Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27039 |
| ensemblid | ENSG00000078795.17 |
| hgncid | 9012 |
| symbol | PKD2L2 |
| name | polycystin 2 like 2, transient receptor potential cation channel |
| refseq_nuc | NM_001300921.2 |
| refseq_prot | NP_001287850.1 |
| ensembl_nuc | ENST00000508883.6 |
| ensembl_prot | ENSP00000424725.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 137889457 |
| end | 137942747 |
| strand | + |
| ver | v1.2 |
| region | chr5:137889457-137942747 |
| region5000 | chr5:137884457-137947747 |
| regionname0 | PKD2L2_chr5_137889457_137942747 |
| regionname5000 | PKD2L2_chr5_137884457_137947747 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 624 | 252 | 50 | 53 | 114 | 6 | 28 | 84 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0002 | 0/0 | 624 | 66 | 27 | 18 | 7 | 8 | 6 | 6 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0003 | 1/0 | 624 | 12 | 11 | 0 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0004 | 0/0 | 624 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0005 | 0/0 | 624 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0006 | 0/0 | 624 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0007 | 0/0 | 624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| a0008 | 0/0 | 624 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | MAEAS others(619): Show |
chr5 | 137884457 | 137947747 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1872 | 251 | 49 | 53 | 114 | 6 | 28 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0001c0012 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0002c0002 | 0/0 | 1872 | 58 | 21 | 18 | 7 | 6 | 6 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0002c0004 | 0/0 | 1872 | 5 | 5 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0002c0005 | 0/0 | 1872 | 3 | 1 | 0 | 0 | 2 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0003c0003 | 0/0 | 1872 | 10 | 10 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0003c0007 | 1/0 | 1872 | 2 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0004c0006 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0005c0011 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0006c0009 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0007c0010 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 | ||
| a0008c0008 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | ATGGC others(1867): Show |
chr5 | 137884457 | 137947747 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2291 | 250 | 49 | 53 | 113 | 6 | 28 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0001c0001t0003 | 0/0 | 2291 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0001c0012t0001 | 0/0 | 2291 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0002c0002t0001 | 0/0 | 2291 | 58 | 21 | 18 | 7 | 6 | 6 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0002c0004t0001 | 0/0 | 2291 | 5 | 5 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0002c0005t0002 | 0/0 | 2291 | 3 | 1 | 0 | 0 | 2 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0003c0003t0001 | 0/0 | 2291 | 10 | 10 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0003c0007t0001 | 1/0 | 2291 | 2 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0004c0006t0001 | 0/0 | 2291 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0005c0011t0001 | 0/0 | 2291 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0006c0009t0001 | 0/0 | 2291 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0007c0010t0001 | 0/0 | 2291 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| a0008c0008t0001 | 0/0 | 2291 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | AGGCG others(2286): Show |
chr5 | 137884457 | 137947747 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0005 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0001c0012t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0005t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0005t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0002c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0007t0001g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0003c0007t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0004c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0004c0006t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0005c0011t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0006c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0007c0010t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| a0008c0008t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0045 | EUR | GBR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0305 | EUR | FIN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0052 | EUR | FIN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | FIN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00639 | hp2 | a0005 | c0011 | t0001 | g0056 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01516 | hp2 | a0002 | c0005 | t0002 | g0100 | EUR | IBS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01517 | hp2 | a0002 | c0005 | t0002 | g0101 | EUR | IBS | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01884 | hp2 | a0001 | c0012 | t0001 | g0024 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0080 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02071 | hp1 | a0006 | c0009 | t0001 | g0178 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0089 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0009 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0086 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03098 | hp2 | a0004 | c0006 | t0001 | g0129 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03195 | hp2 | a0007 | c0010 | t0001 | g0072 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03209 | hp1 | a0002 | c0004 | t0001 | g0088 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0082 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03486 | hp2 | a0003 | c0007 | t0001 | g0230 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03540 | hp1 | a0004 | c0006 | t0001 | g0115 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0087 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0067 | SAS | STU | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | YRI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | YRI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19030 | hp2 | a0002 | c0004 | t0001 | g0090 | AFR | LWK | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | LWK | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | GIH | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0031 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | ACB | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0023 | AFR | MSL | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| HG06807 | hp2 | a0008 | c0008 | t0001 | g0035 | AFR | USA | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | USA | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | USA | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | LWK | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| NA21309 | hp2 | a0002 | c0005 | t0002 | g0099 | AFR | LWK | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0292 | REF | REF | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| homoSapiens | grch38p0 | a0003 | c0007 | t0001 | g0229 | REF | REF | PKD2L2_chr5_137884457_137947747 | PKD2L2 | chr5 | 137884457 | 137947747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137892530 | T | G | 1 | a0004 | 2 | HG03098.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.184T>G | p.Ser62Ala | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/15 | 219/2291 | 184/1875 | 62/624 | chr5 | 137892530 | |||
| chr5:137908828 | G | A | 4 | a0001 a0004 a0006 others(1): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
missense_variant | MODERATE | c.1210G>A | p.Val404Ile | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/15 | 1245/2291 | 1210/1875 | 404/624 | chr5 | 137908828 | |||
| chr5:137908883 | C | T | 1 | a0005 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1265C>T | p.Ala422Val | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/15 | 1300/2291 | 1265/1875 | 422/624 | chr5 | 137908883 | |||
| chr5:137908915 | G | A | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1297G>A | p.Val433Ile | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/15 | 1332/2291 | 1297/1875 | 433/624 | chr5 | 137908915 | |||
| chr5:137921698 | C | T | 1 | a0007 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1391C>T | p.Pro464Leu | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/15 | 1426/2291 | 1391/1875 | 464/624 | chr5 | 137921698 | |||
| chr5:137923490 | T | C | 7 | a0001 a0002 a0004 others(4): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
missense_variant | MODERATE | c.1520T>C | p.Leu507Pro | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/15 | 1555/2291 | 1520/1875 | 507/624 | chr5 | 137923490 | |||
| chr5:137925885 | G | A | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1627G>A | p.Gly543Arg | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/15 | 1662/2291 | 1627/1875 | 543/624 | chr5 | 137925885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137894394 | A | G | 3 | a0001c0012 a0002c0004 a0003c0003 |
16 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.309A>G | p.Ser103Ser | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/15 | 344/2291 | 309/1875 | 103/624 | chr5 | 137894394 | |||
| chr5:137925923 | C | T | 1 | a0002c0005 | 3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1665C>T | p.Asp555Asp | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/15 | 1700/2291 | 1665/1875 | 555/624 | chr5 | 137925923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137942443 | C | T | 1 | a0002c0005t0002 | 3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*77C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 15/15 | 6033 | chr5 | 137942443 | ||||||
| chr5:137942729 | T | C | 1 | a0001c0001t0003 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 15/15 | 6319 | chr5 | 137942729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:137889650 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.31+128C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137889650 | |||||||
| chr5:137889698 | G | A | 6 | a0001c0001t0001g0022 a0002c0002t0001g0017 a0002c0002t0001g0018 others(3): Show |
6 | HG01069.hp2 HG01070.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+176G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137889698 | |||||||
| chr5:137889972 | G | T | 1 | a0001c0001t0001g0306 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.31+450G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137889972 | |||||||
| chr5:137890037 | C | A | 10 | a0001c0012t0001g0024 a0003c0003t0001g0009 a0003c0003t0001g0023 others(7): Show |
11 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-444C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137890037 | |||||||
| chr5:137890039 | C | T | 1 | a0002c0002t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.32-442C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137890039 | |||||||
| chr5:137890207 | G | C | 81 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(78): Show |
83 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.32-274G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137890207 | |||||||
| chr5:137890384 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.32-97C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 1/14 | chr5 | 137890384 | |||||||
| chr5:137890598 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.133+16T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137890598 | |||||||
| chr5:137890659 | A | G | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG02055.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.133+77A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137890659 | |||||||
| chr5:137890752 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.133+170A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137890752 | |||||||
| chr5:137890937 | C | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(70): Show |
82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.133+355C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137890937 | |||||||
| chr5:137891207 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+625T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137891207 | |||||||
