Item | Value |
---|---|
geneid | 835 |
ensemblid | ENSG00000106144.20 |
hgncid | 1503 |
symbol | CASP2 |
name | caspase 2 |
refseq_nuc | NM_032982.4 |
refseq_prot | NP_116764.2 |
ensembl_nuc | ENST00000310447.10 |
ensembl_prot | ENSP00000312664.5 |
mane_status | MANE Select |
chr | chr7 |
start | 143288351 |
end | 143307696 |
strand | + |
ver | v1.2 |
region | chr7:143288351-143307696 |
region5000 | chr7:143283351-143312696 |
regionname0 | CASP2_chr7_143288351_143307696 |
regionname5000 | CASP2_chr7_143283351_143312696 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 452 | 235 | 82 | 49 | 68 | 12 | 22 | 46 | CASP2_chr7_143283351_143312696 | CASP2 | MAAPS others(447): Show |
chr7 | 143283351 | 143312696 |
a0002 | 0/0 | 452 | 10 | 2 | 5 | 0 | 1 | 2 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | MAAPS others(447): Show |
chr7 | 143283351 | 143312696 |
a0003 | 0/0 | 452 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | MAAPS others(447): Show |
chr7 | 143283351 | 143312696 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1356 | 229 | 78 | 47 | 68 | 12 | 22 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 | ||
a0001c0003 | 0/0 | 1356 | 3 | 3 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 | ||
a0001c0004 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 | ||
a0001c0006 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 | ||
a0002c0002 | 0/0 | 1356 | 8 | 2 | 4 | 0 | 1 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 | ||
a0002c0005 | 0/0 | 1356 | 2 | 0 | 1 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 | ||
a0003c0007 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | ATGGC others(1351): Show |
chr7 | 143283351 | 143312696 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4089 | 158 | 54 | 30 | 49 | 10 | 13 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0002 | 0/0 | 4090 | 17 | 5 | 4 | 6 | 0 | 2 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0003 | 0/0 | 4088 | 11 | 5 | 1 | 4 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4083): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0004 | 0/0 | 4088 | 6 | 0 | 2 | 2 | 0 | 2 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4083): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0005 | 0/0 | 4089 | 5 | 0 | 0 | 3 | 0 | 2 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0006 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0009 | 0/0 | 4089 | 2 | 1 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0011 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0012 | 0/0 | 4089 | 2 | 0 | 2 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0013 | 0/0 | 4090 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0015 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0016 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0017 | 0/0 | 4088 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4083): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0018 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0019 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0020 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0021 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0023 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0024 | 0/0 | 4088 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4083): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0025 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0026 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0027 | 0/0 | 4089 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0028 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0029 | 0/0 | 4089 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0030 | 0/0 | 4088 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4083): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0031 | 0/0 | 4090 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0032 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0034 | 0/0 | 4089 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0035 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0036 | 0/0 | 4090 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0001c0001t0037 | 0/0 | 4090 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0001c0003t0006 | 0/0 | 4089 | 3 | 3 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0004t0014 | 0/0 | 4089 | 2 | 0 | 2 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0001c0006t0033 | 0/0 | 4088 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4083): Show |
chr7 | 143283351 | 143312696 |
a0002c0002t0001 | 0/0 | 4089 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0002c0002t0007 | 0/0 | 4089 | 3 | 0 | 2 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0002c0002t0008 | 0/0 | 4090 | 2 | 0 | 1 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0002c0002t0010 | 0/0 | 4089 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
a0002c0005t0008 | 0/0 | 4090 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0002c0005t0022 | 0/0 | 4090 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4085): Show |
chr7 | 143283351 | 143312696 |
a0003c0007t0001 | 0/0 | 4089 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | GCAGT others(4084): Show |
chr7 | 143283351 | 143312696 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 6 | 7 | 16 | 0 | 4 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0002 | 0/0 | 8 | 1 | 3 | 1 | 1 | 2 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0003 | 0/0 | 9 | 5 | 2 | 1 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0005 | 1/0 | 9 | 0 | 0 | 8 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0013 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0004g0001 