Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57047 |
| ensemblid | ENSG00000163746.13 |
| hgncid | 16494 |
| symbol | PLSCR2 |
| name | phospholipid scramblase 2 |
| refseq_nuc | NM_001395437.1 |
| refseq_prot | NP_001382366.1 |
| ensembl_nuc | ENST00000696113.1 |
| ensembl_prot | ENSP00000512407.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 146433288 |
| end | 146469561 |
| strand | - |
| ver | v1.2 |
| region | chr3:146433288-146469561 |
| region5000 | chr3:146428288-146474561 |
| regionname0 | PLSCR2_chr3_146433288_146469561 |
| regionname5000 | PLSCR2_chr3_146428288_146474561 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 224 | 351 | 79 | 57 | 167 | 12 | 34 | 132 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | MPAPP others(219): Show |
chr3 | 146428288 | 146474561 |
| a0002 | 0/0 | 224 | 12 | 0 | 1 | 11 | 0 | 0 | 10 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | MPAPP others(219): Show |
chr3 | 146428288 | 146474561 |
| a0003 | 0/0 | 224 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | MPAPP others(219): Show |
chr3 | 146428288 | 146474561 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 672 | 349 | 78 | 57 | 166 | 12 | 34 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | ATGCC others(667): Show |
chr3 | 146428288 | 146474561 | ||
| a0001c0003 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | ATGCC others(667): Show |
chr3 | 146428288 | 146474561 | ||
| a0001c0004 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | ATGCC others(667): Show |
chr3 | 146428288 | 146474561 | ||
| a0002c0002 | 0/0 | 672 | 12 | 0 | 1 | 11 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | ATGCC others(667): Show |
chr3 | 146428288 | 146474561 | ||
| a0003c0005 | 0/0 | 672 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | ATGCC others(667): Show |
chr3 | 146428288 | 146474561 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1185 | 161 | 42 | 25 | 73 | 8 | 11 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0002 | 0/0 | 1185 | 85 | 12 | 15 | 44 | 2 | 12 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0003 | 0/0 | 1185 | 84 | 9 | 17 | 47 | 2 | 9 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0004 | 0/0 | 1185 | 14 | 14 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0005 | 0/0 | 1185 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0006 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0007 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0001t0008 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0003t0001 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0001c0004t0002 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0002c0002t0001 | 0/0 | 1185 | 12 | 0 | 1 | 11 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| a0003c0005t0001 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | AGACG others(1180): Show |
chr3 | 146428288 | 146474561 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 19 | 0 | 5 | 12 | 2 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0004 | 1/0 | 18 | 1 | 3 | 10 | 2 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0007 | 0/0 | 6 | 2 | 0 | 1 | 0 | 3 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0021 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0002 | 0/0 | 31 | 6 | 5 | 17 | 1 | 2 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0001 | 0/0 | 34 | 0 | 8 | 18 | 1 | 7 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0004g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0001c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0002c0002t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| a0003c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | GBR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | IBS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0024 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0024 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0094 | AFR | YRI | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18987 | hp2 | a0001 | c0004 | t0002 | g0075 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19030 | hp1 | a0003 | c0005 | t0001 | g0040 | AFR | LWK | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ASW | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | GIH | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | USA | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | USA | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | USA | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0021 | REF | REF | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | PLSCR2_chr3_146428288_146474561 | PLSCR2 | chr3 | 146428288 | 146474561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146449302 | T | A | 1 | a0002 | 12 | HG01257.hp2 NA18747.hp1 NA18977.hp1 others(9): Show |
missense_variant | MODERATE | c.549A>T | p.Arg183Ser | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/8 | 795/1185 | 549/675 | 183/224 | chr3 | 146449302 | |||
| chr3:146455348 | C | T | 1 | a0003 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.212G>A | p.Arg71Gln | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/8 | 458/1185 | 212/675 | 71/224 | chr3 | 146455348 | |||
| chr3:146469497 | G | A | 1 | a0001 | 14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
splice_region_variant | LOW | c.-182C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/8 | chr3 | 146469497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146455349 | G | T | 1 | a0001c0004 | 1 | NA18987.hp2 | synonymous_variant | LOW | c.211C>A | p.Arg71Arg | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/8 | 457/1185 | 211/675 | 71/224 | chr3 | 146455349 | |||
| chr3:146459872 | C | G | 1 | a0001c0003 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.33G>C | p.Pro11Pro | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/8 | 279/1185 | 33/675 | 11/224 | chr3 | 146459872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146433388 | T | G | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0004t0002 |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 8/8 | 8404 | chr3 | 146433388 | ||||||
| chr3:146433478 | C | T | 1 | a0001c0001t0005 | 2 | HG03927.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*74G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 8/8 | 8314 | chr3 | 146433478 | ||||||
| chr3:146433495 | T | G | 1 | a0001c0001t0007 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 8/8 | 8297 | chr3 | 146433495 | ||||||
| chr3:146459949 | T | A | 1 | a0001c0001t0008 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-45A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/8 | 45 | chr3 | 146459949 | ||||||
| chr3:146460028 | C | T | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(3): Show |
173 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
5_prime_UTR_variant | MODIFIER | c.-124G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/8 | 124 | chr3 | 146460028 | ||||||
| chr3:146460064 | G | T | 1 | a0001c0001t0006 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/8 | 160 | chr3 | 146460064 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146433584 | T | A | 1 | a0001c0001t0003g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.*35-67A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146433584 | |||||||
| chr3:146433719 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*35-202T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146433719 | |||||||
| chr3:146433742 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.*35-225A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146433742 | |||||||
| chr3:146433744 | C | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.*35-227G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146433744 | |||||||
| chr3:146433768 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.*35-251A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146433768 | |||||||
| chr3:146433776 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.*35-259G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146433776 | |||||||
| chr3:146434056 | G | C | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*35-539C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434056 | |||||||
| chr3:146434128 | T | A | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*35-611A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434128 | |||||||
| chr3:146434141 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0147 |
9 | HG00639.hp2 HG01071.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.*35-624G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434141 | |||||||
| chr3:146434142 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.*35-625C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434142 | |||||||
| chr3:146434148 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.*35-631T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434148 | |||||||
| chr3:146434223 | A | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.*35-706T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434223 | |||||||
| chr3:146434286 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*35-769A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434286 | |||||||
| chr3:146434379 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG01255.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.*35-862A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434379 | |||||||
| chr3:146434426 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.*35-909C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434426 | |||||||
| chr3:146434459 | G | GAAGAAAC others(325): Show |