| chr5:137891558 | C | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.134-922C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137891558 | |||||||
| chr5:137891686 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.134-794T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137891686 | |||||||
| chr5:137891688 | A | AT | 10 | a0001c0012t0001g0024 a0003c0003t0001g0009 a0003c0003t0001g0023 others(7): Show |
11 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-784dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 137891688 | ||||||
| chr5:137891697 | C | CT | 10 | a0001c0001t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0094 others(7): Show |
10 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-773dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 137891697 | ||||||
| chr5:137891867 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.134-613T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137891867 | |||||||
| chr5:137892183 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.134-297G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137892183 | |||||||
| chr5:137892290 | A | G | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.134-190A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137892290 | |||||||
| chr5:137892298 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.134-182G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137892298 | |||||||
| chr5:137892374 | T | C | 69 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(66): Show |
71 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.134-106T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 2/14 | chr5 | 137892374 | |||||||
| chr5:137892819 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.267+206T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137892819 | |||||||
| chr5:137892836 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.267+223G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137892836 | |||||||
| chr5:137892956 | A | G | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01993.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+343A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137892956 | |||||||
| chr5:137892963 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
79 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.267+350G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137892963 | |||||||
| chr5:137893482 | C | A | 1 | a0002c0002t0001g0106 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.267+869C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893482 | |||||||
| chr5:137893504 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-849C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893504 | |||||||
| chr5:137893543 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.268-810C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893543 | |||||||
| chr5:137893721 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.268-632G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893721 | |||||||
| chr5:137893725 | C | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(69): Show |
74 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.268-628C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893725 | |||||||
| chr5:137893738 | G | T | 1 | a0002c0002t0001g0106 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.268-615G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893738 | |||||||
| chr5:137893779 | G | A | 1 | a0003c0003t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.268-574G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893779 | |||||||
| chr5:137893959 | G | A | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.268-394G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893959 | |||||||
| chr5:137893975 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.268-378G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137893975 | |||||||
| chr5:137894245 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0232 a0001c0001t0001g0306 |
5 | HG00408.hp1 NA18612.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-108T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 3/14 | chr5 | 137894245 | |||||||
| chr5:137894637 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02145.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.524+28T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137894637 | |||||||
| chr5:137894778 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.524+169G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137894778 | |||||||
| chr5:137895133 | G | C | 1 | a0002c0002t0001g0106 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.524+524G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895133 | |||||||
| chr5:137895159 | C | T | 15 | a0001c0012t0001g0024 a0002c0004t0001g0086 a0002c0004t0001g0087 others(12): Show |
16 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+550C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895159 | |||||||
| chr5:137895199 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.524+590G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895199 | |||||||
| chr5:137895274 | T | A | 1 | a0002c0002t0001g0041 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.524+665T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895274 | |||||||
| chr5:137895472 | T | TA | 20 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0112 others(17): Show |
21 | HG01081.hp1 HG01361.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.524+884dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137895472 | ||||||
| chr5:137895472 | TA | T | 7 | a0001c0001t0001g0040 a0001c0001t0001g0219 a0001c0001t0001g0221 others(4): Show |
7 | HG00609.hp2 HG01074.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.524+884delA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137895472 | ||||||
| chr5:137895472 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.524+873_524+884del others(12): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137895472 | ||||||
| chr5:137895627 | T | C | 1 | a0002c0005t0002g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524+1018T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895627 | |||||||
| chr5:137895635 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.524+1026T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895635 | |||||||
| chr5:137895695 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.524+1086T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895695 | |||||||
| chr5:137895771 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.524+1162A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895771 | |||||||
| chr5:137895853 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.524+1244G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895853 | |||||||
| chr5:137895877 | C | CA | 13 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0118 others(10): Show |
13 | HG01175.hp2 HG02735.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.524+1285dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137895877 | ||||||
| chr5:137895877 | C | CAA | 7 | a0001c0001t0001g0092 a0001c0001t0001g0111 a0002c0002t0001g0093 others(4): Show |
7 | HG01243.hp2 HG01361.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.524+1284_524+1285d others(4): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137895877 | ||||||
| chr5:137895877 | CAA | C | 46 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(43): Show |
47 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.524+1284_524+1285d others(4): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137895877 | ||||||
| chr5:137895895 | G | T | 46 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(43): Show |
47 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.524+1286G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137895895 | |||||||
| chr5:137896043 | G | A | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.524+1434G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896043 | |||||||
| chr5:137896092 | G | A | 3 | a0001c0012t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 |
3 | HG01884.hp2 HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.524+1483G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896092 | |||||||
| chr5:137896110 | C | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(69): Show |
74 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.524+1501C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896110 | |||||||
| chr5:137896196 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.524+1587G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896196 | |||||||
| chr5:137896491 | G | A | 1 | a0001c0012t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+1882G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896491 | |||||||
| chr5:137896612 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.524+2003A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896612 | |||||||
| chr5:137896825 | T | C | 1 | a0002c0002t0001g0041 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.524+2216T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896825 | |||||||
| chr5:137896886 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.524+2277G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896886 | |||||||
| chr5:137896926 | GT | G | 46 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(43): Show |
47 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.524+2328delT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137896926 | ||||||
| chr5:137896967 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.524+2358G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137896967 | |||||||
| chr5:137897028 | TTATTA | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.524+2426_524+2430d others(7): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897028 | ||||||
| chr5:137897033 | A | ATAT | 3 | a0002c0002t0001g0018 a0002c0002t0001g0199 a0003c0003t0001g0031 |
3 | HG00323.hp2 HG01070.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.525-2442_525-2440d others(5): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897033 | ||||||
| chr5:137897033 | ATAT | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(73): Show |
81 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.525-2442_525-2440d others(5): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897033 | ||||||
| chr5:137897033 | ATATTAT | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(117): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.525-2445_525-2440d others(8): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897033 | ||||||
| chr5:137897033 | ATATTATT others(2): Show |
A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
87 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.525-2448_525-2440d others(11): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897033 | ||||||
| chr5:137897033 | ATATTATT others(5): Show |
A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0157 others(3): Show |
7 | HG00621.hp2 HG01361.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.525-2451_525-2440d others(14): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897033 | ||||||
| chr5:137897041 | AT | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.524+2434delT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897041 | ||||||
| chr5:137897120 | G | T | 2 | a0001c0001t0001g0214 a0002c0002t0001g0215 |
2 | HG01433.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.525-2396G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137897120 | |||||||
| chr5:137897767 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.525-1749C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137897767 | |||||||
| chr5:137897780 | G | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(12): Show |
18 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.525-1736G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137897780 | |||||||
| chr5:137897937 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.525-1579A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137897937 | |||||||
| chr5:137897969 | A | AT | 8 | a0001c0001t0001g0120 a0001c0001t0001g0202 a0001c0001t0001g0203 others(5): Show |
8 | HG00408.hp2 HG02135.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-1532dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 137897969 | ||||||