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0005g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0012g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0016g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0018g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0019g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0021g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0023g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0024g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0025g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0026g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0027g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0029g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0031g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0032g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0034g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0035g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0036g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0003t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0003t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0003t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0004t0014g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0001c0006t0033g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0002t0007g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0002t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0002t0008g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0002t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0002t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0005t0008g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0002c0005t0022g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
a0003c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0007 | t0001 | g0002 | EUR | GBR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00140 | hp2 | a0002 | c0002 | t0007 | g0015 | EUR | GBR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00323 | hp2 | a0001 | c0001 | t0028 | g0001 | EUR | FIN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00639 | hp2 | a0001 | c0001 | t0035 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00642 | hp1 | a0001 | c0001 | t0032 | g0100 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00735 | hp1 | a0002 | c0002 | t0008 | g0033 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0101 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00741 | hp1 | a0001 | c0001 | t0012 | g0021 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01069 | hp2 | a0001 | c0001 | t0024 | g0020 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01071 | hp1 | a0001 | c0001 | t0012 | g0021 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01106 | hp1 | a0001 | c0001 | t0017 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01109 | hp1 | a0002 | c0002 | t0007 | g0102 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01175 | hp2 | a0002 | c0002 | t0007 | g0015 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01255 | hp1 | a0001 | c0001 | t0026 | g0099 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01346 | hp1 | a0002 | c0005 | t0008 | g0014 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01433 | hp2 | a0001 | c0001 | t0018 | g0001 | AMR | CLM | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01884 | hp1 | a0001 | c0003 | t0006 | g0111 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01891 | hp2 | a0001 | c0006 | t0033 | g0035 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01934 | hp2 | a0001 | c0004 | t0014 | g0001 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG01978 | hp2 | a0001 | c0001 | t0023 | g0001 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0031 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02055 | hp2 | a0001 | c0001 | t0037 | g0032 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02145 | hp2 | a0001 | c0003 | t0006 | g0112 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02148 | hp1 | a0001 | c0004 | t0014 | g0001 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02451 | hp1 | a0001 | c0001 | t0016 | g0054 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02523 | hp1 | a0001 | c0001 | t0030 | g0082 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02602 | hp1 | a0002 | c0002 | t0008 | g0033 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02723 | hp1 | a0002 | c0002 | t0010 | g0015 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0079 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02886 | hp2 | a0001 | c0003 | t0006 | g0113 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03041 | hp2 | a0001 | c0001 | t0031 | g0046 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0052 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03130 | hp1 | a0002 | c0002 | t0010 | g0014 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03195 | hp2 | a0001 | c0001 | t0015 | g0031 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03491 | hp2 | a0001 | c0001 | t0020 | g0007 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03579 | hp1 | a0001 | c0001 | t0027 | g0049 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0007 | SAS | BEB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG04184 | hp2 | a0002 | c0005 | t0022 | g0014 | SAS | BEB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG04204 | hp2 | a0001 | c0001 | t0025 | g0002 | SAS | STU | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18942 | hp1 | a0001 | c0001 | t0029 | g0084 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18964 | hp1 | a0001 | c0001 | t0019 | g0007 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA20805 | hp1 | a0001 | c0001 | t0021 | g0064 | EUR | TSI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02109 | hp1 | a0001 | c0001 | t0034 | g0073 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0107 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02486 | hp2 | a0001 | c0001 | t0015 | g0032 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0006 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | USA | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
HG06807 | hp2 | a0001 | c0001 | t0036 | g0053 | AFR | USA | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0069 | REF | REF | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | CASP2_chr7_143283351_143312696 | CASP2 | chr7 | 143283351 | 143312696 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143294268 | G | C | 1 | a0002 | 10 | HG00140.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
missense_variant | MODERATE | c.514G>C | p.Val172Leu | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 5/11 | 619/4089 | 514/1359 | 172/452 | chr7 | 143294268 | |||
chr7:143294285 | G | T | 1 | a0003 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.531G>T | p.Lys177Asn | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 5/11 | 636/4089 | 531/1359 | 177/452 | chr7 | 143294285 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143288476 | G | A | 1 | a0001c0006 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.21G>A | p.Gly7Gly | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/11 | 126/4089 | 21/1359 | 7/452 | chr7 | 143288476 | |||
