Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7107 |
| ensemblid | ENSG00000077585.14 |
| hgncid | 11862 |
| symbol | GPR137B |
| name | G protein-coupled receptor 137B |
| refseq_nuc | NM_003272.4 |
| refseq_prot | NP_003263.1 |
| ensembl_nuc | ENST00000366592.8 |
| ensembl_prot | ENSP00000355551.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 236142539 |
| end | 236208907 |
| strand | + |
| ver | v1.2 |
| region | chr1:236142539-236208907 |
| region5000 | chr1:236137539-236213907 |
| regionname0 | GPR137B_chr1_236142539_236208907 |
| regionname5000 | GPR137B_chr1_236137539_236213907 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 383 | 91 | 69 | 171 | 10 | 40 | 131 | GPR137B_chr1_236137539_236213907 | GPR137B | MRPER others(394): Show |
chr1 | 236137539 | 236213907 |
| a0002 | 0/0 | 200 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | MRPER others(195): Show |
chr1 | 236137539 | 236213907 |
| a0003 | 0/0 | 399 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | MRPER others(394): Show |
chr1 | 236137539 | 236213907 |
| a0004 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | MRPER others(394): Show |
chr1 | 236137539 | 236213907 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 373 | 86 | 67 | 169 | 9 | 40 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 | ||
| a0001c0002 | 0/0 | 1197 | 7 | 5 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 | ||
| a0001c0006 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 | ||
| a0001c0007 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 | ||
| a0001c0008 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 | ||
| a0002c0003 | 0/0 | 1207 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1202): Show |
chr1 | 236137539 | 236213907 | ||
| a0003c0004 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 | ||
| a0004c0005 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | ATGAG others(1192): Show |
chr1 | 236137539 | 236213907 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2033 | 188 | 38 | 41 | 83 | 3 | 21 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0002 | 0/0 | 2034 | 93 | 30 | 14 | 43 | 0 | 6 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0003 | 0/0 | 2033 | 56 | 1 | 8 | 32 | 3 | 12 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0004 | 0/0 | 2034 | 10 | 7 | 1 | 0 | 2 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0005 | 0/0 | 2033 | 8 | 0 | 0 | 8 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0006 | 0/0 | 2034 | 5 | 3 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0007 | 0/0 | 2034 | 6 | 5 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0008 | 0/0 | 2032 | 2 | 0 | 0 | 1 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2027): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0009 | 0/0 | 2034 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0010 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0011 | 0/0 | 2032 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2027): Show |
chr1 | 236137539 | 236213907 |
| a0001c0001t0012 | 0/0 | 2033 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0002t0001 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0002t0002 | 0/0 | 2034 | 5 | 3 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0002t0006 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2029): Show |
chr1 | 236137539 | 236213907 |
| a0001c0006t0001 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0007t0001 | 0/0 | 2033 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0001c0008t0001 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0002c0003t0001 | 0/0 | 2043 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2038): Show |
chr1 | 236137539 | 236213907 |
| a0003c0004t0001 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| a0004c0005t0001 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | GTTTT others(2028): Show |
chr1 | 236137539 | 236213907 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0009g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0011g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0006t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0001c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0003c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| a0004c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0012 | g0257 | EUR | GBR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0235 | EUR | FIN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00280 | hp2 | a0001 | c0007 | t0001 | g0003 | EUR | FIN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0269 | EUR | FIN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00544 | hp1 | a0001 | c0006 | t0001 | g0322 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0272 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0291 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0320 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0254 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0371 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0161 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0240 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0365 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0370 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0019 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0309 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0296 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0144 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0344 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0289 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0358 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0136 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0363 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0359 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0355 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0348 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0354 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0288 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0307 | SAS | STU | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | YRI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | CHB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | CHB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | CHB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18950 | hp1 | a0001 | c0008 | t0001 | g0099 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18986 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18992 | hp2 | a0004 | c0005 | t0001 | g0113 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | LWK | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19078 | hp1 | a0001 | c0001 | t0011 | g0364 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | YRI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | ASW | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | ASW | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0297 | EUR | TSI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0295 | EUR | TSI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0306 | EUR | TSI | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0250 | SAS | GIH | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0369 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0366 | AMR | CLM | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | ACB | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | USA | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | USA | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0190 | REF | REF | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | GPR137B_chr1_236137539_236213907 | GPR137B | chr1 | 236137539 | 236213907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236178488 | T | TAAAGACG others(3): Show |
1 | a0002 | 1 | HG01192.hp2 | frameshift_variant | HIGH | c.542_551dupAGACGGGA others(2): Show |
p.Asn184fs | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/7 | 636/2033 | 552/1200 | 184/399 | INFO_REALIGN_3_PRIME | chr1 | 236178488 | ||
| chr1:236205210 | G | A | 1 | a0003 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1051G>A | p.Asp351Asn | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/7 | 1135/2033 | 1051/1200 | 351/399 | chr1 | 236205210 | |||
| chr1:236208130 | T | C | 1 | a0004 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.1172T>C | p.Leu391Ser | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 1256/2033 | 1172/1200 | 391/399 | chr1 | 236208130 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236142760 | C | T | 1 | a0001c0002 | 7 | HG01106.hp2 HG01169.hp2 HG02647.hp1 others(4): Show |
synonymous_variant | LOW | c.138C>T | p.Thr46Thr | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/7 | 222/2033 | 138/1200 | 46/399 | chr1 | 236142760 | |||
| chr1:236142784 | G | T | 1 | a0001c0008 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.162G>T | p.Ala54Ala | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/7 | 246/2033 | 162/1200 | 54/399 | chr1 | 236142784 | |||
| chr1:236142874 | C | T | 1 | a0001c0007 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.252C>T | p.Leu84Leu | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/7 | 336/2033 | 252/1200 | 84/399 | chr1 | 236142874 | |||
| chr1:236183813 | C | T | 1 | a0001c0006 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.873C>T | p.Tyr291Tyr | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/7 | 957/2033 | 873/1200 | 291/399 | chr1 | 236183813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236142562 | G | T | 1 | a0001c0001t0005 | 8 | NA18973.hp1 NA18979.hp2 NA18987.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-61G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/7 | 61 | chr1 | 236142562 | ||||||
| chr1:236142585 | G | A | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(1): Show |
68 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(65): Show |
5_prime_UTR_variant | MODIFIER | c.-38G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/7 | 38 | chr1 | 236142585 | ||||||
| chr1:236208286 | A | G | 1 | a0001c0001t0009 | 2 | HG02976.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*128A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 128 | chr1 | 236208286 | ||||||
| chr1:236208319 | G | C | 1 | a0001c0001t0012 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 161 | chr1 | 236208319 | ||||||
| chr1:236208393 | A | T | 2 | a0001c0001t0008 a0001c0001t0011 |
3 | HG03831.hp1 NA18986.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*235A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 235 | chr1 | 236208393 | ||||||
| chr1:236208455 | G | GT | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(5): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*306dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 307 | INFO_REALIGN_3_PRIME | chr1 | 236208455 | |||||
| chr1:236208531 | T | C | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(3): Show |
116 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*373T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 373 | chr1 | 236208531 | ||||||
| chr1:236208726 | AG | A | 2 | a0001c0001t0008 a0001c0001t0011 |
3 | HG03831.hp1 NA18986.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*570delG | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 570 | INFO_REALIGN_3_PRIME | chr1 | 236208726 | |||||
| chr1:236208892 | C | G | 2 | a0001c0001t0006 a0001c0002t0006 |
6 | HG00735.hp2 HG01099.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*734C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 7/7 | 734 | chr1 | 236208892 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:236143235 | A | C | 151 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(148): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.414+199A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236143235 | |||||||
| chr1:236143525 | A | G | 231 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(228): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.414+489A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236143525 | |||||||
| chr1:236143563 | G | A | 1 | a0001c0001t0005g0016 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.414+527G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236143563 | |||||||
| chr1:236143632 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(11): Show |
15 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.414+596C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236143632 | |||||||
| chr1:236143661 | G | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0138 others(90): Show |
99 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.414+625G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236143661 | |||||||
| chr1:236143994 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.414+958G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236143994 | |||||||
| chr1:236144060 | G | T | 152 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(149): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.414+1024G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236144060 | |||||||
| chr1:236144086 | C | CT | 34 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0115 others(31): Show |
34 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.414+1065dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236144086 | ||||||
| chr1:236144086 | CT | C | 223 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(220): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.414+1065delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236144086 | ||||||
| chr1:236144086 | CTT | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(15): Show |
19 | HG00544.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.414+1064_414+1065d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236144086 | ||||||
| chr1:236144304 | A | G | 6 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+1268A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236144304 | |||||||
| chr1:236144365 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
7 | HG02109.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+1329G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236144365 | |||||||
| chr1:236144409 | CAAAAA | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0152 others(70): Show |
78 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+1376_414+1380d others(7): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236144409 | ||||||
| chr1:236144498 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0149 others(2): Show |
6 | HG01884.hp2 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+1462A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236144498 | |||||||
| chr1:236144566 | T | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
7 | HG02109.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+1530T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236144566 | |||||||
| chr1:236144634 | C | A | 2 | a0001c0001t0003g0229 a0001c0001t0003g0230 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.414+1598C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236144634 | |||||||
| chr1:236145243 | T | A | 297 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(294): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.414+2207T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145243 | |||||||
| chr1:236145267 | C | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0110 others(29): Show |
32 | HG01099.hp2 HG01109.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.414+2231C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145267 | |||||||
| chr1:236145338 | C | G | 1 | a0001c0001t0008g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.414+2302C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145338 | |||||||
| chr1:236145356 | A | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01099.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+2320A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145356 | |||||||
| chr1:236145375 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+2339G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145375 | |||||||
| chr1:236145376 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+2340G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145376 | |||||||
| chr1:236145377 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+2341C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145377 | |||||||
| chr1:236145379 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+2343G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145379 | |||||||
| chr1:236145414 | A | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
7 | HG02109.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+2378A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145414 | |||||||
| chr1:236145639 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.414+2603G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145639 | |||||||
| chr1:236145647 | G | A | 7 | a0001c0001t0001g0159 a0001c0001t0002g0157 a0001c0001t0002g0158 others(4): Show |
7 | HG00558.hp2 HG00621.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+2611G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145647 | |||||||
| chr1:236145723 | G | GT | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0218 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+2688dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236145723 | ||||||
| chr1:236145758 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414+2722C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145758 | |||||||
| chr1:236145866 | A | T | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0323 others(49): Show |
54 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.414+2830A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145866 | |||||||
| chr1:236145872 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0037 others(88): Show |
97 | HG00438.hp2 HG00733.hp2 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.414+2836T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145872 | |||||||
| chr1:236145946 | C | T | 4 | a0001c0001t0003g0319 a0001c0001t0003g0320 a0001c0001t0004g0318 others(1): Show |
4 | HG01106.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+2910C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236145946 | |||||||
| chr1:236146098 | T | C | 3 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0006g0019 |
3 | HG01169.hp2 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.414+3062T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146098 | |||||||
| chr1:236146145 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.414+3109A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146145 | |||||||
| chr1:236146149 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0037 others(88): Show |
97 | HG00438.hp2 HG00733.hp2 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.414+3113C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146149 | |||||||
| chr1:236146207 | C | T | 2 | a0001c0001t0003g0229 a0001c0001t0003g0230 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.414+3171C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146207 | |||||||
| chr1:236146217 | T | A | 285 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(282): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.414+3181T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146217 | |||||||
| chr1:236146221 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
7 | HG02109.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+3185G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146221 | |||||||
| chr1:236146245 | C | G | 10 | a0001c0001t0001g0043 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | NA18941.hp2 NA18942.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+3209C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146245 | |||||||
| chr1:236146296 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0002g0022 |
2 | HG00741.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.414+3260T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146296 | |||||||
| chr1:236146334 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0037 others(87): Show |
96 | HG00438.hp2 HG00733.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.414+3298G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146334 | |||||||
| chr1:236146503 | C | T | 9 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(6): Show |
9 | HG01243.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+3467C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146503 | |||||||
| chr1:236146504 | A | G | 249 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(246): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.414+3468A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146504 | |||||||
| chr1:236146544 | G | C | 8 | a0001c0001t0002g0040 a0001c0002t0001g0023 a0001c0002t0002g0018 others(5): Show |
8 | HG01106.hp2 HG01169.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+3508G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146544 | |||||||
| chr1:236146589 | G | T | 5 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0312 others(2): Show |
5 | HG01978.hp2 HG02273.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+3553G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146589 | |||||||
| chr1:236146618 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.414+3582C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146618 | |||||||
| chr1:236146724 | A | C | 249 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(246): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.414+3688A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146724 | |||||||
| chr1:236146744 | A | T | 7 | a0001c0002t0001g0023 a0001c0002t0002g0018 a0001c0002t0002g0020 others(4): Show |
7 | HG01106.hp2 HG01169.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+3708A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146744 | |||||||
| chr1:236146818 | C | T | 1 | a0001c0001t0007g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.414+3782C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146818 | |||||||
| chr1:236146860 | C | T | 1 | a0001c0001t0005g0070 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.414+3824C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236146860 | |||||||
| chr1:236147060 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.414+4024C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147060 | |||||||
| chr1:236147132 | C | T | 48 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0072 others(45): Show |
48 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.414+4096C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147132 | |||||||
| chr1:236147269 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.414+4233T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147269 | |||||||
| chr1:236147272 | C | T | 6 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+4236C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147272 | |||||||
| chr1:236147285 | G | C | 45 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0072 others(42): Show |
45 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.414+4249G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147285 | |||||||
| chr1:236147313 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.414+4277C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147313 | |||||||
| chr1:236147529 | G | A | 24 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0111 others(21): Show |
24 | HG01099.hp2 HG02040.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.414+4493G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147529 | |||||||
| chr1:236147562 | C | T | 2 | a0001c0001t0003g0313 a0001c0001t0003g0314 |
2 | NA19076.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.414+4526C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147562 | |||||||
| chr1:236147563 | A | G | 6 | a0001c0001t0001g0211 a0001c0001t0002g0207 a0001c0001t0002g0208 others(3): Show |
7 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+4527A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147563 | |||||||
| chr1:236147821 | G | A | 3 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0006g0019 |
3 | HG01169.hp2 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.414+4785G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147821 | |||||||
| chr1:236147881 | G | C | 8 | a0001c0001t0001g0160 a0001c0001t0001g0215 a0001c0001t0001g0216 others(5): Show |
8 | HG01981.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+4845G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147881 | |||||||
| chr1:236147927 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0149 others(2): Show |
6 | HG01884.hp2 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+4891G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236147927 | |||||||
| chr1:236148181 | G | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.414+5145G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148181 | |||||||
| chr1:236148261 | C | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0218 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+5225C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148261 | |||||||
| chr1:236148272 | C | A | 1 | a0001c0001t0003g0231 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.414+5236C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148272 | |||||||
| chr1:236148327 | G | A | 44 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0072 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.414+5291G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148327 | |||||||
| chr1:236148341 | C | T | 1 | a0001c0001t0003g0013 | 2 | HG00673.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.414+5305C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148341 | |||||||
| chr1:236148344 | G | A | 2 | a0001c0001t0004g0235 a0001c0001t0004g0236 |
2 | HG00280.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.414+5308G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148344 | |||||||
| chr1:236148398 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.414+5362C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148398 | |||||||
| chr1:236148586 | T | C | 338 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.414+5550T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148586 | |||||||
| chr1:236148629 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.414+5593G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148629 | |||||||
| chr1:236148692 | G | T | 3 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0006g0019 |
3 | HG01169.hp2 HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.414+5656G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148692 | |||||||