1 | a0001c0001t0001g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*35-943_*35-942ins others(332): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434459 | |||||||
| chr3:146434459 | G | GAAGAAAC others(326): Show |
1 | a0001c0001t0001g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*35-943_*35-942ins others(333): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434459 | |||||||
| chr3:146434459 | G | GAAGAAAC others(327): Show |
1 | a0001c0001t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*35-943_*35-942ins others(334): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434459 | |||||||
| chr3:146434535 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.*35-1018A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434535 | |||||||
| chr3:146434588 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*35-1071A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434588 | |||||||
| chr3:146434639 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*35-1122T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434639 | |||||||
| chr3:146434648 | T | C | 1 | a0001c0001t0003g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.*35-1131A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434648 | |||||||
| chr3:146434692 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.*35-1175G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434692 | |||||||
| chr3:146434827 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.*35-1310A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434827 | |||||||
| chr3:146434975 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.*35-1458T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146434975 | |||||||
| chr3:146435013 | C | G | 1 | a0001c0001t0004g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*35-1496G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435013 | |||||||
| chr3:146435132 | T | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(14): Show |
44 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.*35-1615A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435132 | |||||||
| chr3:146435243 | T | G | 1 | a0001c0001t0003g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*35-1726A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435243 | |||||||
| chr3:146435270 | C | T | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*35-1753G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435270 | |||||||
| chr3:146435351 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.*35-1834A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435351 | |||||||
| chr3:146435494 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | NA18965.hp1 NA18971.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.*35-1977C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435494 | |||||||
| chr3:146435548 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*35-2031G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435548 | |||||||
| chr3:146435734 | C | A | 5 | a0001c0001t0001g0124 a0001c0001t0001g0143 a0001c0001t0001g0145 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35-2217G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435734 | |||||||
| chr3:146435747 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*35-2230G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146435747 | |||||||
| chr3:146436021 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.*35-2504A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436021 | |||||||
| chr3:146436056 | C | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(42): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.*35-2539G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436056 | |||||||
| chr3:146436087 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.*35-2570C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436087 | |||||||
| chr3:146436148 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*35-2631G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436148 | |||||||
| chr3:146436197 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*35-2680G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436197 | |||||||
| chr3:146436242 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.*35-2725A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436242 | |||||||
| chr3:146436274 | A | G | 1 | a0001c0001t0005g0024 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.*35-2757T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436274 | |||||||
| chr3:146436367 | G | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.*35-2850C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436367 | |||||||
| chr3:146436448 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*35-2931C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436448 | |||||||
| chr3:146436688 | G | T | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*35-3171C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436688 | |||||||
| chr3:146436736 | TTCC | T | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*35-3222_*35-3220d others(5): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436736 | |||||||
| chr3:146436824 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.*35-3307C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436824 | |||||||
| chr3:146436953 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0183 |
4 | HG02129.hp1 NA18947.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.*35-3436T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436953 | |||||||
| chr3:146436982 | G | T | 45 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(42): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.*35-3465C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146436982 | |||||||
| chr3:146437014 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*35-3497G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437014 | |||||||
| chr3:146437147 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.*35-3630T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437147 | |||||||
| chr3:146437170 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.*35-3653A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437170 | |||||||
| chr3:146437249 | T | C | 1 | a0001c0001t0003g0118 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.*35-3732A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437249 | |||||||
| chr3:146437309 | T | C | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*35-3792A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437309 | |||||||
| chr3:146437400 | C | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*35-3883G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437400 | |||||||
| chr3:146437463 | C | A | 1 | a0001c0001t0005g0024 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.*35-3946G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437463 | |||||||
| chr3:146437522 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*35-4005A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437522 | |||||||
| chr3:146437666 | C | T | 87 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(84): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.*34+4092G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437666 | |||||||
| chr3:146437746 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.*34+4012A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437746 | |||||||
| chr3:146437747 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.*34+4011C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437747 | |||||||
| chr3:146437893 | T | C | 1 | a0001c0001t0004g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.*34+3865A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146437893 | |||||||
| chr3:146438000 | C | T | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*34+3758G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438000 | |||||||
| chr3:146438023 | C | T | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*34+3735G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438023 | |||||||
| chr3:146438196 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*34+3562T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438196 | |||||||
| chr3:146438492 | C | G | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*34+3266G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438492 | |||||||
| chr3:146438582 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.*34+3176C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438582 | |||||||
| chr3:146438602 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*34+3156G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438602 | |||||||
| chr3:146438813 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*34+2945G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438813 | |||||||
| chr3:146438834 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*34+2924A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438834 | |||||||
| chr3:146438913 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.*34+2845G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438913 | |||||||
| chr3:146438916 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*34+2842A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438916 | |||||||
| chr3:146438929 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0046 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.*34+2829A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438929 | |||||||
| chr3:146438966 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0160 |
