Item | Value |
---|---|
geneid | 389158 |
ensemblid | ENSG00000231213.7 |
hgncid | 19952 |
symbol | PLSCR5 |
name | phospholipid scramblase family member 5 |
refseq_nuc | NM_001085420.2 |
refseq_prot | NP_001078889.1 |
ensembl_nuc | ENST00000443512.2 |
ensembl_prot | ENSP00000390111.1 |
mane_status | MANE Select |
chr | chr3 |
start | 146585837 |
end | 146605346 |
strand | - |
ver | v1.2 |
region | chr3:146585837-146605346 |
region5000 | chr3:146580837-146610346 |
regionname0 | PLSCR5_chr3_146585837_146605346 |
regionname5000 | PLSCR5_chr3_146580837_146610346 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 271 | 405 | 86 | 62 | 191 | 18 | 46 | 151 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | MASKD others(266): Show |
chr3 | 146580837 | 146610346 |
a0002 | 0/0 | 271 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | MASKD others(266): Show |
chr3 | 146580837 | 146610346 |
a0003 | 0/0 | 271 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | MASKD others(266): Show |
chr3 | 146580837 | 146610346 |
a0004 | 0/0 | 271 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | MASKD others(266): Show |
chr3 | 146580837 | 146610346 |
a0005 | 0/0 | 271 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | MASKD others(266): Show |
chr3 | 146580837 | 146610346 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 813 | 405 | 86 | 62 | 191 | 18 | 46 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATGGC others(808): Show |
chr3 | 146580837 | 146610346 | ||
a0002c0002 | 0/0 | 813 | 6 | 6 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATGGC others(808): Show |
chr3 | 146580837 | 146610346 | ||
a0003c0003 | 0/0 | 813 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATGGC others(808): Show |
chr3 | 146580837 | 146610346 | ||
a0004c0005 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATGGC others(808): Show |
chr3 | 146580837 | 146610346 | ||
a0005c0004 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATGGC others(808): Show |
chr3 | 146580837 | 146610346 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1100 | 309 | 66 | 48 | 157 | 11 | 26 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1095): Show |
chr3 | 146580837 | 146610346 |
a0001c0001t0002 | 0/1 | 1099 | 92 | 17 | 14 | 34 | 6 | 20 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1094): Show |
chr3 | 146580837 | 146610346 |
a0001c0001t0003 | 0/0 | 1099 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1094): Show |
chr3 | 146580837 | 146610346 |
a0001c0001t0004 | 0/0 | 1099 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1094): Show |
chr3 | 146580837 | 146610346 |
a0002c0002t0001 | 0/0 | 1100 | 6 | 6 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1095): Show |
chr3 | 146580837 | 146610346 |
a0003c0003t0001 | 0/0 | 1100 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1095): Show |
chr3 | 146580837 | 146610346 |
a0004c0005t0001 | 0/0 | 1100 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1095): Show |
chr3 | 146580837 | 146610346 |
a0005c0004t0001 | 0/0 | 1100 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | ATATG others(1095): Show |
chr3 | 146580837 | 146610346 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 58 | 8 | 9 | 35 | 1 | 5 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0002 | 1/0 | 56 | 13 | 11 | 21 | 3 | 7 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0003 | 0/0 | 37 | 0 | 9 | 22 | 0 | 6 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0017 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0019 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0022 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0028 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0045 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0005 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0006 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0008 | 0/1 | 8 | 0 | 2 | 0 | 3 | 2 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0012 | 0/0 | 6 | 1 | 1 | 0 | 0 | 4 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0030 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0002c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0003c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0004c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
a0005c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | GBR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | FIN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | FIN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0138 | EUR | FIN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0102 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03579 | hp2 | a0004 | c0005 | t0001 | g0114 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | YRI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19006 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19043 | hp2 | a0005 | c0004 | t0001 | g0122 | AFR | LWK | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ASW | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | TSI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | TSI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | GIH | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | USA | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | LWK | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0008 | REF | REF | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | PLSCR5_chr3_146580837_146610346 | PLSCR5 | chr3 | 146580837 | 146610346 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:146591865 | G | A | 1 | a0003 | 3 | NA18964.hp2 NA19006.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.470C>T | p.Pro157Leu | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/8 | 604/1100 | 470/816 | 157/271 | chr3 | 146591865 | |||
chr3:146593972 | A | C | 1 | a0005 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.401T>G | p.Val134Gly | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/8 | 535/1100 | 401/816 | 134/271 | chr3 | 146593972 | |||
chr3:146594045 | G | T | 1 | a0002 | 6 | HG02280.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.328C>A | p.Arg110Ser | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/8 | 462/1100 | 328/816 | 110/271 | chr3 | 146594045 | |||
chr3:146600461 | C | A | 1 | a0004 | 1 | HG03579.hp2 | missense_variant&splice_region_variant | MODERATE | c.16G>T | p.Ala6Ser | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/8 | 150/1100 | 16/816 | 6/271 | chr3 | 146600461 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:146585876 | AT | A | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*110delA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 8/8 | 197 | chr3 | 146585876 | ||||||
chr3:146586060 | C | A | 1 | a0001c0001t0004 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 7/8 | 14 | chr3 | 146586060 | ||||||
chr3:146586069 | G | A | 1 | a0001c0001t0003 | 3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 7/8 | 5 | chr3 | 146586069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:146585963 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.*45-21C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 7/7 | chr3 | 146585963 | |||||||
chr3:146585986 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*44+44T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 7/7 | chr3 | 146585986 | |||||||
chr3:146586171 | A | G | 4 | a0002c0002t0001g0025 a0002c0002t0001g0100 a0002c0002t0001g0101 others(1): Show |
6 | HG02280.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-59T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586171 | |||||||
