Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283554 |
| ensemblid | ENSG00000180998.12 |
| hgncid | 25445 |
| symbol | GPR137C |
| name | G protein-coupled receptor 137C |
| refseq_nuc | NM_001099652.2 |
| refseq_prot | NP_001093122.1 |
| ensembl_nuc | ENST00000321662.11 |
| ensembl_prot | ENSP00000315106.6 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 52552836 |
| end | 52637713 |
| strand | + |
| ver | v1.2 |
| region | chr14:52552836-52637713 |
| region5000 | chr14:52547836-52642713 |
| regionname0 | GPR137C_chr14_52552836_52637713 |
| regionname5000 | GPR137C_chr14_52547836_52642713 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 429 | 204 | 52 | 22 | 100 | 5 | 24 | 77 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(424): Show |
chr14 | 52547836 | 52642713 |
| a0002 | 0/0 | 429 | 88 | 13 | 20 | 38 | 7 | 10 | 28 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(424): Show |
chr14 | 52547836 | 52642713 |
| a0003 | 1/0 | 429 | 26 | 16 | 2 | 6 | 0 | 1 | 4 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(424): Show |
chr14 | 52547836 | 52642713 |
| a0004 | 0/0 | 429 | 24 | 0 | 3 | 18 | 0 | 3 | 14 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(424): Show |
chr14 | 52547836 | 52642713 |
| a0005 | 0/0 | 429 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(424): Show |
chr14 | 52547836 | 52642713 |
| a0006 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(424): Show |
chr14 | 52547836 | 52642713 |
| a0007 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | MRVSV others(417): Show |
chr14 | 52547836 | 52642713 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1287 | 181 | 45 | 14 | 95 | 4 | 22 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0001c0005 | 0/0 | 1287 | 15 | 6 | 4 | 5 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0001c0006 | 0/0 | 1287 | 7 | 0 | 4 | 0 | 1 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0001c0007 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0002c0002 | 0/0 | 1287 | 88 | 13 | 20 | 38 | 7 | 10 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0003c0003 | 1/0 | 1287 | 26 | 16 | 2 | 6 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0004c0004 | 0/0 | 1287 | 24 | 0 | 3 | 18 | 0 | 3 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0005c0008 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0005c0009 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0006c0010 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1282): Show |
chr14 | 52547836 | 52642713 | ||
| a0007c0011 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | ATGAG others(1261): Show |
chr14 | 52547836 | 52642713 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4200 | 101 | 22 | 4 | 56 | 2 | 17 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0002 | 0/1 | 4200 | 26 | 5 | 7 | 7 | 2 | 4 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0003 | 0/0 | 4200 | 29 | 0 | 1 | 28 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0004 | 0/0 | 4200 | 11 | 11 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0008 | 0/0 | 4200 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0009 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0010 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0013 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0014 | 0/0 | 4200 | 2 | 0 | 1 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0015 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0016 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0019 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0021 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0022 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0001t0025 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0005t0005 | 0/0 | 4200 | 8 | 0 | 3 | 5 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0005t0007 | 0/0 | 4200 | 6 | 6 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0005t0017 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0006t0006 | 0/0 | 4200 | 7 | 0 | 4 | 0 | 1 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0001c0007t0008 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0002c0002t0001 | 0/0 | 4200 | 82 | 12 | 17 | 37 | 7 | 9 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0002c0002t0012 | 0/0 | 4200 | 3 | 0 | 2 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0002c0002t0018 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0002c0002t0020 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0002c0002t0024 | 0/0 | 4218 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4213): Show |
chr14 | 52547836 | 52642713 |
| a0003c0003t0001 | 1/0 | 4200 | 13 | 7 | 1 | 3 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0003c0003t0002 | 0/0 | 4200 | 5 | 1 | 1 | 3 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0003c0003t0009 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0003c0003t0010 | 0/0 | 4200 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0003c0003t0011 | 0/0 | 4200 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0003c0003t0023 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0004c0004t0001 | 0/0 | 4200 | 23 | 0 | 3 | 17 | 0 | 3 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0004c0004t0008 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0005c0008t0001 | 0/0 | 4200 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0005c0009t0001 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0006c0010t0001 | 0/0 | 4200 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4195): Show |
chr14 | 52547836 | 52642713 |
| a0007c0011t0002 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | AGTGC others(4174): Show |
chr14 | 52547836 | 52642713 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0008g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0008g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0013g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0014g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0014g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0019g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0021g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0022g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0001t0025g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0005g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0007g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0005t0017g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0006t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0001c0007t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0012g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0012g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0018g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0020g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0002c0002t0024g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0010g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0003c0003t0023g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0004c0004t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0005c0008t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0005c0009t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0006c0010t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| a0007c0011t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0118 | EUR | GBR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0052 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0066 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0116 | EUR | FIN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00408 | hp2 | a0004 | c0004 | t0001 | g0271 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00621 | hp1 | a0001 | c0001 | t0008 | g0304 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0130 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0237 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00642 | hp1 | a0001 | c0006 | t0006 | g0204 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00735 | hp1 | a0004 | c0004 | t0001 | g0042 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00735 | hp2 | a0001 | c0006 | t0006 | g0192 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00738 | hp1 | a0002 | c0002 | t0020 | g0144 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG00738 | hp2 | a0001 | c0005 | t0005 | g0194 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01074 | hp2 | a0005 | c0008 | t0001 | g0166 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01099 | hp2 | a0002 | c0002 | t0012 | g0051 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01168 | hp1 | a0001 | c0005 | t0005 | g0008 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01169 | hp1 | a0001 | c0005 | t0005 | g0008 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01243 | hp2 | a0001 | c0005 | t0017 | g0293 | AMR | PUR | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01257 | hp1 | a0001 | c0006 | t0006 | g0200 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01258 | hp1 | a0002 | c0002 | t0012 | g0109 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0134 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01496 | hp1 | a0004 | c0004 | t0001 | g0025 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | CLM | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0086 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01515 | hp2 | a0001 | c0006 | t0006 | g0203 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0087 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | IBS | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0332 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01943 | hp2 | a0001 | c0006 | t0006 | g0199 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01978 | hp2 | a0001 | c0001 | t0021 | g0172 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01993 | hp1 | a0004 | c0004 | t0001 | g0020 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0071 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02015 | hp1 | a0004 | c0004 | t0001 | g0273 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02040 | hp2 | a0006 | c0010 | t0001 | g0250 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0185 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02132 | hp2 | a0004 | c0004 | t0001 | g0023 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02257 | hp1 | a0007 | c0011 | t0002 | g0167 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02258 | hp2 | a0001 | c0007 | t0008 | g0156 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0143 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02615 | hp2 | a0001 | c0005 | t0007 | g0003 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02622 | hp1 | a0003 | c0003 | t0023 | g0281 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02717 | hp1 | a0003 | c0003 | t0011 | g0284 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02717 | hp2 | a0001 | c0005 | t0007 | g0003 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02723 | hp1 | a0003 | c0003 | t0009 | g0047 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02818 | hp1 | a0001 | c0005 | t0007 | g0297 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02818 | hp2 | a0002 | c0002 | t0018 | g0081 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0160 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02895 | hp2 | a0003 | c0003 | t0009 | g0048 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0163 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0085 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02965 | hp1 | a0003 | c0003 | t0011 | g0283 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03041 | hp1 | a0001 | c0005 | t0007 | g0296 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03130 | hp1 | a0003 | c0003 | t0011 | g0282 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03130 | hp2 | a0001 | c0005 | t0007 | g0003 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03195 | hp2 | a0001 | c0001 | t0025 | g0186 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03239 | hp2 | a0004 | c0004 | t0001 | g0041 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03453 | hp2 | a0003 | c0003 | t0010 | g0285 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0238 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03491 | hp1 | a0001 | c0006 | t0006 | g0202 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ESN | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03579 | hp1 | a0003 | c0003 | t0010 | g0286 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03831 | hp2 | a0004 | c0004 | t0001 | g0232 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0061 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG04199 | hp1 | a0004 | c0004 | t0001 | g0269 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG04204 | hp1 | a0002 | c0002 | t0012 | g0050 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | STU | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18747 | hp1 | a0004 | c0004 | t0001 | g0265 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0089 | EAS | CHB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18947 | hp2 | a0004 | c0004 | t0001 | g0223 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18953 | hp2 | a0004 | c0004 | t0001 | g0274 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18957 | hp2 | a0001 | c0005 | t0005 | g0198 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0093 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18966 | hp2 | a0001 | c0005 | t0005 | g0197 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18968 | hp2 | a0004 | c0004 | t0001 | g0191 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18977 | hp2 | a0004 | c0004 | t0001 | g0261 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18980 | hp2 | a0001 | c0001 | t0019 | g0038 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18985 | hp1 | a0001 | c0005 | t0005 | g0196 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18985 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18991 | hp1 | a0002 | c0002 | t0024 | g0135 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18992 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA18999 | hp2 | a0004 | c0004 | t0008 | g0315 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19003 | hp1 | a0004 | c0004 | t0001 | g0039 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19003 | hp2 | a0005 | c0009 | t0001 | g0224 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19007 | hp1 | a0001 | c0005 | t0005 | g0007 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19009 | hp1 | a0001 | c0001 | t0008 | g0310 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19011 | hp1 | a0004 | c0004 | t0001 | g0013 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19012 | hp1 | a0004 | c0004 | t0001 | g0033 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19058 | hp1 | a0004 | c0004 | t0001 | g0195 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19063 | hp2 | a0001 | c0005 | t0005 | g0007 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19083 | hp1 | a0004 | c0004 | t0001 | g0018 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0059 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19086 | hp1 | a0001 | c0001 | t0022 | g0289 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19087 | hp1 | a0004 | c0004 | t0001 | g0248 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19087 | hp2 | a0004 | c0004 | t0001 | g0044 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ASW | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | ASW | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0331 | EUR | TSI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20905 | hp1 | a0001 | c0006 | t0006 | g0201 | SAS | GIH | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | GIH | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0217 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0161 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20300 | hp1 | a0001 | c0005 | t0007 | g0295 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA20300 | hp2 | a0003 | c0003 | t0002 | g0072 | AFR | USA | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0165 | AFR | LWK | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0188 | REF | REF | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0110 | REF | REF | GPR137C_chr14_52547836_52642713 | GPR137C | chr14 | 52547836 | 52642713 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52553226 | A | G | 5 | a0001 a0004 a0005 others(2): Show |
231 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(228): Show |
missense_variant | MODERATE | c.79A>G | p.Ser27Gly | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 391/4200 | 79/1290 | 27/429 | chr14 | 52553226 | |||
| chr14:52553246 | CGCTGCAG others(14): Show |
C | 1 | a0007 | 1 | HG02257.hp1 | disruptive_inframe_deletion | MODERATE | c.101_121delCTGCAGCC others(13): Show |
p.Ala34_Ala40del | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 413/4200 | 101/1290 | 34/429 | INFO_REALIGN_3_PRIME | chr14 | 52553246 | ||
| chr14:52553256 | T | TCCCCCCC others(39): Show |
1 | a0006 | 1 | HG02040.hp2 | frameshift_variant | HIGH | c.110_111insCCCCCCCT others(38): Show |
p.Gly38fs | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 423/4200 | 111/1290 | 37/429 | INFO_REALIGN_3_PRIME | chr14 | 52553256 | ||
| chr14:52553259 | G | C | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.112G>C | p.Gly38Arg | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 424/4200 | 112/1290 | 38/429 | chr14 | 52553259 | |||
| chr14:52553260 | G | C | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.113G>C | p.Gly38Ala | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 425/4200 | 113/1290 | 38/429 | chr14 | 52553260 | |||
| chr14:52553262 | G | C | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.115G>C | p.Ala39Pro | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 427/4200 | 115/1290 | 39/429 | chr14 | 52553262 | |||
| chr14:52553271 | C | G | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.124C>G | p.Pro42Ala | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 436/4200 | 124/1290 | 42/429 | chr14 | 52553271 | |||
| chr14:52553559 | A | G | 1 | a0005 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.412A>G | p.Thr138Ala | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 724/4200 | 412/1290 | 138/429 | chr14 | 52553559 | |||
| chr14:52553560 | C | T | 1 | a0005 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.413C>T | p.Thr138Met | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 725/4200 | 413/1290 | 138/429 | chr14 | 52553560 | |||
| chr14:52632184 | G | A | 2 | a0002 a0004 |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
missense_variant | MODERATE | c.742G>A | p.Val248Ile | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/7 | 1054/4200 | 742/1290 | 248/429 | chr14 | 52632184 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52553228 | C | T | 1 | a0001c0006 | 7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
synonymous_variant | LOW | c.81C>T | p.Ser27Ser | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 393/4200 | 81/1290 | 27/429 | chr14 | 52553228 | |||
| chr14:52553258 | A | C | 1 | a0006c0010 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.111A>C | p.Ser37Ser | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 423/4200 | 111/1290 | 37/429 | chr14 | 52553258 | |||
| chr14:52553273 | G | C | 1 | a0006c0010 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.126G>C | p.Pro42Pro | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 438/4200 | 126/1290 | 42/429 | chr14 | 52553273 | |||
| chr14:52553561 | G | C | 1 | a0005c0008 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.414G>C | p.Thr138Thr | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 726/4200 | 414/1290 | 138/429 | chr14 | 52553561 | |||
| chr14:52632210 | G | C | 1 | a0001c0005 | 15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
synonymous_variant | LOW | c.768G>C | p.Leu256Leu | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/7 | 1080/4200 | 768/1290 | 256/429 | chr14 | 52632210 | |||
| chr14:52633881 | C | T | 1 | a0001c0007 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1047C>T | p.Phe349Phe | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/7 | 1359/4200 | 1047/1290 | 349/429 | chr14 | 52633881 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52552902 | T | C | 1 | a0001c0006t0006 | 7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-246T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | chr14 | 52552902 | |||||||
| chr14:52552922 | C | G | 1 | a0002c0002t0012 | 3 | HG01099.hp2 HG01258.hp1 HG04204.hp1 |
5_prime_UTR_variant | MODIFIER | c.-226C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 226 | chr14 | 52552922 | ||||||
| chr14:52552989 | G | A | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(2): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-159G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/7 | 159 | chr14 | 52552989 | ||||||
| chr14:52635133 | G | A | 1 | a0001c0001t0015 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 18 | chr14 | 52635133 | ||||||
| chr14:52635282 | A | G | 1 | a0001c0001t0025 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 167 | chr14 | 52635282 | ||||||
| chr14:52635359 | A | C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 244 | chr14 | 52635359 | ||||||
| chr14:52635363 | A | AACCCCCC others(61): Show |
1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248_*249insACCCCC others(62): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 249 | chr14 | 52635363 | ||||||
| chr14:52635364 | T | C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*249T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 249 | chr14 | 52635364 | ||||||
| chr14:52635366 | CTGACTTT others(43): Show |
C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252_*301delTGACTT others(44): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 252 | chr14 | 52635366 | ||||||
| chr14:52635418 | A | C | 1 | a0002c0002t0024 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 303 | chr14 | 52635418 | ||||||
| chr14:52635419 | C | T | 4 | a0001c0001t0010 a0003c0003t0010 a0003c0003t0011 others(1): Show |
7 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*304C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 304 | chr14 | 52635419 | ||||||
| chr14:52635684 | A | G | 1 | a0001c0001t0022 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 569 | chr14 | 52635684 | ||||||
| chr14:52635704 | G | A | 1 | a0001c0001t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 589 | chr14 | 52635704 | ||||||
| chr14:52635733 | G | A | 1 | a0001c0001t0013 | 2 | HG02886.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*618G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 618 | chr14 | 52635733 | ||||||
| chr14:52635743 | G | A | 1 | a0001c0005t0017 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*628G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 628 | chr14 | 52635743 | ||||||
| chr14:52635941 | T | C | 1 | a0002c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 826 | chr14 | 52635941 | ||||||
| chr14:52635966 | A | C | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
75 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*851A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 851 | chr14 | 52635966 | ||||||
| chr14:52636081 | C | T | 1 | a0002c0002t0020 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 966 | chr14 | 52636081 | ||||||
| chr14:52636268 | T | C | 2 | a0001c0001t0010 a0003c0003t0010 |
3 | HG03453.hp2 HG03579.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1153 | chr14 | 52636268 | ||||||
| chr14:52636425 | G | A | 1 | a0001c0001t0014 | 2 | HG00639.hp2 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1310G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1310 | chr14 | 52636425 | ||||||
| chr14:52636754 | A | C | 1 | a0003c0003t0023 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1639A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1639 | chr14 | 52636754 | ||||||
| chr14:52636838 | G | A | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0021 others(2): Show |
61 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1723G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1723 | chr14 | 52636838 | ||||||
| chr14:52636956 | A | G | 3 | a0001c0005t0005 a0001c0005t0007 a0001c0005t0017 |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1841A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1841 | chr14 | 52636956 | ||||||
| chr14:52636995 | G | T | 1 | a0001c0001t0019 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1880G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1880 | chr14 | 52636995 | ||||||