chr7:143291552 | G | A | 1 | a0001c0004 | 2 | HG01934.hp2 HG02148.hp1 |
synonymous_variant | LOW | c.87G>A | p.Val29Val | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/11 | 192/4089 | 87/1359 | 29/452 | chr7 | 143291552 | |||
chr7:143291633 | G | A | 1 | a0002c0005 | 2 | HG01346.hp1 HG04184.hp2 |
synonymous_variant | LOW | c.168G>A | p.Leu56Leu | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/11 | 273/4089 | 168/1359 | 56/452 | chr7 | 143291633 | |||
chr7:143292676 | C | T | 1 | a0001c0003 | 3 | HG01884.hp1 HG02145.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.453C>T | p.Tyr151Tyr | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/11 | 558/4089 | 453/1359 | 151/452 | chr7 | 143292676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143288362 | C | A | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG01106.hp1 HG01433.hp2 |
5_prime_UTR_variant | MODIFIER | c.-94C>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/11 | 94 | chr7 | 143288362 | ||||||
chr7:143288372 | G | C | 1 | a0001c0001t0009 | 2 | HG00735.hp2 HG02109.hp2 |
5_prime_UTR_variant | MODIFIER | c.-84G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/11 | 84 | chr7 | 143288372 | ||||||
chr7:143288450 | C | A | 1 | a0001c0001t0019 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6C>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/11 | 6 | chr7 | 143288450 | ||||||
chr7:143305078 | C | T | 4 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0036 others(1): Show |
6 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 7 | chr7 | 143305078 | ||||||
chr7:143305153 | C | T | 1 | a0001c0001t0035 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 82 | chr7 | 143305153 | ||||||
chr7:143305389 | C | T | 1 | a0001c0001t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*318C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 318 | chr7 | 143305389 | ||||||
chr7:143305621 | G | A | 1 | a0001c0001t0020 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 550 | chr7 | 143305621 | ||||||
chr7:143305649 | C | T | 1 | a0001c0001t0034 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 578 | chr7 | 143305649 | ||||||
chr7:143305673 | T | C | 1 | a0001c0001t0021 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*602T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 602 | chr7 | 143305673 | ||||||
chr7:143305897 | C | T | 1 | a0001c0001t0016 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*826C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 826 | chr7 | 143305897 | ||||||
chr7:143306184 | G | T | 1 | a0001c0006t0033 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1113G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1113 | chr7 | 143306184 | ||||||
chr7:143306239 | T | A | 5 | a0002c0002t0007 a0002c0002t0008 a0002c0002t0010 others(2): Show |
9 | HG00140.hp2 HG00735.hp1 HG01109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1168T>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1168 | chr7 | 143306239 | ||||||
chr7:143306249 | C | CT | 7 | a0001c0001t0002 a0001c0001t0031 a0001c0001t0032 others(4): Show |
24 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1203dupT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1204 | INFO_REALIGN_3_PRIME | chr7 | 143306249 | |||||
chr7:143306249 | CT | C | 4 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0017 others(1): Show |
10 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1203delT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1203 | INFO_REALIGN_3_PRIME | chr7 | 143306249 | |||||
chr7:143306349 | C | T | 3 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 |
7 | HG02129.hp2 HG02738.hp1 HG03491.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1278C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1278 | chr7 | 143306349 | ||||||
chr7:143306355 | C | T | 2 | a0001c0001t0015 a0001c0001t0037 |
3 | HG02055.hp2 HG02486.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1284C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1284 | chr7 | 143306355 | ||||||
chr7:143306474 | G | A | 1 | a0001c0001t0023 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1403G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1403 | chr7 | 143306474 | ||||||
chr7:143306525 | G | C | 2 | a0001c0001t0012 a0001c0001t0024 |
3 | HG00741.hp1 HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1454G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1454 | chr7 | 143306525 | ||||||
chr7:143306567 | T | C | 1 | a0001c0001t0025 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1496T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1496 | chr7 | 143306567 | ||||||
chr7:143306569 | T | A | 2 | a0001c0001t0006 a0001c0003t0006 |
4 | HG01884.hp1 HG02145.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1498T>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1498 | chr7 | 143306569 | ||||||
chr7:143306569 | T | TA | 3 | a0001c0001t0011 a0001c0001t0013 a0002c0005t0022 |
5 | HG02559.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1517dupA | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1518 | INFO_REALIGN_3_PRIME | chr7 | 143306569 | |||||
chr7:143306569 | TA | T | 4 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0030 others(1): Show |
14 | HG00642.hp1 HG01069.hp2 HG01109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1517delA | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1517 | INFO_REALIGN_3_PRIME | chr7 | 143306569 | |||||
chr7:143306570 | A | T | 4 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0037 others(1): Show |
11 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1499A>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1499 | chr7 | 143306570 | ||||||
chr7:143306742 | C | T | 1 | a0001c0001t0020 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1671 | chr7 | 143306742 | ||||||
chr7:143306768 | T | C | 1 | a0001c0006t0033 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1697T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1697 | chr7 | 143306768 | ||||||
chr7:143306828 | C | A | 1 | a0001c0004t0014 | 2 | HG01934.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1757C>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1757 | chr7 | 143306828 | ||||||
chr7:143306953 | A | G | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02523.hp1 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1882A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1882 | chr7 | 143306953 | ||||||