2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*34+2792G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146438966 | |||||||
| chr3:146439151 | G | A | 87 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(84): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.*34+2607C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439151 | |||||||
| chr3:146439394 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*34+2364G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439394 | |||||||
| chr3:146439512 | A | C | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*34+2246T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439512 | |||||||
| chr3:146439618 | A | G | 1 | a0001c0001t0003g0035 | 2 | HG01517.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.*34+2140T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439618 | |||||||
| chr3:146439677 | A | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.*34+2081T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439677 | |||||||
| chr3:146439775 | C | T | 1 | a0001c0001t0004g0038 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.*34+1983G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439775 | |||||||
| chr3:146439815 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*34+1943G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439815 | |||||||
| chr3:146439834 | G | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*34+1924C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439834 | |||||||
| chr3:146439902 | G | C | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*34+1856C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439902 | |||||||
| chr3:146439903 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.*34+1855C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146439903 | |||||||
| chr3:146440009 | T | C | 38 | a0001c0001t0003g0001 a0001c0001t0003g0011 a0001c0001t0003g0016 others(35): Show |
84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.*34+1749A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440009 | |||||||
| chr3:146440019 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+1739A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440019 | |||||||
| chr3:146440068 | C | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*34+1690G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440068 | |||||||
| chr3:146440443 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*34+1315C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440443 | |||||||
| chr3:146440452 | A | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0015 others(40): Show |
83 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.*34+1306T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440452 | |||||||
| chr3:146440472 | T | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(14): Show |
44 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.*34+1286A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440472 | |||||||
| chr3:146440543 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(57): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.*34+1215G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440543 | |||||||
| chr3:146440577 | G | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.*34+1181C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440577 | |||||||
| chr3:146440608 | T | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.*34+1150A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440608 | |||||||
| chr3:146440676 | G | C | 45 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(42): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.*34+1082C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440676 | |||||||
| chr3:146440733 | C | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0001c0001t0002g0059 |
3 | HG01261.hp2 HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.*34+1025G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440733 | |||||||
| chr3:146440770 | G | GT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(22): Show |
52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.*34+987dupA | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440770 | |||||||
| chr3:146440772 | T | A | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*34+986A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440772 | |||||||
| chr3:146440921 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.*34+837T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440921 | |||||||
| chr3:146440969 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.*34+789T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146440969 | |||||||
| chr3:146441065 | T | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*34+693A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441065 | |||||||
| chr3:146441098 | T | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*34+660A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441098 | |||||||
| chr3:146441123 | T | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0064 |
2 | HG00741.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.*34+635A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441123 | |||||||
| chr3:146441167 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.*34+591C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441167 | |||||||
| chr3:146441393 | A | G | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*34+365T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441393 | |||||||
| chr3:146441492 | T | C | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.*34+266A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441492 | |||||||
| chr3:146441678 | A | G | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*34+80T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 7/7 | chr3 | 146441678 | |||||||
| chr3:146441977 | T | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.646-156A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146441977 | |||||||
| chr3:146442060 | A | G | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.646-239T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442060 | |||||||
| chr3:146442063 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0137 |
3 | HG00099.hp1 HG00741.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.646-242G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442063 | |||||||
| chr3:146442068 | G | T | 1 | a0001c0001t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.646-247C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442068 | |||||||
| chr3:146442095 | C | T | 1 | a0001c0001t0003g0028 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.646-274G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442095 | |||||||
| chr3:146442216 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.646-395A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442216 | |||||||
| chr3:146442271 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.646-450G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442271 | |||||||
| chr3:146442283 | A | G | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.646-462T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442283 | |||||||
| chr3:146442384 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-563T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442384 | |||||||
| chr3:146442469 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-648A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442469 | |||||||
| chr3:146442753 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.646-932T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442753 | |||||||
| chr3:146442802 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.646-981A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442802 | |||||||
| chr3:146442836 | A | C | 1 | a0001c0001t0005g0024 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.646-1015T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442836 | |||||||
| chr3:146442840 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.646-1019T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442840 | |||||||
| chr3:146442851 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.646-1030G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146442851 | |||||||
| chr3:146443011 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1190T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443011 | |||||||
| chr3:146443168 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.646-1347C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443168 | |||||||
| chr3:146443180 | T | G | 1 | a0001c0001t0003g0112 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.646-1359A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443180 | |||||||
| chr3:146443198 | A | G | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.646-1377T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443198 | |||||||
| chr3:146443310 | C | A | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.646-1489G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443310 | |||||||
| chr3:146443481 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.646-1660C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443481 | |||||||
| chr3:146443496 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-1675T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443496 | |||||||
| chr3:146443718 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-1897A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443718 | |||||||
| chr3:146443809 | C | T | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.646-1988G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443809 | |||||||