| chr5:137897969 | A | T | 4 | a0001c0001t0001g0239 a0002c0005t0002g0099 a0002c0005t0002g0100 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1547A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137897969 | |||||||
| chr5:137898044 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.525-1472G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137898044 | |||||||
| chr5:137898101 | G | A | 43 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(40): Show |
44 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.525-1415G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137898101 | |||||||
| chr5:137898235 | G | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525-1281G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137898235 | |||||||
| chr5:137898601 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.525-915G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137898601 | |||||||
| chr5:137899049 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.525-467T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137899049 | |||||||
| chr5:137899125 | T | G | 3 | a0001c0001t0001g0128 a0004c0006t0001g0115 a0004c0006t0001g0129 |
3 | HG01243.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.525-391T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137899125 | |||||||
| chr5:137899336 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0201 |
2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.525-180C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 4/14 | chr5 | 137899336 | |||||||
| chr5:137900036 | A | T | 15 | a0001c0001t0001g0235 a0001c0001t0001g0280 a0001c0001t0001g0281 others(12): Show |
15 | HG00621.hp1 HG02015.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.746+299A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137900036 | |||||||
| chr5:137900234 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.746+497G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137900234 | |||||||
| chr5:137900257 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.746+520T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137900257 | |||||||
| chr5:137900597 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.746+860G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137900597 | |||||||
| chr5:137900664 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.746+927C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137900664 | |||||||
| chr5:137901018 | C | G | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.746+1281C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901018 | |||||||
| chr5:137901131 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.746+1394T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901131 | |||||||
| chr5:137901136 | C | CA | 38 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(35): Show |
39 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.746+1412dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 137901136 | ||||||
| chr5:137901144 | A | C | 7 | a0001c0001t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0094 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.746+1407A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901144 | |||||||
| chr5:137901146 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.746+1409A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901146 | |||||||
| chr5:137901192 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG01975.hp2 HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.746+1455G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901192 | |||||||
| chr5:137901220 | T | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG01361.hp2 HG02735.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+1483T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901220 | |||||||
| chr5:137901270 | T | C | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.746+1533T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901270 | |||||||
| chr5:137901283 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.746+1546A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901283 | |||||||
| chr5:137901340 | T | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.746+1603T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901340 | |||||||
| chr5:137901409 | T | TG | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02698.hp2 HG02735.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+1674dupG | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 137901409 | ||||||
| chr5:137901411 | GA | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.746+1685delA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 137901411 | ||||||
| chr5:137901412 | A | G | 40 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(37): Show |
41 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.746+1675A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901412 | |||||||
| chr5:137901437 | T | C | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.746+1700T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901437 | |||||||
| chr5:137901523 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0301 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+1786G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901523 | |||||||
| chr5:137901538 | T | A | 1 | a0001c0001t0001g0241 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.746+1801T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901538 | |||||||
| chr5:137901788 | G | A | 8 | a0001c0001t0001g0092 a0002c0002t0001g0044 a0002c0002t0001g0093 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.746+2051G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901788 | |||||||
| chr5:137901892 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0301 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+2155A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901892 | |||||||
| chr5:137901900 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.746+2163C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901900 | |||||||
| chr5:137901911 | C | T | 2 | a0002c0002t0001g0199 a0002c0002t0001g0305 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.746+2174C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137901911 | |||||||
| chr5:137901998 | G | GA | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG01516.hp2 HG01517.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.746+2274dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr5 | 137901998 | ||||||
| chr5:137902036 | A | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.746+2299A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137902036 | |||||||
| chr5:137902392 | G | T | 8 | a0001c0001t0001g0092 a0002c0002t0001g0044 a0002c0002t0001g0093 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.746+2655G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137902392 | |||||||
| chr5:137902531 | A | G | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.746+2794A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137902531 | |||||||
| chr5:137902758 | G | A | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.746+3021G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137902758 | |||||||
| chr5:137902918 | G | A | 47 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0068 others(44): Show |
48 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.746+3181G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137902918 | |||||||
| chr5:137903071 | G | C | 1 | a0002c0002t0001g0045 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.747-3135G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903071 | |||||||
| chr5:137903276 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.747-2930T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903276 | |||||||
| chr5:137903578 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.747-2628G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903578 | |||||||
| chr5:137903673 | A | G | 1 | a0007c0010t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.747-2533A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903673 | |||||||
| chr5:137903753 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.747-2453T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903753 | |||||||
| chr5:137903812 | A | G | 7 | a0001c0001t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0094 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.747-2394A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903812 | |||||||
| chr5:137903993 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.747-2213C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137903993 | |||||||
| chr5:137904172 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.747-2034G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137904172 | |||||||
| chr5:137904258 | C | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747-1948C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137904258 | |||||||
| chr5:137904397 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.747-1809G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137904397 | |||||||
| chr5:137904434 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.747-1772A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137904434 | |||||||
| chr5:137904878 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.747-1328G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137904878 | |||||||
| chr5:137905120 | G | T | 4 | a0002c0002t0001g0095 a0002c0002t0001g0096 a0002c0002t0001g0097 others(1): Show |
4 | HG01243.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.747-1086G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137905120 | |||||||
| chr5:137905288 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.747-918G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137905288 | |||||||
| chr5:137905754 | A | C | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747-452A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137905754 | |||||||
| chr5:137905832 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.747-374A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137905832 | |||||||
| chr5:137906070 | C | G | 1 | a0002c0002t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.747-136C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137906070 | |||||||
| chr5:137906167 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
257 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.747-39T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137906167 | |||||||
| chr5:137906198 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.747-8T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 5/14 | chr5 | 137906198 | |||||||
| chr5:137906716 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.975+282T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | chr5 | 137906716 | |||||||
| chr5:137906762 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0039 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+328C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | chr5 | 137906762 | |||||||
| chr5:137906770 | TG | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
247 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.975+341delG | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 137906770 | ||||||
| chr5:137907011 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.975+577C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | chr5 | 137907011 | |||||||
| chr5:137907104 | T | C | 58 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0277 others(55): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.976-638T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | chr5 | 137907104 | |||||||
| chr5:137907187 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.976-555G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | chr5 | 137907187 | |||||||
| chr5:137907481 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.976-261C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 6/14 | chr5 | 137907481 | |||||||
| chr5:137908007 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1146+95C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908007 | |||||||
| chr5:137908052 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1146+140T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908052 | |||||||
| chr5:137908086 | A | G | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1146+174A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908086 | |||||||
