Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84457 |
| ensemblid | ENSG00000165443.12 |
| hgncid | 29378 |
| symbol | PHYHIPL |
| name | phytanoyl-CoA 2-hydroxylase interacting protein like |
| refseq_nuc | NM_032439.4 |
| refseq_prot | NP_115815.2 |
| ensembl_nuc | ENST00000373880.9 |
| ensembl_prot | ENSP00000362987.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 59176643 |
| end | 59247770 |
| strand | + |
| ver | v1.2 |
| region | chr10:59176643-59247770 |
| region5000 | chr10:59171643-59252770 |
| regionname0 | PHYHIPL_chr10_59176643_59247770 |
| regionname5000 | PHYHIPL_chr10_59171643_59252770 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 376 | 110 | 55 | 7 | 34 | 1 | 13 | 27 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | MEVPR others(371): Show |
chr10 | 59171643 | 59252770 |
| a0002 | 0/0 | 376 | 92 | 29 | 15 | 36 | 1 | 11 | 25 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | MEVPR others(371): Show |
chr10 | 59171643 | 59252770 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1128 | 109 | 54 | 7 | 34 | 1 | 13 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | ATGGA others(1123): Show |
chr10 | 59171643 | 59252770 | ||
| a0001c0003 | 0/0 | 1128 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | ATGGA others(1123): Show |
chr10 | 59171643 | 59252770 | ||
| a0002c0002 | 0/0 | 1128 | 91 | 29 | 14 | 36 | 1 | 11 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | ATGGA others(1123): Show |
chr10 | 59171643 | 59252770 | ||
| a0002c0004 | 0/0 | 1128 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | ATGGA others(1123): Show |
chr10 | 59171643 | 59252770 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3522 | 63 | 44 | 4 | 10 | 0 | 5 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0002 | 0/0 | 3522 | 34 | 1 | 1 | 24 | 1 | 7 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0003 | 0/0 | 3522 | 4 | 3 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0004 | 0/0 | 3521 | 3 | 3 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3516): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0005 | 0/0 | 3522 | 2 | 2 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0007 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0009 | 0/0 | 3522 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0001t0011 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0001c0003t0001 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0002c0002t0001 | 0/0 | 3522 | 88 | 27 | 14 | 35 | 1 | 11 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0002c0002t0006 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0002c0002t0008 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0002c0002t0010 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| a0002c0004t0001 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | AGAGC others(3517): Show |
chr10 | 59171643 | 59252770 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0011g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00597 | hp2 | a0002 | c0002 | t0010 | g0162 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01071 | hp1 | a0002 | c0004 | t0001 | g0137 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0164 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02622 | hp2 | a0002 | c0002 | t0008 | g0100 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0041 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0160 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0197 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03516 | hp1 | a0002 | c0002 | t0006 | g0113 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0175 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | ASW | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0128 | EUR | TSI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0023 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59245484 | G | C | 1 | a0002 | 92 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(89): Show |
missense_variant | MODERATE | c.1024G>C | p.Val342Leu | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1235/3521 | 1024/1131 | 342/376 | chr10 | 59245484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59245303 | G | A | 1 | a0001c0003 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.843G>A | p.Val281Val | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1054/3521 | 843/1131 | 281/376 | chr10 | 59245303 | |||
| chr10:59245444 | C | T | 1 | a0002c0004 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.984C>T | p.Val328Val | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1195/3521 | 984/1131 | 328/376 | chr10 | 59245444 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59176707 | C | T | 1 | a0001c0001t0011 | 1 | HG01123.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/5 | 147 | chr10 | 59176707 | ||||||
| chr10:59176796 | C | T | 1 | a0002c0002t0010 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/5 | 58 | chr10 | 59176796 | ||||||
| chr10:59245720 | C | T | 1 | a0001c0001t0009 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 129 | chr10 | 59245720 | ||||||
| chr10:59245795 | T | C | 1 | a0001c0001t0003 | 4 | HG00639.hp2 HG02486.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*204T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 204 | chr10 | 59245795 | ||||||
| chr10:59245856 | T | C | 1 | a0001c0001t0005 | 2 | HG03453.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*265T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 265 | chr10 | 59245856 | ||||||
| chr10:59246005 | G | A | 1 | a0002c0002t0006 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 414 | chr10 | 59246005 | ||||||
| chr10:59246501 | C | T | 1 | a0002c0002t0008 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 910 | chr10 | 59246501 | ||||||
| chr10:59246650 | G | A | 2 | a0001c0001t0002 a0001c0001t0009 |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1059G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1059 | chr10 | 59246650 | ||||||
| chr10:59246776 | A | G | 1 | a0001c0001t0007 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1185A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1185 | chr10 | 59246776 | ||||||
| chr10:59247009 | C | T | 1 | a0001c0001t0011 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1418 | chr10 | 59247009 | ||||||
| chr10:59247042 | G | GA | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(10): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1458dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1459 | INFO_REALIGN_3_PRIME | chr10 | 59247042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59177071 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+112C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177071 | |||||||
| chr10:59177147 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.106+188G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177147 | |||||||
| chr10:59177305 | T | C | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+346T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177305 | |||||||
| chr10:59177449 | T | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+490T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177449 | |||||||
| chr10:59177453 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.106+494T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177453 | |||||||
| chr10:59177495 | G | C | 1 | a0002c0002t0001g0025 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106+536G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177495 | |||||||
| chr10:59177550 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106+591C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177550 | |||||||
| chr10:59177696 | T | C | 4 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+737T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177696 | |||||||
| chr10:59177730 | A | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+771A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177730 | |||||||
| chr10:59177785 | G | GAGTCTGC others(12): Show |
1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+827_106+845dup others(19): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59177785 | ||||||
| chr10:59178013 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+1054A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178013 | |||||||
| chr10:59178241 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01167.hp1 HG02622.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1282A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178241 | |||||||
| chr10:59178259 | A | G | 1 | a0002c0002t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.106+1300A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178259 | |||||||
| chr10:59178364 | G | A | 1 | a0002c0002t0001g0025 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106+1405G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178364 | |||||||
| chr10:59178655 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+1696C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178655 | |||||||
| chr10:59178679 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+1720C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178679 | |||||||
| chr10:59178689 | A | C | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+1730A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178689 | |||||||
| chr10:59178770 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.106+1811A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178770 | |||||||
| chr10:59178851 | C | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+1892C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178851 | |||||||
| chr10:59178898 | A | G | 1 | a0002c0002t0001g0188 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.106+1939A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178898 | |||||||
| chr10:59179246 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
115 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.106+2287G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179246 | |||||||
| chr10:59179302 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
115 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.106+2343A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179302 | |||||||
| chr10:59179458 | C | T | 2 | a0002c0002t0001g0186 a0002c0002t0001g0187 |
2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.106+2499C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179458 | |||||||
| chr10:59179462 | C | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+2503C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179462 | |||||||
| chr10:59179540 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+2581A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179540 | |||||||
| chr10:59179743 | A | G | 1 | a0002c0002t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.106+2784A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179743 | |||||||
| chr10:59179754 | A | T | 2 | a0002c0002t0001g0182 a0002c0002t0001g0183 |
2 | HG02135.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.106+2795A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179754 | |||||||
| chr10:59179765 | ATATT | A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(30): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+2809_106+2812d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179765 | ||||||
| chr10:59179842 | T | TAC | 32 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(29): Show |
33 | HG00738.hp2 HG01071.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.106+2926_106+2927d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | T | TACAC | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
16 | HG00738.hp1 HG02015.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+2924_106+2927d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | T | TACACAC | 12 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
12 | HG01106.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.106+2922_106+2927d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02647.hp1 NA18947.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.106+2920_106+2927d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | TAC | T | 19 | a0001c0001t0001g0103 a0001c0001t0002g0049 a0001c0001t0002g0050 others(16): Show |
19 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+2926_106+2927d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | TACAC | T | 32 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(29): Show |
33 | HG00558.hp1 HG00597.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.106+2924_106+2927d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | TACACAC | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
21 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.106+2922_106+2927d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0111 others(8): Show |
11 | HG00639.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+2920_106+2927d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59179842 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106+2914_106+2927d others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | ||||||
| chr10:59180101 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106+3142A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180101 | |||||||
| chr10:59180249 | C | CAT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+3298_106+3299d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180249 | ||||||
| chr10:59180255 | T | TACAC | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+3297_106+3298i others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180255 | ||||||
| chr10:59180257 | T | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+3298T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180257 | |||||||
| chr10:59180257 | T | TAC | 49 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
50 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.106+3318_106+3319d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | ||||||
| chr10:59180257 | T | TACAC | 2 | a0001c0001t0001g0094 a0002c0002t0001g0190 |
2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.106+3316_106+3319d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | ||||||
| chr10:59180257 | T | TACACAC | 47 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(44): Show |
49 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.106+3314_106+3319d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | ||||||
| chr10:59180257 | T | TACACACA others(1): Show |
2 | a0001c0001t0002g0043 a0001c0001t0002g0189 |
2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.106+3312_106+3319d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | ||||||
| chr10:59180257 | T | TATAC | 5 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 others(2): Show |
5 | HG02145.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+3299_106+3300i others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | ||||||
| chr10:59180259 | C | T | 6 | a0002c0002t0001g0114 a0002c0002t0001g0118 a0002c0002t0001g0119 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+3300C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180259 | |||||||
| chr10:59180279 | T | C | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0042 others(1): Show |
4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+3320T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180279 | |||||||
| chr10:59180294 | A | AAT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01167.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+3347_106+3348d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180294 | ||||||
| chr10:59180294 | AATATATA others(30): Show |
A | 1 | a0002c0002t0001g0117 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.106+3349_106+3385d others(39): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180294 | ||||||
| chr10:59180313 | A | AGTAT | 2 | a0001c0001t0001g0020 a0001c0001t0001g0022 |
2 | HG01433.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.106+3355_106+3358d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180313 | ||||||
| chr10:59180313 | A | AGTATGTG others(3): Show |
1 | a0001c0001t0004g0010 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+3358_106+3359i others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180313 | ||||||