| chr3:146443983 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-2162T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146443983 | |||||||
| chr3:146444202 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.646-2381C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444202 | |||||||
| chr3:146444225 | T | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.646-2404A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444225 | |||||||
| chr3:146444240 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.646-2419G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444240 | |||||||
| chr3:146444283 | T | C | 1 | a0001c0001t0001g0012 | 4 | NA18941.hp1 NA19001.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-2462A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444283 | |||||||
| chr3:146444495 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.646-2674T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444495 | |||||||
| chr3:146444637 | G | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(42): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.646-2816C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444637 | |||||||
| chr3:146444684 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.646-2863G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444684 | |||||||
| chr3:146444730 | A | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.646-2909T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444730 | |||||||
| chr3:146444790 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.646-2969C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444790 | |||||||
| chr3:146444826 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0146 |
2 | NA19077.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.646-3005A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444826 | |||||||
| chr3:146444919 | G | C | 88 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.646-3098C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444919 | |||||||
| chr3:146444931 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-3110G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146444931 | |||||||
| chr3:146445120 | C | T | 1 | a0001c0001t0008g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.646-3299G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146445120 | |||||||
| chr3:146445263 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.646-3442G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146445263 | |||||||
| chr3:146445526 | T | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.645+3680A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146445526 | |||||||
| chr3:146445658 | C | A | 1 | a0001c0001t0004g0006 | 7 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.645+3548G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146445658 | |||||||
| chr3:146445790 | G | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.645+3416C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146445790 | |||||||
| chr3:146445854 | T | G | 1 | a0001c0001t0003g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+3352A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146445854 | |||||||
| chr3:146446258 | C | T | 10 | a0001c0001t0002g0026 a0001c0001t0002g0034 a0001c0001t0002g0056 others(7): Show |
12 | HG00140.hp1 HG01109.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+2948G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446258 | |||||||
| chr3:146446346 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.645+2860A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446346 | |||||||
| chr3:146446487 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.645+2719A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446487 | |||||||
| chr3:146446547 | G | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.645+2659C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446547 | |||||||
| chr3:146446567 | A | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.645+2639T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446567 | |||||||
| chr3:146446895 | C | T | 1 | a0001c0001t0003g0108 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.645+2311G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446895 | |||||||
| chr3:146446936 | C | A | 1 | a0001c0001t0003g0113 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.645+2270G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446936 | |||||||
| chr3:146446970 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.645+2236G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446970 | |||||||
| chr3:146446982 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.645+2224T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146446982 | |||||||
| chr3:146447060 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+2146A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447060 | |||||||
| chr3:146447091 | C | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
22 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.645+2115G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447091 | |||||||
| chr3:146447092 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.645+2114C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447092 | |||||||
| chr3:146447158 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.645+2048A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447158 | |||||||
| chr3:146447404 | C | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.645+1802G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447404 | |||||||
| chr3:146447429 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1777G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447429 | |||||||
| chr3:146447460 | C | G | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645+1746G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447460 | |||||||
| chr3:146447567 | A | C | 1 | a0001c0001t0001g0027 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.645+1639T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447567 | |||||||
| chr3:146447576 | G | T | 1 | a0001c0001t0008g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.645+1630C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447576 | |||||||
| chr3:146447630 | C | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(22): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.645+1576G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447630 | |||||||
| chr3:146447700 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.645+1506G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447700 | |||||||
| chr3:146447722 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.645+1484A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447722 | |||||||
| chr3:146447808 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.645+1398A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447808 | |||||||
| chr3:146447842 | G | A | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645+1364C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447842 | |||||||
| chr3:146447933 | C | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.645+1273G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146447933 | |||||||
| chr3:146448037 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0163 |
4 | HG01433.hp2 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+1169G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146448037 | |||||||
| chr3:146448236 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.645+970A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146448236 | |||||||
| chr3:146448342 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.645+864A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146448342 | |||||||
| chr3:146448555 | G | C | 1 | a0001c0001t0003g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.645+651C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146448555 | |||||||
| chr3:146448616 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.645+590C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146448616 | |||||||
| chr3:146449045 | G | A | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+161C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146449045 | |||||||
| chr3:146449194 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.645+12C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 6/7 | chr3 | 146449194 | |||||||
| chr3:146449387 | A | C | 3 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0001c0001t0002g0059 |
3 | HG01261.hp2 HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.484-20T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449387 | |||||||
| chr3:146449462 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.484-95A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449462 | |||||||
| chr3:146449472 | C | T | 2 | a0002c0002t0001g0131 a0002c0002t0001g0171 |
2 | HG01257.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.484-105G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449472 | |||||||
| chr3:146449565 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.484-198C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449565 | |||||||
| chr3:146449631 | AAT | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.484-266_484-265del others(2): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449631 | |||||||
| chr3:146449704 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-337G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449704 | |||||||
| chr3:146449754 | A | G | 1 | a0001c0001t0003g0016 | 3 | NA18963.hp1 NA18998.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.484-387T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449754 | |||||||
