Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 147463 |
| ensemblid | ENSG00000154065.17 |
| hgncid | 27110 |
| symbol | ANKRD29 |
| name | ankyrin repeat domain 29 |
| refseq_nuc | NM_173505.4 |
| refseq_prot | NP_775776.2 |
| ensembl_nuc | ENST00000592179.6 |
| ensembl_prot | ENSP00000468354.1 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 23598926 |
| end | 23662911 |
| strand | - |
| ver | v1.2 |
| region | chr18:23598926-23662911 |
| region5000 | chr18:23593926-23667911 |
| regionname0 | ANKRD29_chr18_23598926_23662911 |
| regionname5000 | ANKRD29_chr18_23593926_23667911 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 301 | 346 | 87 | 56 | 150 | 12 | 39 | 121 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCRMS others(296): Show |
chr18 | 23593926 | 23667911 |
| a0002 | 0/0 | 301 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCRMS others(296): Show |
chr18 | 23593926 | 23667911 |
| a0003 | 0/0 | 301 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCRMS others(296): Show |
chr18 | 23593926 | 23667911 |
| a0004 | 0/0 | 301 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCRMS others(296): Show |
chr18 | 23593926 | 23667911 |
| a0005 | 0/0 | 301 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCKMS others(296): Show |
chr18 | 23593926 | 23667911 |
| a0006 | 0/0 | 301 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCRMS others(296): Show |
chr18 | 23593926 | 23667911 |
| a0007 | 0/0 | 301 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | MCRMS others(296): Show |
chr18 | 23593926 | 23667911 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 903 | 336 | 78 | 55 | 150 | 12 | 39 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0001c0002 | 0/0 | 903 | 8 | 8 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0001c0003 | 0/0 | 903 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0002c0009 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0003c0007 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0004c0005 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0005c0004 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0006c0008 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 | ||
| a0007c0006 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | ATGTG others(898): Show |
chr18 | 23593926 | 23667911 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3387 | 131 | 25 | 19 | 69 | 3 | 15 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0002 | 0/1 | 3387 | 59 | 8 | 16 | 20 | 5 | 9 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0003 | 0/0 | 3387 | 40 | 0 | 11 | 24 | 4 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0004 | 0/0 | 3387 | 28 | 0 | 2 | 23 | 0 | 3 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0005 | 0/0 | 3387 | 10 | 0 | 1 | 0 | 0 | 9 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0006 | 0/0 | 3387 | 11 | 10 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0007 | 0/0 | 3387 | 10 | 0 | 0 | 10 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0008 | 0/0 | 3388 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3383): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0009 | 0/0 | 3387 | 6 | 5 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0010 | 0/0 | 3387 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0011 | 0/0 | 3387 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0012 | 0/0 | 3387 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0014 | 0/0 | 3387 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0015 | 0/0 | 3387 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0016 | 0/0 | 3387 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0017 | 0/0 | 3387 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0018 | 0/0 | 3387 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0019 | 1/0 | 3387 | 2 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0020 | 0/0 | 3387 | 2 | 0 | 1 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0022 | 0/0 | 3388 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3383): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0023 | 0/0 | 3387 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0024 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0025 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0026 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0027 | 0/0 | 3387 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0028 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0029 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0030 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0001t0031 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0002t0001 | 0/0 | 3387 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0002t0008 | 0/0 | 3388 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3383): Show |
chr18 | 23593926 | 23667911 |
| a0001c0002t0013 | 0/0 | 3387 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0001c0003t0002 | 0/0 | 3387 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0002c0009t0021 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0003c0007t0005 | 0/0 | 3387 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0004c0005t0001 | 0/0 | 3387 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0005c0004t0001 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0006c0008t0001 | 0/0 | 3387 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| a0007c0006t0004 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | GCGCC others(3382): Show |
chr18 | 23593926 | 23667911 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0261 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0009g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0010g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0014g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0014g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0014g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0016g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0016g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0017g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0017g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0018g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0018g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0019g0309 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0020g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0020g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0022g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0023g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0024g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0025g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0026g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0027g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0028g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0029g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0030g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0001t0031g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0013g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0002t0013g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0002c0009t0021g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0003c0007t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0004c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0005c0004t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0006c0008t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| a0007c0006t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | GBR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0246 | EUR | GBR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0310 | EUR | GBR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00558 | hp1 | a0002 | c0009 | t0021 | g0012 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00741 | hp1 | a0001 | c0001 | t0027 | g0298 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG00741 | hp2 | a0003 | c0007 | t0005 | g0196 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01106 | hp2 | a0004 | c0005 | t0001 | g0168 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0013 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0322 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01175 | hp1 | a0001 | c0001 | t0019 | g0136 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0275 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01358 | hp1 | a0001 | c0001 | t0020 | g0320 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0195 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | IBS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | IBS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0202 | EUR | IBS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0131 | EUR | IBS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0132 | EUR | IBS | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01884 | hp1 | a0001 | c0002 | t0013 | g0311 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0329 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0058 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | CDX | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0327 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0098 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PEL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02572 | hp1 | a0001 | c0001 | t0030 | g0321 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02572 | hp2 | a0001 | c0001 | t0024 | g0208 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02602 | hp2 | a0001 | c0001 | t0020 | g0319 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02630 | hp2 | a0005 | c0004 | t0001 | g0018 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0097 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02698 | hp1 | a0006 | c0008 | t0001 | g0143 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0324 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0316 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0297 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0334 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0025 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02886 | hp2 | a0001 | c0002 | t0013 | g0317 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0336 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0335 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0328 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0182 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03041 | hp2 | a0001 | c0001 | t0022 | g0015 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0061 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0332 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03139 | hp1 | a0001 | c0001 | t0029 | g0318 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0016 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0081 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0194 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0032 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0326 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0124 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0045 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0333 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03540 | hp1 | a0001 | c0001 | t0028 | g0112 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0017 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0257 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0193 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0279 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0026 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0027 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04184 | hp2 | a0001 | c0001 | t0023 | g0169 | SAS | BEB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | YRI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | YRI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0066 | EAS | CHB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0300 | AFR | YRI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0323 | AFR | YRI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18945 | hp2 | a0007 | c0006 | t0004 | g0028 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18947 | hp2 | a0001 | c0001 | t0026 | g0127 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18964 | hp1 | a0001 | c0001 | t0018 | g0243 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18988 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18997 | hp2 | a0001 | c0001 | t0025 | g0099 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19009 | hp2 | a0001 | c0001 | t0018 | g0276 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19030 | hp2 | a0001 | c0002 | t0013 | g0312 | AFR | LWK | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0330 | AFR | YRI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0235 | AFR | ASW | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0272 | EUR | TSI | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | GIH | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02109 | hp1 | a0001 | c0002 | t0008 | g0314 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0331 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | USA | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | USA | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA20300 | hp2 | a0001 | c0001 | t0031 | g0325 | AFR | USA | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0204 | AFR | LWK | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0261 | REF | REF | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0019 | g0309 | REF | REF | ANKRD29_chr18_23593926_23667911 | ANKRD29 | chr18 | 23593926 | 23667911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:23601272 | C | T | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.860G>A | p.Arg287His | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 1041/3387 | 860/906 | 287/301 | chr18 | 23601272 | |||
| chr18:23612105 | G | T | 1 | a0007 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.809C>A | p.Ser270Tyr | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/10 | 990/3387 | 809/906 | 270/301 | chr18 | 23612105 | |||
| chr18:23612189 | T | C | 1 | a0006 | 1 | HG02698.hp1 | missense_variant&splice_region_variant | MODERATE | c.725A>G | p.Asn242Ser | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/10 | 906/3387 | 725/906 | 242/301 | chr18 | 23612189 | |||
| chr18:23638874 | C | G | 1 | a0004 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.305G>C | p.Gly102Ala | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/10 | 486/3387 | 305/906 | 102/301 | chr18 | 23638874 | |||
| chr18:23646203 | T | C | 1 | a0002 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.217A>G | p.Asn73Asp | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/10 | 398/3387 | 217/906 | 73/301 | chr18 | 23646203 | |||
| chr18:23662723 | C | T | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.8G>A | p.Arg3Lys | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | 189/3387 | 8/906 | 3/301 | chr18 | 23662723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:23634138 | G | A | 1 | a0001c0002 | 8 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.342C>T | p.Thr114Thr | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/10 | 523/3387 | 342/906 | 114/301 | chr18 | 23634138 | |||
| chr18:23649137 | C | T | 1 | a0001c0003 | 2 | HG01175.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.78G>A | p.Ala26Ala | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/10 | 259/3387 | 78/906 | 26/301 | chr18 | 23649137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:23599079 | T | C | 1 | a0001c0001t0027 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2147A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 2147 | chr18 | 23599079 | ||||||
| chr18:23599094 | C | T | 1 | a0001c0001t0007 | 10 | NA18747.hp2 NA18951.hp1 NA18971.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2132G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 2132 | chr18 | 23599094 | ||||||
| chr18:23599143 | T | C | 1 | a0001c0001t0018 | 2 | NA18964.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2083A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 2083 | chr18 | 23599143 | ||||||
| chr18:23599180 | T | A | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(31): Show |
286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*2046A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 2046 | chr18 | 23599180 | ||||||
| chr18:23599204 | C | T | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0023 others(2): Show |
35 | HG00558.hp1 HG00597.hp1 HG01928.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2022G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 2022 | chr18 | 23599204 | ||||||
| chr18:23599276 | C | T | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0020 |
52 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1950G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 1950 | chr18 | 23599276 | ||||||
| chr18:23599283 | C | G | 1 | a0001c0001t0026 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1943G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 1943 | chr18 | 23599283 | ||||||
| chr18:23599583 | C | A | 2 | a0001c0001t0014 a0001c0002t0013 |
6 | HG01884.hp1 HG02886.hp2 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1643G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 1643 | chr18 | 23599583 | ||||||
| chr18:23600136 | A | T | 1 | a0001c0001t0025 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1090T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 1090 | chr18 | 23600136 | ||||||
| chr18:23600265 | A | G | 1 | a0001c0001t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 961 | chr18 | 23600265 | ||||||
| chr18:23600399 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(35): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*827T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 827 | chr18 | 23600399 | ||||||
| chr18:23600470 | T | C | 1 | a0001c0001t0023 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 756 | chr18 | 23600470 | ||||||
| chr18:23600508 | T | C | 1 | a0001c0001t0009 | 6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*718A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 718 | chr18 | 23600508 | ||||||
| chr18:23600521 | C | T | 6 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0016 others(3): Show |
36 | HG00558.hp1 HG00597.hp1 HG01109.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 705 | chr18 | 23600521 | ||||||
| chr18:23600581 | C | T | 1 | a0001c0001t0031 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*645G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 645 | chr18 | 23600581 | ||||||
| chr18:23600632 | T | G | 2 | a0001c0001t0005 a0003c0007t0005 |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*594A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 594 | chr18 | 23600632 | ||||||
| chr18:23600776 | A | C | 1 | a0001c0001t0009 | 6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*450T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 450 | chr18 | 23600776 | ||||||
| chr18:23600853 | T | C | 1 | a0001c0001t0028 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 373 | chr18 | 23600853 | ||||||
| chr18:23600877 | C | T | 3 | a0001c0001t0005 a0001c0001t0010 a0003c0007t0005 |
15 | HG00741.hp2 HG01433.hp1 HG02647.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*349G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 349 | chr18 | 23600877 | ||||||
| chr18:23600963 | A | C | 3 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0029 |
5 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*263T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 263 | chr18 | 23600963 | ||||||
| chr18:23601125 | C | CT | 3 | a0001c0001t0008 a0001c0001t0022 a0001c0002t0008 |