chr3:146586322 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.778-210T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586322 | |||||||
chr3:146586396 | A | T | 41 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(38): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.778-284T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586396 | |||||||
chr3:146586397 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0123 others(3): Show |
10 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-285T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586397 | |||||||
chr3:146586407 | G | C | 1 | a0001c0001t0001g0038 | 2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.778-295C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586407 | |||||||
chr3:146586412 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-300C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586412 | |||||||
chr3:146586507 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.778-395G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586507 | |||||||
chr3:146586658 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0092 a0001c0001t0001g0124 |
8 | NA18965.hp1 NA18972.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-546C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586658 | |||||||
chr3:146586682 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(104): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.778-570G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586682 | |||||||
chr3:146586718 | C | A | 41 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(38): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.778-606G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586718 | |||||||
chr3:146586750 | G | GA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(104): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.778-639dupT | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586750 | |||||||
chr3:146586761 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01070.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.778-649C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586761 | |||||||
chr3:146586810 | G | A | 42 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0076 others(39): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.778-698C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586810 | |||||||
chr3:146586853 | T | A | 20 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(17): Show |
51 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.778-741A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586853 | |||||||
chr3:146586855 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.778-743G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586855 | |||||||
chr3:146586919 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.778-807T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146586919 | |||||||
chr3:146587021 | A | G | 20 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(17): Show |
51 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.778-909T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587021 | |||||||
chr3:146587106 | T | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(38): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.778-994A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587106 | |||||||
chr3:146587152 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.778-1040A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587152 | |||||||
chr3:146587216 | C | A | 41 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(38): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.778-1104G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587216 | |||||||
chr3:146587228 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.778-1116G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587228 | |||||||
chr3:146587440 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0123 others(3): Show |
10 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-1328C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587440 | |||||||
chr3:146587629 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-1517C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587629 | |||||||
chr3:146587749 | T | A | 14 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0030 others(11): Show |
27 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.778-1637A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587749 | |||||||
chr3:146587758 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0095 |
2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.778-1646T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587758 | |||||||
chr3:146587796 | T | C | 1 | a0001c0001t0002g0016 | 4 | HG01255.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-1684A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587796 | |||||||
chr3:146587852 | T | TTGTATA | 11 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0052 others(8): Show |
14 | HG00438.hp1 HG02486.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-1746_778-1741d others(8): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587852 | |||||||
chr3:146587998 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(53): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.777+1655C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146587998 | |||||||
chr3:146588012 | A | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+1641T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588012 | |||||||
chr3:146588165 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.777+1488T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588165 | |||||||
chr3:146588202 | G | A | 1 | a0002c0002t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.777+1451C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588202 | |||||||
chr3:146588218 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.777+1435G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588218 | |||||||
chr3:146588278 | G | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(6): Show |
14 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.777+1375C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588278 | |||||||
chr3:146588466 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.777+1187T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588466 | |||||||
chr3:146588492 | AACAAAAA others(21): Show |
A | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.777+1133_777+1160d others(30): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588492 | |||||||
chr3:146588517 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.777+1136A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588517 | |||||||
chr3:146588528 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+1125C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588528 | |||||||
chr3:146588568 | T | TAC | 18 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.777+1083_777+1084d others(4): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588568 | |||||||
chr3:146588581 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.777+1072T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588581 | |||||||
chr3:146588677 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0056 others(2): Show |
11 | HG01255.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.777+976A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588677 | |||||||