| chr14:52637035 | C | T | 1 | a0001c0001t0021 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1920C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 1920 | chr14 | 52637035 | ||||||
| chr14:52637671 | T | C | 1 | a0001c0005t0005 | 8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2556T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 7/7 | 2556 | chr14 | 52637671 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52553905 | C | T | 1 | a0001c0001t0004g0332 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.444+314C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52553905 | |||||||
| chr14:52553974 | G | A | 1 | a0002c0002t0001g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.444+383G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52553974 | |||||||
| chr14:52554002 | C | T | 1 | a0002c0002t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444+411C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554002 | |||||||
| chr14:52554154 | C | G | 32 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(29): Show |
32 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.444+563C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554154 | |||||||
| chr14:52554164 | T | C | 34 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
34 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.444+573T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554164 | |||||||
| chr14:52554373 | A | G | 1 | a0001c0001t0003g0330 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.444+782A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554373 | |||||||
| chr14:52554389 | C | T | 34 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
34 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.444+798C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554389 | |||||||
| chr14:52554457 | G | C | 1 | a0002c0002t0001g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.444+866G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554457 | |||||||
| chr14:52554550 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.444+959A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554550 | |||||||
| chr14:52554671 | C | T | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+1080C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554671 | |||||||
| chr14:52554713 | TA | T | 229 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(226): Show |
239 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.444+1136delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52554713 | ||||||
| chr14:52554715 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+1124A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554715 | |||||||
| chr14:52554790 | T | A | 2 | a0003c0003t0009g0047 a0003c0003t0009g0048 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.444+1199T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554790 | |||||||
| chr14:52554825 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+1234G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52554825 | |||||||
| chr14:52555229 | C | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+1638C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555229 | |||||||
| chr14:52555465 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+1874C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555465 | |||||||
| chr14:52555841 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+2250C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555841 | |||||||
| chr14:52555956 | A | C | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | NA18959.hp2 NA18993.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+2365A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555956 | |||||||
| chr14:52555992 | T | G | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+2401T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52555992 | |||||||
| chr14:52556001 | T | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+2410T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556001 | |||||||
| chr14:52556030 | C | T | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.444+2439C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556030 | |||||||
| chr14:52556117 | C | T | 8 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0003c0003t0010g0285 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+2526C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556117 | |||||||
| chr14:52556119 | T | G | 16 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(13): Show |
16 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+2528T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556119 | |||||||
| chr14:52556148 | G | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(78): Show |
84 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.444+2557G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556148 | |||||||
| chr14:52556171 | G | A | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+2580G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556171 | |||||||
| chr14:52556376 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.444+2785C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556376 | |||||||
| chr14:52556391 | C | CT | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
238 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.444+2813dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52556391 | ||||||
| chr14:52556416 | C | T | 25 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0005 others(22): Show |
27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.444+2825C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556416 | |||||||
| chr14:52556509 | TGA | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+2926_444+2927d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52556509 | ||||||
| chr14:52556565 | C | G | 8 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 others(5): Show |
8 | HG00609.hp1 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+2974C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556565 | |||||||
| chr14:52556796 | T | G | 8 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0003c0003t0010g0285 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+3205T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556796 | |||||||
| chr14:52556847 | A | G | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+3256A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556847 | |||||||
| chr14:52556865 | A | G | 2 | a0003c0003t0001g0133 a0003c0003t0001g0134 |
2 | HG01433.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.444+3274A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556865 | |||||||
| chr14:52556889 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
186 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.444+3298G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52556889 | |||||||
| chr14:52557039 | T | C | 2 | a0002c0002t0012g0050 a0002c0002t0012g0051 |
2 | HG01099.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.444+3448T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557039 | |||||||
| chr14:52557129 | T | C | 177 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
184 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.444+3538T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557129 | |||||||
| chr14:52557196 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+3605C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557196 | |||||||
| chr14:52557197 | A | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.444+3606A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557197 | |||||||
| chr14:52557400 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.444+3809A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557400 | |||||||
| chr14:52557628 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.444+4037C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557628 | |||||||
| chr14:52557658 | G | A | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+4067G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557658 | |||||||
| chr14:52557739 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.444+4148A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557739 | |||||||
| chr14:52557888 | T | G | 1 | a0001c0006t0006g0192 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.444+4297T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52557888 | |||||||
| chr14:52558103 | C | A | 1 | a0004c0004t0001g0013 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.444+4512C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558103 | |||||||
| chr14:52558103 | C | CA | 106 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(103): Show |
109 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.444+4527dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52558103 | ||||||
| chr14:52558103 | C | CAAA | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+4525_444+4527d others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52558103 | ||||||
| chr14:52558148 | GT | G | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+4558delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558148 | |||||||
| chr14:52558161 | A | G | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+4570A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558161 | |||||||
| chr14:52558201 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.444+4610G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558201 | |||||||
| chr14:52558296 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+4705G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558296 | |||||||
| chr14:52558305 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+4714C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558305 | |||||||
| chr14:52558315 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.444+4724T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558315 | |||||||
| chr14:52558409 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.444+4818T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558409 | |||||||
| chr14:52558446 | A | C | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+4855A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558446 | |||||||
| chr14:52558483 | G | A | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+4892G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558483 | |||||||
| chr14:52558637 | G | C | 25 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0005 others(22): Show |
27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.444+5046G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558637 | |||||||
| chr14:52558740 | T | A | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.444+5149T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558740 | |||||||
| chr14:52558799 | A | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.444+5208A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558799 | |||||||
| chr14:52558896 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | NA18960.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.444+5305A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558896 | |||||||
| chr14:52558932 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+5341A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52558932 | |||||||
| chr14:52559392 | CAAAA | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+5804_444+5807d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52559392 | ||||||
| chr14:52559403 | C | A | 1 | a0003c0003t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+5812C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559403 | |||||||
| chr14:52559595 | A | T | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+6004A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559595 | |||||||
| chr14:52559614 | G | A | 8 | a0002c0002t0001g0053 a0002c0002t0001g0054 a0002c0002t0001g0055 others(5): Show |
8 | HG02080.hp2 NA18945.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.444+6023G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559614 | |||||||
| chr14:52559654 | A | G | 7 | a0001c0006t0006g0192 a0001c0006t0006g0199 a0001c0006t0006g0200 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+6063A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559654 | |||||||
| chr14:52559926 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0015g0217 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+6335C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52559926 | |||||||
| chr14:52560161 | A | G | 1 | a0002c0002t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444+6570A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560161 | |||||||
| chr14:52560171 | T | C | 1 | a0002c0002t0001g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.444+6580T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560171 | |||||||
| chr14:52560193 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.444+6602T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560193 | |||||||
| chr14:52560261 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.444+6670G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560261 | |||||||
| chr14:52560267 | T | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG01346.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.444+6676T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560267 | |||||||
| chr14:52560426 | G | A | 1 | a0003c0003t0001g0061 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.444+6835G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560426 | |||||||
| chr14:52560440 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.444+6849G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560440 | |||||||
| chr14:52560478 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.444+6887G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560478 | |||||||
| chr14:52560669 | G | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+7078G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560669 | |||||||
| chr14:52560739 | A | G | 26 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0005 others(23): Show |
28 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.444+7148A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560739 | |||||||
| chr14:52560776 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+7185A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560776 | |||||||
| chr14:52560817 | G | T | 1 | a0001c0001t0001g0292 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.444+7226G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560817 | |||||||
| chr14:52560896 | G | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+7305G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52560896 | |||||||
| chr14:52561030 | A | G | 1 | a0001c0001t0003g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.444+7439A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561030 | |||||||
| chr14:52561099 | GGTTATTA | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(80): Show |
86 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.444+7517_444+7523d others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52561099 | ||||||
| chr14:52561151 | G | A | 6 | a0002c0002t0001g0012 a0002c0002t0001g0062 a0002c0002t0001g0063 others(3): Show |
6 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+7560G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561151 | |||||||
| chr14:52561190 | C | T | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
238 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.444+7599C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561190 | |||||||
| chr14:52561198 | A | G | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+7607A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561198 | |||||||
| chr14:52561316 | C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+7725C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561316 | |||||||
| chr14:52561334 | G | A | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+7743G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561334 | |||||||
| chr14:52561346 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.444+7755G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561346 | |||||||
| chr14:52561382 | A | G | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+7791A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561382 | |||||||
| chr14:52561431 | G | A | 1 | a0003c0003t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.444+7840G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561431 | |||||||
| chr14:52561456 | G | A | 25 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0005 others(22): Show |
27 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.444+7865G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561456 | |||||||
| chr14:52561564 | A | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+7973A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561564 | |||||||
| chr14:52561740 | AT | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG00438.hp2 HG00558.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.444+8150delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561740 | |||||||
| chr14:52561768 | A | C | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+8177A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561768 | |||||||
| chr14:52561966 | A | G | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+8375A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52561966 | |||||||
| chr14:52562017 | T | G | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+8426T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562017 | |||||||
| chr14:52562044 | G | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+8453G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562044 | |||||||
| chr14:52562065 | G | A | 3 | a0003c0003t0011g0282 a0003c0003t0011g0283 a0003c0003t0011g0284 |
3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.444+8474G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562065 | |||||||
| chr14:52562168 | AAAAAC | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+8581_444+8585d others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52562168 | ||||||
| chr14:52562188 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.444+8597A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562188 | |||||||
| chr14:52562403 | A | G | 3 | a0002c0002t0001g0128 a0002c0002t0001g0129 a0003c0003t0002g0130 |
3 | HG00621.hp2 NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.444+8812A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562403 | |||||||
| chr14:52562494 | G | A | 2 | a0003c0003t0010g0285 a0003c0003t0010g0286 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444+8903G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562494 | |||||||
| chr14:52562517 | G | A | 1 | a0004c0004t0001g0018 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.444+8926G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562517 | |||||||
| chr14:52562620 | A | G | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+9029A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562620 | |||||||
| chr14:52562835 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+9244G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52562835 | |||||||
| chr14:52563121 | G | C | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.444+9530G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563121 | |||||||
| chr14:52563358 | TACTC | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+9770_444+9773d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52563358 | ||||||
| chr14:52563430 | A | C | 1 | a0002c0002t0001g0288 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.444+9839A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563430 | |||||||
| chr14:52563479 | A | G | 1 | a0003c0003t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.444+9888A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563479 | |||||||
| chr14:52563601 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444+10010G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563601 | |||||||
| chr14:52563647 | A | AAC | 3 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0190 |
3 | HG01069.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.444+10070_444+1007 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52563647 | ||||||
| chr14:52563750 | A | G | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+10159A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563750 | |||||||
| chr14:52563937 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.444+10346T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563937 | |||||||
| chr14:52563962 | T | C | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+10371T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52563962 | |||||||
| chr14:52564005 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(84): Show |
90 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.444+10414G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564005 | |||||||
| chr14:52564120 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+10529C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564120 | |||||||
| chr14:52564269 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444+10678C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564269 | |||||||
| chr14:52564270 | G | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+10679G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564270 | |||||||
| chr14:52564274 | C | CA | 127 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.444+10701dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | ||||||
| chr14:52564274 | C | CAA | 72 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0145 others(69): Show |
74 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.444+10700_444+1070 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | ||||||
| chr14:52564274 | C | CAAA | 10 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(7): Show |
10 | HG01261.hp1 HG02074.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+10699_444+1070 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | ||||||
| chr14:52564274 | C | CAAAA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(10): Show |
14 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+10698_444+1070 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564274 | ||||||
| chr14:52564523 | T | C | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+10932T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564523 | |||||||
| chr14:52564539 | T | C | 3 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0190 |
3 | HG01069.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.444+10948T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564539 | |||||||
| chr14:52564552 | A | G | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+10961A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564552 | |||||||
| chr14:52564616 | T | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+11025T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564616 | |||||||
| chr14:52564643 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+11052A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564643 | |||||||
| chr14:52564967 | CA | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+11380delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52564967 | ||||||
| chr14:52564978 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.444+11387G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52564978 | |||||||
| chr14:52565046 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+11455G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565046 | |||||||
| chr14:52565085 | G | C | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+11494G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565085 | |||||||
| chr14:52565300 | T | C | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+11709T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565300 | |||||||
| chr14:52565403 | T | G | 1 | a0002c0002t0001g0073 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.444+11812T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565403 | |||||||
| chr14:52565575 | C | G | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+11984C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565575 | |||||||
| chr14:52565816 | A | G | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+12225A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565816 | |||||||
| chr14:52565860 | T | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+12269T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565860 | |||||||
| chr14:52565921 | G | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+12330G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565921 | |||||||