| chr10:59180314 | G | GTA | 4 | a0001c0001t0002g0042 a0001c0001t0002g0058 a0002c0002t0001g0144 others(1): Show |
4 | HG02027.hp1 HG03831.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3402_106+3403d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | G | GTATA | 5 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0002c0002t0001g0145 others(2): Show |
5 | HG02015.hp1 HG02698.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+3400_106+3403d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | G | GTATATA | 2 | a0002c0002t0001g0147 a0002c0002t0001g0188 |
2 | HG00673.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.106+3398_106+3403d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | G | GTATATAT others(1): Show |
2 | a0002c0002t0001g0148 a0002c0002t0001g0149 |
2 | HG01884.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.106+3396_106+3403d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0040 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.106+3392_106+3403d others(14): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | G | GTATGTGT others(7): Show |
1 | a0001c0001t0004g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.106+3358_106+3359i others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTA | G | 8 | a0001c0001t0001g0196 a0001c0001t0002g0032 a0001c0001t0002g0053 others(5): Show |
8 | HG00558.hp2 HG01433.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+3402_106+3403d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATA | G | 16 | a0001c0001t0001g0024 a0001c0001t0001g0109 a0001c0001t0002g0052 others(13): Show |
16 | HG00738.hp2 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+3400_106+3403d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATA | G | 10 | a0001c0001t0001g0099 a0001c0001t0001g0193 a0001c0001t0001g0194 others(7): Show |
10 | HG00733.hp1 HG01071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+3398_106+3403d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(1): Show |
G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0108 a0001c0001t0002g0036 others(14): Show |
17 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.106+3396_106+3403d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(3): Show |
G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0076 others(16): Show |
19 | HG02258.hp2 HG02280.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+3394_106+3403d others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(5): Show |
G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(19): Show |
24 | HG00639.hp2 HG01167.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.106+3392_106+3403d others(14): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(7): Show |
G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0077 others(7): Show |
11 | HG01891.hp1 HG01891.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+3390_106+3403d others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(9): Show |
G | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(15): Show |
18 | HG02622.hp2 HG03041.hp1 HG03225.hp1 others(15): Show |
intron_variant | MODIFIER | c.106+3388_106+3403d others(18): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(11): Show |
G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+3386_106+3403d others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(13): Show |
G | 2 | a0001c0001t0001g0091 a0001c0003t0001g0090 |
2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+3384_106+3403d others(22): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+3378_106+3403d others(28): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(21): Show |
G | 32 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0129 others(29): Show |
33 | HG00558.hp1 HG00597.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.106+3376_106+3403d others(30): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180314 | GTATATAT others(23): Show |
G | 1 | a0002c0002t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+3374_106+3403d others(32): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | ||||||
| chr10:59180316 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0004g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.106+3358_106+3359i others(14): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180316 | ||||||
| chr10:59180318 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0021 |
2 | HG03704.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.106+3359A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180318 | |||||||
| chr10:59180322 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0011g0023 |
2 | HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.106+3363A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180322 | |||||||
| chr10:59180324 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.106+3365A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180324 | |||||||
| chr10:59180326 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG02027.hp2 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.106+3367A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180326 | |||||||
| chr10:59180328 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.106+3379_106+3380i others(19): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180328 | ||||||
| chr10:59180328 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0003g0012 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+3369A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180328 | |||||||
| chr10:59180330 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+3371A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180330 | |||||||
| chr10:59180342 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+3383A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180342 | |||||||
| chr10:59180346 | A | T | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+3387A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180346 | |||||||
| chr10:59180359 | T | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+3400T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180359 | |||||||
| chr10:59180375 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01167.hp1 HG02622.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3416C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180375 | |||||||
| chr10:59180383 | A | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+3424A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180383 | |||||||
| chr10:59180535 | C | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+3576C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180535 | |||||||
| chr10:59180559 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+3600C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180559 | |||||||
| chr10:59180752 | T | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.106+3793T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180752 | |||||||
| chr10:59180798 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02258.hp2 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.106+3839G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180798 | |||||||
| chr10:59181315 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(31): Show |
35 | HG01884.hp1 HG01891.hp1 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.106+4356A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181315 | |||||||
| chr10:59181567 | G | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+4608G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181567 | |||||||
| chr10:59181616 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+4657C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181616 | |||||||
| chr10:59181618 | A | C | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+4659A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181618 | |||||||
| chr10:59181642 | G | A | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.106+4683G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181642 | |||||||
| chr10:59181831 | C | CAA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+4873_106+4874d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59181831 | ||||||
| chr10:59182200 | G | T | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+5241G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182200 | |||||||
| chr10:59182347 | G | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+5388G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182347 | |||||||
| chr10:59182725 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.106+5766A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182725 | |||||||
| chr10:59182735 | G | A | 1 | a0002c0002t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.106+5776G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182735 | |||||||
| chr10:59182757 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+5798G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182757 | |||||||
| chr10:59182774 | G | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(126): Show |
132 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.106+5815G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182774 | |||||||
| chr10:59182794 | G | T | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+5835G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182794 | |||||||
| chr10:59183043 | G | T | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+6084G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183043 | |||||||
| chr10:59183135 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
114 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.106+6176G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183135 | |||||||
| chr10:59183145 | T | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+6186T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183145 | |||||||
| chr10:59183270 | A | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+6311A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183270 | |||||||
| chr10:59183374 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+6415A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183374 | |||||||
| chr10:59183512 | G | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+6553G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183512 | |||||||
| chr10:59183516 | C | T | 6 | a0002c0002t0001g0114 a0002c0002t0001g0118 a0002c0002t0001g0119 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+6557C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183516 | |||||||
| chr10:59183634 | A | G | 2 | a0001c0001t0001g0091 a0001c0003t0001g0090 |
2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+6675A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183634 | |||||||
| chr10:59183678 | A | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+6719A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183678 | |||||||
| chr10:59183692 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+6733C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183692 | |||||||
| chr10:59183710 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.106+6751C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183710 | |||||||
| chr10:59183729 | G | T | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+6770G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183729 | |||||||
| chr10:59183806 | TGTA | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+6850_106+6852d others(5): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59183806 | ||||||
| chr10:59184012 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+7053T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184012 | |||||||
| chr10:59184060 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0061 |
2 | HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.106+7101A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184060 | |||||||
| chr10:59184174 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.106+7215C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184174 | |||||||
| chr10:59184262 | A | G | 2 | a0002c0002t0001g0117 a0002c0002t0001g0128 |
2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.106+7303A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184262 | |||||||
| chr10:59184342 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.106+7383C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184342 | |||||||
| chr10:59184402 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+7443C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184402 | |||||||
| chr10:59184495 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0108 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.106+7536C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184495 | |||||||
| chr10:59184540 | A | G | 2 | a0002c0002t0001g0170 a0002c0002t0001g0181 |
2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.106+7581A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184540 | |||||||
| chr10:59184564 | A | G | 2 | a0001c0001t0001g0091 a0001c0003t0001g0090 |
2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+7605A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184564 | |||||||
| chr10:59184569 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
114 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.106+7610G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184569 | |||||||
| chr10:59184612 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.106+7653C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184612 | |||||||
| chr10:59184613 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+7654G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184613 | |||||||
| chr10:59184627 | GT | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+7680delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184627 | ||||||
| chr10:59184785 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.106+7826C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184785 | |||||||
| chr10:59184803 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+7844C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184803 | |||||||
| chr10:59184843 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(191): Show |
198 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.106+7884T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184843 | |||||||
| chr10:59184984 | A | AT | 5 | a0001c0001t0001g0079 a0002c0002t0001g0130 a0002c0002t0001g0147 others(2): Show |
5 | HG00673.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+8049dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184984 | ||||||
| chr10:59184984 | AT | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0062 others(69): Show |
75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.106+8049delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184984 | ||||||
| chr10:59184984 | ATT | A | 26 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(23): Show |
26 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.106+8048_106+8049d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184984 | ||||||
| chr10:59185057 | C | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+8098C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185057 | |||||||
| chr10:59185084 | A | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+8125A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185084 | |||||||
| chr10:59185151 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.106+8192C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185151 | |||||||
| chr10:59185200 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0004g0007 a0001c0001t0004g0010 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+8241C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185200 | |||||||
| chr10:59185201 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+8242G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185201 | |||||||
| chr10:59185219 | T | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+8260T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185219 | |||||||
| chr10:59185285 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG00639.hp2 HG00673.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+8326C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185285 | |||||||