chr3:146588691 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.777+962T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588691 | |||||||
chr3:146588777 | TA | T | 10 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(7): Show |
15 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.777+875delT | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588777 | |||||||
chr3:146588786 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.777+867A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588786 | |||||||
chr3:146588826 | A | C | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.777+827T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588826 | |||||||
chr3:146588943 | A | AT | 4 | a0001c0001t0002g0008 a0001c0001t0002g0137 a0001c0001t0002g0139 others(1): Show |
10 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.777+709dupA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588943 | |||||||
chr3:146588965 | T | C | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.777+688A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588965 | |||||||
chr3:146588979 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.777+674A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146588979 | |||||||
chr3:146589108 | A | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0005c0004t0001g0122 |
5 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+545T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589108 | |||||||
chr3:146589219 | T | G | 1 | a0001c0001t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.777+434A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589219 | |||||||
chr3:146589225 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.777+428G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589225 | |||||||
chr3:146589252 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.777+401T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589252 | |||||||
chr3:146589283 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+370A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589283 | |||||||
chr3:146589353 | C | CA | 11 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.777+299dupT | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589353 | |||||||
chr3:146589487 | G | A | 1 | a0001c0001t0001g0010 | 7 | NA18951.hp2 NA18988.hp2 NA19063.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+166C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589487 | |||||||
chr3:146589532 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.777+121G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589532 | |||||||
chr3:146589552 | T | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+101A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589552 | |||||||
chr3:146589584 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(59): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.777+69C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 6/7 | chr3 | 146589584 | |||||||
chr3:146589848 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.616-34G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146589848 | |||||||
chr3:146589868 | A | G | 1 | a0001c0001t0001g0039 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.616-54T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146589868 | |||||||
chr3:146589934 | A | G | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.616-120T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146589934 | |||||||
chr3:146589945 | T | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.616-131A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146589945 | |||||||
chr3:146590043 | T | G | 1 | a0001c0001t0001g0023 | 3 | HG01243.hp2 HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.616-229A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590043 | |||||||
chr3:146590262 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.616-448G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590262 | |||||||
chr3:146590412 | T | G | 1 | a0001c0001t0001g0031 | 3 | HG01167.hp2 HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.616-598A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590412 | |||||||
chr3:146590778 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.615+942C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590778 | |||||||
chr3:146590796 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.615+924T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590796 | |||||||
chr3:146590808 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.615+912G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590808 | |||||||
chr3:146590865 | G | C | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.615+855C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590865 | |||||||
chr3:146590866 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.615+854G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590866 | |||||||
chr3:146590867 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.615+853A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590867 | |||||||
chr3:146590868 | G | GTCACCCC others(8): Show |
1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.615+851_615+852ins others(15): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590868 | |||||||
chr3:146590880 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.615+840A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590880 | |||||||
chr3:146590962 | C | A | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.615+758G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590962 | |||||||
chr3:146590996 | T | TTG | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.615+723_615+724ins others(2): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590996 | |||||||
chr3:146590997 | G | GT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(57): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.615+722dupA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590997 | |||||||
chr3:146590997 | G | GTT | 18 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0058 others(15): Show |
36 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.615+721_615+722dup others(2): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590997 | |||||||
chr3:146590997 | G | GTTT | 17 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0141 others(14): Show |
41 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.615+720_615+722dup others(3): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590997 | |||||||
chr3:146590997 | G | T | 6 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0126 others(3): Show |
14 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.615+723C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146590997 | |||||||
chr3:146591010 | G | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0123 others(2): Show |
8 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.615+710C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591010 | |||||||
chr3:146591116 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.615+604T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591116 | |||||||
chr3:146591166 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.615+554C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591166 | |||||||
chr3:146591181 | AT | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.615+538delA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591181 | |||||||
chr3:146591226 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0005c0004t0001g0122 |