chr7:143306962 | C | T | 1 | a0002c0002t0010 | 2 | HG02723.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1891C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1891 | chr7 | 143306962 | ||||||
chr7:143306963 | C | T | 3 | a0001c0001t0028 a0001c0001t0029 a0001c0001t0030 |
3 | HG00323.hp2 HG02523.hp1 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1892C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1892 | chr7 | 143306963 | ||||||
chr7:143306982 | T | G | 1 | a0001c0001t0026 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1911T>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 1911 | chr7 | 143306982 | ||||||
chr7:143307088 | C | T | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 2017 | chr7 | 143307088 | ||||||
chr7:143307465 | T | C | 1 | a0001c0001t0031 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2394T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 11/11 | 2394 | chr7 | 143307465 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143288686 | C | G | 3 | a0001c0003t0006g0111 a0001c0003t0006g0112 a0001c0003t0006g0113 |
3 | HG01884.hp1 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.74+157C>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143288686 | |||||||
chr7:143288845 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.74+316C>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143288845 | |||||||
chr7:143288998 | G | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+469G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143288998 | |||||||
chr7:143289076 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.74+547G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289076 | |||||||
chr7:143289097 | G | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+568G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289097 | |||||||
chr7:143289242 | C | T | 1 | a0001c0003t0006g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.74+713C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289242 | |||||||
chr7:143289299 | C | T | 1 | a0001c0001t0001g0009 | 5 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+770C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289299 | |||||||
chr7:143289408 | G | C | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+879G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289408 | |||||||
chr7:143289481 | C | T | 1 | a0001c0001t0003g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.74+952C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289481 | |||||||
chr7:143289588 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.74+1059A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289588 | |||||||
chr7:143289591 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0016 |
6 | HG00733.hp2 HG01099.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+1062G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289591 | |||||||
chr7:143289771 | A | G | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+1242A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289771 | |||||||
chr7:143289805 | T | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(10): Show |
24 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.74+1276T>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289805 | |||||||
chr7:143289820 | A | G | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+1291A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143289820 | |||||||
chr7:143290049 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.75-1491C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143290049 | |||||||
chr7:143290055 | C | CT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0104 others(15): Show |
25 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.75-1462dupT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 143290055 | ||||||
chr7:143290055 | C | CTT | 6 | a0001c0001t0001g0034 a0001c0001t0009g0107 a0001c0001t0015g0032 others(3): Show |
8 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-1463_75-1462dup others(2): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 143290055 | ||||||
chr7:143290055 | C | CTTT | 1 | a0001c0001t0001g0009 | 5 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.75-1464_75-1462dup others(3): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 143290055 | ||||||
chr7:143290055 | CT | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
14 | HG02257.hp1 HG02451.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.75-1462delT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 143290055 | ||||||
chr7:143290095 | G | C | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.75-1445G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143290095 | |||||||
chr7:143290545 | C | CAT | 64 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(61): Show |
89 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.75-992_75-991dupAT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 143290545 | ||||||
chr7:143290720 | C | T | 1 | a0001c0001t0032g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.75-820C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143290720 | |||||||
chr7:143290881 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.75-659C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143290881 | |||||||
chr7:143291183 | G | A | 1 | a0001c0001t0013g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75-357G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143291183 | |||||||
chr7:143291484 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0075 a0001c0001t0003g0076 |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-56A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 1/10 | chr7 | 143291484 | |||||||
chr7:143291730 | G | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.225+40G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | chr7 | 143291730 | |||||||
chr7:143291761 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.225+71G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | chr7 | 143291761 | |||||||
chr7:143291780 | C | CT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(49): Show |
112 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.225+110dupT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTT | 11 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0057 others(8): Show |