| chr14:52565941 | G | T | 2 | a0001c0001t0001g0218 a0001c0001t0015g0217 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+12350G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52565941 | |||||||
| chr14:52566147 | C | T | 1 | a0001c0001t0003g0323 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.444+12556C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566147 | |||||||
| chr14:52566155 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
33 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.444+12564C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566155 | |||||||
| chr14:52566198 | C | T | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
238 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.444+12607C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566198 | |||||||
| chr14:52566306 | T | G | 1 | a0001c0006t0006g0199 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.444+12715T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566306 | |||||||
| chr14:52566398 | T | G | 3 | a0001c0001t0002g0171 a0001c0001t0002g0173 a0001c0001t0021g0172 |
3 | HG01943.hp1 HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.444+12807T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566398 | |||||||
| chr14:52566430 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+12839A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566430 | |||||||
| chr14:52566445 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.444+12854T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566445 | |||||||
| chr14:52566544 | T | A | 1 | a0001c0001t0015g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.444+12953T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566544 | |||||||
| chr14:52566545 | A | T | 1 | a0002c0002t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.444+12954A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566545 | |||||||
| chr14:52566813 | T | C | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+13222T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566813 | |||||||
| chr14:52566833 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+13242C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566833 | |||||||
| chr14:52566940 | T | A | 2 | a0004c0004t0001g0020 a0004c0004t0001g0025 |
2 | HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.444+13349T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52566940 | |||||||
| chr14:52567027 | C | T | 2 | a0004c0004t0001g0041 a0004c0004t0001g0042 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.444+13436C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567027 | |||||||
| chr14:52567061 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444+13470C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567061 | |||||||
| chr14:52567108 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.444+13517G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567108 | |||||||
| chr14:52567279 | T | C | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+13688T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567279 | |||||||
| chr14:52567309 | C | T | 1 | a0004c0004t0001g0273 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.444+13718C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567309 | |||||||
| chr14:52567311 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444+13720C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567311 | |||||||
| chr14:52567352 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.444+13761A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567352 | |||||||
| chr14:52567391 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+13800A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567391 | |||||||
| chr14:52567551 | A | C | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.444+13960A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567551 | |||||||
| chr14:52567568 | A | G | 2 | a0001c0001t0001g0270 a0004c0004t0001g0271 |
2 | HG00408.hp1 HG00408.hp2 |
intron_variant | MODIFIER | c.444+13977A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567568 | |||||||
| chr14:52567649 | C | CT | 15 | a0001c0001t0001g0210 a0001c0001t0001g0222 a0001c0001t0001g0278 others(12): Show |
15 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+14069dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567649 | ||||||
| chr14:52567649 | CT | C | 51 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0302 others(48): Show |
51 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.444+14069delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567649 | ||||||
| chr14:52567660 | T | G | 2 | a0001c0001t0003g0301 a0002c0002t0024g0135 |
2 | HG02074.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.444+14069T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567660 | |||||||
| chr14:52567661 | G | T | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.444+14070G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567661 | |||||||
| chr14:52567662 | G | GT | 11 | a0002c0002t0001g0068 a0002c0002t0001g0073 a0002c0002t0001g0119 others(8): Show |
11 | HG00673.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.444+14086dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567662 | ||||||
| chr14:52567662 | G | T | 1 | a0001c0001t0003g0301 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.444+14071G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567662 | |||||||
| chr14:52567662 | GT | G | 50 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(47): Show |
51 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.444+14086delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52567662 | ||||||
| chr14:52567663 | T | G | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.444+14072T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567663 | |||||||
| chr14:52567688 | A | G | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0187 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+14097A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567688 | |||||||
| chr14:52567720 | C | T | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.444+14129C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567720 | |||||||
| chr14:52567728 | C | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+14137C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567728 | |||||||
| chr14:52567844 | G | A | 3 | a0002c0002t0001g0074 a0002c0002t0001g0075 a0002c0002t0001g0076 |
3 | HG00423.hp1 HG02165.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.444+14253G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567844 | |||||||
| chr14:52567879 | C | T | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+14288C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567879 | |||||||
| chr14:52567891 | C | A | 1 | a0002c0002t0001g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.444+14300C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567891 | |||||||
| chr14:52567937 | C | T | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+14346C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52567937 | |||||||
| chr14:52568209 | A | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(20): Show |
25 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.444+14618A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568209 | |||||||
| chr14:52568340 | C | T | 2 | a0001c0001t0016g0185 a0001c0001t0025g0186 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.444+14749C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568340 | |||||||
| chr14:52568356 | T | G | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.444+14765T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568356 | |||||||
| chr14:52568417 | T | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+14826T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568417 | |||||||
| chr14:52568423 | C | A | 1 | a0004c0004t0001g0223 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.444+14832C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568423 | |||||||
| chr14:52568444 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.444+14853C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568444 | |||||||
| chr14:52568448 | G | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+14857G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568448 | |||||||
| chr14:52568457 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.444+14866G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568457 | |||||||
| chr14:52568707 | G | A | 9 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(6): Show |
11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+15116G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568707 | |||||||
| chr14:52568708 | C | T | 9 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(6): Show |
11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.444+15117C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568708 | |||||||
| chr14:52568839 | C | T | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+15248C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568839 | |||||||
| chr14:52568856 | T | C | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.444+15265T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568856 | |||||||
| chr14:52568897 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+15306G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568897 | |||||||
| chr14:52568897 | G | T | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+15306G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568897 | |||||||
| chr14:52568925 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(20): Show |
25 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.444+15334G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568925 | |||||||
| chr14:52568959 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.444+15368C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52568959 | |||||||
| chr14:52569022 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+15431G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569022 | |||||||
| chr14:52569032 | T | C | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.444+15441T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569032 | |||||||
| chr14:52569083 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.444+15492G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569083 | |||||||
| chr14:52569187 | A | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+15596A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569187 | |||||||
| chr14:52569190 | G | A | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.444+15599G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569190 | |||||||
| chr14:52569225 | CAGAA | C | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+15637_444+1564 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52569225 | ||||||
| chr14:52569326 | G | A | 1 | a0004c0004t0008g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.444+15735G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569326 | |||||||
| chr14:52569362 | C | CA | 21 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0225 others(18): Show |
23 | HG00639.hp1 HG00733.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.444+15783dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52569362 | ||||||
| chr14:52569394 | G | A | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+15803G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569394 | |||||||
| chr14:52569621 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+16030C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569621 | |||||||
| chr14:52569636 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+16045G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569636 | |||||||
| chr14:52569651 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | NA18960.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.444+16060G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569651 | |||||||
| chr14:52569657 | A | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+16066A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569657 | |||||||
| chr14:52569685 | G | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+16094G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569685 | |||||||
| chr14:52569787 | C | A | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0187 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+16196C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569787 | |||||||
| chr14:52569833 | T | G | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.444+16242T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569833 | |||||||
| chr14:52569936 | C | T | 1 | a0004c0004t0001g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.444+16345C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569936 | |||||||
| chr14:52569939 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.444+16348G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52569939 | |||||||
| chr14:52570050 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+16459C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570050 | |||||||
| chr14:52570082 | G | A | 1 | a0002c0002t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444+16491G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570082 | |||||||
| chr14:52570103 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+16512G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570103 | |||||||
| chr14:52570316 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.444+16725A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570316 | |||||||
| chr14:52570337 | C | A | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+16746C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570337 | |||||||
| chr14:52570410 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+16819C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570410 | |||||||
| chr14:52570413 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(34): Show |
40 | HG00280.hp1 HG01069.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+16822C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570413 | |||||||
| chr14:52570436 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0015g0217 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+16845G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570436 | |||||||
| chr14:52570629 | T | TA | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+17043dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52570629 | ||||||
| chr14:52570662 | C | G | 3 | a0001c0006t0006g0199 a0001c0006t0006g0200 a0001c0006t0006g0204 |
3 | HG00642.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.444+17071C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570662 | |||||||
| chr14:52570751 | A | G | 3 | a0001c0006t0006g0199 a0001c0006t0006g0200 a0001c0006t0006g0204 |
3 | HG00642.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.444+17160A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570751 | |||||||
| chr14:52570760 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG01346.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.444+17169C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52570760 | |||||||
| chr14:52571030 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.444+17439A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571030 | |||||||
| chr14:52571145 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(34): Show |
40 | HG00280.hp1 HG01069.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.444+17554C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571145 | |||||||
| chr14:52571146 | G | A | 8 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0003c0003t0010g0285 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+17555G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571146 | |||||||
| chr14:52571234 | C | T | 1 | a0003c0003t0010g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.444+17643C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571234 | |||||||
| chr14:52571298 | C | G | 172 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.444+17707C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571298 | |||||||
| chr14:52571314 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.444+17723A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571314 | |||||||
| chr14:52571459 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
186 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.444+17868A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571459 | |||||||
| chr14:52571502 | G | A | 3 | a0003c0003t0011g0282 a0003c0003t0011g0283 a0003c0003t0011g0284 |
3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.444+17911G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571502 | |||||||
| chr14:52571642 | C | G | 18 | a0001c0001t0001g0011 a0001c0001t0001g0256 a0001c0001t0001g0257 others(15): Show |
19 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.444+18051C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571642 | |||||||
| chr14:52571843 | C | T | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+18252C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571843 | |||||||
| chr14:52571910 | G | T | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.444+18319G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571910 | |||||||
| chr14:52571989 | A | C | 1 | a0002c0002t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+18398A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571989 | |||||||
| chr14:52571992 | T | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+18401T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52571992 | |||||||
| chr14:52572517 | T | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+18926T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572517 | |||||||
| chr14:52572536 | A | G | 2 | a0003c0003t0010g0285 a0003c0003t0010g0286 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444+18945A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572536 | |||||||
| chr14:52572568 | C | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+18977C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572568 | |||||||
| chr14:52572593 | C | A | 1 | a0001c0001t0010g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.444+19002C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52572593 | |||||||
| chr14:52573010 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0221 a0001c0001t0001g0225 others(5): Show |
9 | HG00558.hp1 HG02015.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+19419C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573010 | |||||||
| chr14:52573414 | C | T | 36 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(33): Show |
36 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.444+19823C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573414 | |||||||
| chr14:52573415 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.444+19824G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573415 | |||||||
| chr14:52573443 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444+19852G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573443 | |||||||
| chr14:52573619 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.444+20028C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573619 | |||||||
| chr14:52573634 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.444+20043A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573634 | |||||||
| chr14:52573765 | C | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+20174C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573765 | |||||||
| chr14:52573774 | G | C | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.444+20183G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573774 | |||||||
| chr14:52573781 | C | T | 1 | a0003c0003t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+20190C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573781 | |||||||
| chr14:52573782 | A | G | 1 | a0003c0003t0001g0143 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.444+20191A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573782 | |||||||
| chr14:52573857 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG02145.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.444+20266G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573857 | |||||||
| chr14:52573894 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.444+20303C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52573894 | |||||||
| chr14:52573957 | CAT | C | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+20369_444+2037 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52573957 | ||||||
| chr14:52574003 | T | A | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.444+20412T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574003 | |||||||
| chr14:52574075 | G | A | 8 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0003c0003t0010g0285 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+20484G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574075 | |||||||
| chr14:52574096 | T | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.444+20505T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574096 | |||||||
| chr14:52574151 | G | GA | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(20): Show |
25 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.444+20561dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52574151 | ||||||
| chr14:52574241 | T | C | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.444+20650T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574241 | |||||||
| chr14:52574258 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.444+20667C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574258 | |||||||
| chr14:52574303 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+20712G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574303 | |||||||
| chr14:52574331 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0015g0217 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+20740A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574331 | |||||||
| chr14:52574380 | A | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.444+20789A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574380 | |||||||
| chr14:52574396 | G | C | 4 | a0001c0001t0003g0302 a0001c0001t0003g0303 a0001c0001t0003g0313 others(1): Show |
4 | HG00621.hp1 NA18969.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+20805G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574396 | |||||||
| chr14:52574445 | A | T | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.444+20854A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574445 | |||||||
| chr14:52574488 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.444+20897A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574488 | |||||||
| chr14:52574501 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.444+20910G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574501 | |||||||
| chr14:52574645 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
123 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.444+21054T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574645 | |||||||
| chr14:52574798 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+21207C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574798 | |||||||
| chr14:52574831 | T | C | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
238 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.444+21240T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52574831 | |||||||
| chr14:52575010 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.444+21419G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575010 | |||||||
| chr14:52575102 | G | A | 21 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(18): Show |
23 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.444+21511G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575102 | |||||||
| chr14:52575128 | A | G | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+21537A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575128 | |||||||
| chr14:52575143 | A | G | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+21552A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575143 | |||||||
| chr14:52575149 | C | T | 3 | a0002c0002t0001g0064 a0003c0003t0010g0285 a0003c0003t0010g0286 |
3 | HG00639.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.444+21558C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575149 | |||||||
| chr14:52575200 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+21609T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575200 | |||||||
| chr14:52575548 | C | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.444+21957C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575548 | |||||||