5 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+494G>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591226 | |||||||
chr3:146591289 | G | C | 1 | a0001c0001t0001g0029 | 3 | HG02965.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.615+431C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591289 | |||||||
chr3:146591351 | T | A | 1 | a0001c0001t0001g0028 | 3 | HG01515.hp1 HG01517.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.615+369A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591351 | |||||||
chr3:146591384 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.615+336C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591384 | |||||||
chr3:146591440 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.615+280A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591440 | |||||||
chr3:146591535 | A | G | 9 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(6): Show |
14 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.615+185T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591535 | |||||||
chr3:146591571 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.615+149A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591571 | |||||||
chr3:146591574 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.615+146T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591574 | |||||||
chr3:146591581 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.615+139C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591581 | |||||||
chr3:146591660 | T | C | 1 | a0001c0001t0001g0039 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.615+60A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591660 | |||||||
chr3:146591685 | C | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0013 others(11): Show |
35 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.615+35G>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 5/7 | chr3 | 146591685 | |||||||
chr3:146591921 | T | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.454-40A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146591921 | |||||||
chr3:146591928 | A | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0038 others(13): Show |
59 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.454-47T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146591928 | |||||||
chr3:146592045 | A | G | 9 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(6): Show |
14 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.454-164T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592045 | |||||||
chr3:146592083 | C | T | 1 | a0001c0001t0002g0016 | 4 | HG01255.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-202G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592083 | |||||||
chr3:146592084 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.454-203C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592084 | |||||||
chr3:146592311 | A | AT | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.454-431dupA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592311 | |||||||
chr3:146592437 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.454-556G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592437 | |||||||
chr3:146592441 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.454-560A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592441 | |||||||
chr3:146592586 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
6 | HG02965.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.454-705C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592586 | |||||||
chr3:146592757 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.454-876A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592757 | |||||||
chr3:146592761 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.454-880T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592761 | |||||||
chr3:146592762 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.454-881C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592762 | |||||||
chr3:146592791 | T | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(6): Show |
14 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.454-910A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592791 | |||||||
chr3:146592895 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.454-1014T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592895 | |||||||
chr3:146592934 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(59): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.453+986G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592934 | |||||||
chr3:146592976 | G | C | 1 | a0001c0001t0001g0031 | 3 | HG01167.hp2 HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.453+944C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146592976 | |||||||
chr3:146593194 | T | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.453+726A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593194 | |||||||
chr3:146593239 | A | T | 8 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0030 others(5): Show |
23 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.453+681T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593239 | |||||||
chr3:146593269 | G | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.453+651C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593269 | |||||||
chr3:146593276 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.453+644G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593276 | |||||||
chr3:146593429 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.453+491G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593429 | |||||||
chr3:146593491 | T | C | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.453+429A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593491 | |||||||
chr3:146593590 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0046 |
5 | HG01169.hp2 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+330C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593590 | |||||||
chr3:146593598 | G | T | 1 | a0001c0001t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.453+322C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593598 | |||||||
chr3:146593613 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(1): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.453+307C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593613 | |||||||
chr3:146593649 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.453+271T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593649 | |||||||
chr3:146593679 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.453+241T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593679 | |||||||
chr3:146593709 | A | C | 1 | a0001c0001t0001g0020 | 4 | NA18943.hp1 NA19001.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+211T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593709 | |||||||
chr3:146593732 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.453+188A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593732 | |||||||
chr3:146593802 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.453+118G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 4/7 | chr3 | 146593802 | |||||||
chr3:146594150 | CA | C | 47 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(44): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.233-11delT | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594150 | |||||||
chr3:146594373 | T | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.233-233A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594373 | |||||||