| chr1:236148693 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0002g0120 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.414+5657G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148693 | |||||||
| chr1:236148768 | A | G | 1 | a0001c0001t0011g0364 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.414+5732A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148768 | |||||||
| chr1:236148773 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0027 others(97): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.414+5737C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148773 | |||||||
| chr1:236148886 | C | T | 6 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+5850C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148886 | |||||||
| chr1:236148981 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.414+5945C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236148981 | |||||||
| chr1:236149026 | C | T | 268 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(265): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.414+5990C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149026 | |||||||
| chr1:236149032 | C | T | 6 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0002g0024 others(3): Show |
6 | HG01106.hp2 HG01169.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+5996C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149032 | |||||||
| chr1:236149224 | G | A | 8 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+6188G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149224 | |||||||
| chr1:236149255 | C | CTA | 209 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.414+6219_414+6220i others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149255 | |||||||
| chr1:236149277 | G | GA | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0140 |
3 | HG01243.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.414+6243dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236149277 | ||||||
| chr1:236149471 | G | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0111 others(15): Show |
18 | HG00544.hp1 HG02056.hp2 HG03831.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+6435G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149471 | |||||||
| chr1:236149578 | C | T | 148 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.414+6542C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149578 | |||||||
| chr1:236149616 | C | T | 1 | a0001c0001t0008g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.414+6580C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149616 | |||||||
| chr1:236149756 | C | T | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.414+6720C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149756 | |||||||
| chr1:236149781 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.414+6745C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149781 | |||||||
| chr1:236149827 | T | C | 69 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(66): Show |
70 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.414+6791T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149827 | |||||||
| chr1:236149924 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.414+6888G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149924 | |||||||
| chr1:236149929 | C | T | 21 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0131 others(18): Show |
22 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.414+6893C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236149929 | |||||||
| chr1:236149972 | C | CTG | 6 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0149 others(3): Show |
7 | HG01884.hp2 HG02055.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+6947_414+6948d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236149972 | ||||||
| chr1:236150015 | CTGTGTGT others(9): Show |
C | 2 | a0001c0001t0001g0119 a0001c0001t0002g0120 |
2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.414+6989_414+7004d others(18): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236150015 | ||||||
| chr1:236150023 | G | A | 1 | a0001c0002t0002g0020 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.414+6987G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150023 | |||||||
| chr1:236150027 | C | CTG | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0005g0016 |
3 | HG02647.hp2 HG02922.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.414+7004_414+7005d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236150027 | ||||||
| chr1:236150081 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG01433.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.414+7045G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150081 | |||||||
| chr1:236150173 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0104 others(68): Show |
76 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.414+7137G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150173 | |||||||
| chr1:236150193 | G | A | 338 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.414+7157G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150193 | |||||||
| chr1:236150218 | T | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.414+7182T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150218 | |||||||
| chr1:236150374 | G | T | 2 | a0001c0001t0004g0235 a0001c0001t0004g0236 |
2 | HG00280.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.414+7338G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150374 | |||||||
| chr1:236150380 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.414+7344C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150380 | |||||||
| chr1:236150401 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.414+7365G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150401 | |||||||
| chr1:236150517 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+7481T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150517 | |||||||
| chr1:236150625 | T | A | 1 | a0001c0001t0003g0313 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.414+7589T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150625 | |||||||
| chr1:236150664 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0006g0217 |
3 | HG02723.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.414+7628C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150664 | |||||||
| chr1:236150719 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | NA18964.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.414+7683G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150719 | |||||||
| chr1:236150815 | G | A | 1 | a0001c0001t0003g0013 | 2 | HG00673.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.414+7779G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150815 | |||||||
| chr1:236150862 | C | T | 1 | a0001c0001t0003g0312 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.414+7826C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150862 | |||||||
| chr1:236150864 | C | T | 3 | a0001c0001t0001g0328 a0001c0001t0001g0362 a0001c0001t0002g0361 |
3 | HG00597.hp2 NA18986.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.414+7828C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150864 | |||||||
| chr1:236150962 | C | T | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+7926C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236150962 | |||||||
| chr1:236151286 | C | T | 367 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(364): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.414+8250C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151286 | |||||||
| chr1:236151336 | C | T | 1 | a0001c0001t0003g0248 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.414+8300C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151336 | |||||||
| chr1:236151416 | T | TC | 38 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0079 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.414+8381dupC | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236151416 | ||||||
| chr1:236151417 | C | CCT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
7 | NA18961.hp2 NA18994.hp1 NA19066.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+8381_414+8382i others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151417 | |||||||
| chr1:236151417 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0128 others(61): Show |
69 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.414+8382delA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151417 | |||||||
| chr1:236151417 | CAT | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0041 others(72): Show |
77 | HG00597.hp1 HG01099.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.414+8382_414+8383d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151417 | |||||||
| chr1:236151417 | CATT | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0002g0108 |
3 | HG01243.hp2 HG02818.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.414+8382_414+8384d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151417 | |||||||
| chr1:236151418 | A | AT | 16 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0001t0001g0200 others(13): Show |
16 | HG00597.hp2 HG00621.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+8406dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236151418 | ||||||
| chr1:236151418 | A | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0156 others(3): Show |
6 | HG03041.hp2 NA18747.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+8382A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151418 | |||||||
| chr1:236151418 | A | T | 47 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0072 others(44): Show |
47 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.414+8382A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151418 | |||||||
| chr1:236151418 | AT | A | 25 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(22): Show |
27 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.414+8406delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236151418 | ||||||
| chr1:236151419 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0128 others(61): Show |
69 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.414+8383T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151419 | |||||||
| chr1:236151420 | T | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0041 others(72): Show |
77 | HG00597.hp1 HG01099.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.414+8384T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151420 | |||||||
| chr1:236151421 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0002g0108 |
3 | HG01243.hp2 HG02818.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.414+8385T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151421 | |||||||
| chr1:236151442 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+8406T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151442 | |||||||
| chr1:236151443 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+8407G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151443 | |||||||
| chr1:236151444 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+8408A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151444 | |||||||
| chr1:236151492 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.414+8456C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151492 | |||||||
| chr1:236151572 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+8536C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151572 | |||||||
| chr1:236151605 | G | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0211 a0001c0001t0002g0064 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+8569G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151605 | |||||||
| chr1:236151636 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.414+8600A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151636 | |||||||
| chr1:236151770 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
135 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.414+8734G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151770 | |||||||
| chr1:236151803 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.414+8767A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236151803 | |||||||
| chr1:236152075 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+9039C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152075 | |||||||
| chr1:236152077 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0104 others(62): Show |
70 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.414+9041C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152077 | |||||||
| chr1:236152113 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG03041.hp2 HG03579.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+9077A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152113 | |||||||
| chr1:236152125 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.414+9089C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152125 | |||||||
| chr1:236152191 | G | C | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+9155G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152191 | |||||||
| chr1:236152210 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.414+9174C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152210 | |||||||
| chr1:236152216 | C | CT | 6 | a0001c0001t0001g0119 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+9183dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236152216 | ||||||
| chr1:236152439 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.414+9403G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152439 | |||||||
| chr1:236152469 | G | A | 5 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0002g0163 others(2): Show |
5 | HG02647.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+9433G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152469 | |||||||
| chr1:236152528 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0002g0171 |
2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.414+9492C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152528 | |||||||
| chr1:236152575 | G | A | 35 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(32): Show |
35 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.414+9539G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152575 | |||||||
| chr1:236152826 | G | C | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+9790G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152826 | |||||||
| chr1:236152883 | C | T | 15 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(12): Show |
16 | HG01099.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+9847C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152883 | |||||||
| chr1:236152924 | C | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+9888C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152924 | |||||||
| chr1:236152987 | C | T | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+9951C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236152987 | |||||||
| chr1:236153055 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0002g0028 |
2 | HG00673.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.414+10019C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153055 | |||||||
| chr1:236153059 | G | GA | 37 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0072 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+10036dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236153059 | ||||||
| chr1:236153060 | A | G | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+10024A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153060 | |||||||
| chr1:236153098 | C | A | 3 | a0001c0001t0001g0160 a0001c0001t0007g0161 a0001c0002t0002g0020 |
3 | HG01169.hp2 HG01981.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.414+10062C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153098 | |||||||
| chr1:236153175 | G | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+10139G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153175 | |||||||
| chr1:236153275 | A | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
145 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.414+10239A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153275 | |||||||
| chr1:236153321 | C | A | 1 | a0001c0001t0002g0331 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.414+10285C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153321 | |||||||
| chr1:236153554 | C | T | 1 | a0001c0001t0003g0311 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.414+10518C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153554 | |||||||
| chr1:236153710 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.414+10674C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153710 | |||||||
| chr1:236153741 | A | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+10705A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236153741 | |||||||
| chr1:236154236 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0109 |
2 | HG02080.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.414+11200C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154236 | |||||||
| chr1:236154260 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414+11224T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154260 | |||||||
| chr1:236154293 | C | CT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
204 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.414+11257_414+1125 others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154293 | |||||||
| chr1:236154299 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.414+11263G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154299 | |||||||
| chr1:236154375 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414+11339T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154375 | |||||||
| chr1:236154405 | G | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.414+11369G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154405 | |||||||
| chr1:236154435 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0104 others(65): Show |
74 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.414+11399C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154435 | |||||||
| chr1:236154739 | G | A | 1 | a0001c0001t0012g0257 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.414+11703G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154739 | |||||||
| chr1:236154781 | T | A | 1 | a0001c0001t0003g0312 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.414+11745T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154781 | |||||||
| chr1:236154817 | C | T | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0003g0301 |
3 | NA18946.hp1 NA18980.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.414+11781C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154817 | |||||||
| chr1:236154881 | G | A | 1 | a0001c0001t0003g0250 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.414+11845G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154881 | |||||||
| chr1:236154926 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.414+11890G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154926 | |||||||
| chr1:236154930 | A | G | 1 | a0001c0001t0001g0357 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.414+11894A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154930 | |||||||
| chr1:236154950 | G | T | 1 | a0001c0001t0002g0036 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.414+11914G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236154950 | |||||||
| chr1:236155050 | C | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+12014C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155050 | |||||||
| chr1:236155115 | C | CG | 11 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.414+12081dupG | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236155115 | ||||||
| chr1:236155561 | C | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+12525C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155561 | |||||||
| chr1:236155648 | C | T | 44 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(41): Show |
45 | HG00597.hp1 HG01891.hp1 HG02040.hp2 others(42): Show |
intron_variant | MODIFIER | c.414+12612C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155648 | |||||||
| chr1:236155673 | A | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG01099.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+12637A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155673 | |||||||
| chr1:236155843 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.414+12807T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155843 | |||||||
| chr1:236155940 | C | T | 2 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
2 | HG00621.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.415-12766C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155940 | |||||||
| chr1:236155942 | T | C | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.415-12764T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155942 | |||||||
| chr1:236155980 | C | T | 1 | a0001c0001t0012g0257 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.415-12726C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155980 | |||||||
| chr1:236155984 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415-12722C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236155984 | |||||||
| chr1:236156074 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0065 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.415-12632T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156074 | |||||||
| chr1:236156088 | A | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 others(7): Show |
10 | HG02647.hp2 HG02717.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-12618A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156088 | |||||||
| chr1:236156212 | C | T | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0026 |
3 | HG01106.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-12494C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156212 | |||||||
| chr1:236156276 | C | T | 5 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0002g0192 others(2): Show |
5 | HG00738.hp1 HG01346.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-12430C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156276 | |||||||
| chr1:236156277 | G | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0132 others(5): Show |
8 | HG00741.hp1 HG01099.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-12429G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156277 | |||||||
| chr1:236156309 | C | T | 1 | a0001c0001t0006g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415-12397C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156309 | |||||||
| chr1:236156395 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.415-12311G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156395 | |||||||
| chr1:236156400 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0065 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.415-12306T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156400 | |||||||
| chr1:236156537 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-12169C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156537 | |||||||
| chr1:236156555 | G | A | 34 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(31): Show |
34 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.415-12151G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156555 | |||||||
| chr1:236156599 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415-12107C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156599 | |||||||
| chr1:236156674 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.415-12032C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156674 | |||||||
| chr1:236156824 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0003g0013 |
3 | HG00673.hp1 HG01934.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.415-11882C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156824 | |||||||
| chr1:236156940 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0104 others(64): Show |
72 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.415-11766G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236156940 | |||||||
| chr1:236157193 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0104 others(82): Show |
90 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.415-11513T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157193 | |||||||
| chr1:236157226 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG01243.hp2 HG01433.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-11464dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236157226 | ||||||
| chr1:236157226 | C | CTT | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
104 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.415-11465_415-1146 others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236157226 | ||||||
| chr1:236157226 | C | CTTT | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.415-11466_415-1146 others(7): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236157226 | ||||||
| chr1:236157260 | A | T | 1 | a0001c0001t0001g0015 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.415-11446A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157260 | |||||||
| chr1:236157350 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0002g0022 |
2 | HG00741.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.415-11356A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157350 | |||||||
| chr1:236157361 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.415-11345C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157361 | |||||||
| chr1:236157369 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.415-11337G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157369 | |||||||
| chr1:236157384 | C | T | 9 | a0001c0001t0001g0146 a0001c0001t0001g0202 a0001c0001t0001g0211 others(6): Show |
10 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-11322C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157384 | |||||||
| chr1:236157406 | G | A | 1 | a0001c0001t0003g0258 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.415-11300G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157406 | |||||||
| chr1:236157424 | C | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.415-11282C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157424 | |||||||
| chr1:236157517 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0065 others(39): Show |
43 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.415-11189C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157517 | |||||||
| chr1:236157533 | A | G | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0026 |
3 | HG01106.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-11173A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157533 | |||||||