| chr5:137908286 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1146+374T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908286 | |||||||
| chr5:137908362 | C | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1147-403C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908362 | |||||||
| chr5:137908601 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1147-164A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908601 | |||||||
| chr5:137908622 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
120 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1147-143T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 7/14 | chr5 | 137908622 | |||||||
| chr5:137908999 | A | T | 1 | a0002c0002t0001g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1328+53A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137908999 | |||||||
| chr5:137909085 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1328+139A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909085 | |||||||
| chr5:137909097 | A | C | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1328+151A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909097 | |||||||
| chr5:137909134 | G | T | 1 | a0002c0002t0001g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1328+188G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909134 | |||||||
| chr5:137909281 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1328+335G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909281 | |||||||
| chr5:137909360 | A | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0037 others(4): Show |
7 | HG02145.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1328+414A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909360 | |||||||
| chr5:137909378 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(118): Show |
135 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1328+432C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909378 | |||||||
| chr5:137909531 | A | G | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1328+585A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909531 | |||||||
| chr5:137909538 | AT | A | 70 | a0001c0001t0001g0022 a0001c0001t0001g0180 a0001c0001t0001g0181 others(67): Show |
71 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1328+615delT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137909538 | ||||||
| chr5:137909538 | ATT | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1328+614_1328+615d others(4): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137909538 | ||||||
| chr5:137909538 | ATTT | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0036 others(12): Show |
15 | HG01169.hp2 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1328+613_1328+615d others(5): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137909538 | ||||||
| chr5:137909606 | G | A | 47 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(44): Show |
48 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1328+660G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137909606 | |||||||
| chr5:137910231 | C | CAAT | 70 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0033 others(67): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1328+1327_1328+132 others(7): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910231 | C | CAATAAT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0050 others(30): Show |
37 | HG00544.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1328+1324_1328+132 others(10): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910231 | CAAT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(85): Show |
98 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1328+1327_1328+132 others(7): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910231 | CAATAAT | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0104 a0001c0001t0001g0127 others(27): Show |
32 | HG00140.hp2 HG00408.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1328+1324_1328+132 others(10): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910231 | CAATAATA others(2): Show |
C | 12 | a0001c0001t0001g0012 a0001c0001t0001g0120 a0001c0001t0001g0138 others(9): Show |
13 | HG01169.hp2 HG01884.hp1 HG03490.hp1 others(10): Show |
intron_variant | MODIFIER | c.1328+1321_1328+132 others(13): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910231 | CAATAATA others(5): Show |
C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0186 |
2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1328+1318_1328+132 others(16): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910231 | CAATAATA others(14): Show |
C | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1328+1309_1328+132 others(25): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910231 | ||||||
| chr5:137910247 | AATAATAA others(1): Show |
A | 4 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328+1303_1328+131 others(12): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910247 | ||||||
| chr5:137910333 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1328+1387T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910333 | |||||||
| chr5:137910342 | C | T | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1328+1396C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910342 | |||||||
| chr5:137910435 | A | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1328+1489A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910435 | |||||||
| chr5:137910501 | G | A | 3 | a0002c0002t0001g0044 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | HG02559.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1328+1555G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910501 | |||||||
| chr5:137910544 | G | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1328+1598G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910544 | |||||||
| chr5:137910594 | G | T | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1328+1648G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910594 | |||||||
| chr5:137910712 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1328+1766G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910712 | |||||||
| chr5:137910757 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1328+1811C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910757 | |||||||
| chr5:137910795 | C | CA | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
253 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1328+1860dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137910795 | ||||||
| chr5:137910846 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1328+1900G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910846 | |||||||
| chr5:137910848 | G | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(2): Show |
5 | HG01069.hp2 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1328+1902G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137910848 | |||||||
| chr5:137911296 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1328+2350G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911296 | |||||||
| chr5:137911316 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1328+2370G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911316 | |||||||
| chr5:137911393 | T | G | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1328+2447T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911393 | |||||||
| chr5:137911504 | G | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0297 |
2 | HG02056.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1328+2558G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911504 | |||||||
| chr5:137911601 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1328+2655T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911601 | |||||||
| chr5:137911721 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1328+2775T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911721 | |||||||
| chr5:137911772 | A | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(74): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1328+2826A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137911772 | |||||||
| chr5:137912079 | C | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
258 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1328+3133C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912079 | |||||||
| chr5:137912110 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1328+3164G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912110 | |||||||
| chr5:137912251 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(119): Show |
136 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1328+3305T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912251 | |||||||
| chr5:137912345 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1328+3399C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912345 | |||||||
| chr5:137912474 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02083.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1328+3528C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912474 | |||||||
| chr5:137912509 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(85): Show |
100 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.1328+3563G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912509 | |||||||
| chr5:137912552 | A | G | 15 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1328+3606A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912552 | |||||||
| chr5:137912657 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1328+3711G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912657 | |||||||
| chr5:137912801 | C | CT | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(103): Show |
119 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1328+3858dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137912801 | ||||||
| chr5:137912801 | C | CTT | 7 | a0001c0001t0001g0075 a0001c0001t0001g0127 a0001c0001t0001g0136 others(4): Show |
7 | HG02056.hp1 HG02698.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1328+3857_1328+385 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137912801 | ||||||
| chr5:137912804 | TC | T | 32 | a0001c0001t0001g0138 a0001c0001t0001g0189 a0001c0001t0001g0306 others(29): Show |
33 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1328+3859delC | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912804 | |||||||
| chr5:137912805 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1328+3859C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912805 | |||||||
| chr5:137912864 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1328+3918G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912864 | |||||||
| chr5:137912979 | T | C | 55 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(52): Show |
56 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1328+4033T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137912979 | |||||||
| chr5:137913032 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(117): Show |
134 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1328+4086G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913032 | |||||||
| chr5:137913076 | T | C | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328+4130T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913076 | |||||||
| chr5:137913114 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1328+4168A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913114 | |||||||
| chr5:137913166 | C | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1328+4220C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913166 | |||||||
| chr5:137913184 | C | CT | 10 | a0001c0001t0001g0107 a0001c0001t0001g0197 a0002c0002t0001g0093 others(7): Show |
10 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1328+4257dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137913184 | ||||||
| chr5:137913184 | CT | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1328+4257delT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137913184 | ||||||
| chr5:137913188 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0214 |
2 | HG01346.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1328+4242T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913188 | |||||||
| chr5:137913189 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1328+4243T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913189 | |||||||
| chr5:137913192 | T | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0294 |