chr3:146594545 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.233-405G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594545 | |||||||
chr3:146594635 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.232+406C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594635 | |||||||
chr3:146594743 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.232+298T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594743 | |||||||
chr3:146594752 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232+289G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594752 | |||||||
chr3:146594796 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.232+245T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594796 | |||||||
chr3:146594899 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.232+142T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 3/7 | chr3 | 146594899 | |||||||
chr3:146595099 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.190-16A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595099 | |||||||
chr3:146595101 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.190-18T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595101 | |||||||
chr3:146595104 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.190-21C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595104 | |||||||
chr3:146595105 | G | T | 1 | a0001c0001t0002g0125 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.190-22C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595105 | |||||||
chr3:146595130 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.190-47C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595130 | |||||||
chr3:146595154 | G | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-71C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595154 | |||||||
chr3:146595249 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-166G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595249 | |||||||
chr3:146595253 | A | AT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(13): Show |
31 | HG00408.hp2 HG00609.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.190-171dupA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595253 | |||||||
chr3:146595395 | A | C | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.190-312T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595395 | |||||||
chr3:146595580 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.190-497G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595580 | |||||||
chr3:146595615 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.190-532C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595615 | |||||||
chr3:146595616 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.190-533T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595616 | |||||||
chr3:146595665 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02155.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.190-582G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595665 | |||||||
chr3:146595760 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.190-677G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595760 | |||||||
chr3:146595797 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.190-714C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595797 | |||||||
chr3:146595799 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.190-716A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595799 | |||||||
chr3:146595835 | C | T | 4 | a0002c0002t0001g0025 a0002c0002t0001g0100 a0002c0002t0001g0101 others(1): Show |
6 | HG02280.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-752G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595835 | |||||||
chr3:146595898 | C | T | 2 | a0002c0002t0001g0100 a0002c0002t0001g0102 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.190-815G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595898 | |||||||
chr3:146595918 | A | G | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.190-835T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595918 | |||||||
chr3:146595925 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.190-842A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146595925 | |||||||
chr3:146596015 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0005c0004t0001g0122 |
5 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-932G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596015 | |||||||
chr3:146596098 | AATG | A | 4 | a0002c0002t0001g0025 a0002c0002t0001g0100 a0002c0002t0001g0101 others(1): Show |
6 | HG02280.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1018_190-1016d others(5): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596098 | |||||||
chr3:146596165 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.190-1082A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596165 | |||||||
chr3:146596184 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-1101G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596184 | |||||||
chr3:146596185 | G | A | 1 | a0001c0001t0001g0018 | 4 | NA18960.hp2 NA18994.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-1102C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596185 | |||||||
chr3:146596262 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-1179G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596262 | |||||||
chr3:146596286 | T | G | 1 | a0001c0001t0001g0042 | 2 | NA19068.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.190-1203A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596286 | |||||||
chr3:146596323 | G | T | 2 | a0001c0001t0001g0123 a0005c0004t0001g0122 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.190-1240C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596323 | |||||||
chr3:146596360 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190-1277G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596360 | |||||||
chr3:146596391 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0005c0004t0001g0122 |
5 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1308T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596391 | |||||||
chr3:146596439 | T | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-1356A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596439 | |||||||
chr3:146596473 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.190-1390C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596473 | |||||||
chr3:146596684 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.190-1601A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596684 | |||||||
chr3:146596755 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.190-1672C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596755 | |||||||
chr3:146596936 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.190-1853T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596936 | |||||||
chr3:146596988 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.190-1905A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146596988 | |||||||
chr3:146597339 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-2256C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597339 | |||||||
chr3:146597430 | G | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.190-2347C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597430 | |||||||
chr3:146597434 | A | C | 1 | a0001c0001t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190-2351T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597434 | |||||||