| chr10:59185453 | G | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+8494G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185453 | |||||||
| chr10:59185578 | G | C | 1 | a0002c0002t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106+8619G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185578 | |||||||
| chr10:59185579 | C | T | 1 | a0002c0002t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106+8620C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185579 | |||||||
| chr10:59185598 | A | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
116 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.106+8639A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185598 | |||||||
| chr10:59185629 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+8670G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185629 | |||||||
| chr10:59186064 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+9105G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186064 | |||||||
| chr10:59186122 | C | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+9163C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186122 | |||||||
| chr10:59186133 | A | G | 1 | a0002c0002t0001g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.106+9174A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186133 | |||||||
| chr10:59186264 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106+9305T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186264 | |||||||
| chr10:59186328 | T | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+9369T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186328 | |||||||
| chr10:59186438 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+9479C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186438 | |||||||
| chr10:59186710 | A | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0058 |
2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.106+9751A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186710 | |||||||
| chr10:59186872 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+9913A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186872 | |||||||
| chr10:59186888 | A | G | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | NA18997.hp1 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.106+9929A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186888 | |||||||
| chr10:59187128 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+10169G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187128 | |||||||
| chr10:59187142 | A | G | 10 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0071 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+10183A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187142 | |||||||
| chr10:59187222 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+10263C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187222 | |||||||
| chr10:59187264 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+10305G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187264 | |||||||
| chr10:59187265 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+10306T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187265 | |||||||
| chr10:59187320 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+10361G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187320 | |||||||
| chr10:59187358 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.106+10399C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187358 | |||||||
| chr10:59187364 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+10405G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187364 | |||||||
| chr10:59187556 | G | T | 1 | a0002c0002t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106+10597G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187556 | |||||||
| chr10:59187600 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
115 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.106+10641C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187600 | |||||||
| chr10:59187696 | G | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+10737G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187696 | |||||||
| chr10:59187709 | G | A | 1 | a0002c0002t0001g0131 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.106+10750G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187709 | |||||||
| chr10:59187853 | T | C | 3 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 |
3 | NA18997.hp1 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.106+10894T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187853 | |||||||
| chr10:59187916 | C | G | 1 | a0002c0002t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.106+10957C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187916 | |||||||
| chr10:59187938 | T | C | 2 | a0001c0001t0002g0032 a0002c0002t0001g0116 |
2 | HG02602.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.106+10979T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187938 | |||||||
| chr10:59187984 | T | C | 1 | a0002c0002t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.106+11025T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187984 | |||||||
| chr10:59188084 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+11125C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188084 | |||||||
| chr10:59188402 | G | T | 1 | a0001c0001t0002g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.106+11443G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188402 | |||||||
| chr10:59188446 | A | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+11487A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188446 | |||||||
| chr10:59188525 | A | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+11566A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188525 | |||||||
| chr10:59188538 | A | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+11579A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188538 | |||||||
| chr10:59188727 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+11768T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188727 | |||||||
| chr10:59188748 | G | GT | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+11791dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59188748 | ||||||
| chr10:59188779 | A | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+11820A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188779 | |||||||
| chr10:59189105 | C | A | 4 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+12146C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189105 | |||||||
| chr10:59189141 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+12182T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189141 | |||||||
| chr10:59189719 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106+12760A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189719 | |||||||
| chr10:59189818 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.106+12859A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189818 | |||||||
| chr10:59189982 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0057 |
2 | NA18954.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.106+13023A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189982 | |||||||
| chr10:59190068 | A | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+13109A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190068 | |||||||
| chr10:59190426 | A | G | 1 | a0001c0001t0002g0031 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.106+13467A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190426 | |||||||
| chr10:59190550 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106+13591G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190550 | |||||||
| chr10:59190638 | T | C | 2 | a0002c0002t0001g0136 a0002c0002t0001g0172 |
2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.106+13679T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190638 | |||||||
| chr10:59190934 | T | C | 2 | a0002c0002t0001g0136 a0002c0002t0001g0172 |
2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.106+13975T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190934 | |||||||
| chr10:59191027 | T | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+14068T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59191027 | |||||||
| chr10:59191277 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
116 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.106+14318C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59191277 | |||||||
| chr10:59191403 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02027.hp2 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+14444T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59191403 | |||||||
| chr10:59191902 | G | GA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+14945dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59191902 | ||||||
| chr10:59192033 | T | G | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.106+15074T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192033 | |||||||
| chr10:59192052 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.106+15093G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192052 | |||||||
| chr10:59192053 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+15094C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192053 | |||||||
| chr10:59192130 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+15171T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192130 | |||||||
| chr10:59192257 | G | A | 1 | a0002c0002t0001g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106+15298G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192257 | |||||||
| chr10:59192390 | T | C | 1 | a0001c0001t0003g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+15431T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192390 | |||||||
| chr10:59192394 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+15435T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192394 | |||||||
| chr10:59192534 | T | C | 1 | a0002c0002t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.106+15575T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192534 | |||||||
| chr10:59192536 | G | A | 1 | a0002c0004t0001g0137 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.106+15577G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192536 | |||||||
| chr10:59192586 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+15627C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192586 | |||||||
| chr10:59192601 | CAA | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+15643_106+1564 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192601 | |||||||
| chr10:59192837 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.106+15878G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192837 | |||||||
| chr10:59192899 | A | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+15940A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192899 | |||||||
| chr10:59193152 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16193C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193152 | |||||||
| chr10:59193153 | A | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+16194A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193153 | |||||||
| chr10:59193307 | A | G | 1 | a0002c0002t0001g0180 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.106+16348A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193307 | |||||||
| chr10:59193343 | G | T | 1 | a0002c0002t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+16384G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193343 | |||||||
| chr10:59193359 | A | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+16400A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193359 | |||||||
| chr10:59193409 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16450G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193409 | |||||||
| chr10:59193660 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16701G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193660 | |||||||
| chr10:59193697 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16738T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193697 | |||||||
| chr10:59193836 | G | C | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+16877G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193836 | |||||||
| chr10:59194004 | C | A | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+17045C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194004 | |||||||
| chr10:59194039 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+17080G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194039 | |||||||
| chr10:59194079 | TG | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG02622.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.106+17121delG | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194079 | |||||||
| chr10:59194080 | G | GT | 45 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(42): Show |
45 | HG00639.hp1 HG00733.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.106+17142dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59194080 | ||||||
| chr10:59194080 | G | GTT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0107 others(4): Show |
7 | HG02257.hp2 HG03098.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+17141_106+1714 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59194080 | ||||||
| chr10:59194080 | GT | G | 6 | a0001c0001t0001g0091 a0001c0001t0005g0197 a0001c0001t0005g0198 others(3): Show |
6 | HG00673.hp2 HG02698.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+17142delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59194080 | ||||||
| chr10:59194084 | T | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+17125T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194084 | |||||||
| chr10:59194105 | G | A | 56 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(53): Show |
58 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.106+17146G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194105 | |||||||
| chr10:59194482 | G | A | 6 | a0002c0002t0001g0114 a0002c0002t0001g0118 a0002c0002t0001g0119 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+17523G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194482 | |||||||
| chr10:59194651 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+17692G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194651 | |||||||
| chr10:59194659 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+17700T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194659 | |||||||
| chr10:59194850 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+17891G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194850 | |||||||
| chr10:59195080 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+18121A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195080 | |||||||
| chr10:59195180 | TTAA | T | 34 | a0001c0001t0001g0091 a0001c0001t0002g0001 a0001c0001t0002g0031 others(31): Show |
36 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.106+18222_106+1822 others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195180 | |||||||
| chr10:59195627 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.106+18668T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195627 | |||||||
| chr10:59195670 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+18711T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195670 | |||||||
| chr10:59195706 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.106+18747G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195706 | |||||||
| chr10:59196335 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.106+19376A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196335 | |||||||
| chr10:59196344 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+19385A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196344 | |||||||
| chr10:59196415 | A | AT | 5 | a0001c0001t0001g0078 a0001c0001t0001g0092 a0002c0002t0001g0095 others(2): Show |
5 | HG02723.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+19473dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59196415 | ||||||
| chr10:59196415 | AT | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