| chr3:146449840 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.484-473A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449840 | |||||||
| chr3:146449871 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.484-504T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449871 | |||||||
| chr3:146449925 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.484-558C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146449925 | |||||||
| chr3:146450427 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.484-1060C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146450427 | |||||||
| chr3:146450432 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.484-1065A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146450432 | |||||||
| chr3:146450664 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.484-1297A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146450664 | |||||||
| chr3:146450754 | A | G | 1 | a0001c0001t0003g0167 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.484-1387T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146450754 | |||||||
| chr3:146450838 | C | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0159 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.484-1471G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146450838 | |||||||
| chr3:146450960 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.484-1593T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146450960 | |||||||
| chr3:146451063 | TAC | T | 8 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(5): Show |
17 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.484-1698_484-1697d others(4): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451063 | |||||||
| chr3:146451080 | C | T | 1 | a0001c0001t0003g0107 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.484-1713G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451080 | |||||||
| chr3:146451107 | C | CT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0134 others(5): Show |
10 | HG00642.hp2 HG01433.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-1741dupA | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451107 | |||||||
| chr3:146451107 | CT | C | 87 | a0001c0001t0001g0036 a0001c0001t0001g0085 a0001c0001t0001g0089 others(84): Show |
174 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.484-1741delA | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451107 | |||||||
| chr3:146451107 | CTT | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(17): Show |
46 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.484-1742_484-1741d others(4): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451107 | |||||||
| chr3:146451134 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.484-1767C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451134 | |||||||
| chr3:146451137 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-1770C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451137 | |||||||
| chr3:146451173 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.484-1806C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451173 | |||||||
| chr3:146451271 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.484-1904G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451271 | |||||||
| chr3:146451335 | G | A | 87 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(84): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.484-1968C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451335 | |||||||
| chr3:146451455 | A | T | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.484-2088T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451455 | |||||||
| chr3:146451477 | TA | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(81): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.484-2111delT | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451477 | |||||||
| chr3:146451535 | G | A | 84 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(81): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.484-2168C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451535 | |||||||
| chr3:146451698 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.483+2304G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451698 | |||||||
| chr3:146451699 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.483+2303G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451699 | |||||||
| chr3:146451700 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.483+2302C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451700 | |||||||
| chr3:146451729 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+2273A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451729 | |||||||
| chr3:146451762 | T | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.483+2240A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451762 | |||||||
| chr3:146451887 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.483+2115C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451887 | |||||||
| chr3:146451889 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.483+2113T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451889 | |||||||
| chr3:146451904 | A | AT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.483+2097dupA | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146451904 | |||||||
| chr3:146452025 | G | C | 1 | a0001c0001t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.483+1977C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146452025 | |||||||
| chr3:146452150 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.483+1852A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146452150 | |||||||
| chr3:146452242 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.483+1760T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146452242 | |||||||
| chr3:146452763 | T | G | 1 | a0001c0001t0002g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.483+1239A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146452763 | |||||||
| chr3:146452835 | A | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0104 |
2 | NA18940.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.483+1167T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146452835 | |||||||
| chr3:146452988 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.483+1014T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146452988 | |||||||
| chr3:146453063 | C | A | 1 | a0001c0001t0004g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.483+939G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453063 | |||||||
| chr3:146453124 | A | G | 84 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(81): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.483+878T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453124 | |||||||
| chr3:146453160 | C | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02647.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.483+842G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453160 | |||||||
| chr3:146453173 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+829C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453173 | |||||||
| chr3:146453196 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.483+806A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453196 | |||||||
| chr3:146453259 | G | A | 1 | a0001c0001t0005g0024 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.483+743C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453259 | |||||||
| chr3:146453271 | TCA | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.483+729_483+730del others(2): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453271 | |||||||
| chr3:146453430 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+572T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453430 | |||||||
| chr3:146453518 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.483+484A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453518 | |||||||
| chr3:146453531 | T | C | 3 | a0001c0001t0003g0030 a0001c0001t0003g0118 a0001c0001t0003g0120 |
4 | HG00408.hp1 NA18992.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+471A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453531 | |||||||
| chr3:146453660 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.483+342G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453660 | |||||||
| chr3:146453865 | A | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.483+137T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 5/7 | chr3 | 146453865 | |||||||
| chr3:146454214 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.322-51A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454214 | |||||||
| chr3:146454322 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.322-159C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454322 | |||||||
| chr3:146454325 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.322-162G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454325 | |||||||
| chr3:146454374 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.322-211A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454374 | |||||||
| chr3:146454573 | C | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(81): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.322-410G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454573 | |||||||
| chr3:146454609 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.322-446T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454609 | |||||||