| chr1:236157573 | C | T | 1 | a0001c0001t0003g0297 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.415-11133C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157573 | |||||||
| chr1:236157664 | A | C | 1 | a0001c0001t0002g0225 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.415-11042A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157664 | |||||||
| chr1:236157684 | C | A | 2 | a0001c0001t0002g0199 a0003c0004t0001g0144 |
2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.415-11022C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157684 | |||||||
| chr1:236157727 | C | T | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0026 |
3 | HG01106.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-10979C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157727 | |||||||
| chr1:236157742 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0138 a0001c0001t0001g0151 others(10): Show |
13 | HG00741.hp1 HG01243.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.415-10964G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157742 | |||||||
| chr1:236157814 | C | A | 6 | a0001c0001t0002g0334 a0001c0001t0002g0335 a0001c0001t0002g0336 others(3): Show |
6 | NA18948.hp1 NA18977.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-10892C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157814 | |||||||
| chr1:236157915 | A | G | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415-10791A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157915 | |||||||
| chr1:236157976 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.415-10730G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157976 | |||||||
| chr1:236157984 | G | C | 1 | a0001c0001t0001g0340 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.415-10722G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236157984 | |||||||
| chr1:236158143 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415-10563G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158143 | |||||||
| chr1:236158159 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
214 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.415-10547T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158159 | |||||||
| chr1:236158239 | A | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
162 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.415-10467A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158239 | |||||||
| chr1:236158277 | T | A | 35 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(32): Show |
35 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.415-10429T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158277 | |||||||
| chr1:236158294 | A | C | 1 | a0001c0001t0008g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.415-10412A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158294 | |||||||
| chr1:236158452 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0149 others(2): Show |
6 | HG01884.hp2 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-10254A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158452 | |||||||
| chr1:236158611 | G | A | 39 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(36): Show |
39 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.415-10095G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158611 | |||||||
| chr1:236158676 | C | G | 9 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG01978.hp2 HG02273.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-10030C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158676 | |||||||
| chr1:236158897 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0007g0161 |
2 | HG01981.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.415-9809A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236158897 | |||||||
| chr1:236159227 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0065 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.415-9479T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159227 | |||||||
| chr1:236159315 | AAAAC | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0227 a0001c0001t0001g0238 others(2): Show |
5 | HG00741.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-9377_415-9374d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236159315 | ||||||
| chr1:236159565 | C | A | 4 | a0001c0001t0001g0160 a0001c0001t0002g0214 a0001c0001t0007g0161 others(1): Show |
4 | HG01169.hp2 HG01981.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-9141C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159565 | |||||||
| chr1:236159566 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415-9140G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159566 | |||||||
| chr1:236159684 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0002g0214 a0001c0001t0007g0161 others(1): Show |
4 | HG01169.hp2 HG01981.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-9022C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159684 | |||||||
| chr1:236159765 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.415-8941C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159765 | |||||||
| chr1:236159788 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
213 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.415-8918T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159788 | |||||||
| chr1:236159801 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0150 |
3 | HG01884.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.415-8905C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159801 | |||||||
| chr1:236159968 | C | T | 1 | a0001c0001t0007g0296 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.415-8738C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159968 | |||||||
| chr1:236159969 | G | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415-8737G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236159969 | |||||||
| chr1:236160014 | G | A | 4 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0002g0175 others(1): Show |
4 | HG02717.hp1 HG03471.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-8692G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160014 | |||||||
| chr1:236160222 | C | A | 1 | a0001c0001t0003g0251 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.415-8484C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160222 | |||||||
| chr1:236160241 | G | T | 1 | a0001c0001t0004g0304 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.415-8465G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160241 | |||||||
| chr1:236160258 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.415-8448C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160258 | |||||||
| chr1:236160268 | A | C | 1 | a0001c0002t0006g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.415-8438A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160268 | |||||||
| chr1:236160268 | A | G | 2 | a0001c0001t0001g0328 a0001c0001t0001g0362 |
2 | HG00597.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.415-8438A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160268 | |||||||
| chr1:236160386 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-8320C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160386 | |||||||
| chr1:236160457 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-8249T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160457 | |||||||
| chr1:236160600 | A | G | 1 | a0001c0001t0007g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.415-8106A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160600 | |||||||
| chr1:236160899 | T | G | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-7807T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236160899 | |||||||
| chr1:236160917 | G | GT | 35 | a0001c0001t0001g0044 a0001c0001t0001g0068 a0001c0001t0001g0078 others(32): Show |
36 | HG00280.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.415-7780dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236160917 | ||||||
| chr1:236161025 | G | A | 4 | a0001c0001t0001g0160 a0001c0001t0002g0214 a0001c0001t0007g0161 others(1): Show |
4 | HG01169.hp2 HG01981.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-7681G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161025 | |||||||
| chr1:236161054 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0354 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.415-7652C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161054 | |||||||
| chr1:236161093 | C | T | 7 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0141 others(4): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-7613C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161093 | |||||||
| chr1:236161251 | C | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(1): Show |
4 | HG00735.hp1 HG01358.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-7455C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161251 | |||||||
| chr1:236161314 | G | A | 7 | a0001c0001t0002g0116 a0001c0001t0002g0163 a0001c0001t0002g0165 others(4): Show |
7 | HG01106.hp2 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-7392G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161314 | |||||||
| chr1:236161484 | T | TTCACACC others(16): Show |
7 | a0001c0001t0001g0119 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-7209_415-7208i others(25): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236161484 | ||||||
| chr1:236161498 | C | CGCCTCCC others(16): Show |
149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
157 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.415-7191_415-7190i others(25): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236161498 | ||||||
| chr1:236161498 | C | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG02055.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-7208C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161498 | |||||||
| chr1:236161522 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.415-7184G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161522 | |||||||
| chr1:236161581 | G | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
164 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.415-7125G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161581 | |||||||
| chr1:236161665 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-7041T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161665 | |||||||
| chr1:236161682 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0002g0228 |
2 | HG00438.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.415-7024T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161682 | |||||||
| chr1:236161770 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.415-6936C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161770 | |||||||
| chr1:236161774 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.415-6932G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161774 | |||||||
| chr1:236161900 | A | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(117): Show |
126 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.415-6806A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161900 | |||||||
| chr1:236161984 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.415-6722G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236161984 | |||||||
| chr1:236161986 | AACAG | A | 41 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0067 others(38): Show |
41 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.415-6714_415-6711d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236161986 | ||||||
| chr1:236162286 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(117): Show |
126 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.415-6420G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162286 | |||||||
| chr1:236162432 | G | A | 11 | a0001c0001t0001g0118 a0001c0001t0001g0138 a0001c0001t0001g0139 others(8): Show |
12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-6274G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162432 | |||||||
| chr1:236162467 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(117): Show |
126 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.415-6239C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162467 | |||||||
| chr1:236162606 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(117): Show |
126 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.415-6100G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162606 | |||||||
| chr1:236162651 | C | T | 1 | a0001c0001t0003g0282 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.415-6055C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162651 | |||||||
| chr1:236162660 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-6046C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162660 | |||||||
| chr1:236162680 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.415-6026T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162680 | |||||||
| chr1:236162705 | C | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0027 others(159): Show |
168 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.415-6001C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162705 | |||||||
| chr1:236162755 | G | C | 1 | a0001c0001t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415-5951G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162755 | |||||||
| chr1:236162763 | C | T | 1 | a0001c0001t0006g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415-5943C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162763 | |||||||
| chr1:236162963 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0121 others(15): Show |
19 | HG01106.hp2 HG01109.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.415-5743G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162963 | |||||||
| chr1:236162974 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(117): Show |
126 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.415-5732C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236162974 | |||||||
| chr1:236163063 | C | T | 36 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(33): Show |
36 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.415-5643C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163063 | |||||||
| chr1:236163113 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.415-5593T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163113 | |||||||
| chr1:236163215 | T | G | 1 | a0001c0001t0004g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.415-5491T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163215 | |||||||
| chr1:236163237 | C | T | 6 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 others(3): Show |
6 | HG01106.hp2 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-5469C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163237 | |||||||
| chr1:236163241 | G | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.415-5465G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163241 | |||||||
| chr1:236163446 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18991.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.415-5260G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163446 | |||||||
| chr1:236163895 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(114): Show |
123 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.415-4811A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236163895 | |||||||
| chr1:236163930 | ACATCTCC others(3): Show |
A | 1 | a0001c0001t0002g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-4763_415-4754d others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236163930 | ||||||
| chr1:236164005 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.415-4701C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164005 | |||||||
| chr1:236164136 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0002g0171 |
2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.415-4570T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164136 | |||||||
| chr1:236164138 | C | T | 2 | a0001c0001t0001g0352 a0001c0001t0001g0353 |
2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.415-4568C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164138 | |||||||
| chr1:236164269 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.415-4437G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164269 | |||||||
| chr1:236164309 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415-4397C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164309 | |||||||
| chr1:236164321 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.415-4385G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164321 | |||||||
| chr1:236164419 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0149 others(1): Show |
5 | HG01884.hp2 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-4287G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164419 | |||||||
| chr1:236164499 | A | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0027 others(84): Show |
89 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.415-4207A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164499 | |||||||
| chr1:236164510 | G | A | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG01099.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-4196G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164510 | |||||||
| chr1:236164527 | C | T | 7 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0207 others(4): Show |
7 | HG01169.hp2 HG01981.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-4179C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164527 | |||||||
| chr1:236164710 | T | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0027 others(85): Show |
90 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.415-3996T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164710 | |||||||
| chr1:236164784 | C | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG01099.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-3922C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164784 | |||||||
| chr1:236164787 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415-3919G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236164787 | |||||||
| chr1:236164886 | A | AAG | 4 | a0001c0001t0001g0341 a0001c0001t0002g0095 a0001c0001t0002g0197 others(1): Show |
4 | HG02056.hp1 HG02735.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-3786_415-3785d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236164886 | ||||||
| chr1:236164886 | AAG | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(190): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.415-3786_415-3785d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236164886 | ||||||
| chr1:236164886 | AAGAG | A | 39 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0043 others(36): Show |
40 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(37): Show |
intron_variant | MODIFIER | c.415-3788_415-3785d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236164886 | ||||||
| chr1:236164886 | AAGAGAGA others(5): Show |
A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0100 |
2 | NA18994.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.415-3796_415-3785d others(14): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236164886 | ||||||
| chr1:236164886 | AAGAGAGA others(7): Show |
A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0027 others(82): Show |
87 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.415-3798_415-3785d others(16): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236164886 | ||||||
| chr1:236165017 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.415-3689G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165017 | |||||||
| chr1:236165136 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.415-3570C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165136 | |||||||
| chr1:236165164 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.415-3542G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165164 | |||||||
| chr1:236165190 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0365 a0001c0001t0001g0367 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-3516C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165190 | |||||||
| chr1:236165269 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-3437G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165269 | |||||||
| chr1:236165284 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.415-3422G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165284 | |||||||
| chr1:236165386 | C | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0110 others(36): Show |
41 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.415-3320C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165386 | |||||||
| chr1:236165438 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0137 |
2 | NA18940.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.415-3268G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165438 | |||||||
| chr1:236165468 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415-3238T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165468 | |||||||
| chr1:236165663 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0238 a0001c0001t0001g0281 |
3 | HG01261.hp1 HG03209.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.415-3043C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165663 | |||||||
| chr1:236165906 | T | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0149 a0001c0001t0002g0199 others(3): Show |
6 | HG01109.hp1 HG02723.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-2800T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165906 | |||||||
| chr1:236165942 | C | G | 1 | a0001c0002t0001g0023 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.415-2764C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236165942 | |||||||
| chr1:236166213 | T | C | 97 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0043 others(94): Show |
98 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.415-2493T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166213 | |||||||
| chr1:236166283 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.415-2423G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166283 | |||||||
| chr1:236166288 | T | C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0149 a0001c0001t0001g0177 others(7): Show |
10 | HG01109.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-2418T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166288 | |||||||
| chr1:236166325 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.415-2381T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166325 | |||||||
| chr1:236166391 | C | T | 1 | a0001c0001t0002g0008 | 2 | NA18944.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.415-2315C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166391 | |||||||
| chr1:236166428 | T | G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0215 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-2278T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166428 | |||||||
| chr1:236166456 | GTATATTA others(66): Show |
G | 10 | a0001c0001t0001g0110 a0001c0001t0001g0149 a0001c0001t0001g0177 others(7): Show |
10 | HG01109.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-2244_415-2172d others(75): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166456 | ||||||
| chr1:236166464 | A | AATATATA others(36): Show |
1 | a0001c0001t0002g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.415-2213_415-2171d others(45): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166464 | ||||||
| chr1:236166482 | A | ATGTATAT others(64): Show |
1 | a0001c0001t0001g0083 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.415-2223_415-2222i others(73): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166482 | ||||||
| chr1:236166484 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.415-2222T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166484 | |||||||
| chr1:236166484 | T | TTA | 5 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0215 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-2215_415-2214d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166484 | T | TTATATAT others(65): Show |
8 | a0001c0001t0003g0239 a0001c0001t0003g0243 a0001c0001t0003g0244 others(5): Show |
8 | HG00597.hp1 HG02056.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-2214_415-2213i others(74): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166484 | T | TTATATAT others(64): Show |
47 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0043 others(44): Show |
47 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.415-2214_415-2213i others(73): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166484 | T | TTATATAT others(62): Show |
2 | a0001c0001t0001g0121 a0001c0001t0002g0108 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.415-2214_415-2213i others(71): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166484 | T | TTATATAT others(60): Show |
3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG03041.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.415-2214_415-2213i others(69): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166484 | T | TTATATAT others(64): Show |
1 | a0001c0001t0001g0085 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.415-2214_415-2213i others(73): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166484 | T | TTATATAT others(63): Show |
1 | a0001c0001t0003g0242 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.415-2214_415-2213i others(72): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166484 | ||||||
| chr1:236166491 | T | TATA | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0026 |
3 | HG01106.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-2214_415-2213i others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166491 | ||||||
| chr1:236166491 | T | TATAC | 7 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0120 others(4): Show |
7 | HG01981.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-2214_415-2213i others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236166491 | ||||||
| chr1:236166492 | A | AATATATA others(36): Show |
1 | a0001c0001t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.415-2214_415-2213i others(45): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166492 | |||||||
| chr1:236166492 | A | ATAATATA others(38): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0005 others(2): Show |
6 | HG02109.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-2214_415-2213i others(47): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166492 | |||||||
| chr1:236166493 | C | A | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0005 others(3): Show |
7 | HG02109.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-2213C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166493 | |||||||