28 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.106+19473delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59196415 | ||||||
| chr10:59196518 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+19559C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196518 | |||||||
| chr10:59196576 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.106+19617G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196576 | |||||||
| chr10:59196610 | G | A | 1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.106+19651G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196610 | |||||||
| chr10:59196661 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+19702G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196661 | |||||||
| chr10:59196695 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.106+19736G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196695 | |||||||
| chr10:59196815 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+19856C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196815 | |||||||
| chr10:59196927 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+19968C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196927 | |||||||
| chr10:59197144 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(44): Show |
48 | HG00639.hp1 HG01106.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+20185T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197144 | |||||||
| chr10:59197442 | G | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+20483G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197442 | |||||||
| chr10:59197758 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+20799A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197758 | |||||||
| chr10:59197844 | C | T | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+20885C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197844 | |||||||
| chr10:59198053 | CT | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+21101delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59198053 | ||||||
| chr10:59198153 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+21194G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198153 | |||||||
| chr10:59198332 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+21373C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198332 | |||||||
| chr10:59198339 | T | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+21380T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198339 | |||||||
| chr10:59198385 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+21426A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198385 | |||||||
| chr10:59198431 | AT | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+21480delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59198431 | ||||||
| chr10:59198566 | A | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+21607A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198566 | |||||||
| chr10:59198666 | C | T | 1 | a0002c0004t0001g0137 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.106+21707C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198666 | |||||||
| chr10:59198668 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106+21709C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198668 | |||||||
| chr10:59198669 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106+21710T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198669 | |||||||
| chr10:59198747 | CT | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(105): Show |
111 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.106+21789delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198747 | |||||||
| chr10:59198818 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106+21859T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198818 | |||||||
| chr10:59199000 | G | C | 1 | a0002c0002t0001g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+22041G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199000 | |||||||
| chr10:59199003 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0107 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+22044C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199003 | |||||||
| chr10:59199269 | A | G | 1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.106+22310A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199269 | |||||||
| chr10:59199273 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+22314A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199273 | |||||||
| chr10:59199417 | T | G | 1 | a0001c0001t0002g0043 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.106+22458T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199417 | |||||||
| chr10:59199455 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): Show |
110 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.106+22496C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199455 | |||||||
| chr10:59199469 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.106+22510A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199469 | |||||||
| chr10:59199599 | G | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+22640G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199599 | |||||||
| chr10:59199763 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0086 |
4 | HG02970.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+22804G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199763 | |||||||
| chr10:59199786 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+22827G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199786 | |||||||
| chr10:59200089 | T | C | 1 | a0002c0002t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.106+23130T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200089 | |||||||
| chr10:59200163 | T | A | 1 | a0002c0002t0001g0152 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.106+23204T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200163 | |||||||
| chr10:59200269 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+23310G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200269 | |||||||
| chr10:59200584 | G | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.106+23625G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200584 | |||||||
| chr10:59200622 | A | T | 1 | a0001c0001t0002g0039 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.106+23663A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200622 | |||||||
| chr10:59200626 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+23667G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200626 | |||||||
| chr10:59200814 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.106+23855A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200814 | |||||||
| chr10:59200830 | C | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(8): Show |
11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+23871C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200830 | |||||||
| chr10:59200873 | AG | A | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+23915delG | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200873 | |||||||
| chr10:59200972 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(105): Show |
111 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.106+24013C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200972 | |||||||
| chr10:59200973 | G | A | 2 | a0002c0002t0001g0174 a0002c0002t0001g0182 |
2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.106+24014G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200973 | |||||||
| chr10:59201076 | C | T | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.106+24117C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201076 | |||||||
| chr10:59201166 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106+24207A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201166 | |||||||
| chr10:59201219 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+24260A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201219 | |||||||
| chr10:59201344 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+24385C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201344 | |||||||
| chr10:59201460 | A | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+24501A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201460 | |||||||
| chr10:59201464 | A | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+24505A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201464 | |||||||
| chr10:59201489 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 |
3 | HG03041.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.106+24530A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201489 | |||||||
| chr10:59201550 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+24591G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201550 | |||||||
| chr10:59201580 | G | A | 1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.106+24621G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201580 | |||||||
| chr10:59201728 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(32): Show |
36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.106+24769A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201728 | |||||||
| chr10:59201927 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+24968G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201927 | |||||||
| chr10:59202073 | G | A | 1 | a0002c0002t0001g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.106+25114G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202073 | |||||||
| chr10:59202155 | T | C | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+25196T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202155 | |||||||
| chr10:59202178 | G | T | 1 | a0002c0002t0001g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.106+25219G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202178 | |||||||
| chr10:59202284 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+25325C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202284 | |||||||
| chr10:59202377 | C | G | 1 | a0001c0001t0011g0023 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.106+25418C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202377 | |||||||
| chr10:59202496 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01167.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+25537C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202496 | |||||||
| chr10:59202505 | T | G | 35 | a0001c0001t0001g0091 a0001c0001t0002g0001 a0001c0001t0002g0031 others(32): Show |
37 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.106+25546T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202505 | |||||||
| chr10:59202511 | G | GAATGAC | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+25553_106+2555 others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59202511 | ||||||
| chr10:59202520 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+25561G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202520 | |||||||
| chr10:59202580 | T | C | 4 | a0002c0002t0001g0095 a0002c0002t0001g0101 a0002c0002t0001g0102 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+25621T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202580 | |||||||
| chr10:59202946 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.106+25987G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202946 | |||||||
| chr10:59203103 | A | G | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+26144A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203103 | |||||||
| chr10:59203184 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.106+26225C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203184 | |||||||
| chr10:59203212 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.106+26253A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203212 | |||||||
| chr10:59203215 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.106+26256A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203215 | |||||||
| chr10:59203450 | T | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+26491T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203450 | |||||||
| chr10:59203462 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+26503G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203462 | |||||||
| chr10:59203487 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+26528A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203487 | |||||||
| chr10:59203607 | G | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+26648G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203607 | |||||||
| chr10:59203649 | G | C | 1 | a0002c0002t0001g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.106+26690G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203649 | |||||||
| chr10:59203652 | C | A | 1 | a0002c0002t0001g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.106+26693C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203652 | |||||||
| chr10:59203660 | C | T | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+26701C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203660 | |||||||
| chr10:59203932 | C | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(8): Show |
11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+26973C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203932 | |||||||
| chr10:59203997 | G | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+27038G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203997 | |||||||
| chr10:59204022 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+27063C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204022 | |||||||
| chr10:59204152 | A | G | 1 | a0002c0002t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.106+27193A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204152 | |||||||
| chr10:59204204 | T | G | 1 | a0002c0002t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.106+27245T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204204 | |||||||
| chr10:59204230 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+27271A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204230 | |||||||
| chr10:59204328 | A | ATAAT | 110 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
113 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.106+27370_106+2737 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204328 | ||||||
| chr10:59204473 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+27514G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204473 | |||||||
| chr10:59204506 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(29): Show |
34 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.106+27547G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204506 | |||||||
| chr10:59204660 | G | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
112 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.106+27701G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204660 | |||||||
| chr10:59204729 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.106+27770A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204729 | |||||||
| chr10:59204745 | C | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
112 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.106+27786C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204745 | |||||||
| chr10:59204863 | G | GT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0091 a0001c0001t0002g0043 others(8): Show |
11 | HG00673.hp2 HG01106.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+27923dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204863 | ||||||
| chr10:59204863 | GT | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG00639.hp2 HG01123.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+27923delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204863 | ||||||
| chr10:59204863 | GTT | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 others(2): Show |
5 | HG02145.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+27922_106+2792 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204863 | ||||||
| chr10:59205114 | C | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+28155C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205114 | |||||||
| chr10:59205175 | C | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.106+28216C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205175 | |||||||