chr3:146597471 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.190-2388C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597471 | |||||||
chr3:146597556 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.190-2473G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597556 | |||||||
chr3:146597593 | T | C | 17 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 others(14): Show |
32 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.190-2510A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597593 | |||||||
chr3:146597600 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.190-2517G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597600 | |||||||
chr3:146597684 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.190-2601A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597684 | |||||||
chr3:146597717 | G | A | 5 | a0001c0001t0002g0099 a0002c0002t0001g0025 a0002c0002t0001g0100 others(2): Show |
7 | HG02280.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+2571C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597717 | |||||||
chr3:146597730 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.189+2558C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597730 | |||||||
chr3:146597734 | A | T | 1 | a0001c0001t0002g0016 | 4 | HG01255.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+2554T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597734 | |||||||
chr3:146597831 | A | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0048 others(25): Show |
50 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.189+2457T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146597831 | |||||||
chr3:146598024 | T | C | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.189+2264A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598024 | |||||||
chr3:146598062 | C | T | 9 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(6): Show |
14 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+2226G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598062 | |||||||
chr3:146598097 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0049 |
3 | HG00140.hp1 HG01358.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.189+2191T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598097 | |||||||
chr3:146598236 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.189+2052G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598236 | |||||||
chr3:146598287 | A | G | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.189+2001T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598287 | |||||||
chr3:146598360 | T | A | 1 | a0001c0001t0002g0133 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.189+1928A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598360 | |||||||
chr3:146598462 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.189+1826C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598462 | |||||||
chr3:146598480 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+1808C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598480 | |||||||
chr3:146598508 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+1780T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598508 | |||||||
chr3:146598512 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+1776A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598512 | |||||||
chr3:146598518 | C | T | 7 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(4): Show |
11 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1770G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598518 | |||||||
chr3:146598538 | A | G | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.189+1750T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598538 | |||||||
chr3:146598564 | C | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(8): Show |
18 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+1724G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598564 | |||||||
chr3:146598580 | T | C | 20 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.189+1708A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598580 | |||||||
chr3:146598600 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.189+1688G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146598600 | |||||||
chr3:146599060 | T | C | 1 | a0001c0001t0002g0043 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.189+1228A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599060 | |||||||
chr3:146599134 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.189+1154T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599134 | |||||||
chr3:146599184 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.189+1104A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599184 | |||||||
chr3:146599277 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.189+1011A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599277 | |||||||
chr3:146599308 | T | A | 4 | a0002c0002t0001g0025 a0002c0002t0001g0100 a0002c0002t0001g0101 others(1): Show |
6 | HG02280.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+980A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599308 | |||||||
chr3:146599334 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.189+954G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599334 | |||||||
chr3:146599421 | A | T | 2 | a0001c0001t0001g0123 a0005c0004t0001g0122 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.189+867T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599421 | |||||||
chr3:146599507 | G | T | 17 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 others(14): Show |
32 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.189+781C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599507 | |||||||
chr3:146599514 | CT | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0061 others(10): Show |
20 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+773delA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599514 | |||||||
chr3:146599514 | CTT | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0135 others(19): Show |
39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.189+772_189+773del others(2): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599514 | |||||||
chr3:146599514 | CTTT | C | 19 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0006 others(16): Show |
49 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.189+771_189+773del others(3): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599514 | |||||||
chr3:146599565 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+723C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599565 | |||||||
chr3:146599579 | C | T | 1 | a0001c0001t0002g0013 | 6 | HG02165.hp1 NA18940.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+709G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599579 | |||||||
chr3:146599615 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0136 |
5 | HG02965.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+673C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599615 | |||||||
chr3:146599679 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(79): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.189+608delA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599679 | |||||||
chr3:146599679 | CTT | C | 27 | a0001c0001t0001g0023 a0001c0001t0001g0089 a0001c0001t0002g0005 others(24): Show |
60 | HG00408.hp2 HG00609.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.189+607_189+608del others(2): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599679 | |||||||