| chr1:236166493 | C | T | 13 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0120 others(10): Show |
13 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-2213C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166493 | |||||||
| chr1:236166494 | A | AATATATA others(19): Show |
3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.415-2212_415-2211i others(28): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166494 | |||||||
| chr1:236166504 | T | G | 9 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0091 others(6): Show |
9 | HG00438.hp1 HG00597.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-2202T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166504 | |||||||
| chr1:236166527 | T | G | 5 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0102 others(2): Show |
5 | HG02015.hp2 NA18747.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-2179T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166527 | |||||||
| chr1:236166536 | TACA | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0149 a0001c0001t0001g0177 others(7): Show |
10 | HG01109.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-2169_415-2167d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166536 | |||||||
| chr1:236166600 | T | G | 1 | a0001c0001t0001g0342 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.415-2106T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166600 | |||||||
| chr1:236166610 | A | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0104 others(60): Show |
68 | HG00323.hp1 HG00408.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.415-2096A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166610 | |||||||
| chr1:236166709 | G | A | 1 | a0001c0001t0001g0366 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.415-1997G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166709 | |||||||
| chr1:236166722 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415-1984C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166722 | |||||||
| chr1:236166974 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.415-1732G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236166974 | |||||||
| chr1:236167040 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0002g0228 |
2 | HG00438.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.415-1666C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167040 | |||||||
| chr1:236167115 | G | A | 13 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0120 others(10): Show |
13 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-1591G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167115 | |||||||
| chr1:236167237 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.415-1469A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167237 | |||||||
| chr1:236167368 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.415-1338A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167368 | |||||||
| chr1:236167476 | A | AGGTG | 18 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0001c0001t0001g0211 others(15): Show |
19 | HG01106.hp2 HG01981.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.415-1229_415-1228i others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236167476 | ||||||
| chr1:236167525 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0002g0199 a0001c0001t0006g0145 others(1): Show |
4 | HG01109.hp1 HG02723.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1181G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167525 | |||||||
| chr1:236167569 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.415-1137G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167569 | |||||||
| chr1:236167577 | C | G | 12 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0163 others(9): Show |
12 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1129C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167577 | |||||||
| chr1:236167650 | C | G | 1 | a0001c0001t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415-1056C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167650 | |||||||
| chr1:236167827 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415-879G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236167827 | |||||||
| chr1:236168023 | T | C | 12 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0163 others(9): Show |
12 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-683T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168023 | |||||||
| chr1:236168040 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415-666C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168040 | |||||||
| chr1:236168115 | CTGTT | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0160 others(17): Show |
21 | HG00140.hp2 HG01106.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.415-585_415-582del others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236168115 | ||||||
| chr1:236168148 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415-558C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168148 | |||||||
| chr1:236168165 | A | G | 6 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 others(3): Show |
6 | HG01106.hp2 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-541A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168165 | |||||||
| chr1:236168212 | A | G | 12 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0163 others(9): Show |
12 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-494A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168212 | |||||||
| chr1:236168227 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0215 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-479G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168227 | |||||||
| chr1:236168283 | T | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG02922.hp1 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.415-423T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168283 | |||||||
| chr1:236168372 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.415-334G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168372 | |||||||
| chr1:236168424 | G | GA | 16 | a0001c0001t0001g0029 a0001c0001t0001g0096 a0001c0001t0001g0097 others(13): Show |
16 | HG02055.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.415-265dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236168424 | ||||||
| chr1:236168424 | GA | G | 13 | a0001c0001t0001g0160 a0001c0001t0001g0308 a0001c0001t0001g0328 others(10): Show |
13 | HG00673.hp2 HG01981.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-265delA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 236168424 | ||||||
| chr1:236168519 | T | A | 1 | a0001c0001t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415-187T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168519 | |||||||
| chr1:236168574 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0003g0251 |
2 | NA19002.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.415-132G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168574 | |||||||
| chr1:236168590 | T | C | 12 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0163 others(9): Show |
12 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-116T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168590 | |||||||
| chr1:236168598 | G | T | 1 | a0001c0001t0002g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.415-108G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 1/6 | chr1 | 236168598 | |||||||
| chr1:236168864 | A | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG02922.hp1 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.464+109A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236168864 | |||||||
| chr1:236168869 | G | A | 2 | a0001c0002t0002g0018 a0001c0002t0006g0019 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.464+114G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236168869 | |||||||
| chr1:236168976 | T | C | 12 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0163 others(9): Show |
12 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.464+221T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236168976 | |||||||
| chr1:236169172 | C | CTGCAGG | 21 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0081 others(18): Show |
22 | HG00438.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.464+455_464+460dup others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169172 | C | CTGCAGGT others(5): Show |
25 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0080 others(22): Show |
25 | HG00423.hp2 HG00558.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.464+449_464+460dup others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169172 | C | CTGCAGGT others(11): Show |
32 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0065 others(29): Show |
33 | HG00597.hp1 HG01167.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.464+443_464+460dup others(18): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169172 | C | CTGCAGGT others(17): Show |
1 | a0001c0001t0003g0239 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.464+437_464+460dup others(24): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169172 | C | CTGCAGGT others(35): Show |
1 | a0001c0001t0002g0143 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.464+419_464+460dup others(42): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169172 | CTGCAGG | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0132 others(10): Show |
14 | HG02258.hp1 HG02451.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.464+455_464+460del others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169172 | CTGCAGGT others(5): Show |
C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0150 others(2): Show |
6 | HG01884.hp2 HG02055.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.464+449_464+460del others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169172 | ||||||
| chr1:236169180 | GCAGGTGC others(41): Show |
G | 6 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0207 others(3): Show |
6 | HG01981.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.464+453_464+500del others(48): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169180 | ||||||
| chr1:236169182 | A | G | 1 | a0001c0001t0007g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.464+427A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169182 | |||||||
| chr1:236169192 | GCAGGTGC others(29): Show |
G | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.464+461_464+496del others(36): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169192 | ||||||
| chr1:236169198 | GCAGGTGC others(23): Show |
G | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0026 |
3 | HG01106.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.464+461_464+490del others(30): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169198 | ||||||
| chr1:236169204 | GCAGGTGC others(5): Show |
G | 5 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0215 others(2): Show |
5 | HG02280.hp1 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+455_464+466del others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169204 | ||||||
| chr1:236169210 | G | A | 2 | a0001c0002t0002g0018 a0001c0002t0006g0019 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.464+455G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169210 | |||||||
| chr1:236169210 | G | GCAGGTA | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(1): Show |
4 | HG00733.hp1 HG01192.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+473_464+478dup others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169210 | ||||||
| chr1:236169210 | GCAGGTA | G | 9 | a0001c0001t0001g0110 a0001c0001t0001g0149 a0001c0001t0002g0095 others(6): Show |
9 | HG01106.hp1 HG01109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.464+473_464+478del others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169210 | ||||||
| chr1:236169216 | A | G | 71 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0065 others(68): Show |
72 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.464+461A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169216 | |||||||
| chr1:236169222 | A | G | 1 | a0001c0001t0002g0007 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.464+467A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169222 | |||||||
| chr1:236169228 | A | ACAGGTGC others(5): Show |
1 | a0001c0001t0003g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.464+489_464+500dup others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236169228 | ||||||
| chr1:236169228 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0130 others(64): Show |
72 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.464+473A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169228 | |||||||
| chr1:236169296 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.464+541C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169296 | |||||||
| chr1:236169416 | A | T | 1 | a0001c0001t0003g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.464+661A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169416 | |||||||
| chr1:236169443 | T | G | 12 | a0001c0001t0001g0160 a0001c0001t0002g0064 a0001c0001t0002g0163 others(9): Show |
12 | HG01106.hp2 HG01981.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.464+688T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169443 | |||||||
| chr1:236169490 | T | C | 1 | a0001c0001t0003g0297 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.464+735T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169490 | |||||||
| chr1:236169563 | A | G | 50 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0075 others(47): Show |
52 | HG00280.hp1 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.464+808A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169563 | |||||||
| chr1:236169571 | C | T | 25 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0096 others(22): Show |
25 | HG01106.hp2 HG01981.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.464+816C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169571 | |||||||
| chr1:236169585 | A | G | 4 | a0001c0001t0001g0249 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
4 | NA18980.hp1 NA18987.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+830A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169585 | |||||||
| chr1:236169610 | A | G | 25 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0096 others(22): Show |
25 | HG01106.hp2 HG01981.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.464+855A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169610 | |||||||
| chr1:236169620 | C | A | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0005 others(3): Show |
7 | HG02109.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.464+865C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169620 | |||||||
| chr1:236169777 | C | T | 1 | a0001c0001t0002g0331 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.464+1022C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169777 | |||||||
| chr1:236169908 | C | T | 1 | a0001c0001t0003g0250 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.464+1153C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236169908 | |||||||
| chr1:236170023 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.464+1268G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170023 | |||||||
| chr1:236170039 | C | CA | 28 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0075 others(25): Show |
29 | HG01175.hp1 HG01257.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.464+1309dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170039 | ||||||
| chr1:236170039 | CA | C | 80 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0065 others(77): Show |
82 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.464+1309delA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170039 | ||||||
| chr1:236170039 | CAAA | C | 24 | a0001c0001t0001g0029 a0001c0001t0001g0096 a0001c0001t0001g0097 others(21): Show |
24 | HG01106.hp2 HG01981.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.464+1307_464+1309d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170039 | ||||||
| chr1:236170039 | CAAAA | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0071 others(9): Show |
14 | HG00140.hp2 HG01255.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.464+1306_464+1309d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170039 | ||||||
| chr1:236170039 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0211 a0001c0001t0002g0210 others(1): Show |
5 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+1298_464+1309d others(14): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170039 | ||||||
| chr1:236170131 | T | C | 25 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0096 others(22): Show |
26 | HG01106.hp2 HG02083.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.464+1376T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170131 | |||||||
| chr1:236170164 | G | A | 1 | a0001c0001t0002g0344 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.464+1409G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170164 | |||||||
| chr1:236170173 | A | G | 2 | a0001c0001t0002g0129 a0001c0001t0002g0189 |
2 | NA19012.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.464+1418A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170173 | |||||||
| chr1:236170188 | C | A | 1 | a0001c0001t0003g0297 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.464+1433C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170188 | |||||||
| chr1:236170218 | C | T | 3 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0006g0164 |
3 | HG02717.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.464+1463C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170218 | |||||||
| chr1:236170528 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0002g0108 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.464+1773C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170528 | |||||||
| chr1:236170592 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.464+1837G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170592 | |||||||
| chr1:236170836 | C | T | 25 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0096 others(22): Show |
25 | HG01106.hp2 HG01981.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.464+2081C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236170836 | |||||||
| chr1:236170973 | C | CA | 15 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0123 others(12): Show |
15 | HG01106.hp1 HG01106.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.464+2234dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170973 | ||||||
| chr1:236170997 | G | GAA | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(199): Show |
209 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.464+2243_464+2244i others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236170997 | ||||||
| chr1:236171247 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.464+2492A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171247 | |||||||
| chr1:236171269 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0111 others(10): Show |
15 | HG00140.hp2 HG00323.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.464+2514G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171269 | |||||||
| chr1:236171279 | G | T | 117 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0039 others(114): Show |
119 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.464+2524G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171279 | |||||||
| chr1:236171284 | C | T | 28 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0096 others(25): Show |
28 | HG01106.hp2 HG01981.hp2 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.464+2529C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171284 | |||||||
| chr1:236171417 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.464+2662A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171417 | |||||||
| chr1:236171434 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.464+2679T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171434 | |||||||
| chr1:236171443 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0007g0148 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.464+2688G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171443 | |||||||
| chr1:236171448 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0007g0178 a0001c0001t0007g0209 |
3 | HG02559.hp2 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.464+2693G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171448 | |||||||
| chr1:236171669 | T | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0096 others(10): Show |
13 | HG02083.hp2 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.464+2914T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171669 | |||||||
| chr1:236171678 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0007g0178 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+2923T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171678 | |||||||
| chr1:236171771 | G | A | 3 | a0001c0002t0002g0024 a0001c0002t0002g0025 a0001c0002t0002g0026 |
3 | HG01106.hp2 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.464+3016G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171771 | |||||||
| chr1:236171853 | T | C | 1 | a0001c0001t0003g0297 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.464+3098T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171853 | |||||||
| chr1:236171930 | T | C | 11 | a0001c0001t0001g0110 a0001c0001t0001g0149 a0001c0001t0001g0177 others(8): Show |
11 | HG01106.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.464+3175T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236171930 | |||||||
| chr1:236172040 | C | CA | 11 | a0001c0001t0001g0041 a0001c0001t0001g0071 a0001c0001t0001g0122 others(8): Show |
11 | HG02015.hp1 HG02040.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.464+3302dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236172040 | ||||||
| chr1:236172040 | C | CAA | 18 | a0001c0001t0001g0029 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
18 | HG01106.hp2 HG02083.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.464+3301_464+3302d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236172040 | ||||||
| chr1:236172040 | C | CAAA | 9 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0259 others(6): Show |
9 | HG01981.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.464+3300_464+3302d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236172040 | ||||||
| chr1:236172267 | A | G | 61 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0043 others(58): Show |
61 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.464+3512A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236172267 | |||||||
| chr1:236172349 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0152 others(57): Show |
65 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.464+3594A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236172349 | |||||||
| chr1:236172524 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.464+3769G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236172524 | |||||||
| chr1:236172740 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0152 others(65): Show |
73 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.464+3985G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236172740 | |||||||
| chr1:236173094 | A | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0153 |
2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.464+4339A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173094 | |||||||
| chr1:236173151 | C | T | 7 | a0001c0001t0001g0110 a0001c0001t0001g0177 a0001c0001t0001g0179 others(4): Show |
7 | HG01106.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.464+4396C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173151 | |||||||
| chr1:236173200 | A | G | 1 | a0001c0001t0002g0339 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.464+4445A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173200 | |||||||
| chr1:236173247 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.464+4492C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173247 | |||||||
| chr1:236173290 | CA | C | 86 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(83): Show |
88 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.464+4550delA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236173290 | ||||||
| chr1:236173338 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(1): Show |
4 | HG00733.hp1 HG01192.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+4583G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173338 | |||||||
| chr1:236173367 | G | A | 1 | a0001c0001t0012g0257 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.464+4612G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173367 | |||||||
| chr1:236173415 | A | G | 1 | a0001c0001t0008g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.464+4660A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173415 | |||||||
| chr1:236173416 | G | A | 1 | a0001c0001t0008g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.464+4661G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173416 | |||||||
| chr1:236173416 | G | GAGGA | 336 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(333): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.464+4666_464+4669d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236173416 | ||||||
| chr1:236173501 | C | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0027 others(89): Show |
95 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.464+4746C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173501 | |||||||
| chr1:236173529 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0072 others(16): Show |
22 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.464+4774T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173529 | |||||||
| chr1:236173705 | C | T | 1 | a0001c0001t0003g0306 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.465-4709C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173705 | |||||||
| chr1:236173759 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(114): Show |
123 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(120): Show |
intron_variant | MODIFIER | c.465-4655T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173759 | |||||||
| chr1:236173761 | C | CTG | 117 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(114): Show |
123 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(120): Show |
intron_variant | MODIFIER | c.465-4652_465-4651i others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236173761 | ||||||