| chr10:59205262 | G | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+28303G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205262 | |||||||
| chr10:59205301 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.106+28342G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205301 | |||||||
| chr10:59205503 | A | T | 1 | a0002c0002t0001g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.106+28544A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205503 | |||||||
| chr10:59205700 | C | T | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.107-28604C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205700 | |||||||
| chr10:59205778 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-28526A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205778 | |||||||
| chr10:59205958 | T | G | 2 | a0002c0002t0001g0176 a0002c0002t0001g0177 |
2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.107-28346T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205958 | |||||||
| chr10:59206493 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(47): Show |
51 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.107-27811G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206493 | |||||||
| chr10:59206596 | A | G | 1 | a0002c0002t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.107-27708A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206596 | |||||||
| chr10:59206714 | A | G | 1 | a0002c0002t0001g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.107-27590A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206714 | |||||||
| chr10:59206946 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(83): Show |
89 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.107-27358G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206946 | |||||||
| chr10:59207092 | C | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-27212C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207092 | |||||||
| chr10:59207432 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0107 others(2): Show |
5 | HG02257.hp2 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-26872G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207432 | |||||||
| chr10:59207755 | G | A | 4 | a0002c0002t0001g0095 a0002c0002t0001g0101 a0002c0002t0001g0102 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-26549G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207755 | |||||||
| chr10:59207788 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107-26516G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207788 | |||||||
| chr10:59207890 | C | CA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(12): Show |
15 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.107-26398dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59207890 | ||||||
| chr10:59207890 | C | CAA | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-26399_107-2639 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59207890 | ||||||
| chr10:59207952 | C | A | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-26352C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207952 | |||||||
| chr10:59208244 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-26060C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208244 | |||||||
| chr10:59208339 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-25965G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208339 | |||||||
| chr10:59208412 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-25892A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208412 | |||||||
| chr10:59208427 | A | G | 1 | a0002c0002t0001g0180 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.107-25877A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208427 | |||||||
| chr10:59208797 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-25507C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208797 | |||||||
| chr10:59208862 | A | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(83): Show |
89 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.107-25442A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208862 | |||||||
| chr10:59208951 | T | C | 2 | a0002c0002t0001g0186 a0002c0002t0001g0187 |
2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.107-25353T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208951 | |||||||
| chr10:59209078 | C | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-25226C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209078 | |||||||
| chr10:59209203 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(20): Show |
24 | HG01884.hp1 HG02015.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.107-25101A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209203 | |||||||
| chr10:59209232 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107-25072A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209232 | |||||||
| chr10:59209413 | A | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.107-24891A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209413 | |||||||
| chr10:59209496 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-24808G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209496 | |||||||
| chr10:59209503 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
113 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.107-24801T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209503 | |||||||
| chr10:59209749 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107-24555C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209749 | |||||||
| chr10:59209796 | C | A | 39 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(36): Show |
41 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.107-24508C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209796 | |||||||
| chr10:59210121 | C | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.107-24183C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210121 | |||||||
| chr10:59210169 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0107 others(2): Show |
5 | HG02257.hp2 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-24135C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210169 | |||||||
| chr10:59210694 | A | G | 6 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG02257.hp2 HG03041.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-23610A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210694 | |||||||
| chr10:59210944 | A | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-23360A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210944 | |||||||
| chr10:59211026 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-23278A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211026 | |||||||
| chr10:59211041 | C | CT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-23262dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211041 | ||||||
| chr10:59211062 | A | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-23242A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211062 | |||||||
| chr10:59211373 | T | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-22931T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211373 | |||||||
| chr10:59211664 | T | TAAA | 49 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0095 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-22616_107-2261 others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211664 | T | TAAAA | 32 | a0001c0001t0002g0189 a0002c0002t0001g0028 a0002c0002t0001g0029 others(29): Show |
32 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.107-22617_107-2261 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211664 | T | TAAAAA | 5 | a0001c0001t0001g0024 a0002c0002t0001g0026 a0002c0002t0001g0027 others(2): Show |
5 | HG01106.hp1 HG01106.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-22618_107-2261 others(9): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211664 | TA | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-22614delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211664 | TAA | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(49): Show |
55 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.107-22615_107-2261 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211664 | TAAA | T | 27 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0078 others(24): Show |
27 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-22616_107-2261 others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211664 | TAAAA | T | 5 | a0001c0001t0002g0034 a0001c0001t0002g0040 a0001c0001t0002g0059 others(2): Show |
5 | HG03453.hp2 HG03491.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-22617_107-2261 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | ||||||
| chr10:59211665 | A | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-22639A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211665 | |||||||
| chr10:59211666 | A | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0096 |
2 | HG02145.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.107-22638A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211666 | |||||||
| chr10:59211667 | A | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(49): Show |
55 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.107-22637A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211667 | |||||||
| chr10:59211668 | A | T | 27 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0078 others(24): Show |
27 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-22636A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211668 | |||||||
| chr10:59211669 | A | T | 3 | a0001c0001t0002g0034 a0001c0001t0002g0040 a0001c0001t0002g0059 |
3 | HG03491.hp1 NA18946.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.107-22635A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211669 | |||||||
| chr10:59211747 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-22557A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211747 | |||||||
| chr10:59211900 | G | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-22404G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211900 | |||||||
| chr10:59211949 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-22355A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211949 | |||||||
| chr10:59212270 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-22034G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59212270 | |||||||
| chr10:59212625 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-21679A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59212625 | |||||||
| chr10:59212875 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-21429G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59212875 | |||||||
| chr10:59213136 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(181): Show |
188 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.107-21168T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213136 | |||||||
| chr10:59213167 | T | TA | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-21126dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59213167 | ||||||
| chr10:59213327 | C | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-20977C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213327 | |||||||
| chr10:59213591 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.107-20713C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213591 | |||||||
| chr10:59213616 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-20688A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213616 | |||||||
| chr10:59213712 | T | C | 40 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(37): Show |
42 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.107-20592T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213712 | |||||||
| chr10:59214313 | CA | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(173): Show |
180 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.107-19983delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59214313 | ||||||
| chr10:59214619 | A | G | 1 | a0002c0002t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.107-19685A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59214619 | |||||||
| chr10:59214668 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(82): Show |
88 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.107-19636C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59214668 | |||||||
| chr10:59214916 | A | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-19388A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59214916 | |||||||
| chr10:59215044 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.107-19260A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215044 | |||||||
| chr10:59215082 | C | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-19222C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215082 | |||||||
| chr10:59215244 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.107-19060A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215244 | |||||||
| chr10:59215264 | A | G | 91 | a0001c0001t0001g0024 a0001c0001t0002g0189 a0002c0002t0001g0003 others(88): Show |
92 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.107-19040A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215264 | |||||||
| chr10:59215410 | T | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-18894T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215410 | |||||||
| chr10:59215583 | T | G | 2 | a0001c0001t0001g0091 a0001c0003t0001g0090 |
2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107-18721T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215583 | |||||||
| chr10:59215638 | T | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-18666T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215638 | |||||||
| chr10:59215710 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-18594A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215710 | |||||||
| chr10:59215733 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-18571C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215733 | |||||||
| chr10:59215835 | GA | G | 92 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0002g0189 others(89): Show |
93 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.107-18457delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59215835 | ||||||
| chr10:59215835 | GAA | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(85): Show |
91 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-18458_107-1845 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59215835 | ||||||
| chr10:59215963 | T | A | 1 | a0002c0002t0001g0142 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.107-18341T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215963 | |||||||
| chr10:59216018 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.107-18286T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216018 | |||||||
| chr10:59216269 | C | A | 1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-18035C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216269 | |||||||
| chr10:59216337 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-17967A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216337 | |||||||
| chr10:59216508 | C | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-17796C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216508 | |||||||
| chr10:59216512 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(82): Show |
88 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.107-17792G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216512 | |||||||
| chr10:59216892 | A | G | 1 | a0002c0002t0001g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-17412A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216892 | |||||||
| chr10:59217003 | ATACTT | A | 3 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0175 |
3 | HG02965.hp2 HG03041.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.107-17291_107-1728 others(9): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59217003 | ||||||
| chr10:59217352 | A | G | 91 | a0001c0001t0001g0024 a0001c0001t0002g0189 a0002c0002t0001g0003 others(88): Show |
92 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.107-16952A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217352 | |||||||