2 | HG01074.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1328+4246T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913192 | |||||||
| chr5:137913487 | G | A | 3 | a0001c0001t0001g0128 a0004c0006t0001g0115 a0004c0006t0001g0129 |
3 | HG01243.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1328+4541G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913487 | |||||||
| chr5:137913491 | A | AT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0084 others(20): Show |
26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1328+4560dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137913491 | ||||||
| chr5:137913828 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1328+4882G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137913828 | |||||||
| chr5:137914031 | C | CT | 5 | a0003c0003t0001g0009 a0003c0003t0001g0025 a0003c0003t0001g0026 others(2): Show |
6 | HG02109.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1328+5124dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTT | C | 11 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0066 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1328+5123_1328+512 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTT | C | 12 | a0002c0002t0001g0045 a0002c0002t0001g0046 a0002c0002t0001g0054 others(9): Show |
12 | HG00140.hp2 HG01192.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1328+5122_1328+512 others(7): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTT | C | 9 | a0002c0002t0001g0041 a0002c0002t0001g0052 a0002c0002t0001g0058 others(6): Show |
9 | HG00323.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1328+5121_1328+512 others(8): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTT | C | 9 | a0002c0002t0001g0010 a0002c0002t0001g0019 a0002c0002t0001g0043 others(6): Show |
10 | HG00741.hp1 HG01109.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1328+5120_1328+512 others(9): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTT | C | 17 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0021 others(14): Show |
17 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1328+5119_1328+512 others(10): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0281 |
2 | HG01175.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1328+5114_1328+512 others(15): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(5): Show |
C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0075 others(16): Show |
21 | HG00408.hp2 HG00438.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1328+5113_1328+512 others(16): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(6): Show |
C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
167 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.1328+5112_1328+512 others(17): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(7): Show |
C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(54): Show |
63 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1328+5111_1328+512 others(18): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0306 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1328+5110_1328+512 others(19): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(10): Show |
C | 1 | a0002c0002t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1328+5108_1328+512 others(21): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(11): Show |
C | 3 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0305 |
3 | HG00280.hp2 HG00323.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1328+5107_1328+512 others(22): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914031 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1328+5105_1328+512 others(24): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137914031 | ||||||
| chr5:137914137 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1328+5191G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137914137 | |||||||
| chr5:137914420 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1328+5474A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137914420 | |||||||
| chr5:137914431 | G | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1328+5485G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137914431 | |||||||
| chr5:137914796 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1328+5850A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137914796 | |||||||
| chr5:137914962 | G | A | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG02055.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1328+6016G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137914962 | |||||||
| chr5:137915180 | G | A | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG02055.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1328+6234G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915180 | |||||||
| chr5:137915461 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1329-6175C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915461 | |||||||
| chr5:137915462 | G | A | 18 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0134 others(15): Show |
18 | HG01081.hp2 HG01123.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1329-6174G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915462 | |||||||
| chr5:137915558 | G | A | 3 | a0002c0002t0001g0045 a0002c0002t0001g0046 a0002c0002t0001g0085 |
3 | HG00140.hp2 HG01192.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1329-6078G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915558 | |||||||
| chr5:137915583 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1329-6053C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915583 | |||||||
| chr5:137915609 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1329-6027C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915609 | |||||||
| chr5:137915640 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
120 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1329-5996C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915640 | |||||||
| chr5:137915654 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1329-5982C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915654 | |||||||
| chr5:137915655 | G | A | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1329-5981G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915655 | |||||||
| chr5:137915766 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1329-5870T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915766 | |||||||
| chr5:137915824 | C | CT | 3 | a0002c0002t0001g0044 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | HG02559.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1329-5808dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137915824 | ||||||
| chr5:137915997 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1329-5639T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137915997 | |||||||
| chr5:137916029 | TTTTTTC | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(133): Show |
154 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1329-5601_1329-559 others(10): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137916029 | ||||||
| chr5:137916030 | TTTTTC | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(84): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1329-5601_1329-559 others(9): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137916030 | ||||||
| chr5:137916245 | G | A | 6 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1329-5391G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916245 | |||||||
| chr5:137916246 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
4 | HG00738.hp2 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329-5390G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916246 | |||||||
| chr5:137916358 | G | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1329-5278G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916358 | |||||||
| chr5:137916426 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1329-5210T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916426 | |||||||
| chr5:137916475 | C | CT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
157 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1329-5139dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137916475 | ||||||
| chr5:137916475 | C | CTT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0103 a0001c0001t0001g0148 others(6): Show |
10 | HG00408.hp2 HG01081.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1329-5140_1329-513 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137916475 | ||||||
| chr5:137916475 | CT | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0084 others(17): Show |
20 | HG00323.hp1 HG01167.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1329-5139delT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137916475 | ||||||
| chr5:137916477 | T | TC | 11 | a0001c0001t0001g0118 a0001c0001t0001g0139 a0001c0001t0001g0183 others(8): Show |
11 | HG01106.hp2 HG01993.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1329-5159_1329-515 others(5): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916477 | |||||||
| chr5:137916478 | T | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329-5158T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916478 | |||||||
| chr5:137916479 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1329-5157T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916479 | |||||||
| chr5:137916590 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(71): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1329-5046G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916590 | |||||||
| chr5:137916641 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1329-4995G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916641 | |||||||
| chr5:137916744 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1329-4892A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137916744 | |||||||
| chr5:137917146 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1329-4490G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917146 | |||||||
| chr5:137917162 | C | CT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
246 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1329-4457dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137917162 | ||||||
| chr5:137917162 | C | CTT | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0152 others(4): Show |
7 | HG01175.hp1 HG02523.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-4458_1329-445 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137917162 | ||||||
| chr5:137917162 | CT | C | 6 | a0002c0002t0001g0081 a0002c0002t0001g0093 a0002c0002t0001g0094 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1329-4457delT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137917162 | ||||||
| chr5:137917216 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1329-4420G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917216 | |||||||
| chr5:137917251 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
30 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1329-4385G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917251 | |||||||
| chr5:137917286 | T | A | 1 | a0002c0002t0001g0047 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1329-4350T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917286 | |||||||
| chr5:137917437 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1329-4199T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917437 | |||||||
| chr5:137917640 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1329-3996T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917640 | |||||||
| chr5:137917828 | C | A | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1329-3808C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137917828 | |||||||
| chr5:137918088 | C | G | 1 | a0001c0001t0001g0282 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1329-3548C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137918088 | |||||||
| chr5:137918323 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1329-3313T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137918323 | |||||||
| chr5:137918695 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1329-2941A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137918695 | |||||||
| chr5:137918734 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1329-2902T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137918734 | |||||||
| chr5:137918844 | C | CT | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