| chr1:236173803 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.465-4611C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173803 | |||||||
| chr1:236173805 | C | T | 1 | a0001c0001t0007g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.465-4609C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173805 | |||||||
| chr1:236173838 | G | A | 1 | a0001c0001t0003g0263 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.465-4576G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173838 | |||||||
| chr1:236173925 | A | G | 1 | a0003c0004t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.465-4489A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236173925 | |||||||
| chr1:236173930 | GA | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0027 others(170): Show |
179 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.465-4477delA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236173930 | ||||||
| chr1:236174127 | A | G | 2 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.465-4287A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174127 | |||||||
| chr1:236174197 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0007g0148 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.465-4217A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174197 | |||||||
| chr1:236174217 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.465-4197A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174217 | |||||||
| chr1:236174273 | T | A | 1 | a0001c0001t0002g0344 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.465-4141T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174273 | |||||||
| chr1:236174424 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.465-3990C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174424 | |||||||
| chr1:236174678 | C | CGTGCTAG others(3): Show |
1 | a0001c0001t0003g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.465-3735_465-3726d others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236174678 | ||||||
| chr1:236174761 | C | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0197 |
2 | NA19011.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.465-3653C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174761 | |||||||
| chr1:236174926 | G | A | 71 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(68): Show |
73 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.465-3488G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174926 | |||||||
| chr1:236174962 | G | C | 1 | a0001c0001t0002g0358 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.465-3452G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236174962 | |||||||
| chr1:236175058 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.465-3356G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236175058 | |||||||
| chr1:236175093 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0007g0148 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.465-3321G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236175093 | |||||||
| chr1:236175322 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0021 others(206): Show |
217 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.465-3092T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236175322 | |||||||
| chr1:236175734 | G | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0027 others(190): Show |
201 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.465-2680G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236175734 | |||||||
| chr1:236175770 | G | A | 69 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0043 others(66): Show |
69 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.465-2644G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236175770 | |||||||
| chr1:236176170 | T | A | 1 | a0001c0001t0003g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.465-2244T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176170 | |||||||
| chr1:236176196 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG01261.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.465-2218G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176196 | |||||||
| chr1:236176271 | A | C | 34 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0001t0001g0076 others(31): Show |
34 | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.465-2143A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176271 | |||||||
| chr1:236176397 | C | G | 1 | a0001c0001t0002g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.465-2017C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176397 | |||||||
| chr1:236176398 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
5 | HG01099.hp1 HG01243.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.465-2016G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176398 | |||||||
| chr1:236176438 | C | T | 11 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0097 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.465-1976C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176438 | |||||||
| chr1:236176513 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.465-1901C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176513 | |||||||
| chr1:236176741 | C | CCTTCCTT | 21 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(18): Show |
21 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.465-1667_465-1661d others(9): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236176741 | ||||||
| chr1:236176754 | C | T | 92 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0039 others(89): Show |
92 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.465-1660C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176754 | |||||||
| chr1:236176778 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.465-1636G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176778 | |||||||
| chr1:236176879 | T | G | 101 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0038 others(98): Show |
101 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.465-1535T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236176879 | |||||||
| chr1:236177175 | G | A | 22 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0141 others(19): Show |
22 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.465-1239G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177175 | |||||||
| chr1:236177264 | G | A | 1 | a0001c0002t0001g0023 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.465-1150G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177264 | |||||||
| chr1:236177459 | G | T | 1 | a0001c0001t0003g0319 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.465-955G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177459 | |||||||
| chr1:236177548 | T | C | 1 | a0001c0001t0003g0313 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.465-866T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177548 | |||||||
| chr1:236177564 | GT | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(266): Show |
280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.465-841delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 236177564 | ||||||
| chr1:236177587 | C | T | 1 | a0001c0001t0001g0366 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.465-827C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177587 | |||||||
| chr1:236177588 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(37): Show |
42 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.465-826G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177588 | |||||||
| chr1:236177680 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.465-734T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177680 | |||||||
| chr1:236177989 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0005 |
4 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.465-425A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236177989 | |||||||
| chr1:236178025 | C | T | 19 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0155 others(16): Show |
19 | HG00735.hp2 HG01099.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.465-389C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236178025 | |||||||
| chr1:236178310 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465-104C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236178310 | |||||||
| chr1:236178355 | A | G | 5 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0008g0112 others(2): Show |
5 | HG00280.hp1 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.465-59A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 2/6 | chr1 | 236178355 | |||||||
| chr1:236178785 | G | GGTTTTTT | 3 | a0001c0001t0001g0211 a0001c0001t0002g0120 a0001c0001t0002g0210 |
3 | HG02257.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687+149_687+150ins others(7): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178785 | |||||||
| chr1:236178785 | G | GT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0169 others(3): Show |
6 | HG01175.hp1 HG01255.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.687+179dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTT | 19 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0083 others(16): Show |
19 | HG00558.hp1 HG00738.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.687+176_687+179dup others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0038 others(51): Show |
57 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.687+175_687+179dup others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTT | 86 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0065 others(83): Show |
88 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.687+174_687+179dup others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT | 42 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0043 others(39): Show |
43 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.687+173_687+179dup others(7): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(1): Show |
10 | a0001c0001t0001g0045 a0001c0001t0001g0123 a0001c0001t0001g0166 others(7): Show |
11 | HG00558.hp2 HG00673.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.687+172_687+179dup others(8): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0182 a0001c0001t0001g0285 a0001c0001t0001g0305 others(5): Show |
8 | HG01257.hp1 HG01358.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+171_687+179dup others(9): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0255 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.687+158_687+159ins others(17): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.687+158_687+159ins others(18): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(12): Show |
1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.687+158_687+159ins others(19): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0001g0054 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.687+158_687+159ins others(20): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(3): Show |
4 | a0001c0001t0001g0206 a0001c0001t0001g0283 a0001c0001t0003g0293 others(1): Show |
4 | HG02055.hp1 HG02683.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+170_687+179dup others(10): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0203 |
2 | HG00741.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.687+169_687+179dup others(11): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0005g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.687+168_687+179dup others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0001g0121 a0001c0001t0003g0229 |
2 | HG03225.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.687+167_687+179dup others(13): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(7): Show |
3 | a0001c0001t0001g0205 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG01934.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.687+166_687+179dup others(14): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(11): Show |
3 | a0001c0001t0003g0012 a0001c0001t0004g0235 a0001c0001t0004g0236 |
4 | HG00280.hp1 HG01069.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+162_687+179dup others(18): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(13): Show |
2 | a0001c0001t0002g0108 a0001c0001t0003g0306 |
2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.687+160_687+179dup others(20): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(14): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0329 a0001c0001t0005g0060 |
3 | HG01261.hp2 HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.687+159_687+179dup others(21): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(15): Show |
4 | a0001c0001t0003g0287 a0001c0001t0003g0297 a0001c0001t0005g0070 others(1): Show |
4 | HG03831.hp1 HG03927.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+158_687+179dup others(22): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(16): Show |
1 | a0001c0001t0001g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.687+157_687+179dup others(23): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(17): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0227 |
2 | HG02698.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.687+156_687+179dup others(24): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(18): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0341 a0001c0001t0005g0066 |
3 | HG02056.hp1 NA18964.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.687+155_687+179dup others(25): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(21): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0356 a0001c0001t0003g0290 |
3 | HG01070.hp2 HG01496.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.687+152_687+179dup others(28): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(22): Show |
4 | a0001c0001t0001g0068 a0001c0001t0001g0238 a0001c0001t0001g0363 others(1): Show |
4 | HG01071.hp2 HG01099.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+151_687+179dup others(29): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(23): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0046 others(1): Show |
4 | HG01981.hp1 HG02040.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+150_687+179dup others(30): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(24): Show |
3 | a0001c0001t0001g0360 a0001c0001t0003g0230 a0001c0001t0003g0288 |
3 | HG03834.hp2 HG04228.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.687+179_687+180ins others(31): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(26): Show |
2 | a0001c0001t0001g0100 a0001c0001t0003g0013 |
3 | HG00673.hp1 HG02523.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.687+179_687+180ins others(33): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | G | GTTTTTTT others(27): Show |
1 | a0001c0001t0005g0061 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.687+179_687+180ins others(34): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GT | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(20): Show |
25 | HG01099.hp2 HG01109.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.687+179delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GTTTT | G | 7 | a0001c0001t0001g0057 a0001c0001t0001g0152 a0001c0001t0002g0116 others(4): Show |
7 | HG02055.hp2 HG03669.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.687+176_687+179del others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GTTTTT | G | 17 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(14): Show |
18 | HG01891.hp1 HG01981.hp2 HG02602.hp1 others(15): Show |
intron_variant | MODIFIER | c.687+175_687+179del others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GTTTTTT | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0160 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.687+174_687+179del others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.687+170_687+179del others(10): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0003g0280 a0001c0001t0003g0317 |
2 | NA18956.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.687+167_687+179del others(13): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178785 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0001g0072 a0001c0001t0003g0315 a0001c0001t0003g0316 |
3 | HG00423.hp2 NA18966.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.687+166_687+179del others(14): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 236178785 | ||||||
| chr1:236178790 | T | G | 12 | a0001c0001t0001g0051 a0001c0001t0001g0218 a0001c0001t0002g0117 others(9): Show |
12 | HG00735.hp2 HG01106.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.687+154T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178790 | |||||||
| chr1:236178791 | T | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(17): Show |
22 | HG01099.hp2 HG01109.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.687+155T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178791 | |||||||
| chr1:236178792 | T | G | 1 | a0001c0001t0002g0273 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.687+156T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178792 | |||||||
| chr1:236178795 | T | G | 3 | a0001c0001t0001g0155 a0001c0001t0002g0208 a0001c0001t0007g0161 |
3 | HG01981.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.687+159T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178795 | |||||||
| chr1:236178796 | T | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0160 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.687+160T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178796 | |||||||
| chr1:236178804 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.687+168T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178804 | |||||||
| chr1:236178815 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0126 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.687+179_687+180ins others(11): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178815 | |||||||
| chr1:236178820 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687+184C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178820 | |||||||
| chr1:236178883 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.687+247C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178883 | |||||||
| chr1:236178935 | C | T | 2 | a0001c0001t0002g0350 a0001c0001t0002g0351 |
2 | HG00423.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.687+299C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178935 | |||||||
| chr1:236178943 | A | G | 5 | a0001c0001t0001g0211 a0001c0001t0002g0120 a0001c0001t0002g0210 others(2): Show |
6 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+307A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178943 | |||||||
| chr1:236178947 | A | G | 5 | a0001c0001t0001g0211 a0001c0001t0002g0120 a0001c0001t0002g0210 others(2): Show |
6 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+311A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178947 | |||||||
| chr1:236178952 | T | C | 5 | a0001c0001t0001g0211 a0001c0001t0002g0120 a0001c0001t0002g0210 others(2): Show |
6 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+316T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236178952 | |||||||
| chr1:236179010 | G | T | 11 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0155 others(8): Show |
11 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.687+374G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179010 | |||||||
| chr1:236179086 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.687+450C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179086 | |||||||
| chr1:236179403 | A | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG00140.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.688-476A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179403 | |||||||
| chr1:236179426 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.688-453C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179426 | |||||||
| chr1:236179448 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0159 others(8): Show |
13 | HG00408.hp2 HG00621.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.688-431G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179448 | |||||||
| chr1:236179760 | A | G | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0002g0163 others(1): Show |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.688-119A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179760 | |||||||
| chr1:236179830 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.688-49G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 3/6 | chr1 | 236179830 | |||||||
| chr1:236180081 | C | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(5): Show |
8 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.837+53C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180081 | |||||||
| chr1:236180210 | A | T | 5 | a0001c0001t0001g0211 a0001c0001t0002g0120 a0001c0001t0002g0210 others(2): Show |
6 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+182A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180210 | |||||||
| chr1:236180211 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+183T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180211 | |||||||
| chr1:236180217 | A | G | 1 | a0001c0001t0002g0358 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.837+189A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180217 | |||||||
| chr1:236180235 | A | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(22): Show |
27 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.837+207A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180235 | |||||||
| chr1:236180375 | C | CTG | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+349_837+350dup others(2): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236180375 | ||||||
| chr1:236180406 | C | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+378C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180406 | |||||||
| chr1:236180451 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+423T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180451 | |||||||
| chr1:236180549 | T | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+521T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180549 | |||||||
| chr1:236180633 | A | AT | 134 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0039 others(131): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.837+623dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236180633 | ||||||
| chr1:236180633 | AT | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0141 others(13): Show |
18 | HG01069.hp2 HG01070.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.837+623delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236180633 | ||||||
| chr1:236180633 | ATT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(30): Show |
35 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.837+622_837+623del others(2): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236180633 | ||||||
| chr1:236180671 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.837+643G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180671 | |||||||
| chr1:236180721 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(30): Show |
35 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.837+693A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180721 | |||||||
| chr1:236180832 | G | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.837+804G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180832 | |||||||
| chr1:236180837 | C | T | 5 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(2): Show |
6 | HG02040.hp1 HG02074.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+809C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180837 | |||||||
| chr1:236180878 | C | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(343): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.837+850C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180878 | |||||||
| chr1:236180897 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.837+869G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180897 | |||||||
| chr1:236180935 | A | G | 5 | a0001c0001t0001g0211 a0001c0001t0002g0120 a0001c0001t0002g0210 others(2): Show |
6 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+907A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180935 | |||||||
| chr1:236180988 | G | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+960G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236180988 | |||||||
| chr1:236181008 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+980C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181008 | |||||||
| chr1:236181026 | A | G | 13 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0215 others(10): Show |
13 | HG01106.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.837+998A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181026 | |||||||
| chr1:236181068 | CAG | C | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+1041_837+1042d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181068 | |||||||
| chr1:236181128 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+1100G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181128 | |||||||
| chr1:236181214 | G | A | 1 | a0001c0001t0002g0361 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.837+1186G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181214 | |||||||
| chr1:236181263 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | NA18941.hp2 NA18942.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+1235T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181263 | |||||||
| chr1:236181336 | ATT | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(34): Show |
39 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.837+1319_837+1320d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181336 | ||||||
| chr1:236181336 | ATTT | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0268 others(3): Show |
6 | HG00741.hp1 HG02451.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+1318_837+1320d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181336 | ||||||
| chr1:236181352 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+1324C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181352 | |||||||
| chr1:236181423 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+1395T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181423 | |||||||
| chr1:236181449 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0003g0294 |
2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.837+1421A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181449 | |||||||
| chr1:236181463 | A | C | 2 | a0001c0001t0001g0328 a0001c0001t0001g0362 |
2 | HG00597.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.837+1435A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181463 | |||||||
| chr1:236181517 | T | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.837+1489T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181517 | |||||||