7 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*100dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 10/10 | 100 | chr18 | 23601125 | ||||||
| chr18:23662774 | G | A | 1 | a0001c0001t0029 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | 44 | chr18 | 23662774 | ||||||
| chr18:23662790 | C | G | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0022 |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-60G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | 60 | chr18 | 23662790 | ||||||
| chr18:23662843 | C | T | 1 | a0002c0009t0021 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | 113 | chr18 | 23662843 | ||||||
| chr18:23662877 | C | A | 1 | a0001c0001t0020 | 2 | HG01358.hp1 HG02602.hp2 |
5_prime_UTR_variant | MODIFIER | c.-147G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | 147 | chr18 | 23662877 | ||||||
| chr18:23662893 | C | A | 1 | a0001c0001t0030 | 1 | HG02572.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-163G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | chr18 | 23662893 | |||||||
| chr18:23662904 | G | A | 3 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0031 |
15 | HG01167.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-174C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/10 | 174 | chr18 | 23662904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:23601795 | G | A | 1 | a0001c0001t0005g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.823-486C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23601795 | |||||||
| chr18:23601890 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.823-581A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23601890 | |||||||
| chr18:23601949 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.823-640C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23601949 | |||||||
| chr18:23602105 | C | T | 6 | a0001c0001t0006g0327 a0001c0001t0015g0014 a0001c0001t0015g0017 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-796G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602105 | |||||||
| chr18:23602130 | G | A | 7 | a0001c0001t0008g0037 a0001c0001t0008g0046 a0001c0001t0008g0047 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-821C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602130 | |||||||
| chr18:23602153 | C | T | 5 | a0001c0001t0012g0030 a0001c0001t0012g0032 a0001c0001t0012g0300 others(2): Show |
5 | HG01109.hp1 HG02818.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-844G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602153 | |||||||
| chr18:23602279 | G | A | 2 | a0001c0001t0009g0022 a0001c0001t0009g0098 |
2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.823-970C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602279 | |||||||
| chr18:23602279 | G | T | 2 | a0001c0001t0017g0058 a0001c0001t0017g0061 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.823-970C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602279 | |||||||
| chr18:23602325 | C | T | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-1016G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602325 | |||||||
| chr18:23602489 | G | A | 6 | a0001c0001t0006g0327 a0001c0001t0015g0014 a0001c0001t0015g0017 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-1180C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602489 | |||||||
| chr18:23602518 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.823-1209G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23602518 | |||||||
| chr18:23603406 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-2097C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603406 | |||||||
| chr18:23603698 | G | T | 50 | a0001c0001t0003g0005 a0001c0001t0003g0051 a0001c0001t0003g0063 others(47): Show |
52 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.823-2389C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603698 | |||||||
| chr18:23603721 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.823-2412A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603721 | |||||||
| chr18:23603822 | G | C | 1 | a0001c0001t0001g0302 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.823-2513C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603822 | |||||||
| chr18:23603912 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(144): Show |
153 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.823-2603C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603912 | |||||||
| chr18:23603936 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0166 |
3 | NA18974.hp2 NA19010.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.823-2627C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603936 | |||||||
| chr18:23603991 | C | G | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.823-2682G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23603991 | |||||||
| chr18:23604016 | T | C | 7 | a0001c0001t0008g0037 a0001c0001t0008g0046 a0001c0001t0008g0047 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.823-2707A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604016 | |||||||
| chr18:23604084 | C | T | 1 | a0001c0001t0002g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.823-2775G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604084 | |||||||
| chr18:23604251 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823-2942T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604251 | |||||||
| chr18:23604589 | G | A | 1 | a0001c0001t0004g0184 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.823-3280C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604589 | |||||||
| chr18:23604703 | G | C | 1 | a0001c0001t0003g0202 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.823-3394C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604703 | |||||||
| chr18:23604735 | T | C | 2 | a0001c0001t0007g0041 a0001c0001t0007g0042 |
2 | NA18982.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.823-3426A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604735 | |||||||
| chr18:23604872 | A | G | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-3563T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23604872 | |||||||
| chr18:23605282 | G | GGCATGCA others(8): Show |
1 | a0001c0001t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.823-3988_823-3974d others(17): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23605282 | |||||||
| chr18:23605312 | C | T | 4 | a0001c0001t0011g0023 a0001c0001t0011g0055 a0001c0001t0011g0059 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-4003G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23605312 | |||||||
| chr18:23605356 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823-4047G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23605356 | |||||||
| chr18:23605409 | C | T | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-4100G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23605409 | |||||||
| chr18:23605758 | C | T | 3 | a0001c0001t0014g0330 a0001c0001t0014g0332 a0001c0001t0014g0333 |
3 | HG03130.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823-4449G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23605758 | |||||||
| chr18:23605939 | G | GTAATTTA others(14): Show |
2 | a0001c0001t0001g0191 a0001c0001t0001g0304 |
2 | HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.823-4651_823-4631d others(23): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23605939 | |||||||
| chr18:23606126 | A | G | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.823-4817T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606126 | |||||||
| chr18:23606132 | C | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0305 a0001c0001t0001g0306 others(2): Show |
6 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-4823G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606132 | |||||||
| chr18:23606183 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.823-4874G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606183 | |||||||
| chr18:23606497 | G | A | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-5188C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606497 | |||||||
| chr18:23606609 | C | T | 1 | a0001c0001t0004g0184 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.823-5300G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606609 | |||||||
| chr18:23606626 | A | G | 4 | a0001c0001t0011g0023 a0001c0001t0011g0055 a0001c0001t0011g0059 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-5317T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606626 | |||||||
| chr18:23606643 | C | G | 50 | a0001c0001t0003g0005 a0001c0001t0003g0051 a0001c0001t0003g0063 others(47): Show |
52 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.823-5334G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606643 | |||||||
| chr18:23606741 | T | C | 1 | a0001c0001t0010g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.822+5351A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606741 | |||||||
| chr18:23606855 | G | C | 6 | a0001c0001t0014g0330 a0001c0001t0014g0332 a0001c0001t0014g0333 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+5237C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606855 | |||||||
| chr18:23606934 | T | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(271): Show |
287 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.822+5158A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23606934 | |||||||
| chr18:23607086 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+5006G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607086 | |||||||
| chr18:23607190 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.822+4902C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607190 | |||||||
| chr18:23607203 | G | A | 5 | a0001c0001t0002g0231 a0001c0001t0002g0244 a0001c0001t0002g0254 others(2): Show |
5 | HG01070.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+4889C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607203 | |||||||
| chr18:23607350 | A | G | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+4742T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607350 | |||||||
| chr18:23607515 | G | A | 1 | a0001c0001t0007g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.822+4577C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607515 | |||||||
| chr18:23607760 | C | T | 1 | a0001c0001t0008g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.822+4332G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607760 | |||||||
| chr18:23607810 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(264): Show |
280 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.822+4282A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607810 | |||||||
| chr18:23607935 | G | A | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0234 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+4157C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23607935 | |||||||
| chr18:23608017 | A | C | 4 | a0001c0001t0005g0193 a0001c0001t0005g0194 a0001c0001t0005g0195 others(1): Show |
4 | HG01433.hp1 HG02738.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+4075T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23608017 | |||||||
| chr18:23608125 | C | T | 4 | a0001c0001t0010g0025 a0001c0001t0010g0096 a0001c0001t0010g0097 others(1): Show |
4 | HG02647.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+3967G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23608125 | |||||||
| chr18:23608278 | C | A | 54 | a0001c0001t0003g0005 a0001c0001t0003g0051 a0001c0001t0003g0063 others(51): Show |
56 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.822+3814G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23608278 | |||||||
| chr18:23608356 | G | A | 2 | a0001c0001t0004g0103 a0001c0001t0004g0105 |
2 | NA19080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.822+3736C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23608356 | |||||||
| chr18:23608360 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0014g0330 a0001c0001t0014g0332 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.822+3732G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23608360 | |||||||
| chr18:23608427 | T | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.822+3665A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23608427 | |||||||
| chr18:23609029 | G | A | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+3063C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609029 | |||||||
| chr18:23609094 | C | CA | 12 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0207 others(9): Show |
12 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.822+2997dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609094 | |||||||
| chr18:23609114 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.822+2978A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609114 | |||||||
| chr18:23609206 | T | C | 10 | a0001c0001t0001g0024 a0001c0001t0006g0331 a0001c0001t0014g0330 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+2886A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609206 | |||||||
| chr18:23609382 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0189 |
2 | HG01123.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.822+2710G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609382 | |||||||
| chr18:23609398 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.822+2694T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609398 | |||||||
| chr18:23609428 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.822+2664C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609428 | |||||||
| chr18:23609467 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.822+2625G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609467 | |||||||
| chr18:23609528 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.822+2564G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609528 | |||||||
| chr18:23609528 | C | T | 1 | a0001c0001t0011g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.822+2564G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609528 | |||||||
| chr18:23609573 | C | T | 2 | a0001c0001t0005g0122 a0001c0001t0005g0124 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.822+2519G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609573 | |||||||
| chr18:23609952 | T | A | 6 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0036 others(3): Show |
10 | NA18943.hp2 NA18948.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+2140A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609952 | |||||||
| chr18:23609956 | G | A | 20 | a0001c0001t0001g0083 a0001c0001t0001g0141 a0001c0001t0001g0145 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+2136C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609956 | |||||||
| chr18:23609977 | C | T | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0017g0058 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+2115G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23609977 | |||||||
| chr18:23610082 | GA | G | 3 | a0001c0001t0010g0025 a0001c0001t0010g0096 a0001c0001t0010g0097 |
3 | HG02647.hp1 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.822+2009delT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610082 | |||||||
| chr18:23610084 | T | A | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+2008A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610084 | |||||||
| chr18:23610086 | T | C | 20 | a0001c0001t0001g0083 a0001c0001t0001g0141 a0001c0001t0001g0145 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+2006A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610086 | |||||||
| chr18:23610152 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.822+1940C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610152 | |||||||
| chr18:23610199 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 |
3 | HG03516.hp2 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.822+1893A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610199 | |||||||
| chr18:23610339 | A | G | 24 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0191 others(21): Show |
24 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.822+1753T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610339 | |||||||
| chr18:23610567 | G | A | 54 | a0001c0001t0003g0005 a0001c0001t0003g0051 a0001c0001t0003g0063 others(51): Show |
56 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.822+1525C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610567 | |||||||
| chr18:23610687 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.822+1405C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610687 | |||||||
| chr18:23610731 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.822+1361T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610731 | |||||||
| chr18:23610748 | T | TCACTG | 4 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 others(1): Show |
4 | HG02257.hp2 HG03516.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+1339_822+1343d others(7): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610748 | |||||||
| chr18:23610811 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0189 |
2 | HG01123.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.822+1281C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23610811 | |||||||
| chr18:23611002 | C | G | 1 | a0001c0001t0008g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.822+1090G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611002 | |||||||
| chr18:23611096 | C | G | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+996G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611096 | |||||||
| chr18:23611116 | C | A | 2 | a0001c0001t0012g0030 a0001c0001t0012g0300 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.822+976G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611116 | |||||||
| chr18:23611116 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.822+976G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611116 | |||||||
| chr18:23611118 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0188 a0001c0001t0001g0191 others(1): Show |
4 | HG03516.hp2 HG03688.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+974G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611118 | |||||||
| chr18:23611204 | A | G | 1 | a0001c0001t0006g0331 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.822+888T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611204 | |||||||
| chr18:23611270 | G | C | 1 | a0001c0002t0013g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.822+822C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611270 | |||||||
| chr18:23611490 | C | A | 54 | a0001c0001t0003g0005 a0001c0001t0003g0051 a0001c0001t0003g0063 others(51): Show |
56 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.822+602G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611490 | |||||||
| chr18:23611560 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.822+532G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611560 | |||||||
| chr18:23611641 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 |
3 | HG03516.hp2 HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.822+451G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611641 | |||||||
| chr18:23611776 | G | A | 2 | a0001c0001t0017g0058 a0001c0001t0017g0061 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.822+316C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611776 | |||||||
| chr18:23611778 | C | T | 1 | a0001c0001t0012g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.822+314G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611778 | |||||||
| chr18:23611871 | G | GA | 18 | a0001c0001t0003g0074 a0001c0001t0005g0026 a0001c0001t0005g0027 others(15): Show |
18 | HG00741.hp2 HG01109.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.822+220dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611871 | |||||||