chr3:146599685 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG00438.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.189+603A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599685 | |||||||
chr3:146599840 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+448A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599840 | |||||||
chr3:146599858 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.189+430G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599858 | |||||||
chr3:146599865 | G | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0029 others(45): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.189+423C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599865 | |||||||
chr3:146599954 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(54): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.189+334C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146599954 | |||||||
chr3:146600000 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0060 others(1): Show |
15 | HG00544.hp1 HG00621.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+288G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146600000 | |||||||
chr3:146600213 | T | A | 31 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0048 others(28): Show |
68 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.189+75A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 2/7 | chr3 | 146600213 | |||||||
chr3:146600476 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0005c0004t0001g0122 |
5 | HG01167.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.14-13C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600476 | |||||||
chr3:146600596 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.14-133G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600596 | |||||||
chr3:146600711 | T | C | 1 | a0002c0002t0001g0102 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.14-248A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600711 | |||||||
chr3:146600725 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.14-262G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600725 | |||||||
chr3:146600737 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0007 others(12): Show |
33 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.14-274A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600737 | |||||||
chr3:146600755 | A | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(59): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.14-292T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600755 | |||||||
chr3:146600756 | T | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(59): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.14-293A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600756 | |||||||
chr3:146600890 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.14-427G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600890 | |||||||
chr3:146600996 | TAA | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-535_14-534delTT | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146600996 | |||||||
chr3:146601056 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0098 |
3 | HG02451.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.14-593G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601056 | |||||||
chr3:146601242 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(79): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.14-779T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601242 | |||||||
chr3:146601271 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.14-808G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601271 | |||||||
chr3:146601310 | T | C | 31 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0048 others(28): Show |
68 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.14-847A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601310 | |||||||
chr3:146601311 | T | A | 1 | a0001c0001t0001g0009 | 7 | NA18965.hp2 NA18990.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.14-848A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601311 | |||||||
chr3:146601360 | AT | A | 18 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0116 others(15): Show |
44 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.14-898delA | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601360 | |||||||
chr3:146601532 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.14-1069A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601532 | |||||||
chr3:146601581 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(76): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.14-1118T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601581 | |||||||
chr3:146601598 | GC | G | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-1136delG | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601598 | |||||||
chr3:146601767 | G | T | 1 | a0001c0001t0002g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.14-1304C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601767 | |||||||
chr3:146601870 | ACT | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0120 a0001c0001t0002g0121 |
10 | HG01070.hp1 HG01071.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-1409_14-1408del others(2): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146601870 | |||||||
chr3:146602113 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1650A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602113 | |||||||
chr3:146602122 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-1659G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602122 | |||||||
chr3:146602124 | C | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0056 others(4): Show |
13 | HG01255.hp2 HG01496.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-1661G>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602124 | |||||||
chr3:146602135 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1672T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602135 | |||||||
chr3:146602136 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1673G>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602136 | |||||||
chr3:146602138 | C | CTTCCTAT others(27): Show |
1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1676_14-1675ins others(34): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602138 | |||||||
chr3:146602140 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1677C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602140 | |||||||
chr3:146602142 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1679T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602142 | |||||||
chr3:146602143 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1680G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602143 | |||||||
chr3:146602159 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(92): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-1696C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602159 | |||||||
chr3:146602174 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1711A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602174 | |||||||
chr3:146602178 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1715C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602178 | |||||||
chr3:146602179 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1716C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602179 | |||||||
chr3:146602180 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1717G>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602180 | |||||||