252 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1329-2777dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137918844 | ||||||
| chr5:137918944 | A | ATG | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1329-2669_1329-266 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137918944 | ||||||
| chr5:137918944 | ATGTGTGT others(19): Show |
A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG00597.hp1 HG00609.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1329-2674_1329-264 others(30): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137918944 | ||||||
| chr5:137918967 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(101): Show |
117 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1329-2669T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137918967 | |||||||
| chr5:137918967 | T | TGA | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01175.hp1 HG01255.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1329-2667_1329-266 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137918967 | ||||||
| chr5:137918967 | T | TGTGA | 4 | a0001c0001t0001g0016 a0001c0001t0001g0237 a0001c0001t0001g0266 others(1): Show |
5 | NA18955.hp2 NA18993.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329-2668_1329-266 others(8): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137918967 | ||||||
| chr5:137918969 | A | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0237 a0001c0001t0001g0265 others(5): Show |
9 | HG01361.hp1 HG02559.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.1329-2667A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137918969 | |||||||
| chr5:137919157 | GTTATT | G | 4 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329-2475_1329-247 others(9): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137919157 | ||||||
| chr5:137919314 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1329-2322T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919314 | |||||||
| chr5:137919497 | G | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1329-2139G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919497 | |||||||
| chr5:137919514 | C | CT | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.1329-2111dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137919514 | ||||||
| chr5:137919526 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1329-2110C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919526 | |||||||
| chr5:137919545 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1329-2091G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919545 | |||||||
| chr5:137919548 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1329-2088C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919548 | |||||||
| chr5:137919574 | TC | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1329-2061delC | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919574 | |||||||
| chr5:137919638 | A | G | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1329-1998A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919638 | |||||||
| chr5:137919652 | C | G | 3 | a0002c0002t0001g0017 a0002c0002t0001g0020 a0002c0002t0001g0021 |
3 | HG01069.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1329-1984C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919652 | |||||||
| chr5:137919654 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1329-1982A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919654 | |||||||
| chr5:137919780 | T | C | 1 | a0002c0002t0001g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1329-1856T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137919780 | |||||||
| chr5:137920278 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1329-1358C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137920278 | |||||||
| chr5:137920599 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1329-1037A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137920599 | |||||||
| chr5:137920660 | G | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0151 |
2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1329-976G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137920660 | |||||||
| chr5:137920736 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1329-900G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137920736 | |||||||
| chr5:137920744 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0259 a0001c0001t0001g0263 others(2): Show |
8 | NA18952.hp1 NA18953.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329-892C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137920744 | |||||||
| chr5:137920756 | T | TA | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1329-865dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137920756 | ||||||
| chr5:137920880 | G | C | 3 | a0002c0002t0001g0044 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | HG02559.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1329-756G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137920880 | |||||||
| chr5:137921013 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1329-623C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137921013 | |||||||
| chr5:137921310 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1329-326G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137921310 | |||||||
| chr5:137921362 | G | GA | 63 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(60): Show |
64 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1329-260dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137921362 | ||||||
| chr5:137921362 | G | GAAA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(143): Show |
164 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1329-262_1329-260d others(5): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137921362 | ||||||
| chr5:137921362 | G | GAAAA | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(76): Show |
88 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1329-263_1329-260d others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 137921362 | ||||||
| chr5:137921493 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1329-143C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137921493 | |||||||
| chr5:137921493 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1329-143C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137921493 | |||||||
| chr5:137921599 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1329-37A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 8/14 | chr5 | 137921599 | |||||||
| chr5:137922159 | T | C | 62 | a0001c0001t0001g0267 a0002c0002t0001g0010 a0002c0002t0001g0017 others(59): Show |
63 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1449+403T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922159 | |||||||
| chr5:137922259 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1449+503C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922259 | |||||||
| chr5:137922260 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1449+504G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922260 | |||||||
| chr5:137922372 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1449+616T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922372 | |||||||
| chr5:137922430 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0001g0147 others(1): Show |
5 | HG02809.hp1 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+674A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922430 | |||||||
| chr5:137922573 | A | G | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1449+817A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922573 | |||||||
| chr5:137922998 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1450-422G>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137922998 | |||||||
| chr5:137923016 | C | CT | 6 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1450-390dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 137923016 | ||||||
| chr5:137923069 | TGGTGCGA others(8): Show |
T | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1450-348_1450-334d others(17): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr5 | 137923069 | ||||||
| chr5:137923221 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1450-199G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137923221 | |||||||
| chr5:137923312 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1450-108G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 9/14 | chr5 | 137923312 | |||||||
| chr5:137923562 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1551+41C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137923562 | |||||||
| chr5:137923614 | C | T | 4 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+93C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137923614 | |||||||
| chr5:137923646 | C | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(74): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1551+125C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137923646 | |||||||
| chr5:137923687 | C | T | 1 | a0002c0004t0001g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1551+166C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137923687 | |||||||
| chr5:137924434 | TTCTATTC others(14): Show |
T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1552-602_1552-582d others(23): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 137924434 | ||||||
| chr5:137924514 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1552-526G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137924514 | |||||||
| chr5:137924661 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1552-379C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137924661 | |||||||
| chr5:137924664 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1552-376A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137924664 | |||||||
| chr5:137924766 | C | T | 1 | a0003c0003t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1552-274C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137924766 | |||||||
| chr5:137924767 | G | A | 1 | a0003c0003t0001g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1552-273G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137924767 | |||||||
| chr5:137924807 | C | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1552-233C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 10/14 | chr5 | 137924807 | |||||||
| chr5:137925381 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1616+277A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 11/14 | chr5 | 137925381 | |||||||
| chr5:137926179 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1671+250A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926179 | |||||||
| chr5:137926263 | C | A | 3 | a0001c0001t0001g0128 a0004c0006t0001g0115 a0004c0006t0001g0129 |
3 | HG01243.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1671+334C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926263 | |||||||
| chr5:137926364 | TA | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1671+447delA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137926364 | ||||||
| chr5:137926385 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1671+456T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926385 | |||||||
| chr5:137926535 | T | C | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1671+606T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926535 | |||||||
| chr5:137926568 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1671+639G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926568 | |||||||
| chr5:137926575 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1671+646C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926575 | |||||||
| chr5:137926624 | C | A | 1 | a0007c0010t0001g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1671+695C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137926624 | |||||||
| chr5:137927101 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1671+1172C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927101 | |||||||
| chr5:137927159 | T | C | 3 | a0002c0002t0001g0044 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | HG02559.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1671+1230T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927159 | |||||||
| chr5:137927275 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1671+1346C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927275 | |||||||