| chr18:23611906 | T | C | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+186A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23611906 | |||||||
| chr18:23612050 | A | T | 16 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 others(13): Show |
16 | HG01167.hp1 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.822+42T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23612050 | |||||||
| chr18:23612080 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.822+12G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 9/9 | chr18 | 23612080 | |||||||
| chr18:23612283 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.724-93C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612283 | |||||||
| chr18:23612297 | G | T | 273 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(270): Show |
286 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.724-107C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612297 | |||||||
| chr18:23612345 | T | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0299 a0001c0001t0027g0298 |
3 | HG00741.hp1 HG01074.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.724-155A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612345 | |||||||
| chr18:23612394 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.724-204T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612394 | |||||||
| chr18:23612643 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0157 a0001c0001t0001g0209 |
3 | HG02486.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.724-453T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612643 | |||||||
| chr18:23612735 | G | C | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.724-545C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612735 | |||||||
| chr18:23612930 | A | G | 6 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(3): Show |
6 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-740T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23612930 | |||||||
| chr18:23613045 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.724-855T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613045 | |||||||
| chr18:23613164 | A | AT | 64 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0040 others(61): Show |
64 | HG00597.hp2 HG01109.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.724-975dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613164 | |||||||
| chr18:23613164 | AT | A | 10 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0207 others(7): Show |
10 | HG01106.hp2 HG02735.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.724-975delA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613164 | |||||||
| chr18:23613274 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.724-1084T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613274 | |||||||
| chr18:23613601 | A | AT | 54 | a0001c0001t0001g0053 a0001c0001t0001g0141 a0001c0001t0001g0158 others(51): Show |
59 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.724-1412dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613601 | |||||||
| chr18:23613622 | C | T | 1 | a0001c0001t0005g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.724-1432G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613622 | |||||||
| chr18:23613735 | C | G | 2 | a0001c0001t0006g0327 a0004c0005t0001g0168 |
2 | HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.724-1545G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613735 | |||||||
| chr18:23613759 | C | T | 10 | a0001c0001t0005g0026 a0001c0001t0005g0122 a0001c0001t0005g0124 others(7): Show |
10 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-1569G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23613759 | |||||||
| chr18:23614132 | G | A | 12 | a0001c0001t0001g0057 a0001c0001t0001g0213 a0001c0001t0006g0331 others(9): Show |
12 | HG00544.hp1 HG01884.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.724-1942C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23614132 | |||||||
| chr18:23614309 | A | C | 2 | a0001c0001t0016g0013 a0001c0001t0016g0016 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.724-2119T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23614309 | |||||||
| chr18:23614668 | C | CA | 22 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0040 others(19): Show |
22 | HG00621.hp1 HG00735.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.724-2479dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23614668 | |||||||
| chr18:23614858 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.724-2668A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23614858 | |||||||
| chr18:23614859 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.724-2669T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23614859 | |||||||
| chr18:23615034 | T | G | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.723+2698A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615034 | |||||||
| chr18:23615143 | G | A | 5 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0221 others(2): Show |
5 | NA18950.hp2 NA18970.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.723+2589C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615143 | |||||||
| chr18:23615286 | G | A | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.723+2446C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615286 | |||||||
| chr18:23615427 | G | A | 1 | a0004c0005t0001g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.723+2305C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615427 | |||||||
| chr18:23615497 | T | C | 2 | a0001c0001t0016g0013 a0001c0001t0016g0016 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.723+2235A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615497 | |||||||
| chr18:23615500 | C | T | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.723+2232G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615500 | |||||||
| chr18:23615578 | T | G | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0128 others(1): Show |
4 | HG02040.hp1 NA18994.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+2154A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615578 | |||||||
| chr18:23615579 | T | G | 12 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(9): Show |
12 | HG00741.hp2 HG01106.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+2153A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615579 | |||||||
| chr18:23615701 | C | T | 2 | a0001c0001t0017g0058 a0001c0001t0017g0061 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.723+2031G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615701 | |||||||
| chr18:23615740 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.723+1992A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615740 | |||||||
| chr18:23615923 | G | A | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1809C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615923 | |||||||
| chr18:23615925 | A | AC | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1806_723+1807i others(3): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615925 | |||||||
| chr18:23615930 | T | C | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1802A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615930 | |||||||
| chr18:23615934 | A | G | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1798T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615934 | |||||||
| chr18:23615942 | T | C | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1790A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615942 | |||||||
| chr18:23615943 | A | ATATATAT others(8): Show |
8 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0194 others(5): Show |
8 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.723+1788_723+1789i others(17): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615943 | |||||||
| chr18:23615943 | A | ATATATAT others(6): Show |
3 | a0001c0001t0005g0122 a0001c0001t0005g0124 a0001c0001t0005g0193 |
3 | HG03490.hp2 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.723+1788_723+1789i others(15): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615943 | |||||||
| chr18:23615944 | A | C | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1788T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615944 | |||||||
| chr18:23615946 | A | C | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1786T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615946 | |||||||
| chr18:23615949 | T | C | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1783A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615949 | |||||||
| chr18:23615954 | AC | A | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1777delG | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615954 | |||||||
| chr18:23615956 | T | C | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1776A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615956 | |||||||
| chr18:23615957 | A | G | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1775T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615957 | |||||||
| chr18:23615963 | ATG | A | 11 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1767_723+1768d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615963 | |||||||
| chr18:23615969 | A | G | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1763T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615969 | |||||||
| chr18:23615970 | T | C | 2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1762A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615970 | |||||||
| chr18:23615974 | C | CTATGTAT others(233): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0031 others(5): Show |
11 | HG01891.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1757_723+1758i others(242): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(263): Show |
1 | a0001c0001t0012g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.723+1757_723+1758i others(272): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(234): Show |
1 | a0001c0001t0001g0207 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.723+1757_723+1758i others(243): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(233): Show |
1 | a0001c0001t0001g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.723+1757_723+1758i others(242): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(143): Show |
1 | a0001c0001t0001g0224 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.723+1608_723+1757d others(152): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(409): Show |
1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.723+1757_723+1758i others(418): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(439): Show |
3 | a0001c0001t0017g0058 a0001c0001t0017g0061 a0001c0001t0029g0318 |
3 | HG02145.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.723+1757_723+1758i others(448): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(203): Show |
16 | a0001c0001t0001g0068 a0001c0001t0001g0107 a0001c0001t0001g0119 others(13): Show |
16 | HG00642.hp2 HG01069.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.723+1757_723+1758i others(212): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(233): Show |
102 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(99): Show |
105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.723+1757_723+1758i others(242): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(263): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(6): Show |
9 | HG02602.hp1 HG03139.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.723+1757_723+1758i others(272): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(293): Show |
1 | a0001c0001t0001g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.723+1757_723+1758i others(302): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(323): Show |
3 | a0001c0001t0005g0027 a0001c0001t0005g0257 a0006c0008t0001g0143 |
3 | HG02698.hp1 HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.723+1757_723+1758i others(332): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(353): Show |
1 | a0001c0001t0009g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.723+1757_723+1758i others(362): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(383): Show |
1 | a0001c0001t0009g0020 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.723+1757_723+1758i others(392): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(413): Show |
2 | a0001c0001t0009g0022 a0001c0001t0009g0098 |
2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.723+1757_723+1758i others(422): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(173): Show |
5 | a0001c0001t0001g0174 a0001c0001t0006g0328 a0001c0001t0006g0329 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+1757_723+1758i others(182): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTATGTAT others(263): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0151 |
2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.723+1757_723+1758i others(272): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | C | CTCTACAC others(362): Show |
2 | a0001c0001t0015g0014 a0001c0001t0015g0017 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.723+1757_723+1758i others(371): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23615974 | CTATGTAT others(23): Show |
C | 6 | a0001c0001t0001g0057 a0001c0001t0002g0102 a0001c0001t0002g0148 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.723+1728_723+1757d others(32): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23615974 | |||||||
| chr18:23616126 | A | ATGTATGT others(337): Show |
1 | a0001c0001t0010g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.723+1605_723+1606i others(346): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(319): Show |
1 | a0001c0001t0004g0245 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.723+1605_723+1606i others(328): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(349): Show |
1 | a0001c0001t0005g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.723+1605_723+1606i others(358): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(529): Show |
2 | a0001c0001t0016g0013 a0001c0001t0016g0016 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.723+1605_723+1606i others(538): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(469): Show |
2 | a0001c0001t0003g0073 a0001c0001t0007g0089 |
2 | HG01928.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.723+1605_723+1606i others(478): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(439): Show |
12 | a0001c0001t0003g0005 a0001c0001t0003g0067 a0001c0001t0003g0070 others(9): Show |
13 | HG00738.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.723+1605_723+1606i others(448): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(409): Show |
36 | a0001c0001t0003g0051 a0001c0001t0003g0063 a0001c0001t0003g0064 others(33): Show |
37 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.723+1605_723+1606i others(418): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(379): Show |
11 | a0001c0001t0003g0186 a0001c0001t0004g0039 a0001c0001t0005g0122 others(8): Show |
11 | HG00741.hp2 HG02615.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1605_723+1606i others(388): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(349): Show |
20 | a0001c0001t0001g0053 a0001c0001t0001g0304 a0001c0001t0004g0001 others(17): Show |
24 | HG00558.hp1 HG01928.hp1 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.723+1605_723+1606i others(358): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(319): Show |
10 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0002g0104 others(7): Show |
11 | HG00597.hp1 HG00597.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.723+1605_723+1606i others(328): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616126 | A | ATGTATGT others(139): Show |
1 | a0004c0005t0001g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.723+1605_723+1606i others(148): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616126 | |||||||
| chr18:23616137 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
154 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.723+1595A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616137 | |||||||
| chr18:23616146 | C | T | 1 | a0001c0001t0010g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.723+1586G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616146 | |||||||
| chr18:23616153 | T | C | 2 | a0001c0001t0006g0327 a0001c0001t0029g0318 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.723+1579A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616153 | |||||||
| chr18:23616172 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.723+1560A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616172 | |||||||
| chr18:23616327 | G | A | 1 | a0001c0001t0002g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.723+1405C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616327 | |||||||
| chr18:23616368 | C | T | 11 | a0001c0001t0001g0057 a0001c0001t0006g0331 a0001c0001t0014g0330 others(8): Show |
11 | HG01884.hp1 HG02723.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+1364G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616368 | |||||||
| chr18:23616417 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723+1315G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616417 | |||||||
| chr18:23616420 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0155 |
2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.723+1312C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616420 | |||||||
| chr18:23616422 | C | T | 6 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 others(3): Show |
6 | HG02015.hp1 HG03516.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+1310G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616422 | |||||||
| chr18:23616526 | G | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0158 a0001c0001t0001g0176 others(5): Show |
8 | HG00621.hp1 NA18956.hp2 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+1206C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616526 | |||||||
| chr18:23616532 | T | TTATACTA others(23): Show |
1 | a0004c0005t0001g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.723+1170_723+1199d others(32): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616532 | |||||||
| chr18:23616548 | T | TAGTATAT others(21): Show |
1 | a0001c0001t0012g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.723+1183_723+1184i others(30): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616548 | |||||||
| chr18:23616548 | T | TAGTATAT others(47): Show |
1 | a0001c0001t0004g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.723+1183_723+1184i others(56): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616548 | |||||||
| chr18:23616548 | T | TAGTATAT others(49): Show |
22 | a0001c0001t0001g0053 a0001c0001t0004g0001 a0001c0001t0004g0004 others(19): Show |
27 | HG00558.hp1 HG00597.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.723+1183_723+1184i others(58): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616548 | |||||||
| chr18:23616548 | T | TAGTATAT others(77): Show |
1 | a0001c0001t0004g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.723+1183_723+1184i others(86): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616548 | |||||||
| chr18:23616550 | G | GTA | 138 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(135): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.723+1180_723+1181d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616550 | |||||||
| chr18:23616550 | G | GTATA | 15 | a0001c0001t0001g0107 a0001c0001t0001g0157 a0001c0001t0001g0188 others(12): Show |
15 | HG01346.hp2 HG01515.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.723+1178_723+1181d others(6): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616550 | |||||||
| chr18:23616550 | G | GTATATAT others(51): Show |