| chr14:52575673 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.444+22082A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575673 | |||||||
| chr14:52575743 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.444+22152T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575743 | |||||||
| chr14:52575915 | G | A | 1 | a0001c0001t0003g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.444+22324G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575915 | |||||||
| chr14:52575929 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.444+22338A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52575929 | |||||||
| chr14:52576088 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-22184C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576088 | |||||||
| chr14:52576163 | C | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-22109C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576163 | |||||||
| chr14:52576182 | A | G | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-22090A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576182 | |||||||
| chr14:52576197 | C | T | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-22075C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576197 | |||||||
| chr14:52576437 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.445-21835G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576437 | |||||||
| chr14:52576509 | T | C | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-21763T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576509 | |||||||
| chr14:52576546 | T | C | 1 | a0002c0002t0001g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.445-21726T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576546 | |||||||
| chr14:52576632 | C | G | 1 | a0006c0010t0001g0250 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.445-21640C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576632 | |||||||
| chr14:52576792 | C | T | 1 | a0004c0004t0001g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.445-21480C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576792 | |||||||
| chr14:52576956 | G | A | 1 | a0001c0001t0003g0305 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.445-21316G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576956 | |||||||
| chr14:52576960 | C | T | 1 | a0005c0008t0001g0166 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.445-21312C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576960 | |||||||
| chr14:52576963 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-21309G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52576963 | |||||||
| chr14:52577056 | G | GGTGCACA others(1): Show |
228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
238 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.445-21216_445-2121 others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577056 | |||||||
| chr14:52577068 | GCTACT | G | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-21197_445-2119 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577068 | ||||||
| chr14:52577123 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-21149G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577123 | |||||||
| chr14:52577134 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445-21138C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577134 | |||||||
| chr14:52577166 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0162 others(12): Show |
17 | HG00558.hp1 HG01074.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.445-21106G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577166 | |||||||
| chr14:52577183 | C | CA | 29 | a0001c0001t0001g0080 a0001c0001t0003g0299 a0001c0001t0003g0300 others(26): Show |
29 | HG00642.hp2 HG00673.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.445-21059dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | C | CAA | 7 | a0001c0001t0003g0317 a0001c0001t0003g0318 a0001c0001t0003g0323 others(4): Show |
7 | HG03579.hp1 NA18953.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-21060_445-2105 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | C | CAAAAAA | 6 | a0003c0003t0009g0047 a0003c0003t0009g0048 a0003c0003t0011g0282 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-21064_445-2105 others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.445-21089C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577183 | |||||||
| chr14:52577183 | CA | C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0002g0005 others(34): Show |
40 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.445-21059delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | CAA | C | 28 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(25): Show |
28 | HG01167.hp1 HG01261.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.445-21060_445-2105 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | CAAA | C | 56 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(53): Show |
59 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.445-21061_445-2105 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | CAAAA | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(8): Show |
11 | HG00099.hp2 HG00738.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-21062_445-2105 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | CAAAAA | C | 39 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(36): Show |
41 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.445-21063_445-2105 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | CAAAAAA | C | 12 | a0001c0005t0005g0198 a0001c0005t0007g0003 a0001c0005t0007g0296 others(9): Show |
14 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.445-21064_445-2105 others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577183 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0330 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.445-21069_445-2105 others(15): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577183 | ||||||
| chr14:52577221 | G | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-21051G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577221 | |||||||
| chr14:52577383 | A | C | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-20889A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577383 | |||||||
| chr14:52577385 | T | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
186 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.445-20887T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577385 | |||||||
| chr14:52577505 | T | TGC | 7 | a0001c0001t0003g0300 a0001c0001t0003g0305 a0001c0001t0003g0312 others(4): Show |
7 | HG01099.hp1 NA18960.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-20756_445-2075 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577505 | ||||||
| chr14:52577507 | C | T | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
93 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.445-20765C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577507 | |||||||
| chr14:52577512 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-20760G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577512 | |||||||
| chr14:52577514 | G | GCACACAC others(1): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0170 a0001c0001t0002g0184 others(2): Show |
6 | HG00280.hp1 HG01069.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-20757_445-2075 others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577514 | G | GCACACAC others(3): Show |
12 | a0001c0001t0002g0049 a0001c0001t0002g0169 a0001c0001t0002g0173 others(9): Show |
12 | HG01192.hp2 HG01884.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-20757_445-2075 others(14): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577514 | G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.445-20757_445-2075 others(16): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577514 | G | GCACACAC others(7): Show |
3 | a0001c0001t0001g0030 a0001c0001t0002g0171 a0001c0001t0002g0179 |
3 | HG00733.hp1 HG02004.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.445-20757_445-2075 others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577514 | G | GCACACAC others(13): Show |
1 | a0001c0001t0002g0182 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.445-20757_445-2075 others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577514 | G | GCACGCAC others(7): Show |
6 | a0001c0001t0001g0021 a0004c0004t0001g0013 a0004c0004t0001g0020 others(3): Show |
6 | HG01496.hp1 HG01993.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-20757_445-2075 others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577514 | G | GCACGCAC others(9): Show |
3 | a0001c0001t0001g0032 a0001c0001t0002g0024 a0001c0001t0002g0031 |
3 | NA18952.hp1 NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.445-20757_445-2075 others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577514 | ||||||
| chr14:52577516 | G | A | 31 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0032 others(28): Show |
32 | HG00280.hp1 HG00733.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.445-20756G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577516 | |||||||
| chr14:52577516 | G | GCA | 20 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(17): Show |
20 | HG00642.hp1 HG00735.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.445-20732_445-2073 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCACA | 3 | a0001c0001t0013g0160 a0002c0002t0012g0050 a0005c0008t0001g0166 |
3 | HG01074.hp2 HG02886.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.445-20734_445-2073 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCACACA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0209 others(7): Show |
13 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-20736_445-2073 others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCACACAC others(1): Show |
5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-20738_445-2073 others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCACACAC others(3): Show |
1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.445-20740_445-2073 others(14): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCACACAC others(5): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0145 |
3 | HG00438.hp2 HG02976.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.445-20742_445-2073 others(16): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCACACAC others(13): Show |
1 | a0001c0001t0002g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.445-20750_445-2073 others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCACAC others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445-20755_445-2075 others(16): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCACAC others(7): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0019g0038 others(1): Show |
4 | HG00558.hp2 NA18975.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-20755_445-2075 others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCACAC others(9): Show |
9 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0035 others(6): Show |
9 | HG01978.hp1 HG02071.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.445-20755_445-2075 others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCACAC others(11): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0043 others(1): Show |
4 | HG00735.hp1 HG02155.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-20755_445-2075 others(22): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCACAC others(13): Show |
1 | a0001c0001t0001g0040 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.445-20755_445-2075 others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCACAC others(17): Show |
1 | a0004c0004t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.445-20755_445-2075 others(28): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCGCAC others(9): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0029 |
2 | HG02055.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.445-20755_445-2075 others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | G | GCGCGCAC others(11): Show |
1 | a0004c0004t0001g0023 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445-20755_445-2075 others(22): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | GCA | G | 81 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
86 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.445-20732_445-2073 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577516 | GCACA | G | 6 | a0001c0001t0001g0193 a0001c0001t0001g0249 a0003c0003t0011g0282 others(3): Show |
6 | HG02717.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-20734_445-2073 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577516 | ||||||
| chr14:52577518 | A | G | 42 | a0001c0001t0003g0299 a0001c0001t0003g0301 a0001c0001t0003g0302 others(39): Show |
42 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.445-20754A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577518 | |||||||
| chr14:52577556 | A | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
11 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-20716A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577556 | |||||||
| chr14:52577592 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-20680G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577592 | |||||||
| chr14:52577598 | CAAAAG | C | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-20671_445-2066 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577598 | ||||||
| chr14:52577701 | G | A | 1 | a0001c0007t0008g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.445-20571G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577701 | |||||||
| chr14:52577743 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.445-20529G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577743 | |||||||
| chr14:52577798 | A | C | 2 | a0001c0001t0001g0218 a0001c0001t0015g0217 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.445-20474A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577798 | |||||||
| chr14:52577799 | C | CA | 103 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0157 others(100): Show |
106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.445-20455dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577799 | ||||||
| chr14:52577799 | C | CAAAA | 25 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0026 others(22): Show |
25 | HG00733.hp1 HG00735.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.445-20458_445-2045 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577799 | ||||||
| chr14:52577799 | C | CAAAAA | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(7): Show |
10 | HG00438.hp2 HG00558.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-20459_445-2045 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52577799 | ||||||
| chr14:52577881 | C | G | 8 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 others(5): Show |
8 | HG00609.hp1 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-20391C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577881 | |||||||
| chr14:52577895 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.445-20377G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577895 | |||||||
| chr14:52577897 | A | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-20375A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52577897 | |||||||
| chr14:52578191 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-20081A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578191 | |||||||
| chr14:52578238 | A | T | 18 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(15): Show |
18 | HG00438.hp1 HG00621.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.445-20034A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578238 | |||||||
| chr14:52578266 | C | T | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.445-20006C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578266 | |||||||
| chr14:52578360 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0042 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.445-19912G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578360 | |||||||
| chr14:52578366 | T | A | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-19906T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578366 | |||||||
| chr14:52578429 | A | G | 1 | a0001c0001t0003g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.445-19843A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578429 | |||||||
| chr14:52578490 | C | G | 1 | a0002c0002t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.445-19782C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578490 | |||||||
| chr14:52578658 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-19614A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578658 | |||||||
| chr14:52578660 | G | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-19612G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578660 | |||||||
| chr14:52578661 | C | A | 14 | a0001c0001t0003g0314 a0001c0001t0003g0317 a0001c0001t0003g0318 others(11): Show |
14 | HG01099.hp1 NA18939.hp2 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.445-19611C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578661 | |||||||
| chr14:52578770 | C | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(20): Show |
25 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.445-19502C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578770 | |||||||
| chr14:52578883 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-19389G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52578883 | |||||||
| chr14:52579046 | C | T | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-19226C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579046 | |||||||
| chr14:52579055 | T | C | 1 | a0004c0004t0008g0315 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.445-19217T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579055 | |||||||
| chr14:52579131 | A | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | NA18960.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.445-19141A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579131 | |||||||
| chr14:52579137 | C | G | 1 | a0003c0003t0001g0067 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445-19135C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579137 | |||||||
| chr14:52579143 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.445-19129C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579143 | |||||||
| chr14:52579182 | G | C | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.445-19090G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579182 | |||||||
| chr14:52579304 | C | T | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | NA18959.hp2 NA18993.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.445-18968C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579304 | |||||||
| chr14:52579358 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.445-18914G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579358 | |||||||
| chr14:52579514 | A | G | 1 | a0004c0004t0001g0013 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.445-18758A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579514 | |||||||
| chr14:52579526 | T | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-18746T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579526 | |||||||
| chr14:52579650 | A | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
228 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.445-18622A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579650 | |||||||
| chr14:52579789 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-18483G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579789 | |||||||
| chr14:52579841 | G | A | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-18431G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579841 | |||||||
| chr14:52579883 | G | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(20): Show |
25 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.445-18389G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579883 | |||||||
| chr14:52579918 | T | C | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-18354T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52579918 | |||||||
| chr14:52580011 | A | G | 1 | a0004c0004t0001g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.445-18261A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580011 | |||||||
| chr14:52580113 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-18159A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580113 | |||||||
| chr14:52580177 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.445-18095A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580177 | |||||||
| chr14:52580277 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445-17995G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580277 | |||||||
| chr14:52580361 | G | GA | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
93 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.445-17902dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52580361 | ||||||
| chr14:52580370 | AT | A | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-17892delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52580370 | ||||||
| chr14:52580529 | T | A | 1 | a0004c0004t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.445-17743T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580529 | |||||||
| chr14:52580584 | G | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.445-17688G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580584 | |||||||
| chr14:52580634 | G | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-17638G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580634 | |||||||
| chr14:52580807 | ATTAT | A | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-17460_445-1745 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52580807 | ||||||
| chr14:52580811 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-17461T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580811 | |||||||
| chr14:52580831 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-17441T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580831 | |||||||
| chr14:52580868 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.445-17404T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580868 | |||||||
| chr14:52580874 | G | A | 3 | a0003c0003t0011g0282 a0003c0003t0011g0283 a0003c0003t0011g0284 |
3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.445-17398G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580874 | |||||||
| chr14:52580909 | A | T | 1 | a0001c0001t0003g0320 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.445-17363A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52580909 | |||||||
| chr14:52581144 | C | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-17128C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581144 | |||||||
| chr14:52581195 | C | CA | 38 | a0001c0001t0001g0225 a0001c0001t0002g0005 a0001c0001t0002g0006 others(35): Show |
42 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.445-17059dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581195 | ||||||
| chr14:52581195 | CA | C | 12 | a0001c0001t0001g0175 a0001c0001t0001g0247 a0001c0001t0001g0258 others(9): Show |
12 | HG00738.hp1 HG01167.hp2 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-17059delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581195 | ||||||
| chr14:52581230 | T | C | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.445-17042T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581230 | |||||||
| chr14:52581245 | A | C | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445-17027A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581245 | |||||||
| chr14:52581247 | C | T | 1 | a0002c0002t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.445-17025C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581247 | |||||||
| chr14:52581290 | C | T | 220 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.445-16982C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581290 | |||||||
| chr14:52581370 | TA | T | 133 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(130): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.445-16885delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581370 | ||||||
| chr14:52581533 | C | CA | 47 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.445-16726dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52581533 | ||||||
| chr14:52581622 | T | A | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-16650T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581622 | |||||||
| chr14:52581631 | A | G | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-16641A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581631 | |||||||