14 | HG00741.hp2 HG01169.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.225+109_225+110dup others(2): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTT | 4 | a0001c0001t0001g0009 a0001c0003t0006g0111 a0001c0003t0006g0112 others(1): Show |
8 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+106_225+110dup others(5): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
33 | HG01069.hp2 HG01099.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.225+104_225+110dup others(7): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(1): Show |
4 | a0001c0001t0001g0068 a0001c0001t0009g0101 a0001c0001t0009g0107 others(1): Show |
5 | HG00735.hp2 HG00741.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+103_225+110dup others(8): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.225+99_225+110dupT others(11): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0002g0042 a0002c0002t0001g0103 a0002c0002t0007g0102 others(1): Show |
5 | HG00735.hp1 HG01109.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+98_225+110dupT others(12): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0002g0072 others(3): Show |
6 | HG00642.hp2 HG01346.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+97_225+110dupT others(13): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0018 a0001c0001t0002g0018 a0002c0002t0007g0015 others(1): Show |
5 | HG00140.hp2 HG01175.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+96_225+110dupT others(14): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0045 a0001c0001t0003g0022 a0001c0001t0003g0075 others(2): Show |
6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+95_225+110dupT others(15): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(10): Show |
5 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
6 | HG02109.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+94_225+110dupT others(16): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0027g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.225+110_225+111ins others(24): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143291780 | CTTTTT | C | 6 | a0001c0001t0015g0031 a0001c0001t0015g0032 a0001c0001t0016g0031 others(3): Show |
6 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+106_225+110del others(5): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 143291780 | ||||||
chr7:143292029 | C | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
14 | HG00642.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-271C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | chr7 | 143292029 | |||||||
chr7:143292103 | G | A | 4 | a0001c0001t0005g0007 a0001c0001t0005g0079 a0001c0001t0019g0007 others(1): Show |
7 | HG02129.hp2 HG02738.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-197G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | chr7 | 143292103 | |||||||
chr7:143292232 | T | C | 1 | a0001c0001t0001g0027 | 2 | NA18974.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.226-68T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | chr7 | 143292232 | |||||||
chr7:143292259 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.226-41G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 2/10 | chr7 | 143292259 | |||||||
chr7:143293114 | G | GT | 7 | a0001c0001t0001g0041 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
7 | HG00642.hp1 HG00741.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.475+431dupT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 143293114 | ||||||
chr7:143293114 | GT | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(54): Show |
82 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.475+431delT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 143293114 | ||||||
chr7:143293127 | T | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG02040.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+429T>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293127 | |||||||
chr7:143293133 | G | T | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.475+435G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293133 | |||||||
chr7:143293135 | G | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0027g0049 others(1): Show |
4 | HG01891.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+437G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293135 | |||||||
chr7:143293181 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.475+483G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293181 | |||||||
chr7:143293182 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.475+484C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293182 | |||||||
chr7:143293351 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.475+653C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293351 | |||||||
chr7:143293420 | G | C | 1 | a0001c0001t0011g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.475+722G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293420 | |||||||
chr7:143293511 | TG | T | 3 | a0001c0001t0027g0049 a0001c0006t0033g0035 a0002c0002t0001g0103 |
3 | HG01891.hp2 HG01952.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.476-718delG | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293511 | |||||||
chr7:143293512 | G | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0047 others(13): Show |
23 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.476-718G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293512 | |||||||
chr7:143293579 | G | A | 8 | a0002c0002t0001g0103 a0002c0002t0007g0015 a0002c0002t0007g0102 others(5): Show |
10 | HG00140.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.476-651G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293579 | |||||||
chr7:143293741 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.476-489G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293741 | |||||||
chr7:143293784 | C | T | 2 | a0001c0001t0009g0101 a0001c0001t0009g0107 |
2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.476-446C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293784 | |||||||
chr7:143293858 | G | C | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.476-372G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293858 | |||||||
chr7:143293919 | A | G | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.476-311A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 4/10 | chr7 | 143293919 | |||||||
chr7:143294432 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.570+108G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 5/10 | chr7 | 143294432 | |||||||