1 | a0001c0001t0004g0250 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.723+1181_723+1182i others(60): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616550 | |||||||
| chr18:23616552 | A | ATATATAT others(47): Show |
2 | a0001c0001t0002g0104 a0001c0001t0004g0138 |
2 | HG00597.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.723+1179_723+1180i others(56): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616552 | |||||||
| chr18:23616565 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(251): Show |
267 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.723+1167G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616565 | |||||||
| chr18:23616567 | C | A | 10 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(7): Show |
10 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+1165G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616567 | |||||||
| chr18:23616574 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.723+1158A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616574 | |||||||
| chr18:23616578 | G | GTA | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0034 others(31): Show |
36 | HG01433.hp1 HG02055.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.723+1152_723+1153d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616578 | |||||||
| chr18:23616578 | G | GTATATAT others(21): Show |
2 | a0001c0001t0016g0013 a0001c0001t0016g0016 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.723+1153_723+1154i others(30): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616578 | |||||||
| chr18:23616578 | GTA | G | 14 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0220 others(11): Show |
14 | HG01167.hp1 HG02015.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.723+1152_723+1153d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616578 | |||||||
| chr18:23616586 | A | AG | 8 | a0001c0001t0003g0079 a0001c0001t0003g0130 a0001c0001t0003g0131 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.723+1145_723+1146i others(3): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616586 | |||||||
| chr18:23616595 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0256 |
2 | NA19003.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.723+1137G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616595 | |||||||
| chr18:23616595 | C | T | 1 | a0001c0001t0006g0324 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723+1137G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616595 | |||||||
| chr18:23616596 | T | A | 1 | a0001c0001t0006g0324 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723+1136A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616596 | |||||||
| chr18:23616597 | A | C | 1 | a0001c0001t0006g0324 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723+1135T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616597 | |||||||
| chr18:23616597 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | NA18943.hp1 NA18947.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.723+1135T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616597 | |||||||
| chr18:23616603 | AC | A | 4 | a0001c0001t0006g0324 a0001c0001t0006g0326 a0001c0001t0031g0325 others(1): Show |
4 | HG02717.hp2 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+1128delG | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616603 | |||||||
| chr18:23616604 | CTATA | C | 6 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 others(3): Show |
6 | HG02015.hp1 HG03516.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+1124_723+1127d others(6): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616604 | |||||||
| chr18:23616789 | T | A | 51 | a0001c0001t0001g0024 a0001c0001t0003g0005 a0001c0001t0003g0051 others(48): Show |
53 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.723+943A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616789 | |||||||
| chr18:23616831 | G | C | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.723+901C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616831 | |||||||
| chr18:23616884 | C | T | 1 | a0004c0005t0001g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.723+848G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616884 | |||||||
| chr18:23616945 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.723+787T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23616945 | |||||||
| chr18:23617023 | A | C | 10 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(7): Show |
10 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+709T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617023 | |||||||
| chr18:23617145 | A | G | 2 | a0001c0001t0017g0058 a0001c0001t0017g0061 |
2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.723+587T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617145 | |||||||
| chr18:23617163 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0304 others(1): Show |
4 | HG02257.hp2 HG03516.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+569C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617163 | |||||||
| chr18:23617215 | T | C | 65 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0044 others(62): Show |
67 | HG00408.hp2 HG00738.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.723+517A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617215 | |||||||
| chr18:23617263 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.723+469C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617263 | |||||||
| chr18:23617442 | C | T | 1 | a0001c0001t0010g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.723+290G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617442 | |||||||
| chr18:23617448 | A | G | 1 | a0001c0001t0002g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.723+284T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617448 | |||||||
| chr18:23617496 | T | A | 1 | a0001c0001t0026g0127 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.723+236A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 8/9 | chr18 | 23617496 | |||||||
| chr18:23617916 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.628-89C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23617916 | |||||||
| chr18:23618166 | G | A | 1 | a0001c0001t0029g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.628-339C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618166 | |||||||
| chr18:23618234 | T | C | 1 | a0001c0001t0029g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.628-407A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618234 | |||||||
| chr18:23618286 | G | A | 8 | a0001c0001t0001g0071 a0001c0001t0001g0144 a0001c0001t0001g0197 others(5): Show |
8 | HG00639.hp2 HG01074.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-459C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618286 | |||||||
| chr18:23618292 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.628-465C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618292 | |||||||
| chr18:23618357 | C | T | 43 | a0001c0001t0003g0005 a0001c0001t0003g0051 a0001c0001t0003g0063 others(40): Show |
45 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.628-530G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618357 | |||||||
| chr18:23618390 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0166 |
3 | NA18974.hp2 NA19010.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.628-563C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618390 | |||||||
| chr18:23618451 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.628-624G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618451 | |||||||
| chr18:23618473 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.628-646G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618473 | |||||||
| chr18:23618531 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0304 |
2 | HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628-704C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618531 | |||||||
| chr18:23618689 | T | C | 1 | a0001c0001t0029g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.627+842A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618689 | |||||||
| chr18:23618861 | GGAA | G | 10 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(7): Show |
10 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+667_627+669del others(3): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23618861 | |||||||
| chr18:23619089 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0031 |
2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.627+442A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619089 | |||||||
| chr18:23619210 | G | A | 4 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 others(1): Show |
4 | HG01167.hp1 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+321C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619210 | |||||||
| chr18:23619219 | A | C | 2 | a0001c0001t0016g0013 a0001c0001t0016g0016 |
2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.627+312T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619219 | |||||||
| chr18:23619224 | ACGCCCCA others(6): Show |
A | 1 | a0001c0001t0001g0229 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.627+294_627+306del others(13): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619224 | |||||||
| chr18:23619226 | GCCCCAGG others(13): Show |
G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0223 others(1): Show |
4 | HG00544.hp1 NA18969.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+285_627+304del others(20): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619226 | |||||||
| chr18:23619238 | CCGGGAGG others(13): Show |
C | 1 | a0001c0001t0002g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627+273_627+292del others(20): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619238 | |||||||
| chr18:23619289 | C | T | 10 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(7): Show |
10 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+242G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619289 | |||||||
| chr18:23619405 | T | C | 1 | a0001c0001t0005g0279 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.627+126A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 7/9 | chr18 | 23619405 | |||||||
| chr18:23619801 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.529-172C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23619801 | |||||||
| chr18:23620332 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529-703A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620332 | |||||||
| chr18:23620503 | C | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(235): Show |
251 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.529-874G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620503 | |||||||
| chr18:23620595 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0122 others(6): Show |
9 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.529-966C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620595 | |||||||
| chr18:23620646 | A | C | 1 | a0004c0005t0001g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.529-1017T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620646 | |||||||
| chr18:23620755 | G | T | 41 | a0001c0001t0001g0019 a0001c0001t0001g0068 a0001c0001t0003g0005 others(38): Show |
43 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.529-1126C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620755 | |||||||
| chr18:23620899 | C | T | 3 | a0001c0001t0006g0334 a0001c0001t0006g0335 a0001c0001t0006g0336 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.529-1270G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620899 | |||||||
| chr18:23620966 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.529-1337G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23620966 | |||||||
| chr18:23621004 | C | T | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG02074.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.529-1375G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621004 | |||||||
| chr18:23621116 | A | T | 1 | a0001c0001t0011g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.529-1487T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621116 | |||||||
| chr18:23621171 | G | T | 1 | a0001c0001t0002g0164 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.529-1542C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621171 | |||||||
| chr18:23621211 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0028g0112 |
2 | HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.529-1582T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621211 | |||||||
| chr18:23621375 | G | A | 44 | a0001c0001t0001g0019 a0001c0001t0001g0068 a0001c0001t0001g0071 others(41): Show |
46 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.529-1746C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621375 | |||||||
| chr18:23621381 | G | A | 1 | a0001c0001t0009g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.529-1752C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621381 | |||||||
| chr18:23621398 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0002g0284 |
2 | HG01099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.529-1769G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621398 | |||||||
| chr18:23621480 | CAA | C | 74 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0145 others(71): Show |
76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.529-1853_529-1852d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621480 | |||||||
| chr18:23621705 | G | T | 2 | a0001c0001t0007g0240 a0001c0001t0007g0252 |
2 | NA18951.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.529-2076C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23621705 | |||||||
| chr18:23622038 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.529-2409G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622038 | |||||||
| chr18:23622115 | A | T | 4 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0002g0087 others(1): Show |
6 | HG00423.hp1 HG02071.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-2486T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622115 | |||||||
| chr18:23622288 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.529-2659C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622288 | |||||||
| chr18:23622426 | C | T | 2 | a0001c0001t0012g0030 a0001c0001t0012g0032 |
2 | HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.529-2797G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622426 | |||||||
| chr18:23622543 | T | C | 13 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0003g0005 others(10): Show |
14 | HG00738.hp1 HG01258.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-2914A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622543 | |||||||
| chr18:23622839 | T | C | 171 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0040 others(168): Show |
180 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.529-3210A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622839 | |||||||
| chr18:23622899 | T | C | 1 | a0001c0001t0002g0035 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.529-3270A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23622899 | |||||||
| chr18:23623147 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.529-3518T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623147 | |||||||
| chr18:23623236 | T | G | 1 | a0001c0001t0004g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.529-3607A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623236 | |||||||
| chr18:23623314 | A | C | 1 | a0001c0001t0001g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.529-3685T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623314 | |||||||
| chr18:23623469 | T | C | 48 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(45): Show |
50 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.529-3840A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623469 | |||||||
| chr18:23623532 | C | A | 26 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(23): Show |
30 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.529-3903G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623532 | |||||||
| chr18:23623544 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.529-3915C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623544 | |||||||
| chr18:23623643 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.529-4014G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623643 | |||||||
| chr18:23623648 | G | GT | 9 | a0001c0001t0001g0151 a0001c0001t0003g0076 a0001c0001t0004g0038 others(6): Show |
9 | HG01109.hp1 HG01934.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-4020dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623648 | |||||||
| chr18:23623736 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.529-4107C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623736 | |||||||
| chr18:23623766 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.529-4137G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623766 | |||||||
| chr18:23623843 | C | T | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.529-4214G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623843 | |||||||
| chr18:23623889 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.529-4260G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623889 | |||||||
| chr18:23623960 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.529-4331T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23623960 | |||||||
| chr18:23624122 | A | C | 3 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG01167.hp1 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-4493T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624122 | |||||||
| chr18:23624302 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.529-4673T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624302 | |||||||
| chr18:23624466 | C | CAAAAAA | 6 | a0001c0001t0001g0024 a0001c0001t0003g0094 a0001c0001t0006g0327 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-4843_529-4838d others(8): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | C | CAAAAAAA | 37 | a0001c0001t0001g0144 a0001c0001t0001g0228 a0001c0001t0001g0256 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.529-4844_529-4838d others(9): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | C | CAAAAAAA others(1): Show |
27 | a0001c0001t0001g0145 a0001c0001t0001g0248 a0001c0001t0001g0249 others(24): Show |
29 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.529-4845_529-4838d others(10): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0230 a0001c0001t0002g0091 a0001c0001t0002g0299 others(4): Show |
7 | HG00741.hp1 HG01123.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-4846_529-4838d others(11): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0092 a0001c0001t0002g0263 a0001c0001t0007g0240 |
3 | HG00735.hp1 NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.529-4847_529-4838d others(12): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0271 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.529-4850_529-4838d others(15): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0238 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.529-4852_529-4838d others(17): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CA | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0029 others(76): Show |
83 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.529-4838delT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAA | C | 17 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0119 others(14): Show |
17 | HG00408.hp2 HG00741.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.529-4839_529-4838d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0002g0274 a0001c0001t0004g0050 a0001c0002t0001g0313 others(1): Show |