| chr14:52581669 | A | G | 2 | a0003c0003t0010g0285 a0003c0003t0010g0286 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.445-16603A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581669 | |||||||
| chr14:52581696 | A | G | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.445-16576A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581696 | |||||||
| chr14:52581814 | T | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-16458T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581814 | |||||||
| chr14:52581976 | G | A | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-16296G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52581976 | |||||||
| chr14:52582060 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-16212T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52582060 | |||||||
| chr14:52582130 | C | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-16142C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52582130 | |||||||
| chr14:52582796 | AAAAT | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-15465_445-1546 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52582796 | ||||||
| chr14:52582935 | A | G | 1 | a0005c0009t0001g0224 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.445-15337A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52582935 | |||||||
| chr14:52583170 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-15102A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583170 | |||||||
| chr14:52583206 | G | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-15066G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583206 | |||||||
| chr14:52583551 | G | T | 216 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(213): Show |
226 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.445-14721G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583551 | |||||||
| chr14:52583611 | C | T | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-14661C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583611 | |||||||
| chr14:52583736 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.445-14536C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583736 | |||||||
| chr14:52583773 | C | CAGA | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-14499_445-1449 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583773 | |||||||
| chr14:52583774 | T | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-14498T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583774 | |||||||
| chr14:52583807 | A | C | 1 | a0003c0003t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.445-14465A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583807 | |||||||
| chr14:52583898 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.445-14374A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583898 | |||||||
| chr14:52583928 | CTG | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-14343_445-1434 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52583928 | |||||||
| chr14:52584214 | A | G | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-14058A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584214 | |||||||
| chr14:52584359 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-13913A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584359 | |||||||
| chr14:52584476 | A | G | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-13796A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584476 | |||||||
| chr14:52584643 | G | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-13629G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584643 | |||||||
| chr14:52584748 | C | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-13524C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584748 | |||||||
| chr14:52584832 | C | G | 3 | a0001c0001t0002g0178 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | NA18968.hp1 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.445-13440C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584832 | |||||||
| chr14:52584859 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.445-13413C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584859 | |||||||
| chr14:52584944 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-13328A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52584944 | |||||||
| chr14:52585011 | C | T | 1 | a0002c0002t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445-13261C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585011 | |||||||
| chr14:52585079 | T | C | 1 | a0002c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445-13193T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585079 | |||||||
| chr14:52585154 | G | A | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(120): Show |
126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.445-13118G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585154 | |||||||
| chr14:52585301 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-12971T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585301 | |||||||
| chr14:52585379 | G | GCT | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-12883_445-1288 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52585379 | ||||||
| chr14:52585449 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.445-12823A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585449 | |||||||
| chr14:52585508 | A | T | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.445-12764A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585508 | |||||||
| chr14:52585671 | T | TA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(12): Show |
16 | HG01074.hp2 HG01261.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.445-12595dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52585671 | ||||||
| chr14:52585741 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-12531G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585741 | |||||||
| chr14:52585994 | G | A | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-12278G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52585994 | |||||||
| chr14:52586069 | G | A | 32 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(29): Show |
32 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.445-12203G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586069 | |||||||
| chr14:52586120 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.445-12152A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586120 | |||||||
| chr14:52586411 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.445-11861A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586411 | |||||||
| chr14:52586506 | A | G | 2 | a0001c0001t0004g0147 a0001c0001t0004g0153 |
2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.445-11766A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586506 | |||||||
| chr14:52586623 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-11649A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586623 | |||||||
| chr14:52586670 | C | T | 1 | a0002c0002t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.445-11602C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586670 | |||||||
| chr14:52586757 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.445-11515T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586757 | |||||||
| chr14:52586772 | T | A | 17 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(14): Show |
19 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.445-11500T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586772 | |||||||
| chr14:52586813 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-11459C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52586813 | |||||||
| chr14:52587110 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.445-11162G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587110 | |||||||
| chr14:52587121 | C | A | 6 | a0003c0003t0001g0067 a0003c0003t0001g0103 a0003c0003t0001g0104 others(3): Show |
6 | HG01433.hp1 HG02145.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-11151C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587121 | |||||||
| chr14:52587182 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.445-11090G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587182 | |||||||
| chr14:52587208 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-11064A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587208 | |||||||
| chr14:52587212 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-11060G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587212 | |||||||
| chr14:52587262 | T | C | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-11010T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587262 | |||||||
| chr14:52587546 | A | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-10726A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587546 | |||||||
| chr14:52587795 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-10477C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587795 | |||||||
| chr14:52587844 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-10428A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587844 | |||||||
| chr14:52587921 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445-10351C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52587921 | |||||||
| chr14:52588099 | G | A | 7 | a0001c0006t0006g0192 a0001c0006t0006g0199 a0001c0006t0006g0200 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-10173G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588099 | |||||||
| chr14:52588227 | C | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-10045C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588227 | |||||||
| chr14:52588247 | C | G | 1 | a0001c0001t0004g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445-10025C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588247 | |||||||
| chr14:52588334 | A | G | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(131): Show |
141 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.445-9938A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588334 | |||||||
| chr14:52588461 | A | G | 1 | a0001c0001t0010g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.445-9811A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588461 | |||||||
| chr14:52588640 | A | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-9632A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588640 | |||||||
| chr14:52588678 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-9594A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588678 | |||||||
| chr14:52588760 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.445-9512G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588760 | |||||||
| chr14:52588818 | G | T | 1 | a0001c0001t0002g0024 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.445-9454G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588818 | |||||||
| chr14:52588855 | T | C | 1 | a0001c0001t0002g0005 | 2 | HG00280.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.445-9417T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588855 | |||||||
| chr14:52588945 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0266 |
3 | HG00423.hp2 HG00609.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.445-9327C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588945 | |||||||
| chr14:52588946 | G | A | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-9326G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52588946 | |||||||
| chr14:52589454 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.445-8818A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52589454 | |||||||
| chr14:52589810 | G | A | 8 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0003c0003t0010g0285 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-8462G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52589810 | |||||||
| chr14:52589889 | T | C | 21 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(18): Show |
23 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.445-8383T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52589889 | |||||||
| chr14:52590062 | T | C | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.445-8210T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590062 | |||||||
| chr14:52590253 | GA | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-8010delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52590253 | ||||||
| chr14:52590263 | G | T | 1 | a0004c0004t0001g0223 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.445-8009G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590263 | |||||||
| chr14:52590265 | T | G | 1 | a0001c0001t0004g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.445-8007T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590265 | |||||||
| chr14:52590387 | T | C | 6 | a0001c0001t0003g0300 a0001c0001t0003g0302 a0001c0001t0003g0303 others(3): Show |
6 | HG00621.hp1 NA18969.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-7885T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590387 | |||||||
| chr14:52590444 | G | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-7828G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590444 | |||||||
| chr14:52590738 | T | C | 2 | a0002c0002t0001g0083 a0002c0002t0001g0106 |
2 | NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.445-7534T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590738 | |||||||
| chr14:52590789 | T | G | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-7483T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590789 | |||||||
| chr14:52590990 | C | A | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-7282C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52590990 | |||||||
| chr14:52591034 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-7238A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591034 | |||||||
| chr14:52591095 | C | T | 5 | a0004c0004t0001g0191 a0004c0004t0001g0223 a0004c0004t0001g0248 others(2): Show |
5 | HG02015.hp1 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-7177C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591095 | |||||||
| chr14:52591536 | G | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-6736G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591536 | |||||||
| chr14:52591981 | C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-6291C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52591981 | |||||||
| chr14:52592012 | C | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-6260C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592012 | |||||||
| chr14:52592239 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-6033A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592239 | |||||||
| chr14:52592274 | G | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-5998G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592274 | |||||||
| chr14:52592278 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-5994T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592278 | |||||||
| chr14:52592392 | A | T | 1 | a0002c0002t0001g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445-5880A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592392 | |||||||
| chr14:52592937 | T | C | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-5335T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52592937 | |||||||
| chr14:52593036 | A | G | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(13): Show |
18 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.445-5236A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593036 | |||||||
| chr14:52593059 | G | A | 2 | a0001c0001t0001g0043 a0004c0004t0001g0023 |
2 | HG02132.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.445-5213G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593059 | |||||||
| chr14:52593160 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445-5112C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593160 | |||||||
| chr14:52593260 | T | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-5012T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593260 | |||||||
| chr14:52593289 | T | G | 2 | a0002c0002t0001g0092 a0002c0002t0001g0120 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.445-4983T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593289 | |||||||
| chr14:52593380 | T | G | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(20): Show |
25 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.445-4892T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593380 | |||||||
| chr14:52593528 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-4744G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593528 | |||||||
| chr14:52593662 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.445-4610G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593662 | |||||||
| chr14:52593745 | C | T | 21 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(18): Show |
23 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.445-4527C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593745 | |||||||
| chr14:52593777 | C | T | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-4495C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593777 | |||||||
| chr14:52593796 | AT | A | 324 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(321): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.445-4469delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52593796 | ||||||
| chr14:52593913 | T | C | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-4359T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52593913 | |||||||
| chr14:52594174 | C | CTG | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-4095_445-4094d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 52594174 | ||||||
| chr14:52594301 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.445-3971T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594301 | |||||||
| chr14:52594335 | T | A | 1 | a0004c0004t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.445-3937T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594335 | |||||||
| chr14:52594394 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0145 a0001c0001t0001g0157 others(81): Show |
87 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.445-3878T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594394 | |||||||
| chr14:52594683 | C | T | 1 | a0002c0002t0001g0068 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445-3589C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594683 | |||||||
| chr14:52594700 | T | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.445-3572T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594700 | |||||||
| chr14:52594787 | T | C | 5 | a0002c0002t0001g0119 a0002c0002t0001g0121 a0002c0002t0001g0126 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-3485T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594787 | |||||||
| chr14:52594957 | C | T | 45 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(42): Show |
45 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.445-3315C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52594957 | |||||||
| chr14:52595152 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-3120C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595152 | |||||||
| chr14:52595177 | C | T | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-3095C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595177 | |||||||
| chr14:52595335 | T | C | 1 | a0002c0002t0001g0107 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.445-2937T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595335 | |||||||
| chr14:52595405 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-2867A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595405 | |||||||
| chr14:52595438 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.445-2834A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595438 | |||||||
| chr14:52595525 | T | G | 1 | a0001c0001t0002g0031 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.445-2747T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595525 | |||||||
| chr14:52595609 | C | T | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445-2663C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595609 | |||||||
| chr14:52595651 | A | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.445-2621A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595651 | |||||||
| chr14:52595716 | G | A | 1 | a0001c0001t0003g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.445-2556G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595716 | |||||||
| chr14:52595817 | G | A | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-2455G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595817 | |||||||
| chr14:52595842 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.445-2430T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595842 | |||||||
| chr14:52595895 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0266 |
3 | HG00423.hp2 HG00609.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.445-2377G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595895 | |||||||
| chr14:52595902 | G | C | 8 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0003c0003t0010g0285 others(5): Show |
8 | HG01496.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-2370G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595902 | |||||||
| chr14:52595997 | G | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
11 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-2275G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52595997 | |||||||
| chr14:52596181 | C | T | 2 | a0001c0001t0004g0151 a0001c0001t0004g0154 |
2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.445-2091C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596181 | |||||||
| chr14:52596197 | C | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-2075C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596197 | |||||||
| chr14:52596235 | G | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445-2037G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596235 | |||||||
| chr14:52596269 | CACGGGTC others(21): Show |
C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-2002_445-1975d others(30): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596269 | |||||||
| chr14:52596317 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1955T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596317 | |||||||
| chr14:52596329 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1943C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596329 | |||||||
| chr14:52596352 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1920C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596352 | |||||||
| chr14:52596354 | A | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1918A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596354 | |||||||
| chr14:52596357 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1915T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596357 | |||||||
| chr14:52596358 | G | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1914G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596358 | |||||||
| chr14:52596360 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1912T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596360 | |||||||
| chr14:52596361 | A | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1911A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596361 | |||||||
| chr14:52596374 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1898T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596374 | |||||||
| chr14:52596378 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1894T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596378 | |||||||
| chr14:52596390 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.445-1882G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596390 | |||||||
| chr14:52596441 | G | A | 2 | a0001c0001t0016g0185 a0001c0001t0025g0186 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.445-1831G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596441 | |||||||
| chr14:52596446 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.445-1826G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596446 | |||||||
| chr14:52596452 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-1820C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596452 | |||||||
| chr14:52596545 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.445-1727C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596545 | |||||||
| chr14:52596664 | C | G | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445-1608C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596664 | |||||||