| chr3:146454667 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.322-504A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454667 | |||||||
| chr3:146454810 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02055.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+429A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454810 | |||||||
| chr3:146454811 | T | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02055.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+428A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454811 | |||||||
| chr3:146454871 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.321+368G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454871 | |||||||
| chr3:146454909 | G | C | 1 | a0001c0001t0003g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.321+330C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454909 | |||||||
| chr3:146454930 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.321+309G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454930 | |||||||
| chr3:146454963 | T | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0041 others(7): Show |
15 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+276A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146454963 | |||||||
| chr3:146455010 | C | G | 2 | a0001c0001t0003g0016 a0001c0001t0003g0103 |
4 | NA18963.hp1 NA18966.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+229G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146455010 | |||||||
| chr3:146455018 | A | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0130 others(4): Show |
23 | HG01257.hp2 HG02056.hp1 NA18747.hp1 others(20): Show |
intron_variant | MODIFIER | c.321+221T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146455018 | |||||||
| chr3:146455059 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+180C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 4/7 | chr3 | 146455059 | |||||||
| chr3:146455590 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.101-131A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146455590 | |||||||
| chr3:146455632 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.101-173T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146455632 | |||||||
| chr3:146455810 | GTATAGTT others(4): Show |
G | 1 | a0001c0001t0001g0170 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.101-362_101-352del others(11): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146455810 | |||||||
| chr3:146455911 | T | C | 1 | a0002c0002t0001g0171 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.101-452A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146455911 | |||||||
| chr3:146455934 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.101-475A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146455934 | |||||||
| chr3:146456085 | G | A | 3 | a0001c0001t0003g0030 a0001c0001t0003g0118 a0001c0001t0003g0120 |
4 | HG00408.hp1 NA18992.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-626C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456085 | |||||||
| chr3:146456335 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.101-876A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456335 | |||||||
| chr3:146456396 | T | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0039 |
4 | HG02818.hp1 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-937A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456396 | |||||||
| chr3:146456456 | T | TG | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-998dupC | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456456 | |||||||
| chr3:146456462 | A | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-1003T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456462 | |||||||
| chr3:146456537 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101-1078A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456537 | |||||||
| chr3:146456672 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.101-1213A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456672 | |||||||
| chr3:146456720 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101-1261C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146456720 | |||||||
| chr3:146457319 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.100+1092G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457319 | |||||||
| chr3:146457577 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+834A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457577 | |||||||
| chr3:146457588 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0043 others(112): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.100+823T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457588 | |||||||
| chr3:146457600 | G | T | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100+811C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457600 | |||||||
| chr3:146457743 | A | G | 1 | a0001c0001t0003g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100+668T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457743 | |||||||
| chr3:146457899 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.100+512A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457899 | |||||||
| chr3:146457901 | TAGG | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.100+507_100+509del others(3): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146457901 | |||||||
| chr3:146458047 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.100+364T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146458047 | |||||||
| chr3:146458081 | T | C | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100+330A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146458081 | |||||||
| chr3:146458212 | G | C | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100+199C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146458212 | |||||||
| chr3:146458288 | C | T | 84 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(81): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.100+123G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 3/7 | chr3 | 146458288 | |||||||
| chr3:146458498 | T | C | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58-45A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146458498 | |||||||
| chr3:146458563 | A | T | 1 | a0001c0001t0003g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.58-110T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146458563 | |||||||
| chr3:146459136 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.58-683A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459136 | |||||||
| chr3:146459206 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.57+642C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459206 | |||||||
| chr3:146459209 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.57+639T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459209 | |||||||
| chr3:146459371 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+477G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459371 | |||||||
| chr3:146459544 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.57+304T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459544 | |||||||
| chr3:146459697 | T | C | 1 | a0001c0001t0005g0024 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.57+151A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459697 | |||||||
| chr3:146459714 | TGTTTACC others(119): Show |
T | 1 | a0001c0001t0002g0042 | 1 | NA18997.hp2 | splice_region_variant&intron_variant | LOW | c.57+8_57+133del | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459714 | |||||||
| chr3:146459807 | GT | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(21): Show |
51 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.57+40delA | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 2/7 | chr3 | 146459807 | |||||||
| chr3:146460136 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(15): Show |
45 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-179-53G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460136 | |||||||
| chr3:146460298 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-179-215G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460298 | |||||||
| chr3:146460314 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(104): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-179-231A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460314 | |||||||
| chr3:146460410 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-179-327C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460410 | |||||||
| chr3:146460443 | G | GA | 76 | a0001c0001t0001g0081 a0001c0001t0001g0155 a0001c0001t0001g0176 others(73): Show |
160 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-179-361dupT | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460443 | |||||||
| chr3:146460443 | G | GAA | 7 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(4): Show |
7 | HG01109.hp2 HG01123.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-179-362_-179-361d others(4): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460443 | |||||||
| chr3:146460443 | GA | G | 30 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
47 | HG00099.hp2 HG00280.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.-179-361delT | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460443 | |||||||
| chr3:146460443 | GAA | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
27 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-179-362_-179-361d others(4): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460443 | |||||||