4 | HG02155.hp2 HG03017.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-4849_529-4838d others(14): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAAAAAAA others(6): Show |
C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0040 others(43): Show |
54 | HG00544.hp2 HG00558.hp1 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.529-4850_529-4838d others(15): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0075 a0001c0001t0001g0083 a0001c0001t0003g0074 others(2): Show |
5 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-4851_529-4838d others(16): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAAAAAAA others(8): Show |
C | 39 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(36): Show |
41 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.529-4852_529-4838d others(17): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0003g0077 a0001c0001t0007g0065 |
2 | NA18964.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.529-4853_529-4838d others(18): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624466 | CAAAAAAA others(11): Show |
C | 1 | a0001c0003t0002g0235 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.529-4855_529-4838d others(20): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624466 | |||||||
| chr18:23624553 | C | T | 3 | a0001c0001t0002g0262 a0001c0001t0002g0266 a0001c0001t0002g0303 |
3 | HG00733.hp2 HG00738.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.529-4924G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624553 | |||||||
| chr18:23624765 | A | G | 1 | a0001c0001t0010g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.528+5088T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624765 | |||||||
| chr18:23624895 | A | T | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.528+4958T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624895 | |||||||
| chr18:23624901 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0003g0079 others(6): Show |
9 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+4952G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23624901 | |||||||
| chr18:23625037 | G | A | 20 | a0001c0001t0001g0111 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG00423.hp2 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.528+4816C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625037 | |||||||
| chr18:23625178 | A | T | 1 | a0001c0001t0004g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.528+4675T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625178 | |||||||
| chr18:23625228 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.528+4625G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625228 | |||||||
| chr18:23625602 | G | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(277): Show |
295 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.528+4251C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625602 | |||||||
| chr18:23625820 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.528+4033A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625820 | |||||||
| chr18:23625832 | A | G | 1 | a0001c0001t0005g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.528+4021T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625832 | |||||||
| chr18:23625839 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.528+4014A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625839 | |||||||
| chr18:23625983 | T | C | 146 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(143): Show |
151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.528+3870A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23625983 | |||||||
| chr18:23626031 | G | T | 1 | a0001c0001t0006g0323 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528+3822C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626031 | |||||||
| chr18:23626082 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.528+3771A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626082 | |||||||
| chr18:23626142 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.528+3711G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626142 | |||||||
| chr18:23626288 | T | G | 6 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(3): Show |
6 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.528+3565A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626288 | |||||||
| chr18:23626352 | C | G | 1 | a0001c0001t0004g0054 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.528+3501G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626352 | |||||||
| chr18:23626400 | G | A | 21 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(18): Show |
21 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.528+3453C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626400 | |||||||
| chr18:23626794 | C | G | 30 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(27): Show |
34 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.528+3059G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626794 | |||||||
| chr18:23626836 | A | G | 21 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(18): Show |
21 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.528+3017T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626836 | |||||||
| chr18:23626859 | G | C | 37 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(34): Show |
37 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.528+2994C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23626859 | |||||||
| chr18:23627051 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.528+2802G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23627051 | |||||||
| chr18:23627131 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.528+2722C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23627131 | |||||||
| chr18:23627145 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.528+2708A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23627145 | |||||||
| chr18:23627684 | A | G | 30 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(27): Show |
34 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.528+2169T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23627684 | |||||||
| chr18:23627755 | A | G | 10 | a0001c0001t0001g0107 a0001c0001t0002g0104 a0001c0001t0004g0006 others(7): Show |
11 | HG00597.hp1 HG00597.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+2098T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23627755 | |||||||
| chr18:23628079 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.528+1774A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628079 | |||||||
| chr18:23628232 | T | C | 206 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(203): Show |
215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.528+1621A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628232 | |||||||
| chr18:23628354 | C | A | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+1499G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628354 | |||||||
| chr18:23628414 | A | C | 173 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0040 others(170): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.528+1439T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628414 | |||||||
| chr18:23628522 | C | T | 9 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(6): Show |
9 | HG01167.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+1331G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628522 | |||||||
| chr18:23628734 | T | C | 172 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0040 others(169): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.528+1119A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628734 | |||||||
| chr18:23628826 | G | A | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+1027C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628826 | |||||||
| chr18:23628833 | CA | C | 28 | a0001c0001t0001g0053 a0001c0001t0001g0151 a0001c0001t0004g0054 others(25): Show |
28 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.528+1019delT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628833 | |||||||
| chr18:23628833 | CAA | C | 29 | a0001c0001t0001g0040 a0001c0001t0001g0056 a0001c0001t0001g0080 others(26): Show |
33 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.528+1018_528+1019d others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628833 | |||||||
| chr18:23628833 | CAAA | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0057 others(98): Show |
104 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.528+1017_528+1019d others(5): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628833 | |||||||
| chr18:23628833 | CAAAA | C | 43 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(40): Show |
45 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.528+1016_528+1019d others(6): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23628833 | |||||||
| chr18:23629495 | C | T | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.528+358G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629495 | |||||||
| chr18:23629591 | G | A | 1 | a0001c0001t0004g0140 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.528+262C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629591 | |||||||
| chr18:23629659 | T | A | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.528+194A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629659 | |||||||
| chr18:23629671 | C | A | 1 | a0001c0001t0006g0322 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.528+182G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629671 | |||||||
| chr18:23629671 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.528+182G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629671 | |||||||
| chr18:23629736 | G | T | 30 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(27): Show |
30 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.528+117C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629736 | |||||||
| chr18:23629798 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0006g0327 |
2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.528+55C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629798 | |||||||
| chr18:23629814 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.528+39C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 6/9 | chr18 | 23629814 | |||||||
| chr18:23630019 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0009g0098 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-68G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630019 | |||||||
| chr18:23630024 | G | A | 142 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0043 others(139): Show |
147 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.430-73C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630024 | |||||||
| chr18:23630095 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.430-144G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630095 | |||||||
| chr18:23630156 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0215 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.430-205C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630156 | |||||||
| chr18:23630215 | C | T | 2 | a0001c0001t0001g0175 a0006c0008t0001g0143 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.430-264G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630215 | |||||||
| chr18:23630222 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.430-271G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630222 | |||||||
| chr18:23630288 | G | A | 2 | a0001c0001t0008g0046 a0003c0007t0005g0196 |
2 | HG00741.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.430-337C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630288 | |||||||
| chr18:23630296 | G | A | 12 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0002g0087 others(9): Show |
14 | HG00423.hp1 HG00597.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.430-345C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630296 | |||||||
| chr18:23630413 | A | G | 176 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(173): Show |
185 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.430-462T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630413 | |||||||
| chr18:23630432 | C | CA | 172 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0040 others(169): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.430-482dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630432 | |||||||
| chr18:23630720 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.430-769C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630720 | |||||||
| chr18:23630761 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.430-810A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630761 | |||||||
| chr18:23630967 | C | CA | 166 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0040 others(163): Show |
175 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.430-1017dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23630967 | |||||||
| chr18:23631108 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0305 a0001c0001t0001g0306 |
4 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-1157G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631108 | |||||||
| chr18:23631143 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.430-1192C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631143 | |||||||
| chr18:23631213 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.430-1262G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631213 | |||||||
| chr18:23631242 | C | CT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0031 others(9): Show |
15 | HG01891.hp2 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.430-1292dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631242 | |||||||
| chr18:23631242 | CT | C | 8 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0244 others(5): Show |
8 | HG00099.hp1 HG00639.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-1292delA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631242 | |||||||
| chr18:23631746 | T | C | 2 | a0001c0001t0011g0023 a0001c0001t0011g0055 |
2 | HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.430-1795A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631746 | |||||||
| chr18:23631754 | G | A | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.430-1803C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631754 | |||||||
| chr18:23631829 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.430-1878C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631829 | |||||||
| chr18:23631862 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.430-1911G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631862 | |||||||
| chr18:23631890 | G | A | 30 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(27): Show |
30 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.430-1939C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631890 | |||||||
| chr18:23631920 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0012g0300 |
2 | HG04199.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.430-1969C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23631920 | |||||||
| chr18:23632053 | C | T | 1 | a0001c0001t0006g0323 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429+1998G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632053 | |||||||
| chr18:23632412 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0006g0327 |
2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.429+1639T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632412 | |||||||
| chr18:23632480 | T | C | 1 | a0001c0001t0017g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+1571A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632480 | |||||||
| chr18:23632529 | G | GTA | 12 | a0001c0001t0006g0323 a0001c0001t0006g0324 a0001c0001t0006g0326 others(9): Show |
12 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+1521_429+1522i others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632529 | |||||||
| chr18:23632529 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0259 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.429+1521_429+1522i others(12): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632529 | |||||||
| chr18:23632529 | G | GTATATAT others(9): Show |
5 | a0001c0001t0005g0027 a0001c0001t0005g0193 a0001c0001t0005g0194 others(2): Show |
5 | HG00741.hp2 HG02738.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+1521_429+1522i others(18): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632529 | |||||||
| chr18:23632529 | G | GTATATAT others(11): Show |
3 | a0001c0001t0005g0026 a0001c0001t0005g0195 a0001c0001t0010g0101 |
3 | HG01433.hp1 HG03834.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.429+1521_429+1522i others(20): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632529 | |||||||
| chr18:23632529 | G | GTATATAT others(17): Show |
1 | a0001c0001t0009g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429+1521_429+1522i others(26): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632529 | |||||||
| chr18:23632529 | G | GTATATAT others(25): Show |
2 | a0001c0001t0009g0020 a0001c0001t0009g0022 |
2 | HG01167.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.429+1521_429+1522i others(34): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632529 | |||||||
| chr18:23632531 | G | A | 24 | a0001c0001t0001g0259 a0001c0001t0005g0026 a0001c0001t0005g0027 others(21): Show |
24 | HG00741.hp2 HG01167.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.429+1520C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(3): Show |
69 | a0001c0001t0001g0057 a0001c0001t0001g0144 a0001c0001t0001g0228 others(66): Show |
71 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.429+1519_429+1520i others(12): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(5): Show |
15 | a0001c0001t0001g0145 a0001c0001t0001g0256 a0001c0001t0001g0258 others(12): Show |
15 | HG00544.hp2 HG00735.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.429+1519_429+1520i others(14): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(9): Show |
3 | a0001c0001t0002g0234 a0001c0001t0002g0280 a0001c0001t0029g0318 |
3 | HG01884.hp2 HG02738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(18): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(17): Show |
8 | a0001c0001t0001g0100 a0001c0001t0006g0328 a0001c0001t0006g0329 others(5): Show |
8 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+1519_429+1520i others(26): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(19): Show |
14 | a0001c0001t0001g0056 a0001c0001t0001g0083 a0001c0001t0003g0051 others(11): Show |
18 | HG00558.hp1 HG02647.hp1 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+1519_429+1520i others(28): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(21): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0080 |
2 | HG04199.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(30): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0040 a0001c0001t0004g0054 |
2 | HG04115.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(32): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(25): Show |
3 | a0001c0001t0001g0294 a0001c0002t0001g0316 a0001c0002t0008g0314 |
3 | HG02109.hp1 HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(34): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(27): Show |
2 | a0001c0002t0001g0315 a0001c0002t0013g0317 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(36): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(29): Show |
2 | a0001c0001t0001g0295 a0001c0002t0001g0313 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(38): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(31): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0296 a0001c0002t0013g0311 |
3 | HG01884.hp1 HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(40): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(35): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0304 a0001c0002t0001g0060 |