chr7:143294508 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.571-89G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 5/10 | chr7 | 143294508 | |||||||
chr7:143294869 | T | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+96T>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143294869 | |||||||
chr7:143294877 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG00438.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.747+104G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143294877 | |||||||
chr7:143294955 | G | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+182G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143294955 | |||||||
chr7:143295050 | C | G | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+277C>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295050 | |||||||
chr7:143295091 | G | A | 1 | a0001c0001t0030g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.747+318G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295091 | |||||||
chr7:143295118 | A | C | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+345A>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295118 | |||||||
chr7:143295150 | C | T | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+377C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295150 | |||||||
chr7:143295217 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.747+444G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295217 | |||||||
chr7:143295228 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0078 |
3 | HG01081.hp1 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.747+455A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295228 | |||||||
chr7:143295316 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.747+543C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295316 | |||||||
chr7:143295495 | A | C | 1 | a0001c0001t0001g0009 | 5 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+722A>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143295495 | |||||||
chr7:143296073 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0061 |
5 | HG02257.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+1300G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296073 | |||||||
chr7:143296160 | T | G | 1 | a0001c0001t0032g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.747+1387T>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296160 | |||||||
chr7:143296234 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.747+1461T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296234 | |||||||
chr7:143296270 | T | C | 1 | a0001c0001t0029g0084 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.747+1497T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296270 | |||||||
chr7:143296297 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.747+1524G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296297 | |||||||
chr7:143296615 | A | G | 1 | a0001c0001t0013g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.747+1842A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296615 | |||||||
chr7:143296693 | C | T | 2 | a0001c0001t0009g0101 a0001c0001t0009g0107 |
2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.747+1920C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296693 | |||||||
chr7:143296694 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.747+1921G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296694 | |||||||
chr7:143296733 | C | CA | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0006t0033g0035 others(8): Show |
13 | HG00140.hp2 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+1974dupA | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 143296733 | ||||||
chr7:143296733 | CA | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(21): Show |
41 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.747+1974delA | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 143296733 | ||||||
chr7:143296777 | TCTTA | T | 1 | a0001c0001t0001g0009 | 5 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+2009_747+2012d others(6): Show |
CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 143296777 | ||||||
chr7:143296890 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0012g0021 others(2): Show |
6 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+2117G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296890 | |||||||
chr7:143296966 | A | G | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.747+2193A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143296966 | |||||||
chr7:143297350 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.748-2573G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297350 | |||||||
chr7:143297448 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0072 |
2 | HG00642.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.748-2475T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297448 | |||||||
chr7:143297559 | G | T | 1 | a0001c0001t0003g0075 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.748-2364G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297559 | |||||||
chr7:143297592 | G | A | 1 | a0001c0001t0006g0077 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.748-2331G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297592 | |||||||
chr7:143297604 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.748-2319G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297604 | |||||||
chr7:143297607 | C | T | 1 | a0001c0001t0001g0013 | 3 | HG01516.hp2 HG01517.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.748-2316C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297607 | |||||||
chr7:143297639 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0075 a0001c0001t0003g0076 |
4 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-2284G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143297639 | |||||||
chr7:143298691 | A | T | 1 | a0001c0001t0013g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.748-1232A>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143298691 | |||||||
chr7:143298724 | G | A | 1 | a0001c0001t0036g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.748-1199G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143298724 | |||||||
chr7:143298926 | C | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0057 others(5): Show |
13 | HG01074.hp1 HG01261.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.748-997C>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143298926 | |||||||
