.345-7020_345-7019i others(7): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596795 | |||||||
| chr14:56596796 | T | A | 95 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(92): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.345-7019T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596796 | |||||||
| chr14:56596808 | C | T | 164 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0275 others(161): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.345-7007C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596808 | |||||||
| chr14:56596871 | G | T | 1 | a0002c0003t0001g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.345-6944G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56596871 | |||||||
| chr14:56597152 | A | T | 2 | a0001c0001t0009g0191 a0001c0001t0009g0194 |
2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.345-6663A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597152 | |||||||
| chr14:56597257 | A | G | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.345-6558A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597257 | |||||||
| chr14:56597293 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.345-6522A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597293 | |||||||
| chr14:56597435 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.345-6380C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597435 | |||||||
| chr14:56597568 | A | G | 15 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(12): Show |
17 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-6247A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597568 | |||||||
| chr14:56597584 | G | A | 1 | a0002c0003t0017g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.345-6231G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597584 | |||||||
| chr14:56597604 | G | A | 2 | a0004c0008t0004g0127 a0004c0008t0004g0128 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.345-6211G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597604 | |||||||
| chr14:56597651 | G | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(116): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.345-6164G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56597651 | |||||||
| chr14:56598139 | C | G | 1 | a0001c0002t0001g0078 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.345-5676C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598139 | |||||||
| chr14:56598148 | G | A | 54 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(51): Show |
59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-5667G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598148 | |||||||
| chr14:56598601 | T | C | 9 | a0003c0007t0001g0247 a0003c0007t0001g0248 a0003c0007t0001g0254 others(6): Show |
9 | HG00140.hp1 HG00735.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-5214T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598601 | |||||||
| chr14:56598625 | A | G | 9 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(6): Show |
9 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-5190A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598625 | |||||||
| chr14:56598819 | T | C | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-4996T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598819 | |||||||
| chr14:56598892 | A | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-4923A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598892 | |||||||
| chr14:56598955 | G | A | 1 | a0004c0008t0004g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.345-4860G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56598955 | |||||||
| chr14:56599056 | T | C | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-4759T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599056 | |||||||
| chr14:56599225 | G | A | 1 | a0002c0006t0003g0276 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.345-4590G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599225 | |||||||
| chr14:56599342 | T | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-4473T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599342 | |||||||
| chr14:56599449 | A | G | 55 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(52): Show |
60 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.345-4366A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599449 | |||||||
| chr14:56599516 | T | C | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
10 | HG00639.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-4299T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599516 | |||||||
| chr14:56599969 | G | C | 1 | a0001c0002t0001g0104 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.345-3846G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599969 | |||||||
| chr14:56599974 | G | T | 1 | a0001c0002t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.345-3841G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599974 | |||||||
| chr14:56599981 | A | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0160 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.345-3834A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599981 | |||||||
| chr14:56599990 | C | G | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.345-3825C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56599990 | |||||||
| chr14:56600002 | T | C | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0002c0005t0001g0272 |
3 | HG02257.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.345-3813T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600002 | |||||||
| chr14:56600027 | A | G | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.345-3788A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600027 | |||||||
| chr14:56600096 | T | G | 1 | a0003c0007t0001g0270 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.345-3719T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600096 | |||||||
| chr14:56600122 | A | G | 3 | a0001c0001t0006g0241 a0004c0008t0004g0127 a0004c0008t0004g0128 |
3 | HG02280.hp2 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.345-3693A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600122 | |||||||
| chr14:56600190 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-3625C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600190 | |||||||
| chr14:56600212 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-3603C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600212 | |||||||
| chr14:56600260 | G | A | 302 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.345-3555G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600260 | |||||||
| chr14:56600264 | G | A | 6 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-3551G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600264 | |||||||
| chr14:56600279 | T | C | 55 | a0001c0001t0002g0275 a0001c0004t0003g0278 a0001c0004t0003g0292 others(52): Show |
60 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.345-3536T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600279 | |||||||
| chr14:56600282 | C | T | 1 | a0003c0007t0001g0258 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.345-3533C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600282 | |||||||
| chr14:56600406 | G | A | 1 | a0001c0001t0009g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.345-3409G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600406 | |||||||
| chr14:56600610 | C | G | 55 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(52): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.345-3205C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600610 | |||||||
| chr14:56600652 | A | G | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-3163A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600652 | |||||||
| chr14:56600748 | C | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-3067C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600748 | |||||||
| chr14:56600977 | C | A | 83 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(80): Show |
88 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.345-2838C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56600977 | |||||||
| chr14:56601006 | G | A | 54 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(51): Show |
59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-2809G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601006 | |||||||
| chr14:56601084 | A | G | 8 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(5): Show |
8 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-2731A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601084 | |||||||
| chr14:56601135 | T | G | 2 | a0001c0002t0001g0046 a0001c0002t0001g0086 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.345-2680T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601135 | |||||||
| chr14:56601152 | T | G | 1 | a0001c0004t0004g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.345-2663T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601152 | |||||||
| chr14:56601157 | C | T | 54 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(51): Show |
59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-2658C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601157 | |||||||
| chr14:56601220 | T | C | 8 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-2595T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601220 | |||||||
| chr14:56601228 | C | G | 5 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-2587C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601228 | |||||||
| chr14:56601253 | G | C | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.345-2562G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601253 | |||||||
| chr14:56601294 | T | C | 1 | a0001c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.345-2521T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601294 | |||||||
| chr14:56601436 | T | C | 1 | a0001c0001t0002g0225 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.345-2379T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601436 | |||||||
| chr14:56601523 | A | G | 54 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(51): Show |
59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-2292A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601523 | |||||||
| chr14:56601847 | C | T | 1 | a0001c0004t0014g0020 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.345-1968C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601847 | |||||||
| chr14:56601871 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-1944C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601871 | |||||||
| chr14:56601895 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-1920C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601895 | |||||||
| chr14:56601922 | T | A | 1 | a0002c0003t0001g0100 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.345-1893T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601922 | |||||||
| chr14:56601942 | T | A | 54 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(51): Show |
59 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.345-1873T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601942 | |||||||
| chr14:56601961 | C | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-1854C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56601961 | |||||||
| chr14:56602077 | A | G | 77 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(74): Show |
82 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.345-1738A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602077 | |||||||
| chr14:56602163 | G | T | 302 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.345-1652G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602163 | |||||||
| chr14:56602214 | A | G | 1 | a0001c0001t0005g0319 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.345-1601A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602214 | |||||||
| chr14:56602227 | T | C | 1 | a0002c0003t0001g0063 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.345-1588T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602227 | |||||||
| chr14:56602348 | G | T | 1 | a0002c0005t0002g0218 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-1467G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602348 | |||||||
| chr14:56602557 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(221): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.345-1258T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602557 | |||||||
| chr14:56602628 | A | G | 4 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1187A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56602628 | |||||||
| chr14:56602746 | C | CAG | 303 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.345-1068_345-1067i others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56602746 | ||||||
| chr14:56603254 | G | GA | 218 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(215): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.345-553dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 56603254 | ||||||
| chr14:56603358 | A | G | 9 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(6): Show |
9 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-457A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603358 | |||||||
| chr14:56603586 | T | G | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-229T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603586 | |||||||
| chr14:56603689 | A | G | 7 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(4): Show |
7 | HG01358.hp1 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-126A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603689 | |||||||
| chr14:56603713 | C | A | 12 | a0002c0006t0003g0022 a0002c0006t0003g0281 a0002c0006t0003g0282 others(9): Show |
13 | NA18965.hp2 NA18979.hp2 NA18980.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-102C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603713 | |||||||
| chr14:56603728 | A | G | 1 | a0004c0008t0006g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.345-87A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603728 | |||||||
| chr14:56603748 | A | G | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.345-67A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603748 | |||||||
| chr14:56603783 | A | G | 303 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.345-32A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 3/15 | chr14 | 56603783 | |||||||
| chr14:56604091 | A | T | 1 | a0001c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.522+99A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604091 | |||||||
| chr14:56604254 | G | A | 6 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+262G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604254 | |||||||
| chr14:56604286 | A | G | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+294A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604286 | |||||||
| chr14:56604323 | T | A | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+331T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604323 | |||||||
| chr14:56604431 | G | A | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.522+439G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604431 | |||||||
| chr14:56604489 | T | C | 1 | a0003c0007t0001g0259 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+497T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604489 | |||||||
| chr14:56604744 | A | T | 1 | a0002c0005t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.522+752A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604744 | |||||||
| chr14:56604751 | A | G | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+759A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604751 | |||||||
| chr14:56604815 | C | T | 290 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(287): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.523-755C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604815 | |||||||
| chr14:56604859 | G | C | 5 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(2): Show |
5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-711G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604859 | |||||||
| chr14:56604929 | T | A | 287 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(284): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.523-641T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56604929 | |||||||
| chr14:56605108 | C | T | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.523-462C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605108 | |||||||