| chr10:59217417 | T | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-16887T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217417 | |||||||
| chr10:59217460 | C | T | 2 | a0002c0002t0001g0131 a0002c0002t0001g0144 |
2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.107-16844C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217460 | |||||||
| chr10:59217655 | T | C | 2 | a0001c0001t0001g0091 a0001c0003t0001g0090 |
2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107-16649T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217655 | |||||||
| chr10:59217748 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107-16556C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217748 | |||||||
| chr10:59218055 | G | A | 1 | a0002c0002t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.107-16249G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218055 | |||||||
| chr10:59218138 | A | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.107-16166A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218138 | |||||||
| chr10:59218311 | C | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(84): Show |
90 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-15993C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218311 | |||||||
| chr10:59218674 | TTTGAGTG others(61): Show |
T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(30): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-15561_107-1549 others(72): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59218674 | ||||||
| chr10:59218677 | G | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(140): Show |
145 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.107-15627G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218677 | |||||||
| chr10:59218745 | G | C | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(30): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-15559G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218745 | |||||||
| chr10:59218905 | A | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-15399A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218905 | |||||||
| chr10:59218920 | A | T | 2 | a0002c0002t0001g0116 a0002c0002t0001g0134 |
2 | NA18970.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.107-15384A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218920 | |||||||
| chr10:59218947 | TC | T | 2 | a0002c0002t0001g0156 a0002c0002t0001g0181 |
2 | HG02300.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.107-15356delC | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218947 | |||||||
| chr10:59219000 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-15304G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219000 | |||||||
| chr10:59219201 | A | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(173): Show |
180 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.107-15103A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219201 | |||||||
| chr10:59219346 | GA | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(43): Show |
47 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-14956delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59219346 | ||||||
| chr10:59219833 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-14471G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219833 | |||||||
| chr10:59219838 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(175): Show |
182 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-14466G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219838 | |||||||
| chr10:59220831 | T | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-13473T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59220831 | |||||||
| chr10:59220843 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(32): Show |
36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-13461A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59220843 | |||||||
| chr10:59221041 | A | G | 6 | a0002c0002t0001g0114 a0002c0002t0001g0118 a0002c0002t0001g0119 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-13263A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221041 | |||||||
| chr10:59221194 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107-13110T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221194 | |||||||
| chr10:59221381 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-12923C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221381 | |||||||
| chr10:59221493 | G | A | 7 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0044 others(4): Show |
9 | NA18950.hp1 NA18956.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-12811G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221493 | |||||||
| chr10:59221564 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.107-12740G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221564 | |||||||
| chr10:59221663 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(86): Show |
92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-12641T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221663 | |||||||
| chr10:59221749 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(86): Show |
92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-12555T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221749 | |||||||
| chr10:59222168 | C | T | 10 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0071 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.107-12136C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222168 | |||||||
| chr10:59222194 | A | G | 35 | a0001c0001t0001g0091 a0001c0001t0002g0001 a0001c0001t0002g0031 others(32): Show |
37 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-12110A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222194 | |||||||
| chr10:59222330 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.107-11974G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222330 | |||||||
| chr10:59222402 | C | A | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-11902C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222402 | |||||||
| chr10:59222473 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(32): Show |
36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-11831A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222473 | |||||||
| chr10:59222574 | G | C | 5 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | NA18941.hp1 NA18947.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-11730G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222574 | |||||||
| chr10:59222716 | TG | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-11580delG | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59222716 | ||||||
| chr10:59222717 | G | T | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107-11587G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222717 | |||||||
| chr10:59222839 | A | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-11465A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222839 | |||||||
| chr10:59222935 | A | G | 1 | a0002c0002t0001g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.107-11369A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222935 | |||||||
| chr10:59223095 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(84): Show |
90 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-11209T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223095 | |||||||
| chr10:59223230 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.107-11074G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223230 | |||||||
| chr10:59223235 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.107-11069A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223235 | |||||||
| chr10:59223453 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.107-10851G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223453 | |||||||
| chr10:59223455 | CTGTT | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-10847_107-1084 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59223455 | ||||||
| chr10:59223498 | A | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(175): Show |
182 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-10806A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223498 | |||||||
| chr10:59223603 | G | A | 2 | a0002c0002t0001g0126 a0002c0002t0001g0128 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.107-10701G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223603 | |||||||
| chr10:59223670 | A | AT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(87): Show |
93 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.107-10624dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59223670 | ||||||
| chr10:59223686 | A | C | 1 | a0002c0002t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.107-10618A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223686 | |||||||
| chr10:59223734 | C | T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(30): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-10570C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223734 | |||||||
| chr10:59223948 | C | T | 1 | a0002c0002t0001g0142 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.107-10356C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223948 | |||||||
| chr10:59224356 | T | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-9948T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224356 | |||||||
| chr10:59224456 | G | GAAACA | 27 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0011g0023 others(24): Show |
27 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.107-9809_107-9805d others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | ||||||
| chr10:59224456 | G | GAAACAAA others(3): Show |
49 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0027 others(46): Show |
50 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-9814_107-9805d others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | ||||||
| chr10:59224456 | G | GAAACAAA others(8): Show |
11 | a0002c0002t0001g0119 a0002c0002t0001g0120 a0002c0002t0001g0126 others(8): Show |
11 | HG00738.hp2 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-9819_107-9805d others(17): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | ||||||
| chr10:59224456 | GAAACA | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG00639.hp2 HG01167.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.107-9809_107-9805d others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | ||||||
| chr10:59224497 | A | AAACAAAA others(11): Show |
1 | a0002c0002t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.107-9805_107-9804i others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | ||||||
| chr10:59224497 | A | AAACAAAA others(8): Show |
2 | a0001c0001t0002g0042 a0001c0001t0002g0053 |
2 | HG03831.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.107-9805_107-9804i others(17): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | ||||||
| chr10:59224497 | A | AAACAAAA others(3): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0078 a0001c0001t0001g0082 others(21): Show |
24 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.107-9805_107-9804i others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | ||||||
| chr10:59224497 | A | AAACAC | 35 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0065 others(32): Show |
35 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-9805_107-9804i others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | ||||||
| chr10:59224497 | A | C | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0067 others(22): Show |
27 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.107-9807A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224497 | |||||||
| chr10:59224509 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-9795A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224509 | |||||||
| chr10:59224712 | A | G | 4 | a0002c0002t0001g0095 a0002c0002t0001g0101 a0002c0002t0001g0102 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-9592A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224712 | |||||||
| chr10:59224900 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0108 |
3 | HG01891.hp1 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.107-9404A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224900 | |||||||
| chr10:59225143 | T | TAAGAAAT others(304): Show |
1 | a0002c0002t0001g0138 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.107-9143_107-9142i others(313): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(308): Show |
1 | a0002c0002t0001g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.107-9143_107-9142i others(317): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(309): Show |
2 | a0002c0002t0001g0177 a0002c0002t0001g0187 |
2 | HG01255.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.107-9143_107-9142i others(318): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(315): Show |
1 | a0002c0002t0001g0163 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.107-9143_107-9142i others(324): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(317): Show |
1 | a0002c0002t0010g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.107-9143_107-9142i others(326): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(321): Show |
2 | a0002c0002t0001g0131 a0002c0002t0001g0179 |
2 | NA18965.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.107-9143_107-9142i others(330): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(322): Show |
43 | a0002c0002t0001g0003 a0002c0002t0001g0026 a0002c0002t0001g0028 others(40): Show |
44 | HG00738.hp1 HG01071.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.107-9143_107-9142i others(331): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(323): Show |
28 | a0002c0002t0001g0025 a0002c0002t0001g0027 a0002c0002t0001g0030 others(25): Show |
28 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.107-9143_107-9142i others(332): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(324): Show |
4 | a0002c0002t0001g0147 a0002c0002t0001g0164 a0002c0002t0001g0182 others(1): Show |
4 | HG00673.hp2 HG02602.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-9143_107-9142i others(333): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(325): Show |
3 | a0002c0002t0001g0123 a0002c0002t0001g0124 a0002c0002t0001g0127 |
3 | HG01433.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107-9143_107-9142i others(334): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(326): Show |
1 | a0002c0002t0001g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107-9143_107-9142i others(335): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225143 | T | TAAGAAAT others(328): Show |
1 | a0002c0002t0001g0178 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.107-9143_107-9142i others(337): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | ||||||
| chr10:59225377 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.107-8927C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225377 | |||||||
| chr10:59225390 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-8914C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225390 | |||||||
| chr10:59225511 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-8793A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225511 | |||||||
| chr10:59225714 | GA | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(86): Show |
92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-8589delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225714 | |||||||
| chr10:59225751 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-8553G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225751 | |||||||
| chr10:59225873 | G | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-8431G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225873 | |||||||
| chr10:59226145 | CAGGAG | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(8): Show |
11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-8156_107-8152d others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59226145 | ||||||
| chr10:59226148 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(75): Show |
81 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.107-8156G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226148 | |||||||