| chr3:146460477 | T | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0014 others(81): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-179-394A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460477 | |||||||
| chr3:146460548 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-179-465A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460548 | |||||||
| chr3:146460632 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-179-549C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460632 | |||||||
| chr3:146460660 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-179-577C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460660 | |||||||
| chr3:146460669 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
28 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-179-586A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460669 | |||||||
| chr3:146460686 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-179-603C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460686 | |||||||
| chr3:146460738 | AC | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-179-656delG | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460738 | |||||||
| chr3:146460818 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-179-735C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460818 | |||||||
| chr3:146460857 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0070 a0001c0001t0002g0071 |
5 | HG02074.hp1 NA18942.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-179-774C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146460857 | |||||||
| chr3:146461053 | A | C | 1 | a0001c0001t0002g0055 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-179-970T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461053 | |||||||
| chr3:146461073 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-179-990T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461073 | |||||||
| chr3:146461145 | T | C | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-179-1062A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461145 | |||||||
| chr3:146461412 | T | C | 3 | a0001c0001t0004g0038 a0001c0001t0004g0188 a0001c0001t0004g0189 |
4 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-179-1329A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461412 | |||||||
| chr3:146461465 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-179-1382G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461465 | |||||||
| chr3:146461521 | G | T | 1 | a0001c0001t0008g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-179-1438C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461521 | |||||||
| chr3:146461749 | G | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(21): Show |
51 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-179-1666C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146461749 | |||||||
| chr3:146462004 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG02055.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-179-1921T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462004 | |||||||
| chr3:146462062 | T | C | 1 | a0001c0001t0001g0023 | 3 | HG00099.hp2 HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-179-1979A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462062 | |||||||
| chr3:146462274 | T | C | 1 | a0001c0003t0001g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-179-2191A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462274 | |||||||
| chr3:146462283 | G | A | 1 | a0001c0001t0001g0008 | 6 | HG00639.hp2 HG01358.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-179-2200C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462283 | |||||||
| chr3:146462420 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-179-2337C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462420 | |||||||
| chr3:146462457 | T | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-179-2374A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462457 | |||||||
| chr3:146462468 | CT | C | 19 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(16): Show |
24 | HG00609.hp2 HG02056.hp2 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.-179-2386delA | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462468 | |||||||
| chr3:146462468 | CTT | C | 72 | a0001c0001t0001g0027 a0001c0001t0001g0125 a0001c0001t0001g0185 others(69): Show |
156 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-179-2387_-179-238 others(6): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462468 | |||||||
| chr3:146462468 | CTTT | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0022 others(31): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.-179-2388_-179-238 others(7): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462468 | |||||||
| chr3:146462614 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-179-2531G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462614 | |||||||
| chr3:146462765 | G | A | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-179-2682C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146462765 | |||||||
| chr3:146463099 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-179-3016A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463099 | |||||||
| chr3:146463181 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-179-3098C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463181 | |||||||
| chr3:146463217 | G | C | 87 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(84): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-179-3134C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463217 | |||||||
| chr3:146463294 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-179-3211C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463294 | |||||||
| chr3:146463415 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-179-3332T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463415 | |||||||
| chr3:146463435 | G | A | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-179-3352C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463435 | |||||||
| chr3:146463589 | C | G | 88 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(85): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.-179-3506G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463589 | |||||||
| chr3:146463674 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-179-3591C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463674 | |||||||
| chr3:146463740 | TC | T | 2 | a0001c0001t0003g0029 a0001c0001t0003g0121 |
3 | NA18942.hp2 NA19070.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-179-3658delG | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463740 | |||||||
| chr3:146463752 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-179-3669T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146463752 | |||||||
| chr3:146464041 | G | A | 1 | a0002c0002t0001g0171 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-179-3958C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146464041 | |||||||
| chr3:146464125 | A | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0182 |
3 | HG02015.hp1 HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-179-4042T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146464125 | |||||||
| chr3:146464306 | T | C | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-179-4223A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146464306 | |||||||
| chr3:146464338 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-179-4255A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146464338 | |||||||
| chr3:146464423 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | HG00140.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-179-4340C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146464423 | |||||||
| chr3:146464562 | A | T | 1 | a0001c0001t0002g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-179-4479T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146464562 | |||||||
| chr3:146465033 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(109): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-180+4462T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465033 | |||||||
| chr3:146465204 | C | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0182 |
3 | HG02015.hp1 HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-180+4291G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465204 | |||||||
| chr3:146465382 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-180+4113T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465382 | |||||||
| chr3:146465481 | T | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(109): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-180+4014A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465481 | |||||||
| chr3:146465482 | T | A | 1 | a0001c0001t0002g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-180+4013A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465482 | |||||||
| chr3:146465498 | C | A | 1 | a0001c0001t0002g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-180+3997G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465498 | |||||||
| chr3:146465550 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-180+3945G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465550 | |||||||
| chr3:146465572 | C | CA | 57 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0084 others(54): Show |
130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-180+3922dupT | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465572 | |||||||
| chr3:146465572 | C | CAA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