| chr14:56605180 | G | C | 1 | a0003c0007t0022g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.523-390G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605180 | |||||||
| chr14:56605262 | G | A | 1 | a0003c0007t0001g0018 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.523-308G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605262 | |||||||
| chr14:56605444 | C | T | 1 | a0001c0004t0016g0306 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.523-126C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605444 | |||||||
| chr14:56605467 | C | CTT | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-103_523-102ins others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605467 | |||||||
| chr14:56605471 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-99A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605471 | |||||||
| chr14:56605476 | A | G | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.523-94A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605476 | |||||||
| chr14:56605485 | T | A | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.523-85T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605485 | |||||||
| chr14:56605544 | A | AG | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-26_523-25insG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605544 | |||||||
| chr14:56605545 | A | T | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-25A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 4/15 | chr14 | 56605545 | |||||||
| chr14:56605703 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.636+20A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605703 | |||||||
| chr14:56605799 | A | G | 2 | a0003c0007t0001g0263 a0003c0007t0022g0265 |
2 | HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.636+116A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605799 | |||||||
| chr14:56605923 | T | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0072 |
2 | NA18957.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.636+240T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605923 | |||||||
| chr14:56605925 | A | C | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+242A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605925 | |||||||
| chr14:56605941 | A | T | 1 | a0002c0003t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.636+258A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605941 | |||||||
| chr14:56605975 | C | T | 53 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(50): Show |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.636+292C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56605975 | |||||||
| chr14:56606107 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.636+424G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606107 | |||||||
| chr14:56606263 | T | C | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+580T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606263 | |||||||
| chr14:56606281 | T | C | 306 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(303): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.636+598T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606281 | |||||||
| chr14:56606564 | A | G | 303 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.636+881A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606564 | |||||||
| chr14:56606759 | G | A | 14 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(11): Show |
16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.636+1076G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606759 | |||||||
| chr14:56606770 | C | G | 53 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(50): Show |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.636+1087C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606770 | |||||||
| chr14:56606833 | T | C | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.636+1150T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606833 | |||||||
| chr14:56606928 | A | G | 141 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(138): Show |
160 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.636+1245A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56606928 | |||||||
| chr14:56607000 | T | A | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.636+1317T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607000 | |||||||
| chr14:56607081 | A | G | 1 | a0006c0010t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.636+1398A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607081 | |||||||
| chr14:56607084 | G | A | 1 | a0012c0014t0024g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.636+1401G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607084 | |||||||
| chr14:56607154 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.636+1471A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607154 | |||||||
| chr14:56607276 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.636+1593C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607276 | |||||||
| chr14:56607485 | C | T | 1 | a0003c0007t0001g0266 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.637-1621C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607485 | |||||||
| chr14:56607584 | C | T | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.637-1522C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607584 | |||||||
| chr14:56607618 | G | A | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1488G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607618 | |||||||
| chr14:56607620 | G | A | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1486G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607620 | |||||||
| chr14:56607623 | T | C | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1483T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607623 | |||||||
| chr14:56607625 | T | A | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1481T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607625 | |||||||
| chr14:56607626 | A | G | 7 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1480A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607626 | |||||||
| chr14:56607627 | T | C | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1479T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607627 | |||||||
| chr14:56607629 | C | A | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1477C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607629 | |||||||
| chr14:56607658 | A | G | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(136): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.637-1448A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607658 | |||||||
| chr14:56607712 | G | A | 1 | a0001c0002t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637-1394G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607712 | |||||||
| chr14:56607712 | G | GTA | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.637-1384_637-1383d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 56607712 | ||||||
| chr14:56607746 | G | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1360G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607746 | |||||||
| chr14:56607802 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637-1304G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607802 | |||||||
| chr14:56607971 | T | G | 4 | a0001c0001t0002g0201 a0001c0001t0002g0207 a0001c0001t0002g0226 others(1): Show |
4 | HG00140.hp2 HG00733.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-1135T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56607971 | |||||||
| chr14:56608041 | T | C | 14 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(11): Show |
16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.637-1065T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608041 | |||||||
| chr14:56608088 | C | G | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-1018C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608088 | |||||||
| chr14:56608189 | A | C | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.637-917A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608189 | |||||||
| chr14:56608304 | G | A | 53 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(50): Show |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.637-802G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | chr14 | 56608304 | |||||||
| chr14:56608636 | T | TGTAGAAA others(6): Show |
1 | a0002c0003t0001g0087 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.637-469_637-457dup others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 56608636 | ||||||
| chr14:56608694 | AATG | A | 53 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(50): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.637-404_637-402del others(3): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr14 | 56608694 | ||||||
| chr14:56609376 | A | G | 1 | a0001c0004t0004g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.816+91A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609376 | |||||||
| chr14:56609453 | A | T | 39 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(36): Show |
41 | HG00621.hp1 HG01358.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.816+168A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609453 | |||||||
| chr14:56609544 | T | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.816+259T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609544 | |||||||
| chr14:56609550 | C | T | 1 | a0001c0002t0001g0096 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.816+265C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609550 | |||||||
| chr14:56609576 | G | A | 4 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0222 others(1): Show |
4 | HG01993.hp1 HG02148.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+291G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609576 | |||||||
| chr14:56609678 | A | C | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+393A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609678 | |||||||
| chr14:56609694 | T | G | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+409T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609694 | |||||||
| chr14:56609811 | A | G | 20 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(17): Show |
22 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.816+526A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609811 | |||||||
| chr14:56609818 | T | G | 2 | a0001c0002t0001g0108 a0002c0003t0001g0109 |
2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.816+533T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609818 | |||||||
| chr14:56609932 | A | T | 1 | a0003c0007t0001g0247 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.816+647A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609932 | |||||||
| chr14:56609955 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.816+670C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609955 | |||||||
| chr14:56609958 | T | G | 1 | a0001c0001t0009g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.816+673T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609958 | |||||||
| chr14:56609959 | T | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.816+674T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56609959 | |||||||
| chr14:56610032 | A | G | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.816+747A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610032 | |||||||
| chr14:56610218 | T | TA | 6 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+941dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610218 | ||||||
| chr14:56610227 | G | T | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.816+942G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610227 | |||||||
| chr14:56610267 | T | G | 39 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(36): Show |
41 | HG00621.hp1 HG01358.hp2 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.816+982T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610267 | |||||||
| chr14:56610270 | T | C | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.816+985T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610270 | |||||||
| chr14:56610303 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0221 |
2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.816+1018C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610303 | |||||||
| chr14:56610323 | C | G | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.816+1038C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610323 | |||||||
| chr14:56610385 | C | T | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.816+1100C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610385 | |||||||
| chr14:56610478 | G | A | 1 | a0001c0004t0014g0020 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.816+1193G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610478 | |||||||
| chr14:56610501 | C | G | 5 | a0001c0001t0009g0191 a0001c0001t0009g0192 a0001c0001t0009g0193 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1216C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610501 | |||||||
| chr14:56610508 | C | T | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.816+1223C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610508 | |||||||
| chr14:56610531 | C | T | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.816+1246C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610531 | |||||||
| chr14:56610532 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.816+1247G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610532 | |||||||
| chr14:56610572 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(24): Show |
31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.816+1287G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610572 | |||||||
| chr14:56610947 | TTTTC | T | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-1278_817-1275d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610947 | ||||||
| chr14:56610951 | C | G | 1 | a0001c0001t0002g0202 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.817-1294C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610951 | |||||||
| chr14:56610963 | C | CT | 6 | a0001c0001t0001g0274 a0002c0005t0001g0014 a0002c0005t0001g0015 others(3): Show |
8 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-1279dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610963 | ||||||
| chr14:56610966 | TC | T | 39 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(36): Show |
41 | HG00609.hp2 HG01071.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.817-1278delC | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610966 | |||||||
| chr14:56610967 | C | CT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0002g0228 others(4): Show |
7 | HG02148.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-1261dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610967 | ||||||
| chr14:56610967 | C | T | 24 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0006g0112 others(21): Show |
26 | HG01433.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.817-1278C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56610967 | |||||||
| chr14:56610967 | CT | C | 18 | a0001c0001t0006g0241 a0001c0002t0001g0002 a0001c0002t0001g0008 others(15): Show |
20 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.817-1261delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 56610967 | ||||||
| chr14:56611006 | A | G | 296 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(293): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.817-1239A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611006 | |||||||
| chr14:56611006 | A | T | 3 | a0001c0001t0002g0230 a0001c0001t0010g0004 a0001c0001t0010g0197 |
6 | HG02074.hp2 NA18942.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-1239A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611006 | |||||||
| chr14:56611027 | C | T | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.817-1218C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611027 | |||||||
| chr14:56611256 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-989G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611256 | |||||||
| chr14:56611258 | A | G | 1 | a0001c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-987A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611258 | |||||||
| chr14:56611306 | A | G | 1 | a0002c0005t0012g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.817-939A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611306 | |||||||