| chr1:236181536 | G | A | 1 | a0001c0001t0003g0274 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.837+1508G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181536 | |||||||
| chr1:236181555 | A | T | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+1527A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181555 | |||||||
| chr1:236181694 | A | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0155 others(5): Show |
8 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.837+1666A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181694 | |||||||
| chr1:236181768 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+1740C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181768 | |||||||
| chr1:236181864 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.837+1836A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181864 | |||||||
| chr1:236181893 | A | ATTTTAAC others(3): Show |
15 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(12): Show |
15 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.837+1869_837+1870i others(12): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181893 | ||||||
| chr1:236181893 | A | ATTTTAAC others(4): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(14): Show |
19 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.837+1869_837+1870i others(13): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181893 | ||||||
| chr1:236181893 | A | ATTTTAAC others(5): Show |
11 | a0001c0001t0001g0090 a0001c0001t0001g0124 a0001c0001t0001g0126 others(8): Show |
12 | HG01167.hp2 HG02109.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+1869_837+1870i others(14): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181893 | ||||||
| chr1:236181893 | A | ATTTTAAC others(6): Show |
211 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(208): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.837+1869_837+1870i others(15): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181893 | ||||||
| chr1:236181893 | A | ATTTTAAC others(7): Show |
40 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(37): Show |
41 | HG00140.hp2 HG00544.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.837+1869_837+1870i others(16): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181893 | ||||||
| chr1:236181893 | A | ATTTTAAC others(8): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0085 |
2 | HG00438.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.837+1869_837+1870i others(17): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236181893 | ||||||
| chr1:236181945 | T | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0325 |
3 | NA18612.hp1 NA18963.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.838-1833T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181945 | |||||||
| chr1:236181951 | C | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.838-1827C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181951 | |||||||
| chr1:236181979 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.838-1799G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181979 | |||||||
| chr1:236181985 | C | T | 2 | a0001c0001t0001g0356 a0001c0001t0003g0313 |
2 | NA18950.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.838-1793C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181985 | |||||||
| chr1:236181996 | G | A | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.838-1782G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236181996 | |||||||
| chr1:236182100 | C | A | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.838-1678C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182100 | |||||||
| chr1:236182173 | C | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.838-1605C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182173 | |||||||
| chr1:236182210 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0127 |
2 | NA19065.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.838-1568A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182210 | |||||||
| chr1:236182238 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.838-1540C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182238 | |||||||
| chr1:236182239 | T | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0189 |
2 | NA19012.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.838-1539T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182239 | |||||||
| chr1:236182363 | G | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.838-1415G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182363 | |||||||
| chr1:236182418 | C | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(40): Show |
45 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.838-1360C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182418 | |||||||
| chr1:236182432 | C | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0155 others(5): Show |
8 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.838-1346C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182432 | |||||||
| chr1:236182440 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.838-1338G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182440 | |||||||
| chr1:236182708 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838-1070C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182708 | |||||||
| chr1:236182733 | T | TCAAA | 294 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(291): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.838-1032_838-1029d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236182733 | ||||||
| chr1:236182753 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.838-1025T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182753 | |||||||
| chr1:236182901 | G | A | 31 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(28): Show |
32 | HG01981.hp2 HG02258.hp2 HG02559.hp2 others(29): Show |
intron_variant | MODIFIER | c.838-877G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182901 | |||||||
| chr1:236182913 | C | T | 64 | a0001c0001t0001g0252 a0001c0001t0002g0001 a0001c0001t0002g0007 others(61): Show |
67 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.838-865C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236182913 | |||||||
| chr1:236183029 | A | G | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.838-749A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183029 | |||||||
| chr1:236183104 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.838-674C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183104 | |||||||
| chr1:236183163 | G | A | 1 | a0001c0001t0003g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.838-615G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183163 | |||||||
| chr1:236183175 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.838-603A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183175 | |||||||
| chr1:236183487 | TGAA | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0330 a0001c0001t0001g0332 |
3 | NA18964.hp1 NA18994.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.838-282_838-280del others(3): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 236183487 | ||||||
| chr1:236183520 | T | G | 1 | a0001c0001t0002g0189 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.838-258T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183520 | |||||||
| chr1:236183529 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0211 a0001c0001t0002g0116 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.838-249C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183529 | |||||||
| chr1:236183602 | A | G | 1 | a0001c0001t0001g0349 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.838-176A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183602 | |||||||
| chr1:236183641 | C | T | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0325 |
3 | NA18612.hp1 NA18963.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.838-137C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 4/6 | chr1 | 236183641 | |||||||
| chr1:236183924 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(47): Show |
54 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.966+18C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236183924 | |||||||
| chr1:236184002 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.966+96C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184002 | |||||||
| chr1:236184179 | C | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(65): Show |
73 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.966+273C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184179 | |||||||
| chr1:236184261 | A | C | 5 | a0001c0001t0002g0214 a0001c0001t0004g0256 a0001c0001t0004g0279 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.966+355A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184261 | |||||||
| chr1:236184282 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.966+376A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184282 | |||||||
| chr1:236184464 | G | A | 28 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(25): Show |
29 | HG01981.hp2 HG02559.hp2 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.966+558G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184464 | |||||||
| chr1:236184631 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.966+725C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184631 | |||||||
| chr1:236184632 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.966+726T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184632 | |||||||
| chr1:236184633 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.966+727C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184633 | |||||||
| chr1:236184641 | T | A | 13 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 others(10): Show |
13 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.966+735T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184641 | |||||||
| chr1:236184705 | A | G | 296 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(293): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(303): Show |
intron_variant | MODIFIER | c.966+799A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184705 | |||||||
| chr1:236184728 | T | G | 1 | a0001c0001t0002g0189 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.966+822T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184728 | |||||||
| chr1:236184730 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.966+824C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184730 | |||||||
| chr1:236184745 | G | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+839G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184745 | |||||||
| chr1:236184770 | G | GT | 61 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(58): Show |
65 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.966+873dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236184770 | ||||||
| chr1:236184770 | G | T | 1 | a0001c0001t0003g0242 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.966+864G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184770 | |||||||
| chr1:236184859 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.966+953C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184859 | |||||||
| chr1:236184869 | C | T | 1 | a0001c0001t0003g0239 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.966+963C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184869 | |||||||
| chr1:236184963 | T | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0045 others(71): Show |
76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.966+1057T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184963 | |||||||
| chr1:236184967 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+1061A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184967 | |||||||
| chr1:236184968 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+1062T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236184968 | |||||||
| chr1:236185063 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+1157G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185063 | |||||||
| chr1:236185120 | G | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(5): Show |
8 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+1214G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185120 | |||||||
| chr1:236185139 | A | T | 2 | a0001c0001t0006g0134 a0001c0001t0006g0164 |
2 | HG01099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.966+1233A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185139 | |||||||
| chr1:236185169 | T | A | 10 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.966+1263T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185169 | |||||||
| chr1:236185354 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+1448G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185354 | |||||||
| chr1:236185487 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+1581C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185487 | |||||||
| chr1:236185560 | T | C | 236 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(233): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.966+1654T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236185560 | |||||||
| chr1:236186021 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.966+2115T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186021 | |||||||
| chr1:236186082 | T | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+2176T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186082 | |||||||
| chr1:236186084 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.966+2178C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186084 | |||||||
| chr1:236186167 | C | G | 2 | a0001c0001t0002g0270 a0001c0001t0002g0273 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.966+2261C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186167 | |||||||
| chr1:236186189 | A | AT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(56): Show |
63 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.966+2292dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186189 | ||||||
| chr1:236186189 | AT | A | 11 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 others(8): Show |
11 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.966+2292delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186189 | ||||||
| chr1:236186195 | TTTTA | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(5): Show |
8 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+2292_966+2295d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186195 | ||||||
| chr1:236186202 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0051 |
2 | HG00741.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.966+2296A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186202 | |||||||
| chr1:236186223 | A | AATAT | 13 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(10): Show |
14 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.966+2319_966+2322d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186223 | ||||||
| chr1:236186223 | A | AATATATA others(226): Show |
1 | a0001c0001t0001g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.966+2322_966+2323i others(235): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186223 | ||||||
| chr1:236186224 | ATATAATA others(31): Show |
A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(116): Show |
126 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(123): Show |
intron_variant | MODIFIER | c.966+2323_966+2360d others(40): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186224 | ||||||
| chr1:236186225 | TATA | T | 135 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(132): Show |
137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.966+2323_966+2325d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186225 | ||||||
| chr1:236186228 | A | ATATAATA others(201): Show |
1 | a0001c0001t0001g0323 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.966+2322_966+2323i others(210): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186228 | A | ATATAATA others(130): Show |
2 | a0001c0001t0002g0214 a0001c0001t0004g0256 |
2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.966+2322_966+2323i others(139): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186228 | A | ATATAATA others(162): Show |
13 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0215 others(10): Show |
13 | HG01106.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.966+2322_966+2323i others(171): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186228 | A | ATATAATA others(121): Show |
1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.966+2322_966+2323i others(130): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186228 | A | ATATAATA others(200): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0284 a0001c0001t0012g0257 |
3 | HG00140.hp1 HG00735.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.966+2322_966+2323i others(209): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186228 | A | ATATAATA others(200): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0206 a0001c0001t0001g0305 |
3 | HG01346.hp2 HG01358.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.966+2322_966+2323i others(209): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186228 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.966+2322A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186228 | |||||||
| chr1:236186253 | T | G | 1 | a0001c0001t0003g0276 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.966+2347T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186253 | |||||||
| chr1:236186254 | A | AATATATA others(245): Show |
1 | a0001c0001t0003g0245 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.966+2355_966+2356i others(254): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186254 | ||||||
| chr1:236186254 | A | AATATATT | 22 | a0001c0001t0001g0045 a0001c0001t0001g0119 a0001c0001t0001g0131 others(19): Show |
22 | HG00140.hp1 HG00735.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.966+2354_966+2355i others(9): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186254 | ||||||
| chr1:236186262 | T | A | 24 | a0001c0001t0001g0045 a0001c0001t0001g0119 a0001c0001t0001g0131 others(21): Show |
24 | HG00140.hp1 HG00735.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.966+2356T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186262 | |||||||
| chr1:236186262 | T | TTATATAT others(126): Show |
3 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 |
3 | HG01243.hp2 HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.966+2363_966+2364i others(135): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(161): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0368 |
3 | HG01069.hp1 HG01071.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.966+2363_966+2364i others(170): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(196): Show |
1 | a0001c0001t0001g0369 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.966+2363_966+2364i others(205): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(280): Show |
12 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0074 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+2363_966+2364i others(289): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(245): Show |
42 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0078 others(39): Show |
42 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.966+2363_966+2364i others(254): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(210): Show |
58 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0065 others(55): Show |
58 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.966+2363_966+2364i others(219): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(242): Show |
1 | a0001c0001t0001g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.966+2363_966+2364i others(251): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(175): Show |
9 | a0001c0001t0001g0039 a0001c0001t0001g0110 a0001c0001t0001g0115 others(6): Show |
9 | HG00438.hp2 HG01109.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+2363_966+2364i others(184): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(175): Show |
3 | a0001c0001t0002g0220 a0001c0001t0002g0225 a0001c0001t0002g0237 |
3 | HG02258.hp2 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.966+2363_966+2364i others(184): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(241): Show |
1 | a0001c0001t0001g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.966+2363_966+2364i others(250): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(242): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0195 |
2 | NA18947.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.966+2363_966+2364i others(251): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(280): Show |
1 | a0001c0001t0001g0366 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.966+2363_966+2364i others(289): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(242): Show |
1 | a0001c0001t0001g0182 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.966+2363_966+2364i others(251): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(96): Show |
26 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0044 others(23): Show |
28 | HG00280.hp2 HG00733.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.966+2374_966+2375i others(105): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(151): Show |
1 | a0001c0001t0001g0002 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.966+2374_966+2375i others(160): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186262 | T | TTATATAT others(206): Show |
1 | a0001c0001t0001g0002 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.966+2374_966+2375i others(215): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186262 | ||||||
| chr1:236186270 | T | A | 122 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(119): Show |
129 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(126): Show |
intron_variant | MODIFIER | c.966+2364T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186270 | |||||||
| chr1:236186277 | A | AATATATA others(59): Show |
4 | a0001c0001t0002g0064 a0001c0001t0002g0199 a0001c0001t0002g0207 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+2374_966+2375i others(68): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186277 | ||||||
| chr1:236186277 | A | AATATATA others(59): Show |
1 | a0001c0001t0003g0289 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.966+2374_966+2375i others(68): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186277 | ||||||
| chr1:236186277 | A | AATATATA others(61): Show |
33 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0046 others(30): Show |
34 | HG00673.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.966+2374_966+2375i others(70): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186277 | ||||||
| chr1:236186277 | A | AATATATA others(116): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0349 others(3): Show |
6 | HG02015.hp1 HG02040.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+2374_966+2375i others(125): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186277 | ||||||
| chr1:236186277 | A | AATATCTA others(100): Show |
3 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0008g0136 |
3 | HG00280.hp1 HG01069.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.966+2374_966+2375i others(109): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186277 | ||||||
| chr1:236186277 | A | ATATATAT others(60): Show |
1 | a0001c0001t0001g0285 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.966+2371_966+2372i others(69): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186277 | |||||||
| chr1:236186277 | A | ATCTATAA others(97): Show |
2 | a0001c0001t0008g0112 a0001c0001t0011g0364 |
2 | NA18986.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.966+2371_966+2372i others(106): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186277 | |||||||
| chr1:236186277 | A | ATTATATA others(61): Show |
1 | a0001c0001t0001g0356 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.966+2371_966+2372i others(70): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186277 | |||||||
| chr1:236186277 | A | T | 151 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0039 others(148): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.966+2371A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186277 | |||||||
| chr1:236186280 | A | ATATAATA others(36): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0002g0117 |
3 | HG00741.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.966+2374_966+2375i others(45): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186280 | |||||||
| chr1:236186280 | A | ATATATAA others(6): Show |
3 | a0001c0001t0001g0118 a0001c0001t0002g0005 a0001c0001t0002g0116 |
4 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+2374_966+2375i others(15): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186280 | |||||||
| chr1:236186280 | A | ATATATTA others(6): Show |
1 | a0003c0004t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.966+2374_966+2375i others(15): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186280 | |||||||
| chr1:236186280 | A | ATATATTA others(29): Show |
2 | a0001c0001t0001g0268 a0001c0001t0001g0271 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.966+2374_966+2375i others(38): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186280 | |||||||
| chr1:236186285 | AAATAATA others(31): Show |
A | 1 | a0001c0001t0003g0276 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.966+2384_966+2421d others(40): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186285 | ||||||
| chr1:236186297 | A | ATATATAT | 25 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(22): Show |
26 | HG01981.hp2 HG02602.hp1 HG02615.hp2 others(23): Show |
intron_variant | MODIFIER | c.966+2399_966+2405d others(9): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186297 | ||||||
| chr1:236186320 | AAAT | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(117): Show |
127 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.966+2419_966+2421d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186320 | ||||||
| chr1:236186332 | AT | A | 157 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0039 others(154): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.966+2428delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236186332 | ||||||
| chr1:236186333 | T | TATATTAT others(74): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0368 a0001c0001t0001g0369 |
4 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+2427_966+2428i others(83): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186333 | |||||||
| chr1:236186339 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 |