3 | HG01243.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.429+1519_429+1520i others(44): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632531 | G | GTATATAT others(39): Show |
1 | a0001c0002t0013g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.429+1519_429+1520i others(48): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632531 | |||||||
| chr18:23632533 | G | A | 154 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0040 others(151): Show |
161 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.429+1518C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632533 | G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0244 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.429+1508_429+1517d others(12): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632533 | G | GTATATAT others(5): Show |
4 | a0001c0001t0002g0265 a0001c0001t0002g0273 a0001c0001t0002g0285 others(1): Show |
4 | HG01243.hp1 HG02148.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1506_429+1517d others(14): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632533 | G | GTATATAT others(7): Show |
41 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0068 others(38): Show |
43 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.429+1504_429+1517d others(16): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632533 | G | GTATATAT others(9): Show |
4 | a0001c0001t0003g0069 a0001c0001t0003g0237 a0001c0001t0017g0058 others(1): Show |
4 | HG02145.hp2 HG03098.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1517_429+1518i others(18): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632533 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.429+1517_429+1518i others(18): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632533 | G | GTGTATAT others(21): Show |
1 | a0001c0001t0004g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.429+1517_429+1518i others(30): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632533 | |||||||
| chr18:23632535 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0011g0055 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.429+1516T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632535 | |||||||
| chr18:23632799 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0087 a0001c0001t0002g0239 |
5 | HG00423.hp1 HG02071.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+1252G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23632799 | |||||||
| chr18:23633064 | T | G | 4 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+987A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633064 | |||||||
| chr18:23633277 | A | T | 1 | a0001c0001t0002g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.429+774T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633277 | |||||||
| chr18:23633454 | G | A | 1 | a0001c0001t0029g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.429+597C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633454 | |||||||
| chr18:23633550 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.429+501A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633550 | |||||||
| chr18:23633567 | T | C | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+484A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633567 | |||||||
| chr18:23633605 | A | G | 144 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(141): Show |
149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.429+446T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633605 | |||||||
| chr18:23633618 | T | C | 1 | a0001c0001t0002g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429+433A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633618 | |||||||
| chr18:23633719 | C | T | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.429+332G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633719 | |||||||
| chr18:23633836 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.429+215A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633836 | |||||||
| chr18:23633887 | T | TA | 144 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(141): Show |
149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.429+163dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633887 | |||||||
| chr18:23633907 | C | T | 1 | a0001c0001t0009g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429+144G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 5/9 | chr18 | 23633907 | |||||||
| chr18:23634238 | A | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0185 |
3 | HG02083.hp2 NA18951.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.331-89T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634238 | |||||||
| chr18:23634278 | G | GT | 56 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0031 others(53): Show |
56 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.331-130dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634278 | |||||||
| chr18:23634278 | G | GTT | 11 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0001g0180 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.331-131_331-130dup others(2): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634278 | |||||||
| chr18:23634278 | GT | G | 47 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0053 others(44): Show |
50 | HG00558.hp1 HG00741.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.331-130delA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634278 | |||||||
| chr18:23634278 | GTTTTTTT others(5): Show |
G | 6 | a0001c0001t0001g0238 a0001c0001t0001g0264 a0001c0001t0002g0263 others(3): Show |
6 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-141_331-130del others(12): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634278 | |||||||
| chr18:23634278 | GTTTTTTT others(6): Show |
G | 81 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0228 others(78): Show |
83 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.331-142_331-130del others(13): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634278 | |||||||
| chr18:23634283 | T | G | 13 | a0001c0001t0004g0004 a0001c0001t0005g0193 a0001c0001t0006g0322 others(10): Show |
14 | HG01167.hp2 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.331-134A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634283 | |||||||
| chr18:23634284 | T | G | 38 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(35): Show |
41 | HG00558.hp1 HG00741.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.331-135A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634284 | |||||||
| chr18:23634285 | T | G | 3 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 |
3 | HG03130.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331-136A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634285 | |||||||
| chr18:23634312 | T | G | 4 | a0001c0001t0001g0057 a0001c0001t0009g0098 a0001c0001t0012g0030 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-163A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634312 | |||||||
| chr18:23634328 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.331-179G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634328 | |||||||
| chr18:23634384 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.331-235C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634384 | |||||||
| chr18:23634392 | C | T | 7 | a0001c0001t0006g0328 a0001c0001t0006g0329 a0001c0001t0008g0037 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.331-243G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23634392 | |||||||
| chr18:23635243 | T | C | 1 | a0001c0001t0026g0127 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.331-1094A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23635243 | |||||||
| chr18:23635290 | T | TA | 9 | a0001c0001t0001g0158 a0001c0001t0001g0171 a0001c0001t0001g0177 others(6): Show |
9 | HG00544.hp1 HG01981.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-1142dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23635290 | |||||||
| chr18:23635405 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.331-1256A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23635405 | |||||||
| chr18:23635892 | G | A | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.331-1743C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23635892 | |||||||
| chr18:23636136 | T | TTGTA | 7 | a0001c0001t0001g0100 a0001c0001t0001g0178 a0001c0001t0001g0223 others(4): Show |
7 | HG02451.hp1 HG02630.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.331-1991_331-1988d others(6): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636136 | |||||||
| chr18:23636225 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0185 |
3 | HG02083.hp2 NA18951.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.331-2076G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636225 | |||||||
| chr18:23636435 | A | T | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.331-2286T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636435 | |||||||
| chr18:23636458 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.331-2309C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636458 | |||||||
| chr18:23636587 | T | A | 2 | a0001c0001t0002g0225 a0001c0001t0002g0287 |
2 | HG02015.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.330+2262A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636587 | |||||||
| chr18:23636666 | C | T | 1 | a0001c0001t0010g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.330+2183G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636666 | |||||||
| chr18:23636753 | T | TGATAAAG others(1): Show |
26 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(23): Show |
30 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.330+2088_330+2095d others(10): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636753 | |||||||
| chr18:23636934 | A | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.330+1915T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23636934 | |||||||
| chr18:23637056 | T | TC | 4 | a0001c0001t0001g0277 a0001c0001t0002g0242 a0001c0001t0002g0260 others(1): Show |
4 | HG00099.hp1 HG00639.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+1792dupG | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637056 | |||||||
| chr18:23637277 | T | C | 1 | a0001c0001t0002g0290 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.330+1572A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637277 | |||||||
| chr18:23637317 | A | G | 3 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG01167.hp1 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.330+1532T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637317 | |||||||
| chr18:23637477 | C | T | 4 | a0001c0001t0004g0173 a0001c0001t0009g0020 a0001c0001t0009g0021 others(1): Show |
4 | HG01167.hp1 HG02280.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+1372G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637477 | |||||||
| chr18:23637561 | C | T | 7 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(4): Show |
7 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+1288G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637561 | |||||||
| chr18:23637567 | C | T | 1 | a0001c0001t0006g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.330+1282G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637567 | |||||||
| chr18:23637592 | C | G | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG00639.hp2 HG01074.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.330+1257G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637592 | |||||||
| chr18:23637613 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.330+1236C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637613 | |||||||
| chr18:23637624 | C | T | 53 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0053 others(50): Show |
57 | HG00558.hp1 HG00741.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.330+1225G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637624 | |||||||
| chr18:23637771 | G | T | 7 | a0001c0001t0001g0107 a0001c0001t0004g0006 a0001c0001t0004g0138 others(4): Show |
8 | HG00597.hp1 HG02074.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.330+1078C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637771 | |||||||
| chr18:23637924 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.330+925G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637924 | |||||||
| chr18:23637944 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.330+905A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637944 | |||||||
| chr18:23637994 | C | CT | 81 | a0001c0001t0001g0056 a0001c0001t0001g0144 a0001c0001t0001g0145 others(78): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.330+854dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637994 | |||||||
| chr18:23637994 | C | CTT | 57 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0053 others(54): Show |
61 | HG00099.hp1 HG00558.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.330+853_330+854dup others(2): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637994 | |||||||
| chr18:23637994 | C | CTTTT | 7 | a0001c0001t0001g0304 a0001c0001t0003g0131 a0001c0001t0003g0132 others(4): Show |
7 | HG01167.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.330+851_330+854dup others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637994 | |||||||
| chr18:23637994 | C | CTTTTT | 46 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(43): Show |
47 | HG00738.hp1 HG01071.hp1 HG01258.hp2 others(44): Show |
intron_variant | MODIFIER | c.330+850_330+854dup others(5): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637994 | |||||||
| chr18:23637994 | CT | C | 6 | a0001c0001t0001g0159 a0001c0001t0004g0006 a0001c0001t0004g0138 others(3): Show |
7 | HG00597.hp1 HG02074.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+854delA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23637994 | |||||||
| chr18:23638036 | C | T | 12 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(9): Show |
12 | HG01167.hp2 HG02717.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.330+813G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23638036 | |||||||
| chr18:23638173 | T | C | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | NA18994.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.330+676A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23638173 | |||||||
| chr18:23638236 | G | A | 5 | a0001c0001t0004g0006 a0001c0001t0004g0138 a0001c0001t0004g0139 others(2): Show |
6 | HG00597.hp1 HG02074.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+613C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23638236 | |||||||
| chr18:23638472 | A | G | 9 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0331 others(6): Show |
9 | HG01167.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+377T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 4/9 | chr18 | 23638472 | |||||||
| chr18:23639000 | G | C | 1 | a0001c0002t0013g0317 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.232-53C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639000 | |||||||
| chr18:23639055 | C | T | 8 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(5): Show |
8 | HG01167.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.232-108G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639055 | |||||||
| chr18:23639216 | C | T | 5 | a0001c0001t0001g0238 a0001c0001t0002g0003 a0001c0001t0002g0035 others(2): Show |
7 | HG00408.hp1 HG00423.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.232-269G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639216 | |||||||
| chr18:23639340 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0305 a0001c0001t0001g0306 others(2): Show |
6 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-393T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639340 | |||||||
| chr18:23639341 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.232-394C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639341 | |||||||
| chr18:23639455 | G | A | 3 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG01167.hp1 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.232-508C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639455 | |||||||
| chr18:23639529 | A | AT | 9 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0165 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.232-583dupA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639529 | |||||||
| chr18:23639529 | AT | A | 129 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0029 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.232-583delA | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639529 | |||||||
| chr18:23639529 | ATT | A | 13 | a0001c0001t0002g0087 a0001c0001t0002g0091 a0001c0001t0002g0254 others(10): Show |
13 | HG01070.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.232-584_232-583del others(2): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639529 | |||||||
| chr18:23639574 | G | A | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232-627C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23639574 | |||||||
| chr18:23640260 | T | G | 62 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0029 others(59): Show |
63 | HG00738.hp1 HG01109.hp2 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.232-1313A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640260 | |||||||
| chr18:23640370 | G | T | 7 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(4): Show |
7 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-1423C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640370 | |||||||
| chr18:23640422 | C | A | 66 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(63): Show |
68 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.232-1475G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640422 | |||||||
| chr18:23640455 | T | C | 1 | a0005c0004t0001g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.232-1508A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640455 | |||||||
| chr18:23640474 | A | G | 3 | a0001c0001t0006g0334 a0001c0001t0006g0335 a0001c0001t0006g0336 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.232-1527T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640474 | |||||||
| chr18:23640717 | A | C | 70 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(67): Show |
72 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.232-1770T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640717 | |||||||
| chr18:23640881 | A | G | 1 | a0001c0001t0009g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232-1934T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640881 | |||||||
| chr18:23640953 | G | C | 2 | a0001c0001t0001g0209 a0001c0001t0024g0208 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.232-2006C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640953 | |||||||
| chr18:23640973 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(6): Show |
9 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-2026G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23640973 | |||||||
| chr18:23641010 | A | G | 3 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG01167.hp1 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.232-2063T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641010 | |||||||
| chr18:23641175 | C | G | 199 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(196): Show |
207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.232-2228G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641175 | |||||||
| chr18:23641291 | C | T | 29 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(26): Show |
33 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.232-2344G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641291 | |||||||
| chr18:23641408 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.232-2461C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641408 | |||||||