7 | HG01123.hp1 HG01433.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.-180+3921_-180+392 others(6): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465572 | |||||||
| chr3:146465862 | T | G | 85 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-180+3633A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465862 | |||||||
| chr3:146465911 | C | T | 1 | a0001c0001t0008g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-180+3584G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146465911 | |||||||
| chr3:146466182 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-180+3313C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466182 | |||||||
| chr3:146466245 | T | TCA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0036 others(111): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.-180+3249_-180+325 others(6): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466245 | |||||||
| chr3:146466400 | G | C | 85 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(82): Show |
172 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-180+3095C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466400 | |||||||
| chr3:146466405 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180+3090C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466405 | |||||||
| chr3:146466433 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(23): Show |
53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-180+3062G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466433 | |||||||
| chr3:146466455 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180+3040G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466455 | |||||||
| chr3:146466458 | C | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-180+3037G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466458 | |||||||
| chr3:146466578 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-180+2917T>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466578 | |||||||
| chr3:146466786 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00597.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-180+2709A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466786 | |||||||
| chr3:146466914 | C | T | 84 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.-180+2581G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466914 | |||||||
| chr3:146466967 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-180+2528A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146466967 | |||||||
| chr3:146467020 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-180+2475C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467020 | |||||||
| chr3:146467248 | T | C | 31 | a0001c0001t0002g0018 a0001c0001t0002g0100 a0001c0001t0003g0001 others(28): Show |
73 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-180+2247A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467248 | |||||||
| chr3:146467402 | G | C | 1 | a0001c0001t0008g0094 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-180+2093C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467402 | |||||||
| chr3:146467532 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0185 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-180+1963T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467532 | |||||||
| chr3:146467553 | T | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0036 others(109): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-180+1942A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467553 | |||||||
| chr3:146467630 | C | CAT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
30 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-180+1863_-180+186 others(6): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467630 | |||||||
| chr3:146467708 | AG | A | 84 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(81): Show |
171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.-180+1786delC | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467708 | |||||||
| chr3:146467750 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0186 |
3 | HG02965.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-180+1745C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467750 | |||||||
| chr3:146467882 | G | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-180+1613C>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467882 | |||||||
| chr3:146467937 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0080 others(21): Show |
51 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.-180+1558G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467937 | |||||||
| chr3:146467944 | A | ATGAGGAT others(16): Show |
1 | a0001c0001t0002g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-180+1528_-180+155 others(27): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146467944 | |||||||
| chr3:146468152 | C | G | 91 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(88): Show |
186 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-180+1343G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468152 | |||||||
| chr3:146468346 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0002g0083 |
2 | HG02523.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-180+1149C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468346 | |||||||
| chr3:146468402 | G | T | 94 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(91): Show |
189 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-180+1093C>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468402 | |||||||
| chr3:146468513 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0036 others(109): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-180+982C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468513 | |||||||
| chr3:146468568 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-180+927A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468568 | |||||||
| chr3:146468569 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-180+926A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468569 | |||||||
| chr3:146468571 | T | A | 1 | a0001c0001t0002g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-180+924A>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468571 | |||||||
| chr3:146468572 | G | GGCAGTAC others(24): Show |
1 | a0001c0001t0002g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-180+922_-180+923i others(33): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468572 | |||||||
| chr3:146468576 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-180+919A>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468576 | |||||||
| chr3:146468632 | C | A | 1 | a0001c0001t0003g0121 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-180+863G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468632 | |||||||
| chr3:146468707 | A | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-180+788T>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468707 | |||||||
| chr3:146468809 | AAAAC | A | 37 | a0001c0001t0001g0027 a0001c0001t0002g0018 a0001c0001t0002g0100 others(34): Show |
84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-180+682_-180+685d others(6): Show |
PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468809 | |||||||
| chr3:146468985 | C | T | 1 | a0001c0001t0005g0024 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-180+510G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146468985 | |||||||
| chr3:146469015 | C | T | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-180+480G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469015 | |||||||
| chr3:146469020 | C | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0036 others(110): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.-180+475G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469020 | |||||||
| chr3:146469043 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-180+452C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469043 | |||||||
| chr3:146469163 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-180+332C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469163 | |||||||
| chr3:146469299 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-180+196A>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469299 | |||||||
| chr3:146469307 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-180+188T>G | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469307 | |||||||
| chr3:146469319 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-180+176C>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469319 | |||||||
| chr3:146469334 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0041 others(100): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-180+161G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469334 | |||||||
| chr3:146469347 | C | T | 1 | a0003c0005t0001g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-180+148G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469347 | |||||||
| chr3:146469373 | C | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0036 others(102): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-180+122G>T | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469373 | |||||||
| chr3:146469435 | C | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0039 |
4 | HG02818.hp1 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180+60G>C | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469435 | |||||||
| chr3:146469471 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0041 others(99): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-180+24G>A | PLSCR2 | ENSG00000163746.13 | transcript | ENST00000696113.1 | protein_coding | 1/7 | chr3 | 146469471 |