| chr14:52596730 | C | T | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-1542C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596730 | |||||||
| chr14:52596895 | T | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-1377T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596895 | |||||||
| chr14:52596903 | G | A | 99 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
106 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.445-1369G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52596903 | |||||||
| chr14:52597032 | C | T | 1 | a0002c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.445-1240C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597032 | |||||||
| chr14:52597169 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445-1103G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597169 | |||||||
| chr14:52597189 | C | T | 2 | a0004c0004t0001g0041 a0004c0004t0001g0042 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.445-1083C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597189 | |||||||
| chr14:52597321 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.445-951C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597321 | |||||||
| chr14:52597465 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.445-807C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597465 | |||||||
| chr14:52597563 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.445-709G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597563 | |||||||
| chr14:52597681 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.445-591T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597681 | |||||||
| chr14:52597737 | T | G | 2 | a0001c0001t0016g0185 a0001c0001t0025g0186 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.445-535T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597737 | |||||||
| chr14:52597845 | A | T | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
238 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.445-427A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597845 | |||||||
| chr14:52597971 | C | T | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445-301C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52597971 | |||||||
| chr14:52598070 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445-202G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52598070 | |||||||
| chr14:52598170 | A | G | 1 | a0001c0001t0003g0307 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.445-102A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 1/6 | chr14 | 52598170 | |||||||
| chr14:52598387 | T | A | 9 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(6): Show |
11 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+72T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598387 | |||||||
| chr14:52598425 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.488+110C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598425 | |||||||
| chr14:52598454 | A | G | 2 | a0001c0005t0005g0008 a0001c0005t0005g0194 |
3 | HG00738.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.488+139A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598454 | |||||||
| chr14:52598542 | C | A | 1 | a0004c0004t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.488+227C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598542 | |||||||
| chr14:52598762 | C | G | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.488+447C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598762 | |||||||
| chr14:52598767 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.488+452T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598767 | |||||||
| chr14:52598808 | A | T | 2 | a0001c0001t0001g0043 a0004c0004t0001g0023 |
2 | HG02132.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.488+493A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598808 | |||||||
| chr14:52598996 | C | T | 58 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
60 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.488+681C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52598996 | |||||||
| chr14:52599171 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.488+856C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599171 | |||||||
| chr14:52599218 | G | C | 2 | a0001c0001t0001g0218 a0001c0001t0015g0217 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489-895G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599218 | |||||||
| chr14:52599228 | T | A | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.489-885T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599228 | |||||||
| chr14:52599250 | G | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(32): Show |
38 | HG00280.hp1 HG01069.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.489-863G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599250 | |||||||
| chr14:52599317 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.489-796A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599317 | |||||||
| chr14:52599434 | C | CT | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.489-663dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 52599434 | ||||||
| chr14:52599434 | CT | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.489-663delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 52599434 | ||||||
| chr14:52599434 | CTT | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489-664_489-663del others(2): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 52599434 | ||||||
| chr14:52599450 | T | A | 1 | a0004c0004t0001g0248 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.489-663T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599450 | |||||||
| chr14:52599464 | C | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.489-649C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599464 | |||||||
| chr14:52599465 | G | A | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(21): Show |
26 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.489-648G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599465 | |||||||
| chr14:52599500 | C | T | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-613C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599500 | |||||||
| chr14:52599579 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489-534G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599579 | |||||||
| chr14:52599673 | A | T | 2 | a0002c0002t0001g0088 a0002c0002t0001g0113 |
2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.489-440A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599673 | |||||||
| chr14:52599686 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.489-427G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599686 | |||||||
| chr14:52599774 | C | T | 44 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0003g0301 others(41): Show |
44 | HG00438.hp1 HG00621.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.489-339C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599774 | |||||||
| chr14:52599795 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489-318A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599795 | |||||||
| chr14:52599827 | A | T | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.489-286A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599827 | |||||||
| chr14:52599833 | C | A | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02615.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-280C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599833 | |||||||
| chr14:52599881 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.489-232A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 2/6 | chr14 | 52599881 | |||||||
| chr14:52600428 | C | CTATTT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(9): Show |
13 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.717+113_717+117dup others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52600428 | ||||||
| chr14:52600428 | C | CTATTTTA others(3): Show |
1 | a0001c0001t0001g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.717+108_717+117dup others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52600428 | ||||||
| chr14:52600428 | CTATTT | C | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(84): Show |
92 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.717+113_717+117del others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52600428 | ||||||
| chr14:52600617 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.717+276T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52600617 | |||||||
| chr14:52600868 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.717+527A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52600868 | |||||||
| chr14:52600963 | G | A | 240 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(237): Show |
250 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.717+622G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52600963 | |||||||
| chr14:52601005 | G | T | 8 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+664G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601005 | |||||||
| chr14:52601035 | A | G | 1 | a0003c0003t0010g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.717+694A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601035 | |||||||
| chr14:52601042 | A | G | 1 | a0001c0006t0006g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.717+701A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601042 | |||||||
| chr14:52601283 | G | A | 2 | a0001c0001t0014g0237 a0001c0001t0014g0238 |
2 | HG00639.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.717+942G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601283 | |||||||
| chr14:52601439 | T | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.717+1098T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601439 | |||||||
| chr14:52601466 | G | A | 2 | a0001c0006t0006g0192 a0001c0006t0006g0201 |
2 | HG00735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.717+1125G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601466 | |||||||
| chr14:52601478 | A | ATG | 8 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0002t0001g0138 others(5): Show |
8 | HG00609.hp1 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.717+1157_717+1158d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | ||||||
| chr14:52601478 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
11 | HG01074.hp2 HG01346.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.717+1137A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601478 | |||||||
| chr14:52601478 | ATG | A | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.717+1157_717+1158d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | ||||||
| chr14:52601478 | ATGTG | A | 20 | a0001c0001t0001g0193 a0001c0005t0005g0007 a0001c0005t0005g0008 others(17): Show |
24 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.717+1155_717+1158d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | ||||||
| chr14:52601478 | ATGTGTG | A | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.717+1153_717+1158d others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601478 | ||||||
| chr14:52601498 | G | A | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.717+1157G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601498 | |||||||
| chr14:52601498 | G | GTA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0158 others(10): Show |
14 | HG01074.hp2 HG01261.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.717+1168_717+1169d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52601498 | ||||||
| chr14:52601500 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.717+1159A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601500 | |||||||
| chr14:52601509 | T | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.717+1168T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601509 | |||||||
| chr14:52601511 | G | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(41): Show |
46 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.717+1170G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601511 | |||||||
| chr14:52601546 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG01346.hp2 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.717+1205T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601546 | |||||||
| chr14:52601563 | T | C | 1 | a0002c0002t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.717+1222T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601563 | |||||||
| chr14:52601664 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717+1323T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601664 | |||||||
| chr14:52601741 | A | C | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+1400A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601741 | |||||||
| chr14:52601809 | C | G | 2 | a0001c0001t0004g0147 a0001c0001t0004g0153 |
2 | HG02280.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.717+1468C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601809 | |||||||
| chr14:52601811 | A | G | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+1470A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601811 | |||||||
| chr14:52601871 | A | C | 11 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(8): Show |
13 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.717+1530A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52601871 | |||||||
| chr14:52602204 | T | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.717+1863T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602204 | |||||||
| chr14:52602359 | C | T | 2 | a0002c0002t0001g0140 a0002c0002t0001g0142 |
2 | NA18970.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.717+2018C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602359 | |||||||
| chr14:52602366 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+2025A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602366 | |||||||
| chr14:52602625 | G | T | 1 | a0002c0002t0001g0075 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.717+2284G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602625 | |||||||
| chr14:52602729 | A | G | 2 | a0002c0002t0001g0083 a0002c0002t0001g0106 |
2 | NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.717+2388A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602729 | |||||||
| chr14:52602733 | G | A | 12 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(9): Show |
14 | HG00642.hp1 HG00735.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.717+2392G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602733 | |||||||
| chr14:52602774 | T | C | 74 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
77 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.717+2433T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602774 | |||||||
| chr14:52602796 | T | G | 5 | a0001c0001t0001g0080 a0002c0002t0001g0116 a0002c0002t0001g0124 others(2): Show |
5 | HG00323.hp2 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.717+2455T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602796 | |||||||
| chr14:52602946 | A | G | 1 | a0001c0001t0019g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.717+2605A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52602946 | |||||||
| chr14:52603460 | C | T | 1 | a0002c0002t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.717+3119C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603460 | |||||||
| chr14:52603496 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(141): Show |
147 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.717+3155T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603496 | |||||||
| chr14:52603531 | T | C | 1 | a0003c0003t0001g0089 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.717+3190T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603531 | |||||||
| chr14:52603608 | C | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+3267C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603608 | |||||||
| chr14:52603609 | G | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0015g0217 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+3268G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603609 | |||||||
| chr14:52603660 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.717+3319G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603660 | |||||||
| chr14:52603747 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+3406C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603747 | |||||||
| chr14:52603857 | C | T | 1 | a0002c0002t0018g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.717+3516C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603857 | |||||||
| chr14:52603888 | T | A | 1 | a0001c0001t0013g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.717+3547T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52603888 | |||||||
| chr14:52604598 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+4257A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604598 | |||||||
| chr14:52604647 | C | T | 7 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(4): Show |
9 | HG00609.hp1 HG00738.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+4306C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604647 | |||||||
| chr14:52604742 | A | G | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+4401A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604742 | |||||||
| chr14:52604997 | C | T | 321 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(318): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.717+4656C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52604997 | |||||||
| chr14:52605184 | G | A | 317 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(314): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.717+4843G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605184 | |||||||
| chr14:52605226 | TTC | T | 4 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0015g0217 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+4887_717+4888d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52605226 | ||||||
| chr14:52605247 | G | T | 30 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(27): Show |
30 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.717+4906G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605247 | |||||||
| chr14:52605572 | T | A | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+5231T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605572 | |||||||
| chr14:52605610 | T | C | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+5269T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605610 | |||||||
| chr14:52605632 | A | G | 2 | a0002c0002t0001g0287 a0002c0002t0001g0288 |
2 | HG01496.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.717+5291A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605632 | |||||||
| chr14:52605737 | C | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(13): Show |
18 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.717+5396C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52605737 | |||||||
| chr14:52606274 | A | G | 2 | a0001c0001t0001g0209 a0003c0003t0001g0143 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.717+5933A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606274 | |||||||
| chr14:52606332 | G | A | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+5991G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606332 | |||||||
| chr14:52606676 | A | G | 2 | a0001c0001t0002g0187 a0007c0011t0002g0167 |
2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.717+6335A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606676 | |||||||
| chr14:52606685 | A | T | 2 | a0001c0001t0001g0045 a0001c0005t0017g0293 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.717+6344A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606685 | |||||||
| chr14:52606903 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0272 |
2 | NA18965.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.717+6562A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606903 | |||||||
| chr14:52606917 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.717+6576G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52606917 | |||||||
| chr14:52607063 | T | C | 2 | a0001c0001t0014g0237 a0001c0001t0014g0238 |
2 | HG00639.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.717+6722T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607063 | |||||||
| chr14:52607210 | G | A | 311 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(308): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.717+6869G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607210 | |||||||
| chr14:52607421 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+7080A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607421 | |||||||
| chr14:52607695 | CA | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0216 a0001c0001t0001g0245 others(14): Show |
18 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.717+7358delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52607695 | ||||||
| chr14:52607874 | C | CA | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+7546dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52607874 | ||||||
| chr14:52607996 | G | T | 49 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
50 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.717+7655G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52607996 | |||||||
| chr14:52608138 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+7797C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608138 | |||||||
| chr14:52608273 | T | A | 1 | a0001c0005t0005g0196 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.717+7932T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608273 | |||||||
| chr14:52608430 | G | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(148): Show |
157 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.717+8089G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608430 | |||||||
| chr14:52608690 | G | T | 1 | a0001c0007t0008g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.717+8349G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608690 | |||||||
| chr14:52608714 | C | CT | 8 | a0001c0001t0001g0228 a0001c0001t0021g0172 a0003c0003t0010g0285 others(5): Show |
8 | HG01978.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+8384dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52608714 | ||||||
| chr14:52608761 | C | G | 2 | a0003c0003t0010g0285 a0003c0003t0010g0286 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.717+8420C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608761 | |||||||
| chr14:52608878 | G | C | 2 | a0003c0003t0010g0285 a0003c0003t0010g0286 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.717+8537G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608878 | |||||||
| chr14:52608982 | G | A | 2 | a0002c0002t0001g0125 a0002c0002t0018g0081 |
2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.717+8641G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52608982 | |||||||
| chr14:52609336 | A | G | 1 | a0001c0001t0003g0327 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.717+8995A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609336 | |||||||
| chr14:52609673 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+9332C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609673 | |||||||
| chr14:52609674 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.717+9333G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609674 | |||||||
| chr14:52609700 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.717+9359G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609700 | |||||||
| chr14:52609732 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.717+9391G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609732 | |||||||
| chr14:52609743 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0001c0001t0001g0164 others(3): Show |
7 | HG01074.hp2 HG02451.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+9402G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609743 | |||||||
| chr14:52609752 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+9411G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609752 | |||||||
| chr14:52609796 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.717+9455G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609796 | |||||||
| chr14:52609796 | G | T | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.717+9455G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52609796 | |||||||
| chr14:52610018 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+9677A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610018 | |||||||