| chr14:56611354 | C | G | 1 | a0001c0004t0004g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.817-891C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611354 | |||||||
| chr14:56611387 | G | T | 5 | a0001c0001t0009g0191 a0001c0001t0009g0192 a0001c0001t0009g0193 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-858G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611387 | |||||||
| chr14:56611447 | G | A | 19 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(16): Show |
19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.817-798G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611447 | |||||||
| chr14:56611594 | T | C | 19 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(16): Show |
19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.817-651T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611594 | |||||||
| chr14:56611741 | A | G | 2 | a0002c0003t0001g0033 a0002c0003t0001g0034 |
2 | NA18956.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.817-504A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611741 | |||||||
| chr14:56611758 | A | G | 1 | a0001c0002t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-487A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611758 | |||||||
| chr14:56611917 | C | T | 1 | a0003c0007t0001g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.817-328C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 6/15 | chr14 | 56611917 | |||||||
| chr14:56612525 | A | G | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.857+240A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612525 | |||||||
| chr14:56612585 | T | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+300T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612585 | |||||||
| chr14:56612699 | C | CT | 22 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(19): Show |
22 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.857+431dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56612699 | ||||||
| chr14:56612699 | CT | C | 8 | a0001c0001t0009g0192 a0001c0002t0001g0040 a0001c0002t0001g0048 others(5): Show |
8 | HG01167.hp2 HG02615.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.857+431delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56612699 | ||||||
| chr14:56612699 | CTT | C | 53 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(50): Show |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.857+430_857+431del others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56612699 | ||||||
| chr14:56612777 | T | A | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+492T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612777 | |||||||
| chr14:56612793 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.857+508C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612793 | |||||||
| chr14:56612799 | C | T | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.857+514C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612799 | |||||||
| chr14:56612839 | G | A | 4 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0098 others(1): Show |
4 | HG00639.hp1 HG00738.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+554G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612839 | |||||||
| chr14:56612973 | T | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+688T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56612973 | |||||||
| chr14:56613254 | T | C | 2 | a0003c0007t0001g0247 a0003c0007t0001g0248 |
2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.857+969T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613254 | |||||||
| chr14:56613513 | A | G | 2 | a0001c0004t0004g0177 a0001c0004t0004g0178 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.857+1228A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613513 | |||||||
| chr14:56613545 | C | T | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+1260C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613545 | |||||||
| chr14:56613741 | A | T | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.857+1456A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613741 | |||||||
| chr14:56613787 | C | T | 1 | a0001c0002t0001g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.857+1502C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613787 | |||||||
| chr14:56613791 | G | A | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+1506G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613791 | |||||||
| chr14:56613894 | G | A | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.857+1609G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613894 | |||||||
| chr14:56613895 | C | CA | 198 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(195): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.857+1625dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | ||||||
| chr14:56613895 | C | CAA | 10 | a0001c0001t0002g0219 a0001c0001t0010g0197 a0001c0004t0004g0178 others(7): Show |
10 | HG00609.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.857+1624_857+1625d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | ||||||
| chr14:56613895 | C | CAAAAAAA others(14): Show |
4 | a0001c0001t0005g0317 a0001c0001t0005g0319 a0001c0001t0005g0321 others(1): Show |
4 | NA18945.hp2 NA18959.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+1625_857+1626i others(23): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | ||||||
| chr14:56613895 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0005g0323 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.857+1625_857+1626i others(24): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | ||||||
| chr14:56613895 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0005g0322 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.857+1625_857+1626i others(25): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56613895 | ||||||
| chr14:56613910 | A | AAAAAAAA others(20): Show |
1 | a0001c0001t0005g0327 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.857+1625_857+1626i others(29): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | |||||||
| chr14:56613910 | A | AAAAAAAA others(15): Show |
3 | a0001c0001t0005g0318 a0001c0001t0008g0315 a0001c0001t0008g0316 |
3 | HG02040.hp2 NA19009.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.857+1625_857+1626i others(24): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | |||||||
| chr14:56613910 | A | AAAAAAAA others(14): Show |
3 | a0001c0001t0005g0325 a0001c0001t0008g0314 a0001c0001t0025g0320 |
3 | HG02738.hp2 NA18967.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.857+1625_857+1626i others(23): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | |||||||
| chr14:56613910 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0005g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.857+1625_857+1626i others(22): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | |||||||
| chr14:56613910 | A | AAAAAAAA others(10): Show |
3 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0126 |
3 | HG02523.hp1 NA18943.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.857+1625_857+1626i others(19): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | |||||||
| chr14:56613910 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0008g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.857+1625_857+1626i others(18): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613910 | |||||||
| chr14:56613988 | C | T | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+1703C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613988 | |||||||
| chr14:56613989 | G | A | 1 | a0010c0013t0001g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.857+1704G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56613989 | |||||||
| chr14:56614022 | C | T | 1 | a0002c0005t0012g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.857+1737C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614022 | |||||||
| chr14:56614219 | T | TA | 107 | a0001c0001t0001g0120 a0001c0001t0001g0273 a0001c0001t0001g0274 others(104): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.858-1707dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56614219 | ||||||
| chr14:56614219 | TA | T | 49 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0198 others(46): Show |
54 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.858-1707delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56614219 | ||||||
| chr14:56614295 | G | A | 53 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(50): Show |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.858-1649G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614295 | |||||||
| chr14:56614597 | A | G | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 |
3 | HG00280.hp2 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.858-1347A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614597 | |||||||
| chr14:56614648 | C | T | 1 | a0006c0010t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.858-1296C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614648 | |||||||
| chr14:56614655 | A | G | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.858-1289A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56614655 | |||||||
| chr14:56614724 | CTTCTGTG | C | 72 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(69): Show |
77 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.858-1211_858-1205d others(9): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 56614724 | ||||||
| chr14:56615127 | T | G | 12 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
12 | HG00639.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.858-817T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615127 | |||||||
| chr14:56615209 | C | G | 1 | a0001c0002t0001g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.858-735C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615209 | |||||||
| chr14:56615377 | A | G | 1 | a0006c0010t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.858-567A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615377 | |||||||
| chr14:56615383 | A | G | 1 | a0001c0002t0001g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.858-561A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615383 | |||||||
| chr14:56615412 | G | A | 1 | a0003c0007t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-532G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615412 | |||||||
| chr14:56615414 | T | A | 1 | a0003c0007t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-530T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615414 | |||||||
| chr14:56615415 | T | G | 1 | a0003c0007t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-529T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615415 | |||||||
| chr14:56615416 | T | A | 1 | a0003c0007t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.858-528T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615416 | |||||||
| chr14:56615500 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.858-444C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615500 | |||||||
| chr14:56615577 | T | C | 1 | a0002c0003t0001g0088 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.858-367T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615577 | |||||||
| chr14:56615731 | G | A | 2 | a0002c0005t0002g0016 a0002c0005t0002g0231 |
3 | HG00099.hp2 HG01934.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.858-213G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615731 | |||||||
| chr14:56615757 | C | T | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.858-187C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615757 | |||||||
| chr14:56615885 | T | G | 5 | a0001c0001t0009g0191 a0001c0001t0009g0192 a0001c0001t0009g0193 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-59T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615885 | |||||||
| chr14:56615930 | A | G | 192 | a0001c0001t0001g0120 a0001c0001t0001g0229 a0001c0001t0001g0273 others(189): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.858-14A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 7/15 | chr14 | 56615930 | |||||||
| chr14:56616073 | A | G | 1 | a0002c0006t0003g0285 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.941+46A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616073 | |||||||
| chr14:56616174 | T | C | 5 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(2): Show |
5 | NA18939.hp1 NA18964.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.941+147T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616174 | |||||||
| chr14:56616207 | A | G | 1 | a0003c0007t0001g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.941+180A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616207 | |||||||
| chr14:56616219 | A | C | 17 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0002c0005t0001g0014 others(14): Show |
19 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.941+192A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616219 | |||||||
| chr14:56616252 | C | A | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.941+225C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616252 | |||||||
| chr14:56616262 | C | G | 1 | a0001c0004t0003g0294 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.941+235C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616262 | |||||||
| chr14:56616408 | A | G | 2 | a0001c0001t0002g0239 a0002c0005t0002g0017 |
3 | HG00642.hp1 HG00738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.941+381A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616408 | |||||||
| chr14:56616644 | A | G | 1 | a0001c0004t0004g0183 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.942-539A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616644 | |||||||
| chr14:56616893 | C | T | 3 | a0002c0005t0012g0131 a0002c0005t0012g0132 a0002c0005t0012g0133 |
3 | HG03017.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.942-290C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56616893 | |||||||
| chr14:56617021 | T | A | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.942-162T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56617021 | |||||||
| chr14:56617110 | T | C | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.942-73T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56617110 | |||||||
| chr14:56617179 | G | A | 89 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(86): Show |
95 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(92): Show |
splice_region_variant&intron_variant | LOW | c.942-4G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 8/15 | chr14 | 56617179 | |||||||
| chr14:56617490 | T | TTTAA | 220 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(217): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1056+194_1056+197d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 56617490 | ||||||
| chr14:56617649 | C | G | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1056+352C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617649 | |||||||
| chr14:56617695 | G | T | 1 | a0002c0003t0001g0087 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1056+398G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617695 | |||||||
| chr14:56617718 | A | G | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1056+421A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617718 | |||||||
| chr14:56617855 | C | T | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1056+558C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56617855 | |||||||
| chr14:56618099 | A | G | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-495A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618099 | |||||||
| chr14:56618304 | C | G | 2 | a0001c0004t0003g0278 a0001c0004t0003g0298 |
2 | NA18984.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1057-290C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618304 | |||||||
| chr14:56618343 | A | G | 8 | a0001c0004t0004g0005 a0001c0004t0004g0182 a0001c0004t0004g0183 others(5): Show |
10 | HG01081.hp2 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1057-251A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618343 | |||||||
| chr14:56618420 | A | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1057-174A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618420 | |||||||
| chr14:56618511 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1057-83A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 9/15 | chr14 | 56618511 | |||||||