| chr18:23641601 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0109 a0001c0001t0001g0141 others(2): Show |
6 | HG00621.hp1 NA19056.hp2 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-2654A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641601 | |||||||
| chr18:23641760 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.232-2813C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641760 | |||||||
| chr18:23641765 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0024g0208 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.232-2818C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641765 | |||||||
| chr18:23641927 | G | A | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-2980C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641927 | |||||||
| chr18:23641972 | C | T | 1 | a0001c0001t0004g0278 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.232-3025G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23641972 | |||||||
| chr18:23642329 | C | T | 29 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(26): Show |
33 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.232-3382G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642329 | |||||||
| chr18:23642468 | G | A | 1 | a0001c0001t0009g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.232-3521C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642468 | |||||||
| chr18:23642793 | A | C | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+3396T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642793 | |||||||
| chr18:23642843 | C | A | 2 | a0001c0001t0020g0319 a0001c0001t0020g0320 |
2 | HG01358.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.231+3346G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642843 | |||||||
| chr18:23642844 | C | T | 2 | a0001c0001t0020g0319 a0001c0001t0020g0320 |
2 | HG01358.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.231+3345G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642844 | |||||||
| chr18:23642952 | G | T | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+3237C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642952 | |||||||
| chr18:23642982 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.231+3207A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23642982 | |||||||
| chr18:23643362 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.231+2827A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23643362 | |||||||
| chr18:23643606 | T | C | 1 | a0001c0001t0005g0027 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.231+2583A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23643606 | |||||||
| chr18:23643692 | G | A | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+2497C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23643692 | |||||||
| chr18:23643966 | A | C | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+2223T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23643966 | |||||||
| chr18:23644063 | C | A | 7 | a0001c0002t0001g0313 a0001c0002t0001g0315 a0001c0002t0001g0316 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+2126G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644063 | |||||||
| chr18:23644093 | T | C | 1 | a0001c0001t0005g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.231+2096A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644093 | |||||||
| chr18:23644155 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0012g0030 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+2034A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644155 | |||||||
| chr18:23644202 | A | C | 1 | a0001c0001t0003g0070 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.231+1987T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644202 | |||||||
| chr18:23644223 | C | G | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.231+1966G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644223 | |||||||
| chr18:23644381 | C | T | 66 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(63): Show |
68 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.231+1808G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644381 | |||||||
| chr18:23644427 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.231+1762C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644427 | |||||||
| chr18:23644683 | C | A | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+1506G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644683 | |||||||
| chr18:23644752 | C | T | 1 | a0001c0001t0011g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.231+1437G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644752 | |||||||
| chr18:23644827 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.231+1362A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644827 | |||||||
| chr18:23644992 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.231+1197C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23644992 | |||||||
| chr18:23645009 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.231+1180A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645009 | |||||||
| chr18:23645018 | C | T | 1 | a0001c0001t0004g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.231+1171G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645018 | |||||||
| chr18:23645021 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.231+1168A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645021 | |||||||
| chr18:23645083 | C | G | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.231+1106G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645083 | |||||||
| chr18:23645094 | T | C | 1 | a0001c0001t0009g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.231+1095A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645094 | |||||||
| chr18:23645125 | A | T | 1 | a0001c0001t0001g0224 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.231+1064T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645125 | |||||||
| chr18:23645188 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.231+1001G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645188 | |||||||
| chr18:23645326 | G | T | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.231+863C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645326 | |||||||
| chr18:23645336 | G | C | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+853C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645336 | |||||||
| chr18:23645372 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.231+817C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645372 | |||||||
| chr18:23645406 | T | C | 8 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(5): Show |
8 | HG01167.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+783A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645406 | |||||||
| chr18:23645430 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.231+759G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645430 | |||||||
| chr18:23645527 | T | G | 29 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(26): Show |
33 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.231+662A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645527 | |||||||
| chr18:23645569 | A | G | 62 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0029 others(59): Show |
63 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.231+620T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23645569 | |||||||
| chr18:23646004 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0012g0030 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+185G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23646004 | |||||||
| chr18:23646025 | C | T | 29 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(26): Show |
33 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.231+164G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 3/9 | chr18 | 23646025 | |||||||
| chr18:23646311 | A | G | 1 | a0001c0001t0010g0101 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.133-24T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646311 | |||||||
| chr18:23646355 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.133-68T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646355 | |||||||
| chr18:23646412 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.133-125A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646412 | |||||||
| chr18:23646604 | A | C | 1 | a0001c0001t0016g0013 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.133-317T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646604 | |||||||
| chr18:23646607 | A | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0304 a0001c0001t0030g0321 |
3 | HG02451.hp1 HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.133-320T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646607 | |||||||
| chr18:23646676 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0107 others(80): Show |
90 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.133-389T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646676 | |||||||
| chr18:23646785 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.133-498A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646785 | |||||||
| chr18:23646837 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.133-550C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646837 | |||||||
| chr18:23646896 | C | T | 7 | a0001c0002t0001g0313 a0001c0002t0001g0315 a0001c0002t0001g0316 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-609G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23646896 | |||||||
| chr18:23647087 | G | A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
33 | HG00738.hp1 HG01109.hp2 HG01258.hp2 others(30): Show |
intron_variant | MODIFIER | c.133-800C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647087 | |||||||
| chr18:23647241 | C | T | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-954G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647241 | |||||||
| chr18:23647711 | G | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0107 others(34): Show |
42 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.132+1372C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647711 | |||||||
| chr18:23647719 | G | C | 1 | a0001c0001t0003g0094 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.132+1364C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647719 | |||||||
| chr18:23647738 | C | A | 13 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0003g0005 others(10): Show |
14 | HG00738.hp1 HG01258.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.132+1345G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647738 | |||||||
| chr18:23647839 | A | G | 3 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0186 |
3 | HG02015.hp1 NA18747.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.132+1244T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647839 | |||||||
| chr18:23647880 | G | A | 70 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0029 others(67): Show |
71 | HG00738.hp1 HG01109.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.132+1203C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647880 | |||||||
| chr18:23647966 | T | C | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1117A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647966 | |||||||
| chr18:23647967 | G | C | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1116C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647967 | |||||||
| chr18:23647968 | G | C | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1115C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647968 | |||||||
| chr18:23647969 | G | C | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1114C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647969 | |||||||
| chr18:23647971 | TCTA | T | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1109_132+1111d others(5): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23647971 | |||||||
| chr18:23648019 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.132+1064C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648019 | |||||||
| chr18:23648019 | G | C | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1064C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648019 | |||||||
| chr18:23648048 | A | G | 86 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0031 others(83): Show |
91 | HG00558.hp1 HG00738.hp1 HG01109.hp2 others(88): Show |
intron_variant | MODIFIER | c.132+1035T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648048 | |||||||
| chr18:23648144 | A | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | HG02074.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.132+939T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648144 | |||||||
| chr18:23648293 | G | C | 1 | a0001c0001t0003g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+790C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648293 | |||||||
| chr18:23648628 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.132+455A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648628 | |||||||
| chr18:23648683 | G | T | 83 | a0001c0001t0001g0088 a0001c0001t0001g0228 a0001c0001t0001g0229 others(80): Show |
85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.132+400C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648683 | |||||||
| chr18:23648812 | T | G | 1 | a0001c0001t0010g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.132+271A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23648812 | |||||||
| chr18:23649075 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.132+8G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 2/9 | chr18 | 23649075 | |||||||
| chr18:23649345 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(6): Show |
9 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.22-152T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649345 | |||||||
| chr18:23649398 | G | C | 1 | a0001c0001t0010g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.22-205C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649398 | |||||||
| chr18:23649416 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.22-223A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649416 | |||||||
| chr18:23649582 | C | G | 2 | a0001c0001t0010g0096 a0001c0001t0010g0097 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.22-389G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649582 | |||||||
| chr18:23649811 | C | T | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-618G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649811 | |||||||
| chr18:23649834 | A | G | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-641T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649834 | |||||||
| chr18:23649874 | C | T | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-681G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649874 | |||||||
| chr18:23649878 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.22-685G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23649878 | |||||||
| chr18:23650250 | A | G | 91 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
96 | HG00558.hp1 HG00738.hp1 HG01109.hp2 others(93): Show |
intron_variant | MODIFIER | c.22-1057T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650250 | |||||||
| chr18:23650374 | G | T | 1 | a0006c0008t0001g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.22-1181C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650374 | |||||||
| chr18:23650429 | C | A | 1 | a0001c0001t0002g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.22-1236G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650429 | |||||||
| chr18:23650502 | G | A | 1 | a0001c0001t0003g0170 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.22-1309C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650502 | |||||||
| chr18:23650552 | ATCT | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0003g0079 others(2): Show |
5 | HG01109.hp2 HG01358.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-1362_22-1360del others(3): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650552 | |||||||
| chr18:23650651 | A | G | 78 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0031 others(75): Show |
83 | HG00558.hp1 HG00738.hp1 HG01109.hp2 others(80): Show |
intron_variant | MODIFIER | c.22-1458T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650651 | |||||||
| chr18:23650723 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0223 |
2 | HG02135.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.22-1530G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650723 | |||||||
| chr18:23650766 | A | G | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-1573T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650766 | |||||||
| chr18:23650787 | T | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.22-1594A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650787 | |||||||
| chr18:23650960 | C | T | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-1767G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23650960 | |||||||
| chr18:23651428 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.22-2235A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23651428 | |||||||
| chr18:23651705 | C | T | 77 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0031 others(74): Show |
82 | HG00558.hp1 HG00738.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.22-2512G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23651705 | |||||||
| chr18:23651827 | T | C | 7 | a0001c0002t0001g0313 a0001c0002t0001g0315 a0001c0002t0001g0316 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-2634A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23651827 | |||||||
| chr18:23651844 | C | A | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.22-2651G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23651844 | |||||||
| chr18:23651889 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.22-2696C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23651889 | |||||||
| chr18:23652093 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0009g0020 a0001c0001t0009g0021 others(6): Show |
10 | HG01109.hp1 HG01167.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.22-2900T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652093 | |||||||
| chr18:23652266 | C | A | 45 | a0001c0001t0001g0111 a0001c0001t0001g0144 a0001c0001t0001g0145 others(42): Show |
47 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.22-3073G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652266 | |||||||
| chr18:23652376 | G | A | 1 | a0007c0006t0004g0028 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.22-3183C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652376 | |||||||
| chr18:23652379 | G | T | 1 | a0001c0001t0002g0163 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.22-3186C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652379 | |||||||
| chr18:23652420 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.22-3227A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652420 | |||||||
| chr18:23652474 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
11 | HG02647.hp2 HG02922.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.22-3281G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652474 | |||||||
| chr18:23652523 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(6): Show |
9 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.22-3330C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652523 | |||||||
| chr18:23652584 | A | G | 1 | a0001c0001t0017g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.22-3391T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652584 | |||||||
| chr18:23652883 | G | A | 29 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(26): Show |