| chr14:52610029 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717+9688C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610029 | |||||||
| chr14:52610091 | A | G | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+9750A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610091 | |||||||
| chr14:52610094 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+9753C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610094 | |||||||
| chr14:52610276 | C | G | 1 | a0002c0002t0001g0129 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.717+9935C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610276 | |||||||
| chr14:52610385 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+10044G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610385 | |||||||
| chr14:52610406 | C | A | 1 | a0002c0002t0001g0137 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.717+10065C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610406 | |||||||
| chr14:52610425 | G | GAGTAC | 3 | a0003c0003t0011g0282 a0003c0003t0011g0283 a0003c0003t0011g0284 |
3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.717+10091_717+1009 others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52610425 | ||||||
| chr14:52610535 | G | C | 317 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(314): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.717+10194G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610535 | |||||||
| chr14:52610568 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.717+10227G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610568 | |||||||
| chr14:52610603 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.717+10262G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610603 | |||||||
| chr14:52610624 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+10283T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610624 | |||||||
| chr14:52610640 | G | A | 7 | a0002c0002t0001g0086 a0002c0002t0001g0087 a0002c0002t0001g0088 others(4): Show |
7 | HG00323.hp2 HG00642.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+10299G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52610640 | |||||||
| chr14:52611307 | A | G | 1 | a0001c0001t0008g0304 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.717+10966A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611307 | |||||||
| chr14:52611314 | T | C | 1 | a0001c0007t0008g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.717+10973T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611314 | |||||||
| chr14:52611340 | A | G | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+10999A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611340 | |||||||
| chr14:52611354 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.717+11013C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611354 | |||||||
| chr14:52611379 | T | C | 1 | a0004c0004t0001g0022 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.717+11038T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611379 | |||||||
| chr14:52611768 | A | C | 1 | a0004c0004t0001g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.717+11427A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611768 | |||||||
| chr14:52611880 | G | A | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.717+11539G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52611880 | |||||||
| chr14:52612082 | G | C | 3 | a0001c0001t0001g0218 a0001c0001t0015g0217 a0003c0003t0001g0143 |
3 | HG02451.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.717+11741G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612082 | |||||||
| chr14:52612205 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.717+11864G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612205 | |||||||
| chr14:52612321 | A | C | 317 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(314): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.717+11980A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612321 | |||||||
| chr14:52612480 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.717+12139G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612480 | |||||||
| chr14:52612568 | T | C | 1 | a0003c0003t0011g0282 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.717+12227T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612568 | |||||||
| chr14:52612749 | A | C | 1 | a0002c0002t0001g0063 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.717+12408A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612749 | |||||||
| chr14:52612853 | A | C | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.717+12512A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52612853 | |||||||
| chr14:52613105 | G | A | 1 | a0006c0010t0001g0250 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.717+12764G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613105 | |||||||
| chr14:52613234 | G | A | 6 | a0003c0003t0010g0285 a0003c0003t0010g0286 a0003c0003t0011g0282 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+12893G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613234 | |||||||
| chr14:52613246 | CA | C | 8 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0179 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+12922delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52613246 | ||||||
| chr14:52613305 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.717+12964A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613305 | |||||||
| chr14:52613546 | A | G | 1 | a0003c0003t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.717+13205A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613546 | |||||||
| chr14:52613568 | T | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0015g0217 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+13227T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613568 | |||||||
| chr14:52613634 | A | T | 1 | a0007c0011t0002g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.717+13293A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613634 | |||||||
| chr14:52613873 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01167.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.717+13532A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52613873 | |||||||
| chr14:52614006 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.717+13665C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614006 | |||||||
| chr14:52614081 | G | C | 4 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0015g0217 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.717+13740G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614081 | |||||||
| chr14:52614123 | C | CT | 12 | a0001c0001t0001g0158 a0002c0002t0001g0054 a0002c0002t0001g0056 others(9): Show |
12 | HG02109.hp1 HG02257.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+13796dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52614123 | ||||||
| chr14:52614161 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.717+13820C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614161 | |||||||
| chr14:52614198 | G | A | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.717+13857G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614198 | |||||||
| chr14:52614207 | A | T | 3 | a0001c0001t0001g0218 a0001c0001t0015g0217 a0003c0003t0001g0143 |
3 | HG02451.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.717+13866A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614207 | |||||||
| chr14:52614223 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.717+13882C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614223 | |||||||
| chr14:52614260 | G | A | 2 | a0002c0002t0001g0088 a0002c0002t0001g0113 |
2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.717+13919G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614260 | |||||||
| chr14:52614369 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.717+14028C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614369 | |||||||
| chr14:52614487 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0159 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.717+14146T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614487 | |||||||
| chr14:52614561 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.717+14220C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614561 | |||||||
| chr14:52614683 | C | G | 1 | a0001c0001t0003g0319 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.717+14342C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614683 | |||||||
| chr14:52614803 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0015g0217 a0003c0003t0001g0143 |
3 | HG02451.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.717+14462G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614803 | |||||||
| chr14:52614892 | T | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02615.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+14551T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52614892 | |||||||
| chr14:52615087 | G | A | 3 | a0003c0003t0011g0282 a0003c0003t0011g0283 a0003c0003t0011g0284 |
3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.717+14746G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615087 | |||||||
| chr14:52615157 | C | G | 1 | a0004c0004t0001g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.717+14816C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615157 | |||||||
| chr14:52615467 | G | GT | 84 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0014 others(81): Show |
88 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.717+15140dupT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52615467 | ||||||
| chr14:52615467 | G | GTT | 105 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0268 others(102): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.717+15139_717+1514 others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52615467 | ||||||
| chr14:52615774 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+15433G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615774 | |||||||
| chr14:52615833 | T | C | 104 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.717+15492T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615833 | |||||||
| chr14:52615995 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0145 others(13): Show |
17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.717+15654A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52615995 | |||||||
| chr14:52616049 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+15708A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616049 | |||||||
| chr14:52616283 | T | TTTTG | 68 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(65): Show |
70 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.718-15853_718-1585 others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52616283 | ||||||
| chr14:52616458 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.718-15702C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616458 | |||||||
| chr14:52616472 | G | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-15688G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616472 | |||||||
| chr14:52616495 | C | T | 328 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(325): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.718-15665C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616495 | |||||||
| chr14:52616574 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-15586G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616574 | |||||||
| chr14:52616758 | A | G | 2 | a0002c0002t0001g0287 a0002c0002t0001g0288 |
2 | HG01496.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.718-15402A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616758 | |||||||
| chr14:52616806 | A | T | 53 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
54 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.718-15354A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616806 | |||||||
| chr14:52616838 | G | A | 10 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(7): Show |
14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.718-15322G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616838 | |||||||
| chr14:52616939 | A | C | 1 | a0002c0002t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.718-15221A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52616939 | |||||||
| chr14:52617129 | A | G | 1 | a0003c0003t0009g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-15031A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617129 | |||||||
| chr14:52617208 | T | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-14952T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617208 | |||||||
| chr14:52617397 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.718-14763G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617397 | |||||||
| chr14:52617401 | G | A | 2 | a0001c0001t0002g0187 a0007c0011t0002g0167 |
2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.718-14759G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617401 | |||||||
| chr14:52617510 | C | T | 106 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0012 others(103): Show |
110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.718-14650C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617510 | |||||||
| chr14:52617590 | C | A | 248 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.718-14570C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617590 | |||||||
| chr14:52617609 | G | T | 1 | a0001c0001t0002g0178 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.718-14551G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617609 | |||||||
| chr14:52617924 | G | A | 3 | a0001c0001t0010g0161 a0003c0003t0010g0285 a0003c0003t0010g0286 |
3 | HG03453.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.718-14236G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617924 | |||||||
| chr14:52617946 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.718-14214A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617946 | |||||||
| chr14:52617950 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.718-14210C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52617950 | |||||||
| chr14:52618032 | G | A | 1 | a0001c0006t0006g0202 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.718-14128G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618032 | |||||||
| chr14:52618035 | G | A | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-14125G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618035 | |||||||
| chr14:52618035 | G | C | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-14125G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618035 | |||||||
| chr14:52618035 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0280 |
2 | HG02155.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.718-14125G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618035 | |||||||
| chr14:52618124 | A | G | 2 | a0002c0002t0001g0100 a0002c0002t0020g0144 |
2 | HG00738.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.718-14036A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618124 | |||||||
| chr14:52618220 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0145 others(13): Show |
17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.718-13940A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618220 | |||||||
| chr14:52618326 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.718-13834A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618326 | |||||||
| chr14:52618646 | G | A | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-13514G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618646 | |||||||
| chr14:52618681 | C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-13479C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618681 | |||||||
| chr14:52618833 | G | A | 8 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(5): Show |
10 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.718-13327G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52618833 | |||||||
| chr14:52619022 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.718-13138C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52619022 | |||||||
| chr14:52619559 | C | T | 11 | a0001c0001t0001g0222 a0001c0001t0001g0230 a0001c0001t0001g0231 others(8): Show |
11 | HG00408.hp1 NA18747.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.718-12601C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52619559 | |||||||
| chr14:52619725 | T | A | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-12435T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52619725 | |||||||
| chr14:52620054 | G | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.718-12106G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620054 | |||||||
| chr14:52620082 | G | T | 2 | a0002c0002t0012g0050 a0002c0002t0012g0051 |
2 | HG01099.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.718-12078G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620082 | |||||||
| chr14:52620195 | A | G | 107 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0002 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.718-11965A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620195 | |||||||
| chr14:52620262 | TAGA | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0005c0009t0001g0224 |
3 | NA18960.hp2 NA18964.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.718-11891_718-1188 others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52620262 | ||||||
| chr14:52620483 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.718-11677A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620483 | |||||||
| chr14:52620530 | G | A | 184 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0014 others(181): Show |
194 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.718-11630G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620530 | |||||||
| chr14:52620946 | T | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-11214T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620946 | |||||||
| chr14:52620973 | A | G | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-11187A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52620973 | |||||||
| chr14:52621035 | A | G | 14 | a0001c0001t0002g0182 a0001c0001t0002g0183 a0002c0002t0001g0069 others(11): Show |
14 | HG01167.hp1 HG01496.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-11125A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621035 | |||||||
| chr14:52621049 | T | A | 8 | a0001c0001t0010g0161 a0003c0003t0009g0047 a0003c0003t0010g0285 others(5): Show |
8 | HG02622.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-11111T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621049 | |||||||
| chr14:52621351 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.718-10809T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621351 | |||||||
| chr14:52621679 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.718-10481T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621679 | |||||||
| chr14:52621741 | T | C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-10419T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52621741 | |||||||
| chr14:52622602 | A | T | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-9558A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622602 | |||||||
| chr14:52622777 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0145 others(13): Show |
17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.718-9383C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622777 | |||||||
| chr14:52622862 | C | T | 11 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(8): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-9298C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622862 | |||||||
| chr14:52622903 | G | T | 52 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0043 others(49): Show |
53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-9257G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52622903 | |||||||
| chr14:52623036 | T | C | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-9124T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623036 | |||||||
| chr14:52623234 | C | A | 321 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(318): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.718-8926C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623234 | |||||||
| chr14:52623273 | A | T | 1 | a0004c0004t0001g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.718-8887A>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623273 | |||||||
| chr14:52623277 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0015g0217 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-8883T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52623277 | |||||||
| chr14:52623667 | C | CTTCATAA others(6): Show |
319 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(316): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.718-8492_718-8480d others(15): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52623667 | ||||||
| chr14:52623687 | A | ATTTTCAT others(3): Show |
1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-8469_718-8468i others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52623687 | ||||||
| chr14:52623894 | TTCATTA | T | 11 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(8): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-8259_718-8254d others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52623894 | ||||||
| chr14:52624129 | C | T | 1 | a0001c0001t0003g0326 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.718-8031C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624129 | |||||||
| chr14:52624163 | G | A | 2 | a0002c0002t0001g0092 a0002c0002t0001g0120 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.718-7997G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624163 | |||||||
| chr14:52624215 | T | TA | 79 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(76): Show |
85 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.718-7931dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624215 | ||||||
| chr14:52624399 | A | C | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.718-7761A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624399 | |||||||
| chr14:52624428 | A | G | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.718-7732A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624428 | |||||||
| chr14:52624580 | C | G | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-7580C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624580 | |||||||
| chr14:52624580 | CG | C | 107 | a0001c0006t0006g0204 a0002c0002t0001g0001 a0002c0002t0001g0002 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.718-7577delG | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624580 | ||||||
| chr14:52624581 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.718-7579G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624581 | |||||||
| chr14:52624641 | C | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.718-7519C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624641 | |||||||
| chr14:52624700 | C | T | 1 | a0002c0002t0020g0144 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.718-7460C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624700 | |||||||
| chr14:52624711 | C | T | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-7449C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624711 | |||||||
| chr14:52624723 | C | CA | 122 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0027 others(119): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.718-7423dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624723 | ||||||
| chr14:52624723 | CA | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0049 others(8): Show |
13 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.718-7423delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52624723 | ||||||
| chr14:52624739 | T | A | 2 | a0001c0001t0001g0218 a0003c0003t0001g0143 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-7421T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624739 | |||||||
| chr14:52624740 | G | C | 2 | a0001c0001t0001g0218 a0003c0003t0001g0143 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-7420G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624740 | |||||||
| chr14:52624823 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718-7337C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624823 | |||||||
| chr14:52624871 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-7289A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52624871 | |||||||
| chr14:52625211 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.718-6949C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625211 | |||||||