| chr14:56618870 | A | G | 3 | a0002c0005t0012g0131 a0002c0005t0012g0132 a0002c0005t0012g0133 |
3 | HG03017.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1226+107A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56618870 | |||||||
| chr14:56618939 | A | G | 52 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(49): Show |
57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1226+176A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56618939 | |||||||
| chr14:56619039 | G | C | 31 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(28): Show |
39 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1226+276G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619039 | |||||||
| chr14:56619071 | A | G | 15 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(12): Show |
17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1226+308A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619071 | |||||||
| chr14:56619654 | ATGGAAGA others(8): Show |
A | 2 | a0005c0009t0001g0135 a0005c0009t0001g0159 |
2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1226+897_1226+911d others(17): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 56619654 | ||||||
| chr14:56619693 | G | C | 1 | a0001c0001t0002g0239 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1226+930G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619693 | |||||||
| chr14:56619721 | T | G | 6 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0203 others(3): Show |
6 | HG00408.hp1 NA18945.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1226+958T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619721 | |||||||
| chr14:56619727 | T | G | 1 | a0001c0001t0002g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1226+964T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619727 | |||||||
| chr14:56619946 | A | T | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1226+1183A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56619946 | |||||||
| chr14:56620062 | C | G | 1 | a0002c0003t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1226+1299C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620062 | |||||||
| chr14:56620240 | C | T | 1 | a0001c0004t0003g0310 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1227-1291C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620240 | |||||||
| chr14:56620287 | T | C | 1 | a0001c0001t0005g0318 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1227-1244T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620287 | |||||||
| chr14:56620300 | A | T | 1 | a0003c0007t0001g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1227-1231A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620300 | |||||||
| chr14:56620361 | C | T | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1227-1170C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620361 | |||||||
| chr14:56620400 | A | G | 83 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(80): Show |
88 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.1227-1131A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620400 | |||||||
| chr14:56620414 | C | A | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1227-1117C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620414 | |||||||
| chr14:56620428 | C | A | 102 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(99): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1227-1103C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620428 | |||||||
| chr14:56620588 | G | A | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-943G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620588 | |||||||
| chr14:56620703 | G | A | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227-828G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620703 | |||||||
| chr14:56620808 | T | A | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1227-723T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56620808 | |||||||
| chr14:56621153 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1227-378G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621153 | |||||||
| chr14:56621161 | G | GCAA | 38 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(35): Show |
41 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1227-370_1227-369i others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621161 | |||||||
| chr14:56621168 | T | C | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1227-363T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621168 | |||||||
| chr14:56621252 | GA | G | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1227-273delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 56621252 | ||||||
| chr14:56621275 | A | G | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1227-256A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621275 | |||||||
| chr14:56621330 | A | AT | 52 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(49): Show |
57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1227-193dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 56621330 | ||||||
| chr14:56621352 | A | T | 199 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(196): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1227-179A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621352 | |||||||
| chr14:56621363 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1227-168A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621363 | |||||||
| chr14:56621451 | T | A | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1227-80T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 10/15 | chr14 | 56621451 | |||||||
| chr14:56621715 | A | T | 52 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(49): Show |
57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1398+13A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56621715 | |||||||
| chr14:56621788 | C | T | 76 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(73): Show |
81 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.1398+86C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56621788 | |||||||
| chr14:56622180 | A | G | 6 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1398+478A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622180 | |||||||
| chr14:56622297 | C | T | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1398+595C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622297 | |||||||
| chr14:56622341 | T | A | 36 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0294 others(33): Show |
39 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1398+639T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622341 | |||||||
| chr14:56622342 | C | A | 38 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(35): Show |
41 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1398+640C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622342 | |||||||
| chr14:56622342 | C | CA | 179 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(176): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1398+663dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 56622342 | ||||||
| chr14:56622342 | C | CAA | 39 | a0001c0001t0001g0144 a0001c0001t0001g0170 a0001c0001t0002g0206 others(36): Show |
39 | HG00438.hp1 HG00621.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.1398+662_1398+663d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 56622342 | ||||||
| chr14:56622381 | C | T | 52 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(49): Show |
57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1398+679C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622381 | |||||||
| chr14:56622521 | G | C | 6 | a0002c0003t0001g0009 a0002c0003t0001g0041 a0002c0003t0001g0063 others(3): Show |
7 | HG00423.hp2 HG02074.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+819G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622521 | |||||||
| chr14:56622699 | G | A | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1398+997G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622699 | |||||||
| chr14:56622752 | A | G | 1 | a0002c0003t0001g0034 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1398+1050A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622752 | |||||||
| chr14:56622821 | G | A | 1 | a0002c0005t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1398+1119G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622821 | |||||||
| chr14:56622827 | T | G | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1398+1125T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622827 | |||||||
| chr14:56622879 | T | G | 210 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(207): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1398+1177T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622879 | |||||||
| chr14:56622894 | C | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1398+1192C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56622894 | |||||||
| chr14:56623191 | T | C | 53 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(50): Show |
58 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.1398+1489T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623191 | |||||||
| chr14:56623308 | C | T | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1398+1606C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623308 | |||||||
| chr14:56623446 | A | G | 1 | a0001c0002t0001g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1398+1744A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623446 | |||||||
| chr14:56623446 | A | T | 1 | a0002c0003t0001g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1398+1744A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623446 | |||||||
| chr14:56623675 | A | G | 1 | a0002c0003t0001g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1399-1707A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623675 | |||||||
| chr14:56623682 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0155 |
3 | HG02027.hp2 HG02040.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1399-1700A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623682 | |||||||
| chr14:56623826 | T | C | 1 | a0002c0005t0013g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1399-1556T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623826 | |||||||
| chr14:56623836 | C | T | 1 | a0002c0005t0012g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1399-1546C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623836 | |||||||
| chr14:56623870 | A | G | 132 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0005g0317 others(129): Show |
149 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1399-1512A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623870 | |||||||
| chr14:56623882 | C | T | 2 | a0001c0001t0002g0219 a0001c0001t0002g0224 |
2 | HG01175.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1399-1500C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56623882 | |||||||
| chr14:56624109 | G | A | 1 | a0001c0001t0009g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1399-1273G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624109 | |||||||
| chr14:56624193 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0160 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1399-1189C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624193 | |||||||
| chr14:56624205 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-1177A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624205 | |||||||
| chr14:56624224 | A | G | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1399-1158A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624224 | |||||||
| chr14:56624349 | G | A | 1 | a0001c0004t0004g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1399-1033G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624349 | |||||||
| chr14:56624403 | G | A | 1 | a0002c0003t0001g0058 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1399-979G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624403 | |||||||
| chr14:56624410 | T | C | 307 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(304): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.1399-972T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624410 | |||||||
| chr14:56624428 | T | G | 307 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(304): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.1399-954T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624428 | |||||||
| chr14:56624431 | T | G | 307 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(304): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.1399-951T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624431 | |||||||
| chr14:56624441 | T | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-941T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624441 | |||||||
| chr14:56624452 | C | A | 1 | a0001c0001t0008g0316 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1399-930C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624452 | |||||||
| chr14:56624602 | C | T | 2 | a0001c0002t0001g0048 a0001c0002t0001g0051 |
2 | NA18982.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1399-780C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624602 | |||||||
| chr14:56624646 | A | G | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-736A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624646 | |||||||
| chr14:56624665 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1399-717C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624665 | |||||||
| chr14:56624671 | G | A | 1 | a0001c0001t0005g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1399-711G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624671 | |||||||
| chr14:56624757 | C | T | 1 | a0002c0005t0012g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1399-625C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624757 | |||||||
| chr14:56624840 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1399-542G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624840 | |||||||
| chr14:56624844 | G | A | 1 | a0003c0007t0022g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1399-538G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624844 | |||||||
| chr14:56624971 | A | G | 3 | a0001c0001t0002g0200 a0001c0001t0002g0214 a0001c0001t0002g0215 |
3 | NA18942.hp1 NA18969.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1399-411A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56624971 | |||||||
| chr14:56625002 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-380A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625002 | |||||||
| chr14:56625147 | G | A | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1399-235G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625147 | |||||||
| chr14:56625313 | A | T | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1399-69A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625313 | |||||||
| chr14:56625320 | A | G | 115 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0002t0001g0001 others(112): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1399-62A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 11/15 | chr14 | 56625320 | |||||||
| chr14:56625721 | T | G | 115 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0002t0001g0001 others(112): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1547+191T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56625721 | |||||||
| chr14:56625867 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1547+337C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56625867 | |||||||
| chr14:56626045 | A | C | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(110): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1547+515A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626045 | |||||||
| chr14:56626069 | C | A | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+539C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626069 | |||||||
| chr14:56626090 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1547+560C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626090 | |||||||
| chr14:56626182 | A | C | 55 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(52): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1547+652A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626182 | |||||||
| chr14:56626221 | C | G | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1547+691C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626221 | |||||||