chr7:143299031 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.748-892C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299031 | |||||||
chr7:143299147 | G | C | 1 | a0001c0001t0001g0034 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.748-776G>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299147 | |||||||
chr7:143299296 | A | C | 1 | a0001c0001t0021g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.748-627A>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299296 | |||||||
chr7:143299328 | A | G | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.748-595A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299328 | |||||||
chr7:143299374 | G | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.748-549G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299374 | |||||||
chr7:143299522 | A | C | 2 | a0001c0001t0009g0101 a0001c0001t0009g0107 |
2 | HG00735.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.748-401A>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299522 | |||||||
chr7:143299722 | G | A | 1 | a0002c0002t0001g0103 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.748-201G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 6/10 | chr7 | 143299722 | |||||||
chr7:143300459 | A | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0072 |
2 | HG00642.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.967+165A>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143300459 | |||||||
chr7:143300533 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0047 others(16): Show |
26 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.967+239T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143300533 | |||||||
chr7:143300765 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.967+471T>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143300765 | |||||||
chr7:143300809 | C | T | 1 | a0001c0001t0036g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.967+515C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143300809 | |||||||
chr7:143300928 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0047 others(16): Show |
26 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.967+634T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143300928 | |||||||
chr7:143301010 | A | T | 1 | a0001c0001t0001g0009 | 5 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+716A>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301010 | |||||||
chr7:143301104 | G | A | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.967+810G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301104 | |||||||
chr7:143301141 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.967+847A>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301141 | |||||||
chr7:143301167 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.967+873A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301167 | |||||||
chr7:143301324 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0003g0026 a0001c0001t0003g0050 |
3 | NA18962.hp2 NA19063.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.967+1030A>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301324 | |||||||
chr7:143301509 | T | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.967+1215T>G | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301509 | |||||||
chr7:143301953 | G | T | 1 | a0001c0001t0031g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.967+1659G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143301953 | |||||||
chr7:143302065 | G | T | 8 | a0002c0002t0001g0103 a0002c0002t0007g0015 a0002c0002t0007g0102 others(5): Show |
10 | HG00140.hp2 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.968-1719G>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143302065 | |||||||
chr7:143302295 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG03710.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.968-1489T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143302295 | |||||||
chr7:143302941 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0021g0064 |
2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.968-843G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143302941 | |||||||
chr7:143303093 | A | C | 1 | a0001c0001t0027g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.968-691A>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143303093 | |||||||
chr7:143303109 | G | GA | 3 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0061 |
7 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.968-666dupA | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 143303109 | ||||||
chr7:143303306 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0027g0049 |
3 | HG02976.hp2 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.968-478T>C | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143303306 | |||||||
chr7:143303395 | G | A | 1 | a0001c0001t0004g0088 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.968-389G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143303395 | |||||||
chr7:143303503 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.968-281C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143303503 | |||||||
chr7:143303513 | C | T | 1 | a0001c0006t0033g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.968-271C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | chr7 | 143303513 | |||||||
chr7:143303621 | AT | A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
5 | HG01069.hp1 HG01256.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-145delT | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 143303621 | ||||||
chr7:143304119 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1117+186C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 9/10 | chr7 | 143304119 | |||||||
chr7:143304560 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0087 others(1): Show |
5 | NA18954.hp2 NA18974.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1118-114C>T | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 9/10 | chr7 | 143304560 | |||||||
chr7:143304597 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1118-77G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 9/10 | chr7 | 143304597 | |||||||
chr7:143304865 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1228-75G>A | CASP2 | ENSG00000106144.20 | transcript | ENST00000310447.10 | protein_coding | 10/10 | chr7 | 143304865 |