| chr10:59226185 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(43): Show |
47 | HG00639.hp1 HG01106.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-8119T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226185 | |||||||
| chr10:59226365 | C | T | 35 | a0001c0001t0001g0091 a0001c0001t0002g0001 a0001c0001t0002g0031 others(32): Show |
37 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-7939C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226365 | |||||||
| chr10:59226555 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(86): Show |
92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-7749A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226555 | |||||||
| chr10:59226827 | C | T | 1 | a0002c0002t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.107-7477C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226827 | |||||||
| chr10:59226946 | A | G | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107-7358A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226946 | |||||||
| chr10:59227036 | A | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-7268A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227036 | |||||||
| chr10:59227149 | A | G | 1 | a0002c0002t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107-7155A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227149 | |||||||
| chr10:59227250 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0062 others(175): Show |
182 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-7054A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227250 | |||||||
| chr10:59227535 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 |
3 | HG03041.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.107-6769A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227535 | |||||||
| chr10:59227621 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-6683A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227621 | |||||||
| chr10:59227855 | T | C | 2 | a0002c0002t0001g0117 a0002c0004t0001g0137 |
2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.107-6449T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227855 | |||||||
| chr10:59227879 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(184): Show |
191 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(188): Show |
intron_variant | MODIFIER | c.107-6425G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227879 | |||||||
| chr10:59227975 | G | GAGAGATA others(11): Show |
1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-6328_107-6327i others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GAGAGATA others(17): Show |
1 | a0001c0001t0002g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.107-6328_107-6327i others(26): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GAGATATA others(13): Show |
5 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0045 others(2): Show |
7 | NA18950.hp1 NA18956.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(22): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GAGATATA others(15): Show |
4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0043 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GAGATATA others(17): Show |
15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0036 others(12): Show |
15 | HG00558.hp2 HG00597.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(26): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GAGATATA others(19): Show |
6 | a0001c0001t0002g0042 a0001c0001t0002g0050 a0001c0001t0002g0058 others(3): Show |
6 | HG00673.hp1 HG02027.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(28): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GAGATATA others(21): Show |
2 | a0001c0001t0002g0037 a0001c0001t0002g0047 |
2 | HG04228.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.107-6328_107-6327i others(30): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATAGATA others(15): Show |
1 | a0001c0001t0001g0002 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-6326_107-6325i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATAT | 3 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02258.hp2 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.107-6320_107-6317d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATAT | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-6322_107-6317d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(15): Show |
1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-6317_107-6316i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(7): Show |
1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-6317_107-6316i others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(9): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | HG00639.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(18): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(11): Show |
1 | a0001c0001t0001g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.107-6317_107-6316i others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(13): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0074 a0001c0001t0001g0084 others(2): Show |
5 | HG01106.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(22): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(15): Show |
23 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0071 others(20): Show |
23 | HG01891.hp1 HG01891.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(17): Show |
6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(26): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(19): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0067 others(3): Show |
6 | HG02886.hp2 NA18941.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(28): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(21): Show |
3 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02109.hp2 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(30): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(25): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(34): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(27): Show |
1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.107-6317_107-6316i others(36): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(29): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0017 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(38): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59227975 | G | GATATATA others(25): Show |
3 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 |
3 | HG00639.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(34): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | ||||||
| chr10:59228333 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 |
3 | HG00639.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.107-5971T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228333 | |||||||
| chr10:59228379 | G | C | 1 | a0001c0001t0002g0059 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.107-5925G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228379 | |||||||
| chr10:59228795 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-5509C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228795 | |||||||
| chr10:59228823 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.107-5481C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228823 | |||||||
| chr10:59228899 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-5405C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228899 | |||||||
| chr10:59228952 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-5352A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228952 | |||||||
| chr10:59229106 | G | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-5198G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229106 | |||||||
| chr10:59229109 | T | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(27): Show |
31 | HG01884.hp1 HG01891.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.107-5195T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229109 | |||||||
| chr10:59229243 | ATAGT | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-5055_107-5052d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59229243 | ||||||
| chr10:59229330 | C | A | 1 | a0002c0002t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.107-4974C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229330 | |||||||
| chr10:59229392 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-4912G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229392 | |||||||
| chr10:59229392 | G | T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(31): Show |
36 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-4912G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229392 | |||||||
| chr10:59229465 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.107-4839G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229465 | |||||||
| chr10:59229506 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107-4798T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229506 | |||||||
| chr10:59229609 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
101 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.107-4695T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229609 | |||||||
| chr10:59229673 | C | CA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(82): Show |
88 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.107-4623dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59229673 | ||||||
| chr10:59229674 | A | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-4630A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229674 | |||||||
| chr10:59229678 | A | AT | 11 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(8): Show |
11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-4626_107-4625i others(3): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229678 | |||||||
| chr10:59229707 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-4597C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229707 | |||||||
| chr10:59229859 | CTTAG | C | 41 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0079 others(38): Show |
43 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-4440_107-4437d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59229859 | ||||||
| chr10:59229915 | A | G | 1 | a0002c0002t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.107-4389A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229915 | |||||||
| chr10:59229997 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-4307A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229997 | |||||||
| chr10:59230057 | T | C | 3 | a0002c0002t0001g0136 a0002c0002t0001g0172 a0002c0002t0001g0173 |
3 | HG02083.hp2 HG02132.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.107-4247T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230057 | |||||||
| chr10:59230117 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107-4187G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230117 | |||||||
| chr10:59230167 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-4137G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230167 | |||||||
| chr10:59230212 | C | CT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(169): Show |
176 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(173): Show |
intron_variant | MODIFIER | c.107-4073dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59230212 | ||||||
| chr10:59230212 | C | CTT | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(11): Show |
14 | HG01106.hp2 HG01123.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.107-4074_107-4073d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59230212 | ||||||
| chr10:59230373 | C | A | 1 | a0002c0002t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-3931C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230373 | |||||||
| chr10:59231107 | AT | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(184): Show |
191 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(188): Show |
intron_variant | MODIFIER | c.107-3189delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59231107 | ||||||
| chr10:59231127 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-3177A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231127 | |||||||
| chr10:59231365 | G | A | 1 | a0002c0002t0001g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.107-2939G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231365 | |||||||
| chr10:59231380 | G | C | 1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-2924G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231380 | |||||||
| chr10:59231719 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
101 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.107-2585C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231719 | |||||||
| chr10:59231871 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-2433G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231871 | |||||||
| chr10:59232006 | T | C | 1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-2298T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232006 | |||||||
| chr10:59232038 | C | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-2266C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232038 | |||||||
| chr10:59232284 | G | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(32): Show |
36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-2020G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232284 | |||||||
| chr10:59232326 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107-1978A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232326 | |||||||
| chr10:59232376 | A | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-1928A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232376 | |||||||
| chr10:59232426 | G | A | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107-1878G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232426 | |||||||
| chr10:59232474 | T | C | 5 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0001c0001t0001g0192 others(2): Show |
5 | HG00639.hp1 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-1830T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232474 | |||||||
| chr10:59232561 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-1743T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232561 | |||||||
| chr10:59232754 | TCTA | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-1546_107-1544d others(5): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59232754 | ||||||
| chr10:59232804 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.107-1500G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232804 | |||||||
| chr10:59232941 | T | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-1363T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232941 | |||||||
| chr10:59233063 | T | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1241T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233063 | |||||||
| chr10:59233205 | C | A | 1 | a0001c0001t0005g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.107-1099C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233205 | |||||||
| chr10:59233209 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01167.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-1095A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233209 | |||||||
| chr10:59233269 | G | A | 3 | a0002c0002t0001g0136 a0002c0002t0001g0172 a0002c0002t0001g0173 |
3 | HG02083.hp2 HG02132.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.107-1035G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233269 | |||||||
| chr10:59233287 | A | G | 1 | a0002c0002t0001g0138 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.107-1017A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233287 | |||||||
| chr10:59233336 | A | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-968A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233336 | |||||||
| chr10:59233382 | G | T | 7 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0044 others(4): Show |
9 | NA18950.hp1 NA18956.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-922G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233382 | |||||||
| chr10:59233577 | T | G | 89 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0026 others(86): Show |