| chr14:56626288 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1547+758C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626288 | |||||||
| chr14:56626403 | T | C | 1 | a0001c0002t0001g0104 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1547+873T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626403 | |||||||
| chr14:56626435 | A | G | 211 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(208): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1547+905A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626435 | |||||||
| chr14:56626614 | A | G | 1 | a0003c0007t0022g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1547+1084A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626614 | |||||||
| chr14:56626779 | C | T | 55 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(52): Show |
60 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1547+1249C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626779 | |||||||
| chr14:56626827 | G | A | 1 | a0001c0001t0008g0314 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1547+1297G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626827 | |||||||
| chr14:56626914 | T | C | 14 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(11): Show |
14 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1547+1384T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626914 | |||||||
| chr14:56626916 | A | G | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+1386A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626916 | |||||||
| chr14:56626966 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547+1436A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56626966 | |||||||
| chr14:56627086 | A | G | 4 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0202 others(1): Show |
5 | NA18947.hp1 NA18952.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547+1556A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627086 | |||||||
| chr14:56627167 | AAT | A | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+1638_1547+163 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627167 | |||||||
| chr14:56627394 | C | G | 1 | a0001c0001t0002g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1547+1864C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627394 | |||||||
| chr14:56627427 | T | C | 1 | a0001c0002t0001g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1547+1897T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627427 | |||||||
| chr14:56627505 | C | T | 1 | a0001c0001t0006g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1547+1975C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627505 | |||||||
| chr14:56627653 | AT | A | 4 | a0002c0003t0001g0058 a0004c0008t0004g0127 a0004c0008t0004g0128 others(1): Show |
4 | HG01256.hp1 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+2128delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56627653 | ||||||
| chr14:56627658 | T | C | 135 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
154 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1547+2128T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627658 | |||||||
| chr14:56627658 | TC | T | 32 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(29): Show |
34 | HG00621.hp1 HG01358.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1547+2135delC | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56627658 | ||||||
| chr14:56627664 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1547+2134C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627664 | |||||||
| chr14:56627669 | G | C | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547+2139G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627669 | |||||||
| chr14:56627704 | G | A | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1547+2174G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627704 | |||||||
| chr14:56627823 | T | A | 1 | a0001c0001t0008g0314 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1547+2293T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627823 | |||||||
| chr14:56627846 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547+2316A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627846 | |||||||
| chr14:56627900 | G | A | 1 | a0002c0003t0001g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1547+2370G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56627900 | |||||||
| chr14:56628204 | G | T | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547+2674G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628204 | |||||||
| chr14:56628354 | C | T | 1 | a0001c0001t0006g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1547+2824C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628354 | |||||||
| chr14:56628411 | G | A | 19 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(16): Show |
19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1547+2881G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628411 | |||||||
| chr14:56628422 | A | G | 55 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(52): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1547+2892A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628422 | |||||||
| chr14:56628511 | A | G | 1 | a0001c0002t0019g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1547+2981A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628511 | |||||||
| chr14:56628520 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1547+2990A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628520 | |||||||
| chr14:56628634 | A | G | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1547+3104A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628634 | |||||||
| chr14:56628694 | T | A | 55 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(52): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1547+3164T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628694 | |||||||
| chr14:56628809 | C | A | 19 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(16): Show |
19 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1547+3279C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628809 | |||||||
| chr14:56628896 | CT | C | 137 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(134): Show |
156 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1547+3378delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56628896 | ||||||
| chr14:56628940 | G | A | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1547+3410G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56628940 | |||||||
| chr14:56629029 | G | T | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1547+3499G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629029 | |||||||
| chr14:56629271 | G | GT | 113 | a0001c0001t0001g0120 a0001c0001t0001g0152 a0001c0001t0001g0155 others(110): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1548-3709dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56629271 | ||||||
| chr14:56629271 | G | GTT | 23 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0215 others(20): Show |
25 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1548-3710_1548-370 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56629271 | ||||||
| chr14:56629273 | T | TG | 3 | a0002c0005t0002g0154 a0002c0005t0002g0156 a0002c0005t0002g0165 |
3 | HG02698.hp2 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1548-3722_1548-372 others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629273 | |||||||
| chr14:56629377 | A | T | 1 | a0002c0006t0003g0281 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1548-3618A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629377 | |||||||
| chr14:56629628 | G | A | 52 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(49): Show |
57 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1548-3367G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629628 | |||||||
| chr14:56629680 | G | T | 283 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(280): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1548-3315G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629680 | |||||||
| chr14:56629774 | A | G | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1548-3221A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629774 | |||||||
| chr14:56629843 | T | G | 1 | a0001c0001t0009g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1548-3152T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629843 | |||||||
| chr14:56629859 | ACC | A | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1548-3134_1548-313 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56629859 | ||||||
| chr14:56629867 | G | A | 1 | a0002c0003t0020g0097 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1548-3128G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629867 | |||||||
| chr14:56629902 | G | C | 6 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548-3093G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629902 | |||||||
| chr14:56629939 | G | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-3056G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56629939 | |||||||
| chr14:56630021 | A | G | 2 | a0001c0004t0003g0295 a0001c0004t0003g0310 |
2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1548-2974A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630021 | |||||||
| chr14:56630042 | G | GA | 34 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(31): Show |
36 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1548-2942dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56630042 | ||||||
| chr14:56630042 | G | GAA | 38 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(35): Show |
41 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1548-2943_1548-294 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56630042 | ||||||
| chr14:56630259 | T | G | 299 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(296): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1548-2736T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630259 | |||||||
| chr14:56630314 | A | G | 2 | a0001c0001t0002g0200 a0001c0001t0002g0214 |
2 | NA18942.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1548-2681A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630314 | |||||||
| chr14:56630384 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1548-2611A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630384 | |||||||
| chr14:56630421 | T | G | 1 | a0001c0004t0004g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1548-2574T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630421 | |||||||
| chr14:56630423 | A | G | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-2572A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630423 | |||||||
| chr14:56630466 | T | C | 1 | a0001c0004t0004g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1548-2529T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630466 | |||||||
| chr14:56630472 | C | CT | 16 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0002c0005t0001g0014 others(13): Show |
18 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1548-2514dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56630472 | ||||||
| chr14:56630573 | C | T | 1 | a0003c0007t0001g0270 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1548-2422C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630573 | |||||||
| chr14:56630577 | A | G | 1 | a0002c0006t0003g0309 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1548-2418A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630577 | |||||||
| chr14:56630688 | C | T | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
10 | HG00639.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1548-2307C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630688 | |||||||
| chr14:56630904 | C | T | 3 | a0002c0005t0001g0172 a0002c0005t0001g0173 a0002c0005t0001g0234 |
3 | HG02257.hp1 HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1548-2091C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630904 | |||||||
| chr14:56630905 | G | A | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-2090G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630905 | |||||||
| chr14:56630972 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1548-2023G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630972 | |||||||
| chr14:56630975 | G | A | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1548-2020G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630975 | |||||||
| chr14:56630982 | T | A | 15 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(12): Show |
17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-2013T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56630982 | |||||||
| chr14:56631024 | A | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-1971A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631024 | |||||||
| chr14:56631118 | A | ACAAGCTC others(1): Show |
15 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(12): Show |
17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-1877_1548-187 others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631118 | |||||||
| chr14:56631177 | C | T | 14 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(11): Show |
16 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1548-1818C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631177 | |||||||
| chr14:56631226 | C | T | 15 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0158 others(12): Show |
17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1548-1769C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631226 | |||||||
| chr14:56631262 | C | T | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1548-1733C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631262 | |||||||
| chr14:56631361 | G | A | 50 | a0001c0001t0001g0229 a0001c0001t0002g0006 a0001c0001t0002g0121 others(47): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.1548-1634G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631361 | |||||||
| chr14:56631400 | ATCACCTG others(3): Show |
A | 1 | a0013c0019t0001g0050 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1548-1591_1548-158 others(14): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56631400 | ||||||
| chr14:56631491 | T | C | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-1504T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631491 | |||||||
| chr14:56631516 | C | T | 1 | a0001c0001t0008g0124 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1548-1479C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631516 | |||||||
| chr14:56631622 | C | CA | 171 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(168): Show |
193 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1548-1357dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56631622 | ||||||
| chr14:56631629 | A | AAC | 108 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(105): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1548-1365_1548-136 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56631629 | ||||||
| chr14:56631642 | A | G | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-1353A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631642 | |||||||
| chr14:56631700 | G | C | 1 | a0001c0004t0003g0295 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1548-1295G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631700 | |||||||
| chr14:56631748 | T | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(24): Show |
31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1548-1247T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631748 | |||||||
| chr14:56631815 | A | G | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1548-1180A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631815 | |||||||
| chr14:56631839 | G | A | 131 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(128): Show |
148 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1548-1156G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631839 | |||||||
| chr14:56631867 | T | A | 301 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(298): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1548-1128T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631867 | |||||||
| chr14:56631872 | G | A | 2 | a0001c0004t0004g0179 a0001c0004t0004g0180 |
2 | HG01243.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1548-1123G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631872 | |||||||
| chr14:56631961 | C | T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(21): Show |