| chr5:137927545 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
258 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1671+1616A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927545 | |||||||
| chr5:137927630 | T | C | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1671+1701T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927630 | |||||||
| chr5:137927783 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1671+1854G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927783 | |||||||
| chr5:137927814 | T | C | 10 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0235 others(7): Show |
10 | HG00621.hp1 HG02083.hp1 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.1671+1885T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927814 | |||||||
| chr5:137927830 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1671+1901C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927830 | |||||||
| chr5:137927961 | C | T | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1671+2032C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137927961 | |||||||
| chr5:137928250 | A | C | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1671+2321A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137928250 | |||||||
| chr5:137928254 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1671+2325A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137928254 | |||||||
| chr5:137928383 | CA | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1671+2474delA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137928383 | ||||||
| chr5:137928383 | CAA | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1671+2473_1671+247 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137928383 | ||||||
| chr5:137928581 | G | A | 1 | a0004c0006t0001g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1671+2652G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137928581 | |||||||
| chr5:137928590 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1671+2661C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137928590 | |||||||
| chr5:137928598 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1671+2669A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137928598 | |||||||
| chr5:137928752 | T | C | 6 | a0001c0001t0001g0227 a0002c0002t0001g0093 a0002c0002t0001g0094 others(3): Show |
6 | HG01243.hp2 HG01993.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1671+2823T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137928752 | |||||||
| chr5:137929232 | C | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(117): Show |
134 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1671+3303C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929232 | |||||||
| chr5:137929235 | G | A | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+3306G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929235 | |||||||
| chr5:137929264 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1671+3335C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929264 | |||||||
| chr5:137929448 | C | T | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1671+3519C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929448 | |||||||
| chr5:137929455 | C | A | 1 | a0002c0002t0001g0195 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1671+3526C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929455 | |||||||
| chr5:137929534 | C | CA | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(87): Show |
103 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1671+3630dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137929534 | ||||||
| chr5:137929534 | C | CAA | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
118 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1671+3629_1671+363 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137929534 | ||||||
| chr5:137929534 | C | CAAA | 59 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0120 others(56): Show |
60 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1671+3628_1671+363 others(7): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137929534 | ||||||
| chr5:137929534 | C | CAAAA | 20 | a0001c0001t0001g0011 a0001c0001t0001g0110 a0001c0001t0001g0145 others(17): Show |
21 | HG00735.hp1 HG01243.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.1671+3627_1671+363 others(8): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137929534 | ||||||
| chr5:137929569 | C | A | 2 | a0002c0002t0001g0047 a0002c0002t0001g0049 |
2 | HG02027.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1671+3640C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929569 | |||||||
| chr5:137929570 | G | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1671+3641G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929570 | |||||||
| chr5:137929844 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1671+3915T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929844 | |||||||
| chr5:137929908 | A | C | 61 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(58): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1671+3979A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137929908 | |||||||
| chr5:137930006 | CCAAA | C | 9 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0154 others(6): Show |
9 | HG00423.hp2 HG00621.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+4080_1671+408 others(8): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137930006 | ||||||
| chr5:137930394 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1671+4465C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137930394 | |||||||
| chr5:137930444 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1671+4515G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137930444 | |||||||
| chr5:137930448 | G | A | 3 | a0002c0002t0001g0044 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | HG02559.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1671+4519G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137930448 | |||||||
| chr5:137930571 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(105): Show |
121 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1671+4642T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137930571 | |||||||
| chr5:137930587 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1671+4658C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137930587 | |||||||
| chr5:137930664 | T | TA | 19 | a0001c0001t0001g0134 a0001c0001t0001g0160 a0001c0001t0001g0181 others(16): Show |
19 | HG00735.hp2 HG01243.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.1671+4752dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137930664 | ||||||
| chr5:137930664 | TA | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0159 a0001c0001t0001g0169 others(3): Show |
6 | HG02523.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671+4752delA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137930664 | ||||||
| chr5:137930767 | C | CA | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+4839dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137930767 | ||||||
| chr5:137930933 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG01257.hp1 HG01361.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1672-4864C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137930933 | |||||||
| chr5:137931127 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1672-4670T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931127 | |||||||
| chr5:137931200 | G | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1672-4597G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931200 | |||||||
| chr5:137931212 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1672-4585G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931212 | |||||||
| chr5:137931307 | T | C | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1672-4490T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931307 | |||||||
| chr5:137931362 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1672-4435C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931362 | |||||||
| chr5:137931381 | T | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0237 a0001c0001t0001g0241 others(6): Show |
10 | HG00597.hp2 HG02015.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.1672-4416T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931381 | |||||||
| chr5:137931692 | C | G | 29 | a0002c0002t0001g0041 a0002c0002t0001g0045 a0002c0002t0001g0046 others(26): Show |
29 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1672-4105C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931692 | |||||||
| chr5:137931977 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1672-3820C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137931977 | |||||||
| chr5:137932606 | A | G | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1672-3191A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932606 | |||||||
| chr5:137932629 | G | A | 4 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-3168G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932629 | |||||||
| chr5:137932805 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1672-2992T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932805 | |||||||
| chr5:137932842 | G | A | 3 | a0002c0002t0001g0117 a0002c0002t0001g0193 a0002c0002t0001g0220 |
3 | HG02451.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1672-2955G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932842 | |||||||
| chr5:137932866 | G | A | 1 | a0002c0004t0001g0086 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1672-2931G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932866 | |||||||
| chr5:137932890 | G | A | 4 | a0002c0002t0001g0095 a0002c0002t0001g0194 a0002c0002t0001g0195 others(1): Show |
4 | HG00741.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-2907G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932890 | |||||||
| chr5:137932898 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1672-2899A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932898 | |||||||
| chr5:137932900 | A | G | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG02055.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1672-2897A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137932900 | |||||||
| chr5:137933004 | T | C | 4 | a0001c0001t0001g0137 a0001c0001t0001g0184 a0001c0001t0001g0224 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1672-2793T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933004 | |||||||
| chr5:137933044 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1672-2753A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933044 | |||||||
| chr5:137933050 | C | CA | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(160): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1672-2731dupA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137933050 | ||||||
| chr5:137933050 | C | CAA | 27 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(24): Show |
32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1672-2732_1672-273 others(6): Show |
PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 137933050 | ||||||
| chr5:137933154 | A | G | 4 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-2643A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933154 | |||||||
| chr5:137933157 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1672-2640G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933157 | |||||||
| chr5:137933186 | A | C | 1 | a0002c0002t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1672-2611A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933186 | |||||||
| chr5:137933225 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
258 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1672-2572C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933225 | |||||||
| chr5:137933564 | T | G | 1 | a0001c0001t0001g0012 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1672-2233T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137933564 | |||||||
| chr5:137934093 | A | T | 1 | a0001c0001t0001g0176 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1672-1704A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934093 | |||||||
| chr5:137934187 | G | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1672-1610G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934187 | |||||||