90 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-727T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233577 | |||||||
| chr10:59233883 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-421C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233883 | |||||||
| chr10:59233911 | T | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-393T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233911 | |||||||
| chr10:59233915 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-389C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233915 | |||||||
| chr10:59233997 | T | G | 88 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0026 others(85): Show |
89 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.107-307T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233997 | |||||||
| chr10:59234021 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-283C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59234021 | |||||||
| chr10:59234153 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.107-151G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59234153 | |||||||
| chr10:59234697 | T | C | 2 | a0002c0002t0001g0176 a0002c0002t0001g0177 |
2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.303+197T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59234697 | |||||||
| chr10:59234797 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.303+297C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59234797 | |||||||
| chr10:59235246 | A | G | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.303+746A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235246 | |||||||
| chr10:59235322 | T | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.303+822T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235322 | |||||||
| chr10:59235558 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-925G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235558 | |||||||
| chr10:59235614 | A | T | 89 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0026 others(86): Show |
90 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.304-869A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235614 | |||||||
| chr10:59235654 | G | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.304-829G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235654 | |||||||
| chr10:59235713 | G | T | 1 | a0001c0001t0002g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.304-770G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235713 | |||||||
| chr10:59235824 | C | T | 1 | a0001c0001t0007g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.304-659C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235824 | |||||||
| chr10:59235825 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(27): Show |
31 | HG01884.hp1 HG01891.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.304-658G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235825 | |||||||
| chr10:59235828 | A | G | 1 | a0002c0002t0001g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.304-655A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235828 | |||||||
| chr10:59236250 | A | G | 8 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0009 others(5): Show |
8 | HG00639.hp2 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-233A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59236250 | |||||||
| chr10:59236320 | A | G | 1 | a0002c0002t0001g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.304-163A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59236320 | |||||||
| chr10:59236355 | TTCCCTTC others(15): Show |
T | 2 | a0002c0002t0001g0145 a0002c0002t0001g0146 |
2 | HG02698.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.304-120_304-99delT others(21): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr10 | 59236355 | ||||||
| chr10:59236465 | T | C | 1 | a0002c0002t0001g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.304-18T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59236465 | |||||||
| chr10:59236693 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.478+36G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59236693 | |||||||
| chr10:59236998 | CT | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(79): Show |
85 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.478+355delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr10 | 59236998 | ||||||
| chr10:59236998 | CTT | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.478+354_478+355del others(2): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr10 | 59236998 | ||||||
| chr10:59237039 | A | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.478+382A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59237039 | |||||||
| chr10:59237806 | T | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.479-782T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59237806 | |||||||
| chr10:59238034 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0067 others(3): Show |
6 | NA18941.hp1 NA18947.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-554G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238034 | |||||||
| chr10:59238090 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.479-498T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238090 | |||||||
| chr10:59238320 | A | T | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.479-268A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238320 | |||||||
| chr10:59238492 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.479-96C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238492 | |||||||
| chr10:59238524 | T | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.479-64T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238524 | |||||||
| chr10:59238995 | C | T | 4 | a0002c0002t0001g0026 a0002c0002t0001g0027 a0002c0002t0001g0028 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+290C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59238995 | |||||||
| chr10:59239033 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.596+328C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239033 | |||||||
| chr10:59239042 | A | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.596+337A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239042 | |||||||
| chr10:59239086 | CTGTT | C | 2 | a0002c0002t0001g0129 a0002c0002t0001g0130 |
2 | NA18990.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.596+383_596+386del others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59239086 | ||||||
| chr10:59239149 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.596+444T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239149 | |||||||
| chr10:59239344 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.596+639G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239344 | |||||||
| chr10:59239427 | C | T | 2 | a0001c0001t0001g0091 a0001c0003t0001g0090 |
2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.596+722C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239427 | |||||||
| chr10:59239436 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.596+731A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239436 | |||||||
| chr10:59239440 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.596+735A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239440 | |||||||
| chr10:59239448 | T | C | 2 | a0002c0002t0001g0170 a0002c0002t0001g0181 |
2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.596+743T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239448 | |||||||
| chr10:59239528 | T | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+823T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239528 | |||||||
| chr10:59239639 | G | T | 1 | a0002c0002t0001g0165 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.596+934G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239639 | |||||||
| chr10:59239768 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.596+1063C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239768 | |||||||
| chr10:59239874 | A | AT | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.596+1170dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59239874 | ||||||
| chr10:59240040 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.596+1335C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240040 | |||||||
| chr10:59240231 | A | G | 2 | a0002c0002t0001g0126 a0002c0002t0001g0128 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.596+1526A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240231 | |||||||
| chr10:59240639 | T | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0006 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.596+1934T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240639 | |||||||
| chr10:59240720 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.596+2015C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240720 | |||||||
| chr10:59240756 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.596+2051A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240756 | |||||||
| chr10:59240842 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.596+2137G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240842 | |||||||
| chr10:59241274 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(186): Show |
193 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(190): Show |
intron_variant | MODIFIER | c.596+2569T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241274 | |||||||
| chr10:59241335 | AT | A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(30): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.596+2631delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241335 | |||||||
| chr10:59241424 | A | G | 2 | a0001c0001t0005g0197 a0001c0001t0005g0198 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.596+2719A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241424 | |||||||
| chr10:59241443 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(97): Show |
103 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.596+2738T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241443 | |||||||
| chr10:59241555 | C | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
101 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.596+2850C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241555 | |||||||
| chr10:59241926 | C | G | 1 | a0001c0001t0002g0039 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.597-3131C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241926 | |||||||
| chr10:59241927 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.597-3130A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241927 | |||||||
| chr10:59242382 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-2675A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242382 | |||||||
| chr10:59242420 | TAGTC | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-2634_597-2631d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59242420 | ||||||
| chr10:59242533 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-2524C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242533 | |||||||
| chr10:59242650 | A | C | 33 | a0001c0001t0002g0001 a0001c0001t0002g0031 a0001c0001t0002g0032 others(30): Show |
35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.597-2407A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242650 | |||||||
| chr10:59242670 | G | T | 1 | a0001c0001t0005g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597-2387G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242670 | |||||||
| chr10:59242671 | A | T | 1 | a0001c0001t0005g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597-2386A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242671 | |||||||
| chr10:59243128 | G | GAA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1918_597-1917d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59243128 | ||||||
| chr10:59243128 | GA | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
91 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.597-1917delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59243128 | ||||||
| chr10:59243261 | C | T | 1 | a0002c0002t0010g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.597-1796C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243261 | |||||||
| chr10:59243301 | T | G | 1 | a0001c0001t0002g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.597-1756T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243301 | |||||||
| chr10:59243429 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-1628C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243429 | |||||||
| chr10:59243923 | T | C | 92 | a0001c0001t0005g0198 a0002c0002t0001g0003 a0002c0002t0001g0005 others(89): Show |
93 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.597-1134T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243923 | |||||||
| chr10:59243990 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597-1067T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243990 | |||||||
| chr10:59244151 | G | A | 89 | a0001c0001t0005g0198 a0002c0002t0001g0003 a0002c0002t0001g0025 others(86): Show |
90 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.597-906G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59244151 | |||||||
| chr10:59244268 | TA | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0107 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-784delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244268 | ||||||
| chr10:59244562 | C | CA | 56 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(53): Show |
59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.597-471dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAA | 20 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0078 others(17): Show |
20 | HG00558.hp2 HG02135.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.597-472_597-471dup others(2): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(2): Show |
5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-474_597-471dup others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAAAAA others(1): Show |
31 | a0002c0002t0001g0003 a0002c0002t0001g0025 a0002c0002t0001g0026 others(28): Show |
32 | HG00733.hp2 HG01123.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.597-478_597-471dup others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAAAAA others(2): Show |
28 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0002c0002t0001g0029 others(25): Show |
28 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.597-479_597-471dup others(9): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAAAAA others(3): Show |
14 | a0002c0002t0001g0030 a0002c0002t0001g0123 a0002c0002t0001g0124 others(11): Show |
14 | HG01071.hp1 HG02083.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.597-480_597-471dup others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAAAAA others(4): Show |
2 | a0002c0002t0001g0117 a0002c0002t0001g0148 |
2 | HG00738.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.597-481_597-471dup others(11): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAAAAA others(5): Show |
2 | a0002c0002t0001g0121 a0002c0002t0010g0162 |
2 | HG00597.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.597-482_597-471dup others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | C | CAAAAAAA others(6): Show |
2 | a0002c0002t0001g0135 a0002c0002t0001g0143 |
2 | HG01106.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.597-483_597-471dup others(13): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | CA | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0065 others(5): Show |
8 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-471delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | CAAAAAAA | C | 7 | a0002c0002t0001g0127 a0002c0002t0001g0141 a0002c0002t0001g0147 others(4): Show |
7 | HG00673.hp2 HG01433.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.597-477_597-471del others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | ||||||
| chr10:59244562 | CAAAAAAA others(5): Show |
C | 3 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0190 |
3 | HG02965.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.597-482_597-471del others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 |