28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1548-1034C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56631961 | |||||||
| chr14:56632158 | C | T | 6 | a0002c0003t0001g0009 a0002c0003t0001g0041 a0002c0003t0001g0063 others(3): Show |
7 | HG00423.hp2 HG02074.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-837C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632158 | |||||||
| chr14:56632167 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1548-828G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632167 | |||||||
| chr14:56632185 | T | G | 18 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(15): Show |
18 | HG00621.hp1 HG01358.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1548-810T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632185 | |||||||
| chr14:56632248 | C | T | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1548-747C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632248 | |||||||
| chr14:56632417 | A | G | 1 | a0003c0007t0001g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1548-578A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632417 | |||||||
| chr14:56632462 | C | T | 1 | a0011c0016t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1548-533C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632462 | |||||||
| chr14:56632574 | C | CT | 115 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0002t0001g0001 others(112): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1548-414dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56632574 | ||||||
| chr14:56632619 | C | CT | 6 | a0001c0002t0001g0036 a0001c0002t0001g0066 a0001c0002t0001g0075 others(3): Show |
6 | NA18939.hp2 NA18959.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1548-370dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 56632619 | ||||||
| chr14:56632792 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1548-203G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 12/15 | chr14 | 56632792 | |||||||
| chr14:56633234 | T | G | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724+63T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633234 | |||||||
| chr14:56633235 | A | G | 1 | a0001c0001t0005g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1724+64A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633235 | |||||||
| chr14:56633258 | A | ATT | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+97_1724+98dup others(2): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633258 | ||||||
| chr14:56633258 | AT | A | 31 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(28): Show |
33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1724+98delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633258 | ||||||
| chr14:56633258 | ATTTT | A | 7 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(4): Show |
8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1724+95_1724+98del others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633258 | ||||||
| chr14:56633292 | T | G | 1 | a0007c0017t0007g0024 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1724+121T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633292 | |||||||
| chr14:56633434 | T | G | 1 | a0001c0001t0002g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1724+263T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633434 | |||||||
| chr14:56633550 | T | A | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1724+379T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633550 | |||||||
| chr14:56633607 | T | C | 40 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(37): Show |
42 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1724+436T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633607 | |||||||
| chr14:56633612 | G | A | 1 | a0002c0003t0001g0063 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1724+441G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633612 | |||||||
| chr14:56633614 | G | A | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+443G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633614 | |||||||
| chr14:56633731 | A | T | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+560A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633731 | |||||||
| chr14:56633794 | T | TCA | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724+636_1724+637d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56633794 | ||||||
| chr14:56633808 | A | G | 7 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(4): Show |
7 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724+637A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633808 | |||||||
| chr14:56633874 | A | G | 1 | a0003c0007t0001g0261 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1724+703A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56633874 | |||||||
| chr14:56634333 | A | G | 4 | a0001c0002t0001g0002 a0001c0002t0001g0071 a0001c0002t0001g0084 others(1): Show |
9 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1725-566A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634333 | |||||||
| chr14:56634334 | G | T | 37 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(34): Show |
39 | HG00621.hp1 HG01081.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1725-565G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634334 | |||||||
| chr14:56634408 | A | C | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725-491A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634408 | |||||||
| chr14:56634516 | A | T | 1 | a0002c0003t0001g0069 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1725-383A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634516 | |||||||
| chr14:56634534 | C | T | 185 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(182): Show |
199 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1725-365C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634534 | |||||||
| chr14:56634535 | C | G | 304 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(301): Show |
335 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.1725-364C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634535 | |||||||
| chr14:56634679 | G | T | 279 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(276): Show |
308 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.1725-220G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634679 | |||||||
| chr14:56634694 | G | T | 287 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(284): Show |
316 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.1725-205G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634694 | |||||||
| chr14:56634709 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1725-190G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | chr14 | 56634709 | |||||||
| chr14:56634842 | C | CA | 11 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0166 others(8): Show |
13 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725-42dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 56634842 | ||||||
| chr14:56634964 | A | G | 213 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(210): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1778+12A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56634964 | |||||||
| chr14:56635288 | C | T | 1 | a0002c0005t0012g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1778+336C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635288 | |||||||
| chr14:56635447 | T | C | 1 | a0001c0001t0009g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1778+495T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635447 | |||||||
| chr14:56635469 | T | TGTTAAAG others(9): Show |
7 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(4): Show |
8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1778+518_1778+533d others(18): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635469 | ||||||
| chr14:56635738 | C | T | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1779-770C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635738 | |||||||
| chr14:56635771 | T | C | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1779-737T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635771 | |||||||
| chr14:56635775 | G | A | 1 | a0001c0002t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1779-733G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635775 | |||||||
| chr14:56635816 | G | A | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
27 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1779-692G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56635816 | |||||||
| chr14:56635844 | A | AAT | 62 | a0001c0001t0001g0171 a0001c0001t0002g0006 a0001c0001t0002g0121 others(59): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1779-650_1779-649d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635844 | ||||||
| chr14:56635844 | AAT | A | 44 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(41): Show |
47 | HG00621.hp1 HG01081.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1779-650_1779-649d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635844 | ||||||
| chr14:56635980 | G | GCATAATT others(16): Show |
5 | a0002c0006t0003g0281 a0002c0006t0003g0288 a0002c0006t0003g0289 others(2): Show |
5 | NA18979.hp2 NA19002.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.1779-527_1779-505d others(25): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56635980 | ||||||
| chr14:56636012 | G | A | 1 | a0001c0001t0006g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1779-496G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56636012 | |||||||
| chr14:56636158 | G | A | 4 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(1): Show |
4 | NA18959.hp1 NA18967.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1779-350G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56636158 | |||||||
| chr14:56636225 | T | TAACAATA others(6): Show |
7 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(4): Show |
8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1779-281_1779-269d others(15): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 56636225 | ||||||
| chr14:56636504 | C | G | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1779-4C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 14/15 | chr14 | 56636504 | |||||||
| chr14:56636661 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+63A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56636661 | |||||||
| chr14:56636663 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+65A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56636663 | |||||||
| chr14:56636780 | G | A | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+182G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56636780 | |||||||
| chr14:56636794 | GAAT | G | 7 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(4): Show |
8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1869+201_1869+203d others(5): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56636794 | ||||||
| chr14:56637007 | C | T | 25 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(22): Show |
25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+409C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637007 | |||||||
| chr14:56637044 | G | A | 5 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(2): Show |
5 | HG01433.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+446G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637044 | |||||||
| chr14:56637068 | T | C | 1 | a0001c0002t0001g0108 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1869+470T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637068 | |||||||
| chr14:56637230 | T | C | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1869+632T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637230 | |||||||
| chr14:56637268 | C | T | 288 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(285): Show |
317 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.1869+670C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637268 | |||||||
| chr14:56637321 | G | C | 2 | a0001c0002t0001g0108 a0002c0003t0001g0109 |
2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1869+723G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637321 | |||||||
| chr14:56637392 | A | C | 4 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0222 others(1): Show |
4 | HG01993.hp1 HG02148.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+794A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637392 | |||||||
| chr14:56637409 | G | A | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+811G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637409 | |||||||
| chr14:56637423 | C | T | 102 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0002t0001g0001 others(99): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1869+825C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637423 | |||||||
| chr14:56637435 | T | C | 1 | a0004c0008t0004g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1869+837T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637435 | |||||||
| chr14:56637522 | A | G | 8 | a0002c0005t0001g0014 a0002c0005t0001g0015 a0002c0005t0001g0166 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1869+924A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637522 | |||||||
| chr14:56637714 | G | A | 1 | a0002c0006t0003g0279 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1869+1116G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637714 | |||||||
| chr14:56637853 | T | TCCCTGCT others(13): Show |
20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+1269_1869+127 others(24): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56637853 | ||||||
| chr14:56637877 | G | C | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+1279G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56637877 | |||||||
| chr14:56637923 | TTGTGAGT others(2): Show |
T | 4 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(1): Show |
4 | NA18959.hp1 NA18967.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+1332_1869+134 others(13): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56637923 | ||||||
| chr14:56637948 | AG | A | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+1353delG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56637948 | ||||||
| chr14:56638073 | G | GCTAACCA others(21): Show |
31 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(28): Show |
33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1869+1476_1869+150 others(32): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56638073 | ||||||
| chr14:56638133 | A | G | 247 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(244): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1869+1535A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638133 | |||||||
| chr14:56638191 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+1593A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638191 | |||||||
| chr14:56638257 | C | A | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1869+1659C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638257 | |||||||
| chr14:56638268 | A | G | 5 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0004c0008t0004g0127 others(2): Show |
5 | HG02257.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869+1670A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638268 | |||||||
| chr14:56638476 | C | T | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+1878C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638476 | |||||||
| chr14:56638511 | T | C | 6 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+1913T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638511 | |||||||
| chr14:56638612 | A | C | 109 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1869+2014A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638612 | |||||||
| chr14:56638638 | A | AATGAGGC others(45): Show |
1 | a0003c0007t0001g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1869+2041_1869+209 others(56): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56638638 | ||||||
| chr14:56638749 | A | G | 1 | a0001c0004t0011g0300 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1869+2151A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638749 | |||||||
| chr14:56638766 | G | C | 1 | a0001c0001t0009g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1869+2168G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638766 | |||||||
| chr14:56638793 | AGCAGG | A | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+2203_1869+220 others(9): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56638793 | ||||||