| chr5:137934256 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1672-1541A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934256 | |||||||
| chr5:137934260 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1672-1537T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934260 | |||||||
| chr5:137934629 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1672-1168C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934629 | |||||||
| chr5:137934736 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1672-1061C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934736 | |||||||
| chr5:137934740 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1672-1057A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934740 | |||||||
| chr5:137934769 | G | A | 2 | a0002c0005t0002g0100 a0002c0005t0002g0101 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1672-1028G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934769 | |||||||
| chr5:137934838 | G | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1672-959G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934838 | |||||||
| chr5:137934874 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1672-923C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934874 | |||||||
| chr5:137934966 | T | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
30 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1672-831T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137934966 | |||||||
| chr5:137935128 | T | C | 7 | a0001c0001t0001g0084 a0002c0002t0001g0114 a0002c0002t0001g0199 others(4): Show |
7 | HG00280.hp2 HG00323.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-669T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935128 | |||||||
| chr5:137935220 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1672-577C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935220 | |||||||
| chr5:137935337 | T | A | 1 | a0001c0001t0001g0161 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1672-460T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935337 | |||||||
| chr5:137935374 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1672-423T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935374 | |||||||
| chr5:137935381 | A | C | 1 | a0002c0002t0001g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1672-416A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935381 | |||||||
| chr5:137935438 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1672-359C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935438 | |||||||
| chr5:137935542 | G | T | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1672-255G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935542 | |||||||
| chr5:137935554 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1672-243A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935554 | |||||||
| chr5:137935576 | C | T | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1672-221C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935576 | |||||||
| chr5:137935651 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0124 others(9): Show |
14 | HG00738.hp1 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1672-146G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935651 | |||||||
| chr5:137935736 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1672-61G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935736 | |||||||
| chr5:137935746 | T | C | 3 | a0002c0002t0001g0117 a0002c0002t0001g0193 a0002c0002t0001g0220 |
3 | HG02451.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1672-51T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 12/14 | chr5 | 137935746 | |||||||
| chr5:137935955 | C | A | 3 | a0002c0005t0002g0099 a0002c0005t0002g0100 a0002c0005t0002g0101 |
3 | HG01516.hp2 HG01517.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1784+46C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 13/14 | chr5 | 137935955 | |||||||
| chr5:137936154 | C | T | 61 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(58): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1785-166C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 13/14 | chr5 | 137936154 | |||||||
| chr5:137936195 | C | T | 47 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(44): Show |
48 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1785-125C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 13/14 | chr5 | 137936195 | |||||||
| chr5:137936279 | T | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1785-41T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 13/14 | chr5 | 137936279 | |||||||
| chr5:137936460 | C | CT | 13 | a0001c0001t0001g0174 a0002c0002t0001g0057 a0002c0002t0001g0058 others(10): Show |
13 | HG01071.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.*17+46dupT | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 137936460 | ||||||
| chr5:137936474 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0141 |
2 | NA18948.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.*17+47G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936474 | |||||||
| chr5:137936494 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.*17+67C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936494 | |||||||
| chr5:137936502 | C | T | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*17+75C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936502 | |||||||
| chr5:137936516 | C | T | 2 | a0002c0004t0001g0086 a0002c0004t0001g0087 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*17+89C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936516 | |||||||
| chr5:137936656 | T | C | 1 | a0001c0001t0001g0297 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.*17+229T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936656 | |||||||
| chr5:137936667 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.*17+240G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936667 | |||||||
| chr5:137936688 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*17+261C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936688 | |||||||
| chr5:137936735 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.*17+308G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137936735 | |||||||
| chr5:137937182 | C | T | 5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0096 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*17+755C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137937182 | |||||||
| chr5:137937226 | C | G | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.*17+799C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137937226 | |||||||
| chr5:137937295 | G | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0297 |
2 | HG02056.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.*17+868G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137937295 | |||||||
| chr5:137937720 | A | G | 2 | a0002c0004t0001g0086 a0002c0004t0001g0087 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*17+1293A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137937720 | |||||||
| chr5:137938043 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.*17+1616A>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938043 | |||||||
| chr5:137938089 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0307 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.*17+1662C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938089 | |||||||
| chr5:137938090 | A | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.*17+1663A>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938090 | |||||||
| chr5:137938192 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.*17+1765T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938192 | |||||||
| chr5:137938342 | A | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.*17+1915A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938342 | |||||||
| chr5:137938528 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.*17+2101T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938528 | |||||||
| chr5:137938652 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*17+2225C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938652 | |||||||
| chr5:137938781 | C | G | 1 | a0001c0001t0001g0014 | 2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.*17+2354C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938781 | |||||||
| chr5:137938797 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*17+2370G>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137938797 | |||||||
| chr5:137939426 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.*18-2958G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137939426 | |||||||
| chr5:137939510 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
253 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.*18-2874T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137939510 | |||||||
| chr5:137939518 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0307 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.*18-2866G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137939518 | |||||||
| chr5:137939701 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*18-2683C>T | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137939701 | |||||||
| chr5:137939952 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*18-2432G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137939952 | |||||||
| chr5:137940237 | T | G | 1 | a0001c0001t0001g0014 | 2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.*18-2147T>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137940237 | |||||||
| chr5:137940279 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.*18-2105C>G | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137940279 | |||||||
| chr5:137940443 | T | A | 1 | a0001c0012t0001g0024 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*18-1941T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137940443 | |||||||
| chr5:137940469 | TA | T | 7 | a0001c0001t0001g0107 a0001c0001t0001g0161 a0001c0001t0001g0236 others(4): Show |
7 | HG01516.hp2 HG01517.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.*18-1900delA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 137940469 | ||||||
| chr5:137940710 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0201 |
2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*18-1674G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137940710 | |||||||
| chr5:137940903 | T | C | 3 | a0002c0004t0001g0088 a0002c0004t0001g0089 a0002c0004t0001g0090 |
3 | HG02145.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*18-1481T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137940903 | |||||||
| chr5:137940979 | C | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(117): Show |
134 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.*18-1405C>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137940979 | |||||||
| chr5:137941031 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.*18-1353G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137941031 | |||||||
| chr5:137941049 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00597.hp1 HG00609.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.*18-1335G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137941049 | |||||||
| chr5:137941063 | G | A | 3 | a0002c0002t0001g0044 a0002c0002t0001g0082 a0002c0002t0001g0083 |
3 | HG02559.hp2 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.*18-1321G>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137941063 | |||||||
| chr5:137941077 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*18-1307T>A | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137941077 | |||||||
| chr5:137941126 | T | C | 2 | a0002c0004t0001g0086 a0002c0004t0001g0087 |
2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*18-1258T>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137941126 | |||||||
| chr5:137941692 | A | C | 4 | a0002c0002t0001g0114 a0002c0002t0001g0199 a0002c0002t0001g0215 others(1): Show |
4 | HG00280.hp2 HG00323.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.*18-692A>C | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | chr5 | 137941692 | |||||||
| chr5:137942286 | A | AAG | 50 | a0002c0002t0001g0010 a0002c0002t0001g0017 a0002c0002t0001g0018 others(47): Show |
51 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.*18-96_*18-95dupGA | PKD2L2 | ENSG00000078795.17 | transcript | ENST00000508883.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 137942286 |