33 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.22-3690C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23652883 | |||||||
| chr18:23653005 | G | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0304 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.22-3812C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653005 | |||||||
| chr18:23653170 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.22-3977G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653170 | |||||||
| chr18:23653397 | C | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0012g0030 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-4204G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653397 | |||||||
| chr18:23653482 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.22-4289G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653482 | |||||||
| chr18:23653598 | T | TCTCCCCT others(28): Show |
1 | a0001c0001t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.22-4440_22-4406dup others(35): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653598 | |||||||
| chr18:23653762 | C | T | 2 | a0001c0001t0002g0233 a0001c0001t0002g0234 |
2 | HG00544.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.22-4569G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653762 | |||||||
| chr18:23653763 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.22-4570C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653763 | |||||||
| chr18:23653862 | T | C | 8 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(5): Show |
8 | HG01167.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.22-4669A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653862 | |||||||
| chr18:23653931 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.22-4738G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653931 | |||||||
| chr18:23653962 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.22-4769T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653962 | |||||||
| chr18:23653996 | G | T | 82 | a0001c0001t0001g0088 a0001c0001t0001g0228 a0001c0001t0001g0229 others(79): Show |
84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.22-4803C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23653996 | |||||||
| chr18:23654198 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0179 a0001c0001t0003g0161 |
3 | HG00408.hp2 NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.22-5005C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654198 | |||||||
| chr18:23654279 | A | AAAAT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0110 a0001c0001t0001g0111 others(14): Show |
19 | HG00735.hp2 HG01074.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.22-5090_22-5087dup others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654279 | |||||||
| chr18:23654279 | AAAAT | A | 102 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0044 others(99): Show |
106 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.22-5090_22-5087del others(4): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654279 | |||||||
| chr18:23654279 | AAAATAAA others(1): Show |
A | 48 | a0001c0001t0001g0019 a0001c0001t0001g0068 a0001c0001t0001g0071 others(45): Show |
49 | HG00738.hp1 HG01109.hp2 HG01258.hp2 others(46): Show |
intron_variant | MODIFIER | c.22-5094_22-5087del others(8): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654279 | |||||||
| chr18:23654279 | AAAATAAA others(9): Show |
A | 1 | a0001c0001t0011g0081 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.22-5102_22-5087del others(16): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654279 | |||||||
| chr18:23654397 | A | T | 1 | a0001c0001t0005g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.22-5204T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654397 | |||||||
| chr18:23654575 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.22-5382G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654575 | |||||||
| chr18:23654618 | C | CA | 25 | a0001c0001t0001g0024 a0001c0001t0001g0185 a0001c0001t0001g0187 others(22): Show |
25 | HG00544.hp1 HG00597.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.22-5426dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654618 | |||||||
| chr18:23654618 | CA | C | 73 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0043 others(70): Show |
78 | HG00558.hp1 HG00738.hp1 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.22-5426delT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654618 | |||||||
| chr18:23654618 | CAA | C | 9 | a0001c0001t0004g0036 a0001c0001t0006g0322 a0001c0001t0006g0323 others(6): Show |
9 | HG01167.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.22-5427_22-5426del others(2): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654618 | |||||||
| chr18:23654744 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.22-5551A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654744 | |||||||
| chr18:23654970 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.22-5777T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23654970 | |||||||
| chr18:23655045 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.22-5852A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655045 | |||||||
| chr18:23655162 | T | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.22-5969A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655162 | |||||||
| chr18:23655246 | G | A | 4 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0282 others(1): Show |
4 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-6053C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655246 | |||||||
| chr18:23655303 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0193 others(6): Show |
9 | HG00741.hp2 HG01433.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.22-6110C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655303 | |||||||
| chr18:23655309 | C | T | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-6116G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655309 | |||||||
| chr18:23655455 | T | A | 7 | a0001c0002t0001g0313 a0001c0002t0001g0315 a0001c0002t0001g0316 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-6262A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655455 | |||||||
| chr18:23655816 | G | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0009g0020 others(2): Show |
6 | HG01167.hp1 HG01243.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.22-6623C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23655816 | |||||||
| chr18:23656006 | T | C | 91 | a0001c0001t0001g0088 a0001c0001t0001g0197 a0001c0001t0001g0198 others(88): Show |
93 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.21+6704A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656006 | |||||||
| chr18:23656009 | C | T | 3 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG01167.hp1 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.21+6701G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656009 | |||||||
| chr18:23656024 | C | T | 2 | a0001c0001t0002g0226 a0001c0001t0002g0292 |
2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.21+6686G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656024 | |||||||
| chr18:23656034 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.21+6676T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656034 | |||||||
| chr18:23656065 | C | G | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.21+6645G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656065 | |||||||
| chr18:23656072 | G | A | 1 | a0001c0001t0009g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.21+6638C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656072 | |||||||
| chr18:23656092 | C | CA | 28 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0106 others(25): Show |
32 | HG01099.hp2 HG01167.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.21+6617dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656092 | |||||||
| chr18:23656092 | CA | C | 9 | a0001c0001t0001g0100 a0001c0001t0002g0035 a0001c0001t0002g0285 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.21+6617delT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656092 | |||||||
| chr18:23656385 | T | G | 1 | a0001c0001t0003g0095 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.21+6325A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656385 | |||||||
| chr18:23656468 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0024g0208 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.21+6242C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656468 | |||||||
| chr18:23656539 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.21+6171T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23656539 | |||||||
| chr18:23657320 | C | T | 1 | a0001c0001t0009g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.21+5390G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657320 | |||||||
| chr18:23657565 | C | A | 1 | a0001c0001t0002g0285 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.21+5145G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657565 | |||||||
| chr18:23657648 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.21+5062C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657648 | |||||||
| chr18:23657680 | C | A | 1 | a0001c0001t0030g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.21+5030G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657680 | |||||||
| chr18:23657693 | T | C | 1 | a0001c0001t0002g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.21+5017A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657693 | |||||||
| chr18:23657720 | T | A | 1 | a0001c0001t0007g0008 | 2 | NA18971.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.21+4990A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657720 | |||||||
| chr18:23657846 | A | G | 1 | a0001c0001t0005g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.21+4864T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657846 | |||||||
| chr18:23657996 | C | T | 7 | a0001c0002t0001g0313 a0001c0002t0001g0315 a0001c0002t0001g0316 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.21+4714G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23657996 | |||||||
| chr18:23658380 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.21+4330G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23658380 | |||||||
| chr18:23658440 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.21+4270A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23658440 | |||||||
| chr18:23658500 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.21+4210G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23658500 | |||||||
| chr18:23658662 | C | A | 2 | a0001c0001t0010g0096 a0001c0001t0010g0097 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.21+4048G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23658662 | |||||||
| chr18:23659070 | C | G | 21 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(18): Show |
21 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.21+3640G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659070 | |||||||
| chr18:23659205 | C | T | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+3505G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659205 | |||||||
| chr18:23659211 | ACTTCAGG others(4): Show |
A | 1 | a0001c0001t0001g0211 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.21+3488_21+3498del others(11): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659211 | |||||||
| chr18:23659378 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG00544.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.21+3332A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659378 | |||||||
| chr18:23659391 | C | T | 111 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0024 others(108): Show |
119 | HG00423.hp1 HG00558.hp1 HG00738.hp1 others(116): Show |
intron_variant | MODIFIER | c.21+3319G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659391 | |||||||
| chr18:23659473 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.21+3237C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659473 | |||||||
| chr18:23659526 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.21+3184G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659526 | |||||||
| chr18:23659529 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.21+3181C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659529 | |||||||
| chr18:23659599 | T | C | 8 | a0001c0001t0030g0321 a0001c0002t0001g0313 a0001c0002t0001g0315 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.21+3111A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659599 | |||||||
| chr18:23659604 | A | G | 99 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0031 others(96): Show |
106 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.21+3106T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659604 | |||||||
| chr18:23659750 | C | CA | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | NA18950.hp2 NA18969.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.21+2959dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659750 | |||||||
| chr18:23659750 | CA | C | 163 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0040 others(160): Show |
171 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.21+2959delT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659750 | |||||||
| chr18:23659761 | A | C | 1 | a0001c0001t0001g0034 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.21+2949T>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659761 | |||||||
| chr18:23659877 | G | T | 72 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(69): Show |
72 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.21+2833C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659877 | |||||||
| chr18:23659986 | C | T | 2 | a0001c0001t0005g0026 a0001c0001t0005g0027 |
2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.21+2724G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23659986 | |||||||
| chr18:23660160 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0009g0020 a0001c0001t0009g0021 others(1): Show |
5 | HG01167.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.21+2550A>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660160 | |||||||
| chr18:23660180 | G | A | 72 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(69): Show |
72 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.21+2530C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660180 | |||||||
| chr18:23660302 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0009g0020 a0001c0001t0009g0021 others(1): Show |
5 | HG01167.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.21+2408A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660302 | |||||||
| chr18:23660535 | C | G | 1 | a0001c0001t0002g0033 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.21+2175G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660535 | |||||||
| chr18:23660587 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0012g0030 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+2123G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660587 | |||||||
| chr18:23660622 | A | T | 1 | a0007c0006t0004g0028 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.21+2088T>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660622 | |||||||
| chr18:23660637 | C | T | 2 | a0001c0001t0005g0026 a0001c0001t0005g0027 |
2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.21+2073G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660637 | |||||||
| chr18:23660647 | A | G | 1 | a0001c0001t0010g0025 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.21+2063T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660647 | |||||||
| chr18:23660774 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.21+1936A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660774 | |||||||
| chr18:23660826 | C | A | 1 | a0001c0001t0002g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.21+1884G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660826 | |||||||
| chr18:23660968 | C | T | 13 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(10): Show |
13 | HG01167.hp2 HG02257.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.21+1742G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23660968 | |||||||
| chr18:23661103 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.21+1607A>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23661103 | |||||||
| chr18:23661104 | T | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 |
3 | HG02976.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.21+1606A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23661104 | |||||||
| chr18:23661477 | G | A | 1 | a0001c0001t0005g0297 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.21+1233C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23661477 | |||||||
| chr18:23661704 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.21+1006G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23661704 | |||||||
| chr18:23661931 | T | A | 2 | a0001c0001t0002g0299 a0001c0001t0027g0298 |
2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.21+779A>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23661931 | |||||||
| chr18:23662024 | G | GA | 5 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0002g0010 others(2): Show |
6 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.21+685dupT | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662024 | |||||||
| chr18:23662110 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.21+600C>G | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662110 | |||||||
| chr18:23662287 | C | T | 1 | a0001c0001t0011g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.21+423G>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662287 | |||||||
| chr18:23662340 | C | G | 328 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(325): Show |
343 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.21+370G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662340 | |||||||
| chr18:23662442 | C | A | 1 | a0001c0001t0006g0327 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.21+268G>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662442 | |||||||
| chr18:23662449 | G | A | 5 | a0001c0001t0015g0014 a0001c0001t0015g0017 a0001c0001t0016g0013 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.21+261C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662449 | |||||||
| chr18:23662456 | G | T | 13 | a0001c0001t0006g0322 a0001c0001t0006g0323 a0001c0001t0006g0324 others(10): Show |
13 | HG01167.hp2 HG02257.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.21+254C>A | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662456 | |||||||
| chr18:23662475 | C | G | 3 | a0001c0001t0009g0020 a0001c0001t0009g0021 a0001c0001t0009g0022 |
3 | HG01167.hp1 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.21+235G>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662475 | |||||||
| chr18:23662508 | G | GGCAAACC | 7 | a0001c0002t0001g0313 a0001c0002t0001g0315 a0001c0002t0001g0316 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.21+195_21+201dupGG others(5): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662508 | |||||||
| chr18:23662596 | G | GGCGGGCA | 4 | a0001c0001t0006g0331 a0001c0001t0014g0330 a0001c0001t0014g0332 others(1): Show |
4 | HG03130.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+107_21+113dupTG others(5): Show |
ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662596 | |||||||
| chr18:23662642 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.21+68T>C | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662642 | |||||||
| chr18:23662700 | G | A | 3 | a0001c0001t0006g0334 a0001c0001t0006g0335 a0001c0001t0006g0336 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.21+10C>T | ANKRD29 | ENSG00000154065.17 | transcript | ENST00000592179.6 | protein_coding | 1/9 | chr18 | 23662700 |