chr3:146602181 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14-1718A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602181 | |||||||
chr3:146602230 | A | T | 33 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0135 others(30): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.14-1767T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602230 | |||||||
chr3:146602231 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(58): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.14-1768T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602231 | |||||||
chr3:146602276 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.14-1813C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602276 | |||||||
chr3:146602297 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.14-1834T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602297 | |||||||
chr3:146602350 | G | A | 2 | a0001c0001t0001g0123 a0005c0004t0001g0122 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.14-1887C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602350 | |||||||
chr3:146602482 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(91): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.14-2019C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602482 | |||||||
chr3:146602516 | T | A | 1 | a0001c0001t0001g0022 | 4 | HG00735.hp2 HG01192.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-2053A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602516 | |||||||
chr3:146602839 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.13+2361C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602839 | |||||||
chr3:146602999 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.13+2201T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146602999 | |||||||
chr3:146603086 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0135 |
4 | HG02965.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+2114T>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603086 | |||||||
chr3:146603216 | G | T | 1 | a0001c0001t0001g0026 | 3 | HG02071.hp2 NA18973.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.13+1984C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603216 | |||||||
chr3:146603221 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
9 | HG00099.hp1 HG00741.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+1979A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603221 | |||||||
chr3:146603223 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(1): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.13+1977G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603223 | |||||||
chr3:146603534 | G | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0048 others(10): Show |
27 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.13+1666C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603534 | |||||||
chr3:146603574 | T | G | 25 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0007 others(22): Show |
53 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.13+1626A>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603574 | |||||||
chr3:146603714 | C | T | 5 | a0001c0001t0002g0099 a0002c0002t0001g0025 a0002c0002t0001g0100 others(2): Show |
7 | HG02280.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+1486G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603714 | |||||||
chr3:146603840 | GTTTA | G | 25 | a0001c0001t0001g0023 a0001c0001t0002g0005 a0001c0001t0002g0007 others(22): Show |
53 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.13+1356_13+1359del others(4): Show |
PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146603840 | |||||||
chr3:146604040 | G | C | 5 | a0001c0001t0002g0008 a0001c0001t0002g0030 a0001c0001t0002g0137 others(2): Show |
13 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+1160C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604040 | |||||||
chr3:146604084 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(58): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.13+1116G>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604084 | |||||||
chr3:146604109 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0016 |
6 | HG01255.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+1091C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604109 | |||||||
chr3:146604191 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0065 others(2): Show |
10 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.13+1009T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604191 | |||||||
chr3:146604433 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0065 others(2): Show |
10 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.13+767G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604433 | |||||||
chr3:146604442 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.13+758G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604442 | |||||||
chr3:146604590 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.13+610T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604590 | |||||||
chr3:146604610 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0002g0063 |
2 | HG02602.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.13+590G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604610 | |||||||
chr3:146604664 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0061 |
3 | HG02129.hp2 NA18948.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.13+536G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604664 | |||||||
chr3:146604666 | G | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0001c0001t0002g0006 others(6): Show |
18 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+534C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604666 | |||||||
chr3:146604671 | C | T | 5 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0049 others(2): Show |
9 | HG00140.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+529G>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604671 | |||||||
chr3:146604755 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.13+445C>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604755 | |||||||
chr3:146604782 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.13+418T>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604782 | |||||||
chr3:146604792 | T | A | 32 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0052 others(29): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.13+408A>T | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604792 | |||||||
chr3:146604843 | G | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0056 others(4): Show |
13 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+357C>A | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604843 | |||||||
chr3:146604899 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0140 others(1): Show |
9 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.13+301A>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146604899 | |||||||
chr3:146605099 | G | C | 1 | a0001c0001t0001g0031 | 3 | HG01167.hp2 HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.13+101C>G | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146605099 | |||||||
chr3:146605114 | A | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0002g0015 others(7): Show |
16 | HG00140.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.13+86T>C | PLSCR5 | ENSG00000231213.7 | transcript | ENST00000443512.2 | protein_coding | 1/7 | chr3 | 146605114 |