| chr14:56638799 | G | A | 4 | a0001c0001t0002g0200 a0001c0001t0002g0214 a0001c0001t0002g0215 others(1): Show |
4 | NA18942.hp1 NA18969.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+2201G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638799 | |||||||
| chr14:56638804 | G | A | 1 | a0001c0004t0003g0294 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1869+2206G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638804 | |||||||
| chr14:56638806 | G | A | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+2208G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638806 | |||||||
| chr14:56638826 | A | G | 1 | a0001c0001t0006g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1869+2228A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638826 | |||||||
| chr14:56638918 | A | T | 7 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(4): Show |
8 | HG01433.hp1 HG02559.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1869+2320A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638918 | |||||||
| chr14:56638925 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+2327A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638925 | |||||||
| chr14:56638929 | C | T | 5 | a0001c0004t0011g0299 a0001c0004t0011g0300 a0001c0004t0011g0301 others(2): Show |
5 | HG01433.hp1 HG02559.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+2331C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638929 | |||||||
| chr14:56638948 | C | G | 1 | a0002c0003t0001g0058 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1869+2350C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56638948 | |||||||
| chr14:56639022 | A | G | 6 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
6 | HG01358.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1869+2424A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639022 | |||||||
| chr14:56639192 | A | G | 2 | a0004c0008t0004g0128 a0004c0008t0004g0175 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1869+2594A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639192 | |||||||
| chr14:56639234 | ACAGGGTA others(12): Show |
A | 38 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
42 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1869+2656_1869+267 others(23): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56639234 | ||||||
| chr14:56639243 | C | A | 1 | a0002c0003t0007g0039 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1869+2645C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639243 | |||||||
| chr14:56639298 | CTA | C | 13 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(10): Show |
15 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1869+2701_1869+270 others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639298 | |||||||
| chr14:56639372 | A | G | 1 | a0004c0008t0004g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1869+2774A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639372 | |||||||
| chr14:56639574 | C | T | 25 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(22): Show |
25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+2976C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639574 | |||||||
| chr14:56639583 | C | T | 14 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(11): Show |
14 | HG00639.hp2 HG01109.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1869+2985C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639583 | |||||||
| chr14:56639584 | G | A | 1 | a0007c0017t0007g0024 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1869+2986G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639584 | |||||||
| chr14:56639590 | T | C | 1 | a0004c0008t0018g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1869+2992T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639590 | |||||||
| chr14:56639704 | C | T | 5 | a0001c0001t0006g0241 a0001c0001t0006g0242 a0001c0001t0006g0243 others(2): Show |
5 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869+3106C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639704 | |||||||
| chr14:56639705 | G | A | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1869+3107G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639705 | |||||||
| chr14:56639777 | T | TCCCACCC others(16): Show |
1 | a0002c0006t0003g0289 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1869+3181_1869+320 others(27): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56639777 | ||||||
| chr14:56639784 | C | T | 25 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(22): Show |
25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3186C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639784 | |||||||
| chr14:56639839 | C | G | 1 | a0001c0001t0009g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1869+3241C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639839 | |||||||
| chr14:56639991 | C | T | 1 | a0001c0001t0008g0315 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1869+3393C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56639991 | |||||||
| chr14:56640001 | A | G | 25 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(22): Show |
25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3403A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640001 | |||||||
| chr14:56640017 | C | G | 2 | a0001c0001t0009g0191 a0001c0001t0009g0194 |
2 | HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1869+3419C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640017 | |||||||
| chr14:56640030 | G | C | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+3432G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640030 | |||||||
| chr14:56640310 | CA | C | 25 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(22): Show |
25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3714delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56640310 | ||||||
| chr14:56640322 | T | A | 25 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(22): Show |
25 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1869+3724T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640322 | |||||||
| chr14:56640346 | G | A | 1 | a0008c0015t0001g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1869+3748G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640346 | |||||||
| chr14:56640640 | C | T | 1 | a0002c0003t0007g0025 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1869+4042C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640640 | |||||||
| chr14:56640657 | G | A | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4059G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640657 | |||||||
| chr14:56640673 | G | C | 1 | a0001c0004t0003g0308 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1869+4075G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640673 | |||||||
| chr14:56640689 | C | T | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+4091C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640689 | |||||||
| chr14:56640796 | C | T | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+4198C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640796 | |||||||
| chr14:56640807 | C | T | 1 | a0001c0011t0001g0313 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1869+4209C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640807 | |||||||
| chr14:56640818 | GA | G | 32 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(29): Show |
34 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1869+4224delA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56640818 | ||||||
| chr14:56640832 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1869+4234G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640832 | |||||||
| chr14:56640899 | G | A | 1 | a0003c0007t0001g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1869+4301G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640899 | |||||||
| chr14:56640928 | G | T | 1 | a0002c0005t0002g0218 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1869+4330G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640928 | |||||||
| chr14:56640956 | GAAAC | G | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1869+4366_1869+436 others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56640956 | ||||||
| chr14:56640975 | A | C | 16 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(13): Show |
16 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1869+4377A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640975 | |||||||
| chr14:56640982 | T | G | 3 | a0001c0002t0001g0052 a0001c0002t0001g0053 a0001c0002t0001g0060 |
3 | HG00741.hp2 HG01993.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1869+4384T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56640982 | |||||||
| chr14:56641032 | T | C | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4434T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641032 | |||||||
| chr14:56641058 | C | T | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4460C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641058 | |||||||
| chr14:56641059 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4461A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641059 | |||||||
| chr14:56641060 | G | C | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4462G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641060 | |||||||
| chr14:56641062 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4464A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641062 | |||||||
| chr14:56641069 | G | C | 102 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0002t0001g0001 others(99): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1869+4471G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641069 | |||||||
| chr14:56641099 | C | T | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4501C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641099 | |||||||
| chr14:56641104 | T | C | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4506T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641104 | |||||||
| chr14:56641115 | T | C | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4517T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641115 | |||||||
| chr14:56641121 | C | T | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4523C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641121 | |||||||
| chr14:56641130 | T | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4532T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641130 | |||||||
| chr14:56641138 | G | A | 95 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(92): Show |
100 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.1869+4540G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641138 | |||||||
| chr14:56641140 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4542A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641140 | |||||||
| chr14:56641145 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4547A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641145 | |||||||
| chr14:56641166 | A | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4568A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641166 | |||||||
| chr14:56641207 | TGATTGTC others(1): Show |
T | 6 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+4614_1869+462 others(12): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56641207 | ||||||
| chr14:56641256 | A | T | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+4658A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641256 | |||||||
| chr14:56641454 | C | T | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+4856C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641454 | |||||||
| chr14:56641518 | C | T | 32 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(29): Show |
34 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1869+4920C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641518 | |||||||
| chr14:56641650 | A | G | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1869+5052A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641650 | |||||||
| chr14:56641723 | A | G | 1 | a0001c0002t0001g0028 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1869+5125A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641723 | |||||||
| chr14:56641751 | G | A | 1 | a0001c0001t0005g0325 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1869+5153G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641751 | |||||||
| chr14:56641817 | G | A | 1 | a0002c0003t0001g0090 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1869+5219G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641817 | |||||||
| chr14:56641884 | TTAAA | T | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1869+5287_1869+529 others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641884 | |||||||
| chr14:56641902 | G | A | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+5304G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641902 | |||||||
| chr14:56641909 | CAAAG | C | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1869+5314_1869+531 others(8): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56641909 | ||||||
| chr14:56641986 | A | T | 2 | a0003c0007t0001g0255 a0003c0007t0001g0257 |
2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1870-5257A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56641986 | |||||||
| chr14:56642112 | T | C | 21 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(18): Show |
24 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1870-5131T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642112 | |||||||
| chr14:56642125 | C | A | 3 | a0004c0008t0004g0127 a0004c0008t0004g0128 a0004c0008t0004g0175 |
3 | HG03195.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1870-5118C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642125 | |||||||
| chr14:56642148 | C | T | 94 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(91): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1870-5095C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642148 | |||||||
| chr14:56642149 | G | C | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870-5094G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642149 | |||||||
| chr14:56642153 | C | T | 35 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(32): Show |
35 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.1870-5090C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642153 | |||||||
| chr14:56642154 | G | A | 8 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0221 others(5): Show |
8 | HG00280.hp2 HG00323.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1870-5089G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642154 | |||||||
| chr14:56642188 | A | C | 2 | a0002c0005t0001g0015 a0002c0005t0001g0166 |
3 | HG01891.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1870-5055A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642188 | |||||||
| chr14:56642220 | G | A | 289 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(286): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1870-5023G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642220 | |||||||
| chr14:56642265 | A | C | 1 | a0001c0001t0005g0327 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1870-4978A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642265 | |||||||
| chr14:56642292 | A | G | 1 | a0001c0004t0003g0293 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1870-4951A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642292 | |||||||
| chr14:56642296 | A | G | 14 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
16 | HG01081.hp2 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870-4947A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642296 | |||||||
| chr14:56642366 | A | G | 14 | a0001c0001t0002g0233 a0001c0001t0002g0235 a0001c0001t0002g0236 others(11): Show |
14 | HG01358.hp1 HG01891.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1870-4877A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642366 | |||||||
| chr14:56642460 | C | A | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-4783C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642460 | |||||||
| chr14:56642461 | G | A | 6 | a0001c0004t0004g0176 a0001c0004t0004g0177 a0001c0004t0004g0178 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-4782G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642461 | |||||||
| chr14:56642497 | A | G | 1 | a0002c0003t0021g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1870-4746A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642497 | |||||||