3 | HG01243.hp2 HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.966+2433A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186339 | |||||||
| chr1:236186340 | T | A | 3 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 |
3 | HG01243.hp2 HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.966+2434T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186340 | |||||||
| chr1:236186341 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 |
3 | HG01243.hp2 HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.966+2435A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186341 | |||||||
| chr1:236186500 | C | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+2594C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186500 | |||||||
| chr1:236186711 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+2805C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236186711 | |||||||
| chr1:236187077 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+3171G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187077 | |||||||
| chr1:236187080 | T | C | 4 | a0001c0001t0004g0256 a0001c0001t0004g0279 a0001c0001t0004g0318 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+3174T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187080 | |||||||
| chr1:236187185 | TG | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0330 a0001c0001t0001g0332 |
3 | NA18964.hp1 NA18994.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.966+3280delG | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187185 | |||||||
| chr1:236187251 | A | T | 1 | a0001c0001t0002g0194 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.966+3345A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187251 | |||||||
| chr1:236187273 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+3367C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187273 | |||||||
| chr1:236187274 | T | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+3368T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187274 | |||||||
| chr1:236187341 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.966+3435T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187341 | |||||||
| chr1:236187356 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0271 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.966+3450T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187356 | |||||||
| chr1:236187471 | G | C | 2 | a0001c0001t0007g0178 a0001c0001t0007g0209 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.966+3565G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187471 | |||||||
| chr1:236187570 | C | T | 5 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0008g0112 others(2): Show |
5 | HG00280.hp1 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+3664C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187570 | |||||||
| chr1:236187593 | T | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+3687T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187593 | |||||||
| chr1:236187692 | T | TCTGTTTT others(15): Show |
146 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(143): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.966+3797_966+3818d others(24): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236187692 | ||||||
| chr1:236187751 | AATC | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+3847_966+3849d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236187751 | ||||||
| chr1:236187790 | T | C | 1 | a0001c0001t0003g0229 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.966+3884T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187790 | |||||||
| chr1:236187802 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+3896C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236187802 | |||||||
| chr1:236188013 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+4107C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188013 | |||||||
| chr1:236188014 | A | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(283): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.966+4108A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188014 | |||||||
| chr1:236188231 | G | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+4325G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188231 | |||||||
| chr1:236188300 | C | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+4394C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188300 | |||||||
| chr1:236188343 | A | C | 2 | a0001c0002t0002g0018 a0001c0002t0006g0019 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.966+4437A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188343 | |||||||
| chr1:236188349 | C | T | 1 | a0001c0001t0004g0295 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.966+4443C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188349 | |||||||
| chr1:236188356 | A | G | 1 | a0001c0001t0002g0331 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.966+4450A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188356 | |||||||
| chr1:236188466 | A | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(135): Show |
146 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(143): Show |
intron_variant | MODIFIER | c.966+4560A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188466 | |||||||
| chr1:236188467 | A | C | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+4561A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188467 | |||||||
| chr1:236188490 | T | G | 1 | a0001c0001t0002g0197 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.966+4584T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188490 | |||||||
| chr1:236188495 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+4589C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188495 | |||||||
| chr1:236188506 | T | G | 3 | a0001c0001t0006g0145 a0001c0001t0006g0217 a0001c0001t0006g0272 |
3 | HG00735.hp2 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.966+4600T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188506 | |||||||
| chr1:236188533 | T | G | 5 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0008g0112 others(2): Show |
5 | HG00280.hp1 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+4627T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188533 | |||||||
| chr1:236188544 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.966+4638G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188544 | |||||||
| chr1:236188617 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0268 others(3): Show |
6 | HG00741.hp1 HG02451.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+4711A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188617 | |||||||
| chr1:236188619 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.966+4713G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188619 | |||||||
| chr1:236188633 | G | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+4727G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188633 | |||||||
| chr1:236188727 | G | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+4821G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188727 | |||||||
| chr1:236188746 | T | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0285 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.966+4840T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188746 | |||||||
| chr1:236188913 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.966+5007A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188913 | |||||||
| chr1:236188928 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+5022C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188928 | |||||||
| chr1:236188961 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+5055C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188961 | |||||||
| chr1:236188967 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.966+5061G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188967 | |||||||
| chr1:236188986 | C | T | 2 | a0001c0001t0002g0270 a0001c0001t0002g0273 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.966+5080C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236188986 | |||||||
| chr1:236189106 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.966+5200T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189106 | |||||||
| chr1:236189125 | C | A | 8 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0092 others(5): Show |
8 | HG00423.hp2 HG02080.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.966+5219C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189125 | |||||||
| chr1:236189130 | A | G | 2 | a0001c0001t0001g0093 a0001c0008t0001g0099 |
2 | HG02080.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.966+5224A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189130 | |||||||
| chr1:236189201 | C | A | 70 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0045 others(67): Show |
72 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.966+5295C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189201 | |||||||
| chr1:236189234 | C | T | 72 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0007 others(69): Show |
76 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.966+5328C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189234 | |||||||
| chr1:236189284 | T | C | 20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG02602.hp1 HG02735.hp2 HG02896.hp1 others(18): Show |
intron_variant | MODIFIER | c.966+5378T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189284 | |||||||
| chr1:236189310 | G | A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(2): Show |
6 | HG02040.hp1 HG02074.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+5404G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189310 | |||||||
| chr1:236189314 | C | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(20): Show |
25 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.966+5408C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189314 | |||||||
| chr1:236189444 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+5538T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189444 | |||||||
| chr1:236189519 | CT | C | 4 | a0001c0001t0001g0191 a0001c0001t0003g0310 a0001c0001t0003g0311 others(1): Show |
4 | HG00738.hp1 HG01978.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+5618delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236189519 | ||||||
| chr1:236189569 | T | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+5663T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189569 | |||||||
| chr1:236189575 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.966+5669C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189575 | |||||||
| chr1:236189694 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+5788T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189694 | |||||||
| chr1:236189877 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+5971C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189877 | |||||||
| chr1:236189927 | A | G | 5 | a0001c0001t0001g0121 a0001c0001t0002g0042 a0001c0001t0002g0108 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+6021A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189927 | |||||||
| chr1:236189946 | C | T | 5 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0008g0112 others(2): Show |
5 | HG00280.hp1 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.966+6040C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236189946 | |||||||
| chr1:236190080 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0003g0315 a0001c0001t0003g0316 others(1): Show |
4 | HG00423.hp2 NA18956.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+6174G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190080 | |||||||
| chr1:236190107 | G | T | 9 | a0001c0001t0002g0022 a0001c0001t0002g0040 a0001c0001t0002g0222 others(6): Show |
9 | HG01106.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+6201G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190107 | |||||||
| chr1:236190141 | G | GCTT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0075 others(79): Show |
87 | HG00733.hp2 HG00735.hp2 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.966+6242_966+6244d others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190141 | ||||||
| chr1:236190144 | T | G | 1 | a0001c0001t0003g0312 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.966+6238T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190144 | |||||||
| chr1:236190148 | C | CTTCT | 33 | a0001c0001t0001g0086 a0001c0001t0001g0141 a0001c0001t0001g0142 others(30): Show |
33 | HG00423.hp1 HG00544.hp2 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.966+6244_966+6245i others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190148 | ||||||
| chr1:236190148 | CT | C | 147 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(144): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.966+6261delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190148 | ||||||
| chr1:236190149 | T | TTC | 8 | a0001c0001t0001g0260 a0001c0001t0001g0359 a0001c0001t0003g0011 others(5): Show |
9 | HG02897.hp1 HG03834.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+6244_966+6245i others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190149 | ||||||
| chr1:236190151 | T | C | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0109 others(9): Show |
12 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+6245T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190151 | |||||||
| chr1:236190152 | T | C | 146 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(143): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.966+6246T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190152 | |||||||
| chr1:236190152 | T | G | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0109 others(9): Show |
12 | HG00423.hp2 HG00735.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+6246T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190152 | |||||||
| chr1:236190153 | T | C | 2 | a0001c0001t0002g0163 a0001c0001t0002g0165 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.966+6247T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190153 | |||||||
| chr1:236190153 | T | G | 146 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(143): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.966+6247T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190153 | |||||||
| chr1:236190154 | T | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0165 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.966+6248T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190154 | |||||||
| chr1:236190221 | A | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+6315A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190221 | |||||||
| chr1:236190247 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+6341C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190247 | |||||||
| chr1:236190277 | CTT | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+6373_966+6374d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190277 | ||||||
| chr1:236190361 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+6455T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190361 | |||||||
| chr1:236190419 | T | C | 17 | a0001c0001t0001g0043 a0001c0001t0001g0115 a0001c0001t0001g0123 others(14): Show |
17 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.966+6513T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190419 | |||||||
| chr1:236190446 | A | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+6540A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190446 | |||||||
| chr1:236190485 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.966+6579A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190485 | |||||||
| chr1:236190631 | T | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(283): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.966+6725T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190631 | |||||||
| chr1:236190647 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+6741T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190647 | |||||||
| chr1:236190663 | ACT | A | 133 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(130): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.966+6762_966+6763d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190663 | ||||||
| chr1:236190727 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0271 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.966+6821G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190727 | |||||||
| chr1:236190792 | ATCTGACG others(8): Show |
A | 1 | a0001c0001t0003g0306 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.966+6905_966+6919d others(17): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236190792 | ||||||
| chr1:236190993 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0021 others(135): Show |
146 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(143): Show |
intron_variant | MODIFIER | c.966+7087T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236190993 | |||||||
| chr1:236191143 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0174 a0001c0001t0002g0184 others(2): Show |
6 | HG01433.hp2 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+7237C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191143 | |||||||
| chr1:236191158 | C | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+7252C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191158 | |||||||
| chr1:236191273 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.966+7367A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191273 | |||||||
| chr1:236191332 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+7426C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191332 | |||||||
| chr1:236191333 | G | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(284): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.966+7427G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191333 | |||||||
| chr1:236191491 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0005 |
4 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+7585G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191491 | |||||||
| chr1:236191500 | T | G | 287 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(284): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.966+7594T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191500 | |||||||
| chr1:236191514 | G | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.966+7608G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191514 | |||||||
| chr1:236191766 | C | G | 6 | a0001c0001t0001g0211 a0001c0001t0002g0210 a0001c0001t0002g0221 others(3): Show |
7 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+7860C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191766 | |||||||
| chr1:236191863 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.966+7957G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191863 | |||||||
| chr1:236191948 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+8042T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236191948 | |||||||
| chr1:236192104 | C | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.966+8198C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192104 | |||||||
| chr1:236192119 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.966+8213T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192119 | |||||||
| chr1:236192157 | C | T | 79 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0007 others(76): Show |
83 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.966+8251C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192157 | |||||||
| chr1:236192263 | C | T | 1 | a0001c0001t0002g0331 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.966+8357C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192263 | |||||||
| chr1:236192276 | C | G | 6 | a0001c0001t0001g0211 a0001c0001t0002g0210 a0001c0001t0002g0221 others(3): Show |
7 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.966+8370C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192276 | |||||||
| chr1:236192361 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0347 |
2 | NA18946.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.966+8455C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192361 | |||||||
| chr1:236192372 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.966+8466T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192372 | |||||||
| chr1:236192376 | G | GA | 15 | a0001c0001t0001g0077 a0001c0001t0001g0101 a0001c0001t0001g0137 others(12): Show |
16 | HG00621.hp1 HG01109.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.966+8483dupA | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236192376 | ||||||
| chr1:236192390 | C | A | 1 | a0001c0001t0002g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.966+8484C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192390 | |||||||
| chr1:236192479 | A | G | 1 | a0001c0001t0007g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.966+8573A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192479 | |||||||
| chr1:236192524 | T | G | 175 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(172): Show |
179 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.966+8618T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192524 | |||||||
| chr1:236192539 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.966+8633G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192539 | |||||||
| chr1:236192585 | T | C | 65 | a0001c0001t0001g0202 a0001c0001t0002g0001 a0001c0001t0002g0007 others(62): Show |
68 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.966+8679T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192585 | |||||||
| chr1:236192605 | C | G | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+8699C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192605 | |||||||
| chr1:236192619 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+8713C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192619 | |||||||
| chr1:236192620 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0191 a0001c0001t0001g0198 others(7): Show |
10 | HG00738.hp1 HG01978.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.966+8714G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192620 | |||||||
| chr1:236192628 | C | T | 20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG02602.hp1 HG02896.hp1 HG02897.hp1 others(18): Show |
intron_variant | MODIFIER | c.966+8722C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192628 | |||||||
| chr1:236192785 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(1): Show |
4 | HG00733.hp1 HG01192.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+8879G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192785 | |||||||
| chr1:236192813 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.966+8907C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192813 | |||||||
| chr1:236192904 | GTTTA | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(188): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.966+9002_966+9005d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236192904 | ||||||
| chr1:236192908 | A | G | 98 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(95): Show |
103 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.966+9002A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236192908 | |||||||
| chr1:236193132 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0051 |
2 | HG00741.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.966+9226C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193132 | |||||||
| chr1:236193133 | G | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0005 |
4 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+9227G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193133 | |||||||
| chr1:236193311 | T | C | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.966+9405T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193311 | |||||||
| chr1:236193378 | C | T | 20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG02602.hp1 HG02896.hp1 HG02897.hp1 others(18): Show |
intron_variant | MODIFIER | c.966+9472C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193378 | |||||||
| chr1:236193598 | G | A | 3 | a0001c0001t0002g0214 a0001c0001t0004g0256 a0001c0001t0004g0279 |
3 | HG02109.hp1 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.966+9692G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193598 | |||||||
| chr1:236193714 | G | C | 6 | a0001c0001t0002g0120 a0001c0001t0002g0214 a0001c0001t0004g0256 others(3): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+9808G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193714 | |||||||
| chr1:236193725 | T | C | 1 | a0001c0001t0003g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.966+9819T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193725 | |||||||
| chr1:236193922 | A | G | 111 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(108): Show |
116 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.966+10016A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236193922 | |||||||
| chr1:236194028 | A | G | 1 | a0001c0001t0003g0301 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.966+10122A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194028 | |||||||
| chr1:236194091 | T | C | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.966+10185T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194091 | |||||||
| chr1:236194232 | AT | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.966+10330delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236194232 | ||||||
| chr1:236194349 | A | G | 1 | a0001c0001t0003g0319 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.966+10443A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194349 | |||||||
| chr1:236194381 | T | C | 7 | a0001c0001t0003g0011 a0001c0001t0003g0274 a0001c0001t0003g0276 others(4): Show |
8 | NA18940.hp1 NA18956.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.966+10475T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194381 | |||||||
| chr1:236194385 | G | A | 298 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.966+10479G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194385 | |||||||
| chr1:236194485 | G | A | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.966+10579G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194485 | |||||||
| chr1:236194610 | G | T | 1 | a0001c0001t0006g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.967-10516G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194610 | |||||||
| chr1:236194755 | C | T | 18 | a0001c0001t0002g0095 a0001c0001t0002g0105 a0001c0001t0002g0157 others(15): Show |
18 | HG00423.hp1 HG00544.hp2 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.967-10371C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194755 | |||||||