| chr14:52625233 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.718-6927C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625233 | |||||||
| chr14:52625254 | C | T | 1 | a0004c0004t0001g0018 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.718-6906C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625254 | |||||||
| chr14:52625255 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.718-6905G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625255 | |||||||
| chr14:52625317 | A | C | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-6843A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625317 | |||||||
| chr14:52625352 | C | T | 2 | a0004c0004t0001g0191 a0004c0004t0001g0274 |
2 | NA18953.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.718-6808C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625352 | |||||||
| chr14:52625481 | C | CA | 7 | a0001c0001t0001g0227 a0001c0005t0005g0007 a0001c0005t0005g0008 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.718-6665dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625481 | ||||||
| chr14:52625532 | CT | C | 19 | a0001c0006t0006g0201 a0002c0002t0001g0002 a0002c0002t0001g0054 others(16): Show |
21 | HG01071.hp2 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.718-6588delT | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTT | C | 40 | a0001c0001t0001g0243 a0002c0002t0001g0046 a0002c0002t0001g0056 others(37): Show |
40 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.718-6589_718-6588d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTT | C | 23 | a0001c0001t0001g0145 a0002c0002t0001g0001 a0002c0002t0001g0012 others(20): Show |
25 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.718-6590_718-6588d others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTT | C | 11 | a0001c0001t0001g0207 a0001c0001t0001g0279 a0002c0002t0001g0063 others(8): Show |
11 | HG00323.hp1 HG01515.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.718-6591_718-6588d others(6): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTT | C | 12 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0226 others(9): Show |
12 | HG01261.hp1 HG01433.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.718-6592_718-6588d others(7): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTT | C | 37 | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0158 others(34): Show |
37 | HG00099.hp2 HG00621.hp1 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.718-6593_718-6588d others(8): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0162 others(27): Show |
32 | HG00408.hp1 HG00558.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.718-6594_718-6588d others(9): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(1): Show |
C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0016 others(34): Show |
40 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.718-6595_718-6588d others(10): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(10): Show |
13 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.718-6596_718-6588d others(11): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0025g0186 a0001c0005t0007g0296 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.718-6597_718-6588d others(12): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(4): Show |
C | 3 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0297 |
5 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-6598_718-6588d others(13): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(5): Show |
C | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-6599_718-6588d others(14): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0179 others(10): Show |
13 | HG00621.hp2 HG01978.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.718-6602_718-6588d others(17): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(9): Show |
C | 58 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0024 others(55): Show |
60 | HG00280.hp1 HG00438.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.718-6603_718-6588d others(18): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0002g0031 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.718-6604_718-6588d others(19): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0001g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.718-6605_718-6588d others(20): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(15): Show |
C | 3 | a0002c0002t0001g0099 a0002c0002t0001g0128 a0002c0002t0001g0129 |
3 | NA18957.hp1 NA18983.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.718-6609_718-6588d others(24): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625532 | CTTTTTTT others(18): Show |
C | 2 | a0001c0001t0001g0045 a0001c0001t0015g0217 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-6612_718-6588d others(27): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52625532 | ||||||
| chr14:52625573 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.718-6587G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625573 | |||||||
| chr14:52625577 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.718-6583C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625577 | |||||||
| chr14:52625703 | C | T | 1 | a0002c0002t0012g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.718-6457C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625703 | |||||||
| chr14:52625715 | C | T | 1 | a0001c0005t0005g0196 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.718-6445C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625715 | |||||||
| chr14:52625776 | G | A | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-6384G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625776 | |||||||
| chr14:52625806 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0221 others(5): Show |
9 | HG00558.hp1 HG02015.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-6354G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625806 | |||||||
| chr14:52625850 | G | T | 6 | a0001c0001t0010g0161 a0003c0003t0010g0285 a0003c0003t0010g0286 others(3): Show |
6 | HG02717.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-6310G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625850 | |||||||
| chr14:52625950 | C | G | 1 | a0001c0001t0016g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.718-6210C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625950 | |||||||
| chr14:52625977 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718-6183A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625977 | |||||||
| chr14:52625998 | A | G | 1 | a0003c0003t0002g0094 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.718-6162A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52625998 | |||||||
| chr14:52626002 | A | G | 10 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(7): Show |
14 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.718-6158A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626002 | |||||||
| chr14:52626007 | C | T | 11 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(8): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-6153C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626007 | |||||||
| chr14:52626455 | T | TA | 16 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0294 others(13): Show |
20 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.718-5693dupA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52626455 | ||||||
| chr14:52626479 | A | G | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0277 |
3 | HG02071.hp2 NA18962.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.718-5681A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626479 | |||||||
| chr14:52626794 | A | C | 12 | a0001c0001t0025g0186 a0001c0005t0005g0007 a0001c0005t0005g0008 others(9): Show |
16 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.718-5366A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626794 | |||||||
| chr14:52626912 | A | G | 3 | a0001c0001t0004g0150 a0001c0001t0004g0152 a0001c0001t0004g0155 |
3 | HG02976.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.718-5248A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626912 | |||||||
| chr14:52626934 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.718-5226C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52626934 | |||||||
| chr14:52627060 | A | G | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.718-5100A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627060 | |||||||
| chr14:52627096 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.718-5064T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627096 | |||||||
| chr14:52627292 | C | G | 144 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(141): Show |
148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.718-4868C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627292 | |||||||
| chr14:52627324 | T | A | 1 | a0001c0001t0002g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.718-4836T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627324 | |||||||
| chr14:52627391 | T | C | 1 | a0001c0001t0015g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.718-4769T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627391 | |||||||
| chr14:52627507 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0157 others(12): Show |
16 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.718-4653G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627507 | |||||||
| chr14:52627526 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.718-4634C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627526 | |||||||
| chr14:52627569 | C | T | 1 | a0001c0001t0002g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.718-4591C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627569 | |||||||
| chr14:52627575 | G | A | 1 | a0001c0001t0003g0301 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.718-4585G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627575 | |||||||
| chr14:52627592 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.718-4568A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627592 | |||||||
| chr14:52627759 | G | A | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-4401G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627759 | |||||||
| chr14:52627837 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.718-4323C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627837 | |||||||
| chr14:52627877 | G | A | 34 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
34 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.718-4283G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627877 | |||||||
| chr14:52627903 | T | C | 3 | a0003c0003t0011g0282 a0003c0003t0011g0283 a0003c0003t0011g0284 |
3 | HG02717.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.718-4257T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52627903 | |||||||
| chr14:52628003 | A | G | 2 | a0001c0001t0013g0160 a0001c0001t0013g0165 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.718-4157A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628003 | |||||||
| chr14:52628104 | T | C | 72 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0024 others(69): Show |
74 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.718-4056T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628104 | |||||||
| chr14:52628127 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.718-4033A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628127 | |||||||
| chr14:52628139 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-4021G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628139 | |||||||
| chr14:52628141 | G | A | 7 | a0002c0002t0001g0012 a0002c0002t0001g0062 a0002c0002t0001g0063 others(4): Show |
7 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-4019G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628141 | |||||||
| chr14:52628303 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.718-3857T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628303 | |||||||
| chr14:52628472 | G | C | 1 | a0002c0002t0001g0129 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.718-3688G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628472 | |||||||
| chr14:52628489 | A | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0016g0185 |
3 | HG01346.hp2 HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718-3671A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628489 | |||||||
| chr14:52628546 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.718-3614A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628546 | |||||||
| chr14:52628884 | C | T | 6 | a0002c0002t0001g0052 a0002c0002t0001g0119 a0002c0002t0001g0121 others(3): Show |
6 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.718-3276C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628884 | |||||||
| chr14:52628887 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.718-3273A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628887 | |||||||
| chr14:52628899 | A | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-3261A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628899 | |||||||
| chr14:52628977 | G | T | 1 | a0001c0001t0003g0314 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.718-3183G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628977 | |||||||
| chr14:52628988 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.718-3172A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52628988 | |||||||
| chr14:52629009 | C | T | 1 | a0003c0003t0009g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-3151C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629009 | |||||||
| chr14:52629367 | C | T | 1 | a0003c0003t0009g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-2793C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629367 | |||||||
| chr14:52629580 | A | G | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-2580A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629580 | |||||||
| chr14:52629603 | A | G | 12 | a0001c0001t0025g0186 a0001c0005t0005g0007 a0001c0005t0005g0008 others(9): Show |
16 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.718-2557A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629603 | |||||||
| chr14:52629632 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.718-2528A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629632 | |||||||
| chr14:52629703 | T | C | 1 | a0001c0001t0003g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.718-2457T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629703 | |||||||
| chr14:52629817 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0159 others(8): Show |
12 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.718-2343C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629817 | |||||||
| chr14:52629853 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0015g0217 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.718-2307A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629853 | |||||||
| chr14:52629887 | G | A | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-2273G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629887 | |||||||
| chr14:52629939 | G | A | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-2221G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629939 | |||||||
| chr14:52629950 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.718-2210C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52629950 | |||||||
| chr14:52630054 | C | T | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.718-2106C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630054 | |||||||
| chr14:52630125 | G | A | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-2035G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630125 | |||||||
| chr14:52630189 | C | T | 1 | a0001c0005t0005g0197 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.718-1971C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630189 | |||||||
| chr14:52630200 | C | A | 11 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(8): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-1960C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630200 | |||||||
| chr14:52630446 | C | CTT | 11 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(8): Show |
15 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.718-1711_718-1710d others(4): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52630446 | ||||||
| chr14:52630453 | T | TAAC | 28 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0145 others(25): Show |
33 | HG00738.hp2 HG01074.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.718-1706_718-1704d others(5): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52630453 | ||||||
| chr14:52630491 | G | T | 107 | a0001c0001t0001g0278 a0002c0002t0001g0001 a0002c0002t0001g0002 others(104): Show |
111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.718-1669G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630491 | |||||||
| chr14:52630694 | ACCCCGCA others(4): Show |
A | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-1455_718-1445d others(13): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52630694 | ||||||
| chr14:52630709 | C | T | 7 | a0002c0002t0001g0069 a0002c0002t0001g0099 a0004c0004t0001g0013 others(4): Show |
7 | HG01496.hp1 HG01993.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-1451C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630709 | |||||||
| chr14:52630888 | A | G | 2 | a0001c0001t0001g0218 a0003c0003t0001g0143 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-1272A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630888 | |||||||
| chr14:52630994 | G | A | 104 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.718-1166G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52630994 | |||||||
| chr14:52631090 | A | G | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG01261.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-1070A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631090 | |||||||
| chr14:52631091 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0162 a0003c0003t0001g0103 others(1): Show |
5 | HG01074.hp2 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-1069T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631091 | |||||||
| chr14:52631142 | G | A | 9 | a0002c0002t0001g0053 a0002c0002t0001g0054 a0002c0002t0001g0055 others(6): Show |
9 | HG02080.hp2 NA18747.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-1018G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631142 | |||||||
| chr14:52631305 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718-855C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631305 | |||||||
| chr14:52631339 | C | G | 1 | a0001c0001t0009g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.718-821C>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631339 | |||||||
| chr14:52631394 | A | G | 1 | a0001c0001t0009g0163 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.718-766A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631394 | |||||||
| chr14:52631438 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0016g0185 |
3 | HG01346.hp2 HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718-722C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631438 | |||||||
| chr14:52631828 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.718-332G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631828 | |||||||
| chr14:52631854 | C | T | 2 | a0001c0001t0003g0326 a0001c0001t0003g0329 |
2 | NA18991.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.718-306C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52631854 | |||||||
| chr14:52631953 | CA | C | 148 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(145): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.718-191delA | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52631953 | ||||||
| chr14:52631953 | CAA | C | 8 | a0001c0001t0010g0161 a0002c0002t0001g0062 a0002c0002t0001g0064 others(5): Show |
8 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-192_718-191del others(2): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 52631953 | ||||||
| chr14:52632069 | A | C | 1 | a0001c0001t0025g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.718-91A>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52632069 | |||||||
| chr14:52632111 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0016g0185 |
3 | HG01346.hp2 HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718-49C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 3/6 | chr14 | 52632111 | |||||||
| chr14:52632350 | ATTAAC | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0235 a0001c0001t0001g0239 |
3 | NA18971.hp2 NA19005.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.867+45_867+49delAC others(3): Show |
GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 52632350 | ||||||
| chr14:52632390 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0008g0310 |
3 | HG00438.hp2 NA18947.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.867+81C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632390 | |||||||
| chr14:52632532 | T | G | 1 | a0001c0005t0017g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.867+223T>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632532 | |||||||
| chr14:52632541 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.867+232T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632541 | |||||||
| chr14:52632575 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0145 others(13): Show |
17 | HG01074.hp2 HG01346.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.867+266T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632575 | |||||||
| chr14:52632577 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.867+268A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632577 | |||||||
| chr14:52632760 | G | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | NA18942.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.867+451G>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632760 | |||||||
| chr14:52632821 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0019g0038 |
2 | NA18980.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.867+512A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632821 | |||||||
| chr14:52632946 | T | A | 4 | a0001c0005t0007g0003 a0001c0005t0007g0295 a0001c0005t0007g0296 others(1): Show |
6 | HG02615.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.868-584T>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632946 | |||||||
| chr14:52632955 | C | T | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.868-575C>T | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52632955 | |||||||
| chr14:52633116 | G | A | 1 | a0001c0001t0013g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.868-414G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52633116 | |||||||
| chr14:52633234 | T | C | 6 | a0001c0005t0005g0007 a0001c0005t0005g0008 a0001c0005t0005g0194 others(3): Show |
8 | HG00738.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.868-296T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 4/6 | chr14 | 52633234 | |||||||
| chr14:52634042 | A | G | 172 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(169): Show |
181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1112+96A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634042 | |||||||
| chr14:52634106 | A | G | 2 | a0001c0001t0001g0218 a0003c0003t0001g0143 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1112+160A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634106 | |||||||
| chr14:52634152 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1112+206A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634152 | |||||||
| chr14:52634212 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0040 others(7): Show |
10 | HG00423.hp2 HG00609.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.1112+266G>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634212 | |||||||
| chr14:52634531 | C | A | 1 | a0001c0001t0002g0187 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113-407C>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634531 | |||||||
| chr14:52634834 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1113-104T>C | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634834 | |||||||
| chr14:52634863 | A | G | 3 | a0002c0002t0012g0050 a0002c0002t0012g0051 a0002c0002t0012g0109 |
3 | HG01099.hp2 HG01258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1113-75A>G | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634863 | |||||||
| chr14:52634904 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1113-34G>A | GPR137C | ENSG00000180998.12 | transcript | ENST00000321662.11 | protein_coding | 6/6 | chr14 | 52634904 |