| chr14:56642530 | G | A | 1 | a0002c0003t0007g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-4713G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642530 | |||||||
| chr14:56642578 | C | A | 1 | a0003c0007t0001g0018 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1870-4665C>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642578 | |||||||
| chr14:56642620 | C | T | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1870-4623C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642620 | |||||||
| chr14:56642673 | G | A | 1 | a0002c0003t0007g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-4570G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642673 | |||||||
| chr14:56642874 | A | G | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0125 others(1): Show |
4 | HG02523.hp1 NA18943.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1870-4369A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642874 | |||||||
| chr14:56642882 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1870-4361G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642882 | |||||||
| chr14:56642944 | G | A | 14 | a0001c0002t0001g0037 a0001c0002t0001g0049 a0001c0002t0001g0059 others(11): Show |
16 | HG00423.hp1 HG00673.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1870-4299G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642944 | |||||||
| chr14:56642944 | G | T | 1 | a0003c0007t0001g0252 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1870-4299G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56642944 | |||||||
| chr14:56643037 | A | G | 5 | a0001c0001t0009g0191 a0001c0001t0009g0192 a0001c0001t0009g0193 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-4206A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643037 | |||||||
| chr14:56643059 | T | G | 1 | a0001c0002t0001g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1870-4184T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643059 | |||||||
| chr14:56643063 | T | C | 1 | a0001c0002t0001g0108 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1870-4180T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643063 | |||||||
| chr14:56643117 | G | T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0153 a0001c0004t0003g0278 others(7): Show |
12 | HG02258.hp2 HG02486.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.1870-4126G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643117 | |||||||
| chr14:56643199 | A | G | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1870-4044A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643199 | |||||||
| chr14:56643250 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1870-3993A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643250 | |||||||
| chr14:56643288 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1870-3955A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643288 | |||||||
| chr14:56643358 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1870-3885C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643358 | |||||||
| chr14:56643415 | A | G | 1 | a0002c0006t0003g0291 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1870-3828A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643415 | |||||||
| chr14:56643418 | A | C | 2 | a0001c0002t0001g0104 a0001c0002t0001g0105 |
2 | NA19002.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1870-3825A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643418 | |||||||
| chr14:56643484 | A | C | 21 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(18): Show |
21 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1870-3759A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643484 | |||||||
| chr14:56643494 | T | C | 1 | a0002c0005t0001g0272 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1870-3749T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643494 | |||||||
| chr14:56643506 | A | G | 1 | a0001c0002t0001g0036 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1870-3737A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643506 | |||||||
| chr14:56643577 | A | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1870-3666A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643577 | |||||||
| chr14:56643582 | C | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1870-3661C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643582 | |||||||
| chr14:56643624 | A | G | 1 | a0002c0005t0002g0218 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1870-3619A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643624 | |||||||
| chr14:56643693 | T | C | 5 | a0001c0001t0009g0191 a0001c0001t0009g0192 a0001c0001t0009g0193 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-3550T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643693 | |||||||
| chr14:56643735 | T | C | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
41 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1870-3508T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643735 | |||||||
| chr14:56643800 | A | G | 4 | a0002c0005t0012g0131 a0002c0005t0012g0132 a0002c0005t0012g0133 others(1): Show |
4 | HG02970.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1870-3443A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643800 | |||||||
| chr14:56643906 | A | G | 2 | a0005c0009t0001g0135 a0005c0009t0001g0159 |
2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1870-3337A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643906 | |||||||
| chr14:56643929 | C | T | 2 | a0001c0001t0001g0120 a0009c0012t0001g0119 |
2 | HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1870-3314C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56643929 | |||||||
| chr14:56644020 | T | A | 1 | a0002c0003t0021g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1870-3223T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644020 | |||||||
| chr14:56644075 | T | G | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1870-3168T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644075 | |||||||
| chr14:56644271 | A | G | 1 | a0002c0003t0017g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1870-2972A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644271 | |||||||
| chr14:56644272 | C | G | 1 | a0003c0007t0001g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1870-2971C>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644272 | |||||||
| chr14:56644286 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1870-2957A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644286 | |||||||
| chr14:56644369 | T | G | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1870-2874T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644369 | |||||||
| chr14:56644498 | T | A | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-2745T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644498 | |||||||
| chr14:56644499 | T | A | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-2744T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644499 | |||||||
| chr14:56644585 | G | C | 187 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1870-2658G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644585 | |||||||
| chr14:56644605 | G | A | 31 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(28): Show |
31 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.1870-2638G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644605 | |||||||
| chr14:56644668 | T | A | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1870-2575T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644668 | |||||||
| chr14:56644707 | G | C | 31 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(28): Show |
33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1870-2536G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644707 | |||||||
| chr14:56644723 | G | A | 1 | a0001c0001t0006g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1870-2520G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644723 | |||||||
| chr14:56644744 | A | G | 2 | a0001c0001t0008g0125 a0004c0008t0018g0118 |
2 | NA19081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1870-2499A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644744 | |||||||
| chr14:56644776 | T | A | 1 | a0001c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1870-2467T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56644776 | |||||||
| chr14:56645028 | A | G | 12 | a0001c0004t0004g0005 a0001c0004t0004g0176 a0001c0004t0004g0177 others(9): Show |
14 | HG01081.hp2 HG01243.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1870-2215A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645028 | |||||||
| chr14:56645086 | T | C | 119 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0001t0002g0233 others(116): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1870-2157T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645086 | |||||||
| chr14:56645167 | T | C | 11 | a0001c0001t0006g0112 a0001c0001t0006g0114 a0001c0001t0006g0115 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1870-2076T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645167 | |||||||
| chr14:56645208 | G | A | 2 | a0001c0011t0001g0313 a0004c0008t0005g0251 |
2 | HG01943.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1870-2035G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645208 | |||||||
| chr14:56645244 | C | CA | 144 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0001t0006g0112 others(141): Show |
161 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1870-1997dupA | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56645244 | ||||||
| chr14:56645257 | A | T | 2 | a0001c0002t0001g0108 a0002c0003t0001g0109 |
2 | NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1870-1986A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645257 | |||||||
| chr14:56645360 | G | A | 134 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0002t0001g0001 others(131): Show |
151 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1870-1883G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645360 | |||||||
| chr14:56645387 | G | A | 9 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(6): Show |
9 | HG00639.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1870-1856G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645387 | |||||||
| chr14:56645452 | A | G | 2 | a0001c0001t0002g0006 a0015c0021t0002g0006 |
3 | NA18952.hp2 NA19004.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1870-1791A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645452 | |||||||
| chr14:56645481 | G | T | 304 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(301): Show |
335 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.1870-1762G>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645481 | |||||||
| chr14:56645501 | G | A | 5 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(2): Show |
5 | NA18939.hp1 NA18964.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-1742G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645501 | |||||||
| chr14:56645502 | G | C | 8 | a0001c0004t0004g0005 a0001c0004t0004g0182 a0001c0004t0004g0183 others(5): Show |
10 | HG01081.hp2 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1870-1741G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645502 | |||||||
| chr14:56645504 | T | G | 1 | a0002c0003t0007g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-1739T>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645504 | |||||||
| chr14:56645505 | A | T | 1 | a0002c0003t0007g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-1738A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645505 | |||||||
| chr14:56645505 | AG | A | 118 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0002t0001g0001 others(115): Show |
135 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1870-1732delG | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56645505 | ||||||
| chr14:56645506 | G | A | 1 | a0002c0003t0007g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1870-1737G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645506 | |||||||
| chr14:56645517 | T | C | 4 | a0002c0005t0012g0131 a0002c0005t0012g0132 a0002c0005t0012g0133 others(1): Show |
4 | HG02970.hp2 HG03017.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1870-1726T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645517 | |||||||
| chr14:56645567 | A | G | 20 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1870-1676A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645567 | |||||||
| chr14:56645627 | AAAACTT | A | 99 | a0001c0001t0001g0153 a0001c0001t0001g0229 a0001c0002t0001g0001 others(96): Show |
114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1870-1612_1870-160 others(10): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56645627 | ||||||
| chr14:56645634 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1870-1609A>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645634 | |||||||
| chr14:56645685 | A | G | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
41 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1870-1558A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645685 | |||||||
| chr14:56645918 | A | G | 2 | a0005c0009t0001g0135 a0005c0009t0001g0159 |
2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1870-1325A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56645918 | |||||||
| chr14:56646065 | G | A | 1 | a0003c0007t0001g0018 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1870-1178G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646065 | |||||||
| chr14:56646104 | T | C | 31 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(28): Show |
33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1870-1139T>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646104 | |||||||
| chr14:56646490 | TTTTG | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
38 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1870-746_1870-743d others(6): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646490 | ||||||
| chr14:56646555 | C | T | 1 | a0001c0001t0005g0318 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1870-688C>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646555 | |||||||
| chr14:56646783 | G | C | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-460G>C | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646783 | |||||||
| chr14:56646852 | G | GT | 47 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
52 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1870-379dupT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646852 | ||||||
| chr14:56646852 | GT | G | 37 | a0001c0002t0001g0079 a0001c0004t0003g0278 a0001c0004t0003g0292 others(34): Show |
39 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1870-379delT | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646852 | ||||||
| chr14:56646852 | GTT | G | 37 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(34): Show |
39 | HG00621.hp1 HG01081.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1870-380_1870-379d others(4): Show |
TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | 56646852 | ||||||
| chr14:56646887 | A | G | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-356A>G | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646887 | |||||||
| chr14:56646932 | A | T | 1 | a0001c0002t0001g0054 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1870-311A>T | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56646932 | |||||||
| chr14:56647076 | G | A | 80 | a0001c0001t0005g0317 a0001c0001t0005g0318 a0001c0001t0005g0319 others(77): Show |
85 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.1870-167G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647076 | |||||||
| chr14:56647098 | T | A | 4 | a0002c0005t0013g0210 a0003c0007t0013g0246 a0003c0007t0013g0264 others(1): Show |
4 | HG03831.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1870-145T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647098 | |||||||
| chr14:56647133 | G | A | 31 | a0001c0004t0003g0278 a0001c0004t0003g0292 a0001c0004t0003g0293 others(28): Show |
33 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1870-110G>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647133 | |||||||
| chr14:56647178 | T | A | 1 | a0001c0002t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1870-65T>A | TMEM260 | ENSG00000070269.14 | transcript | ENST00000261556.11 | protein_coding | 15/15 | chr14 | 56647178 |