| chr1:236194792 | G | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-10334G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194792 | |||||||
| chr1:236194850 | T | C | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.967-10276T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236194850 | |||||||
| chr1:236195223 | CT | C | 110 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(107): Show |
115 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(112): Show |
intron_variant | MODIFIER | c.967-9890delT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236195223 | ||||||
| chr1:236195416 | T | C | 63 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(60): Show |
66 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.967-9710T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236195416 | |||||||
| chr1:236195465 | C | T | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.967-9661C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236195465 | |||||||
| chr1:236195522 | G | A | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.967-9604G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236195522 | |||||||
| chr1:236195645 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.967-9481G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236195645 | |||||||
| chr1:236195691 | A | C | 1 | a0001c0001t0003g0233 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.967-9435A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236195691 | |||||||
| chr1:236195894 | T | C | 305 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(302): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.967-9232T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236195894 | |||||||
| chr1:236196042 | GTTTC | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-9080_967-9077d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236196042 | ||||||
| chr1:236196264 | T | C | 305 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(302): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.967-8862T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196264 | |||||||
| chr1:236196448 | A | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-8678A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196448 | |||||||
| chr1:236196459 | A | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-8667A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196459 | |||||||
| chr1:236196466 | T | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-8660T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196466 | |||||||
| chr1:236196505 | T | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(1): Show |
4 | HG00733.hp1 HG01192.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.967-8621T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196505 | |||||||
| chr1:236196677 | C | T | 1 | a0001c0001t0009g0009 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.967-8449C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196677 | |||||||
| chr1:236196978 | C | T | 109 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(106): Show |
114 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(111): Show |
intron_variant | MODIFIER | c.967-8148C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236196978 | |||||||
| chr1:236197299 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.967-7827T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197299 | |||||||
| chr1:236197510 | T | G | 110 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0076 others(107): Show |
115 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(112): Show |
intron_variant | MODIFIER | c.967-7616T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197510 | |||||||
| chr1:236197594 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0086 others(16): Show |
21 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.967-7532T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197594 | |||||||
| chr1:236197637 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.967-7489C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197637 | |||||||
| chr1:236197740 | G | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-7386G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197740 | |||||||
| chr1:236197756 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.967-7370T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197756 | |||||||
| chr1:236197872 | C | T | 119 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0075 others(116): Show |
125 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(122): Show |
intron_variant | MODIFIER | c.967-7254C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236197872 | |||||||
| chr1:236198038 | T | C | 30 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(27): Show |
31 | HG01981.hp2 HG02559.hp2 HG02602.hp1 others(28): Show |
intron_variant | MODIFIER | c.967-7088T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198038 | |||||||
| chr1:236198183 | T | C | 1 | a0001c0001t0007g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.967-6943T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198183 | |||||||
| chr1:236198269 | A | G | 287 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(284): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.967-6857A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198269 | |||||||
| chr1:236198289 | G | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(284): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.967-6837G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198289 | |||||||
| chr1:236198365 | T | G | 6 | a0001c0001t0001g0211 a0001c0001t0002g0210 a0001c0001t0002g0221 others(3): Show |
7 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-6761T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198365 | |||||||
| chr1:236198511 | T | C | 5 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(2): Show |
6 | HG02040.hp1 HG02074.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-6615T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198511 | |||||||
| chr1:236198602 | G | C | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-6524G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198602 | |||||||
| chr1:236198687 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0003g0306 |
2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.967-6439C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198687 | |||||||
| chr1:236198853 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.967-6273G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198853 | |||||||
| chr1:236198933 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.967-6193T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198933 | |||||||
| chr1:236198974 | C | G | 19 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
20 | HG02602.hp1 HG02896.hp1 HG02897.hp1 others(17): Show |
intron_variant | MODIFIER | c.967-6152C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198974 | |||||||
| chr1:236198988 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0118 others(4): Show |
7 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-6138G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236198988 | |||||||
| chr1:236199212 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0005g0050 |
2 | NA18987.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.967-5914G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199212 | |||||||
| chr1:236199412 | T | G | 1 | a0001c0001t0003g0233 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.967-5714T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199412 | |||||||
| chr1:236199516 | G | A | 1 | a0001c0001t0008g0112 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.967-5610G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199516 | |||||||
| chr1:236199573 | TTGTTATG others(3170): Show |
T | 2 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.967-5550_967-2374d others(2): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236199573 | ||||||
| chr1:236199695 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.967-5431G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199695 | |||||||
| chr1:236199767 | A | G | 1 | a0001c0001t0003g0307 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.967-5359A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199767 | |||||||
| chr1:236199788 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.967-5338T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199788 | |||||||
| chr1:236199939 | A | T | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-5187A>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199939 | |||||||
| chr1:236199979 | T | G | 1 | a0001c0001t0002g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.967-5147T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236199979 | |||||||
| chr1:236200165 | C | G | 20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG02602.hp1 HG02896.hp1 HG02897.hp1 others(18): Show |
intron_variant | MODIFIER | c.967-4961C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236200165 | |||||||
| chr1:236200216 | C | T | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-4910C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236200216 | |||||||
| chr1:236200473 | G | A | 1 | a0001c0001t0001g0369 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.967-4653G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236200473 | |||||||
| chr1:236200626 | T | G | 1 | a0001c0001t0003g0012 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.967-4500T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236200626 | |||||||
| chr1:236200900 | C | CTT | 179 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(176): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.967-4217_967-4216d others(4): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236200900 | ||||||
| chr1:236200950 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.967-4176G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236200950 | |||||||
| chr1:236201199 | G | T | 178 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(175): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.967-3927G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201199 | |||||||
| chr1:236201322 | G | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | NA19068.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.967-3804G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201322 | |||||||
| chr1:236201371 | G | A | 20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG02602.hp1 HG02896.hp1 HG02897.hp1 others(18): Show |
intron_variant | MODIFIER | c.967-3755G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201371 | |||||||
| chr1:236201416 | A | ATTC | 300 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(297): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.967-3708_967-3707i others(5): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236201416 | ||||||
| chr1:236201416 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.967-3710A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201416 | |||||||
| chr1:236201451 | T | C | 1 | a0001c0001t0002g0361 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.967-3675T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201451 | |||||||
| chr1:236201551 | A | G | 182 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(179): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.967-3575A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201551 | |||||||
| chr1:236201628 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0138 others(5): Show |
9 | HG00741.hp1 HG01243.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.967-3498A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201628 | |||||||
| chr1:236201679 | G | T | 301 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(298): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.967-3447G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201679 | |||||||
| chr1:236201757 | C | A | 2 | a0001c0001t0002g0163 a0001c0001t0002g0165 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.967-3369C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201757 | |||||||
| chr1:236201855 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0271 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.967-3271C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201855 | |||||||
| chr1:236201935 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0005 |
4 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-3191G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201935 | |||||||
| chr1:236201960 | C | T | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-3166C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236201960 | |||||||
| chr1:236202030 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.967-3096C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202030 | |||||||
| chr1:236202063 | C | A | 2 | a0001c0001t0001g0366 a0001c0001t0003g0269 |
2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.967-3063C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202063 | |||||||
| chr1:236202077 | C | T | 5 | a0001c0001t0006g0134 a0001c0001t0006g0145 a0001c0001t0006g0164 others(2): Show |
5 | HG00735.hp2 HG01099.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-3049C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202077 | |||||||
| chr1:236202330 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.967-2796G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202330 | |||||||
| chr1:236202440 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.967-2686G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202440 | |||||||
| chr1:236202448 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.967-2678G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202448 | |||||||
| chr1:236202463 | T | A | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(7): Show |
10 | HG01981.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.967-2663T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202463 | |||||||
| chr1:236202624 | A | G | 1 | a0001c0001t0003g0277 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.967-2502A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202624 | |||||||
| chr1:236202637 | A | G | 111 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(108): Show |
116 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.967-2489A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202637 | |||||||
| chr1:236202811 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0005g0050 |
2 | NA18987.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.967-2315A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202811 | |||||||
| chr1:236202812 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0002g0210 a0001c0001t0009g0009 |
4 | HG02257.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-2314A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202812 | |||||||
| chr1:236202872 | T | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(300): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.967-2254T>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236202872 | |||||||
| chr1:236203051 | A | G | 1 | a0001c0001t0001g0347 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.967-2075A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203051 | |||||||
| chr1:236203052 | T | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(290): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.967-2074T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203052 | |||||||
| chr1:236203139 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.967-1987G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203139 | |||||||
| chr1:236203218 | T | C | 303 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(300): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.967-1908T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203218 | |||||||
| chr1:236203227 | C | A | 303 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(300): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.967-1899C>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203227 | |||||||
| chr1:236203238 | C | T | 105 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(102): Show |
110 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.967-1888C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203238 | |||||||
| chr1:236203670 | T | G | 3 | a0001c0001t0002g0214 a0001c0001t0004g0256 a0001c0001t0004g0279 |
3 | HG02109.hp1 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.967-1456T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203670 | |||||||
| chr1:236203718 | T | C | 2 | a0001c0001t0003g0243 a0001c0001t0003g0244 |
2 | HG02129.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.967-1408T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236203718 | |||||||
| chr1:236204100 | T | TTGAGGGT others(8): Show |
3 | a0001c0001t0002g0214 a0001c0001t0004g0256 a0001c0001t0004g0279 |
3 | HG02109.hp1 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.967-1022_967-1008d others(17): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236204100 | ||||||
| chr1:236204157 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.967-969A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204157 | |||||||
| chr1:236204221 | C | T | 181 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(178): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.967-905C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204221 | |||||||
| chr1:236204331 | G | A | 1 | a0001c0001t0003g0301 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.967-795G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204331 | |||||||
| chr1:236204368 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0005g0016 a0001c0001t0005g0060 others(3): Show |
6 | NA18964.hp2 NA18973.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-758A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204368 | |||||||
| chr1:236204371 | T | G | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0135 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-755T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204371 | |||||||
| chr1:236204560 | C | T | 7 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0005 others(4): Show |
8 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.967-566C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204560 | |||||||
| chr1:236204725 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0268 others(2): Show |
5 | HG00741.hp1 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-401A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204725 | |||||||
| chr1:236204886 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.967-240C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204886 | |||||||
| chr1:236204927 | C | T | 294 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(291): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.967-199C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236204927 | |||||||
| chr1:236205028 | T | C | 5 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0008g0112 others(2): Show |
5 | HG00280.hp1 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-98T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236205028 | |||||||
| chr1:236205058 | G | T | 1 | a0001c0006t0001g0322 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.967-68G>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | chr1 | 236205058 | |||||||
| chr1:236205091 | C | CT | 154 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(151): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.967-34dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr1 | 236205091 | ||||||
| chr1:236205399 | T | C | 7 | a0001c0001t0001g0211 a0001c0001t0002g0210 a0001c0001t0002g0221 others(4): Show |
8 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091+149T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205399 | |||||||
| chr1:236205408 | T | C | 267 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(264): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1091+158T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205408 | |||||||
| chr1:236205558 | G | GAGAT | 3 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG01884.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1091+311_1091+314d others(6): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 236205558 | ||||||
| chr1:236205582 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0002g0210 |
2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1091+332C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205582 | |||||||
| chr1:236205600 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0005 |
4 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091+350G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205600 | |||||||
| chr1:236205836 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0180 |
3 | HG03041.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1091+586G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205836 | |||||||
| chr1:236205918 | C | T | 20 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
21 | HG02602.hp1 HG02896.hp1 HG02897.hp1 others(18): Show |
intron_variant | MODIFIER | c.1091+668C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205918 | |||||||
| chr1:236205953 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1091+703A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205953 | |||||||
| chr1:236205973 | T | G | 2 | a0001c0001t0001g0149 a0001c0001t0007g0148 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1091+723T>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236205973 | |||||||
| chr1:236206705 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1092-1345G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236206705 | |||||||
| chr1:236206748 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1092-1302C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236206748 | |||||||
| chr1:236206758 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0220 |
2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1092-1292C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236206758 | |||||||
| chr1:236206773 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1092-1277C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236206773 | |||||||
| chr1:236206829 | G | GAGGCCAG others(2): Show |
202 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(199): Show |
207 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1092-1220_1092-121 others(13): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 236206829 | ||||||
| chr1:236206829 | G | GAGGCCAG others(11): Show |
1 | a0001c0001t0002g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1092-1212_1092-121 others(22): Show |
GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 236206829 | ||||||
| chr1:236206895 | G | C | 1 | a0002c0003t0001g0254 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1092-1155G>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236206895 | |||||||
| chr1:236206956 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0220 |
2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1092-1094G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236206956 | |||||||
| chr1:236207012 | C | CT | 73 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
77 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.1092-1032dupT | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 236207012 | ||||||
| chr1:236207089 | T | C | 25 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0075 others(22): Show |
26 | HG00741.hp1 HG02602.hp1 HG02896.hp1 others(23): Show |
intron_variant | MODIFIER | c.1092-961T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207089 | |||||||
| chr1:236207102 | A | G | 2 | a0001c0001t0003g0266 a0001c0001t0003g0267 |
2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1092-948A>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207102 | |||||||
| chr1:236207225 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1092-825C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207225 | |||||||
| chr1:236207354 | C | T | 234 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0038 others(231): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.1092-696C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207354 | |||||||
| chr1:236207390 | A | C | 273 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(270): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.1092-660A>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207390 | |||||||
| chr1:236207412 | T | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0051 others(31): Show |
36 | HG00741.hp1 HG01243.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.1092-638T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207412 | |||||||
| chr1:236207530 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1092-520T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207530 | |||||||
| chr1:236207566 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1092-484C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207566 | |||||||
| chr1:236207574 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1092-476G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207574 | |||||||
| chr1:236207579 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0051 others(28): Show |
33 | HG00741.hp1 HG01884.hp2 HG02280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1092-471T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207579 | |||||||
| chr1:236207609 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1092-441C>G | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207609 | |||||||
| chr1:236207775 | G | A | 5 | a0001c0001t0002g0022 a0001c0002t0002g0020 a0001c0002t0002g0024 others(2): Show |
5 | HG01106.hp2 HG01169.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092-275G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207775 | |||||||
| chr1:236207866 | G | A | 6 | a0001c0001t0007g0148 a0001c0001t0007g0161 a0001c0001t0007g0178 others(3): Show |
6 | HG01981.hp2 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1092-184G>A | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207866 | |||||||
| chr1:236207960 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(112): Show |
120 | HG00423.hp1 HG00544.hp2 HG00733.hp2 others(117): Show |
intron_variant | MODIFIER | c.1092-90C>T | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236207960 | |||||||
| chr1:236208007 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18991.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1092-43T>C | GPR137B | ENSG00000077585.14 | transcript | ENST00000366592.8 | protein_coding | 6/6 | chr1 | 236208007 |