Item | Value |
---|---|
geneid | 22948 |
ensemblid | ENSG00000150753.12 |
hgncid | 1618 |
symbol | CCT5 |
name | chaperonin containing TCP1 subunit 5 |
refseq_nuc | NM_012073.5 |
refseq_prot | NP_036205.1 |
ensembl_nuc | ENST00000280326.9 |
ensembl_prot | ENSP00000280326.4 |
mane_status | MANE Select |
chr | chr5 |
start | 10250280 |
end | 10266389 |
strand | + |
ver | v1.2 |
region | chr5:10250280-10266389 |
region5000 | chr5:10245280-10271389 |
regionname0 | CCT5_chr5_10250280_10266389 |
regionname5000 | CCT5_chr5_10245280_10271389 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 358 | 88 | 65 | 147 | 16 | 40 | 116 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0002 | 0/0 | 541 | 7 | 0 | 4 | 1 | 0 | 2 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0003 | 0/0 | 541 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0004 | 0/0 | 541 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0005 | 0/0 | 541 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0006 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0007 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
a0008 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | MASMG others(536): Show |
chr5 | 10245280 | 10271389 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1623 | 237 | 35 | 42 | 120 | 15 | 24 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0002 | 1/0 | 1623 | 107 | 43 | 22 | 25 | 1 | 15 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0004 | 0/0 | 1623 | 5 | 5 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0005 | 0/0 | 1623 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0006 | 0/0 | 1623 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0007 | 0/0 | 1623 | 2 | 0 | 1 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0011 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0015 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0001c0016 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0002c0003 | 0/0 | 1623 | 7 | 0 | 4 | 1 | 0 | 2 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0003c0010 | 0/0 | 1623 | 2 | 1 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0004c0008 | 0/0 | 1623 | 2 | 0 | 0 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0005c0009 | 0/0 | 1623 | 2 | 0 | 2 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0006c0012 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0007c0014 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 | ||
a0008c0013 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | ATGGC others(1618): Show |
chr5 | 10245280 | 10271389 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3298 | 143 | 5 | 15 | 106 | 5 | 11 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0002 | 0/0 | 3298 | 69 | 16 | 18 | 13 | 9 | 13 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0005 | 0/0 | 3298 | 8 | 7 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0006 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0007 | 0/0 | 3294 | 4 | 3 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3289): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0009 | 0/0 | 3298 | 3 | 0 | 2 | 0 | 1 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0011 | 0/0 | 3298 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0013 | 0/0 | 3298 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0014 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0015 | 0/0 | 3298 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0016 | 0/0 | 3298 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0017 | 0/0 | 3298 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0018 | 0/0 | 3298 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0001t0019 | 0/0 | 3298 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0002t0003 | 0/0 | 3293 | 50 | 39 | 9 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0002t0004 | 1/0 | 3293 | 49 | 0 | 9 | 23 | 1 | 15 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0002t0008 | 0/0 | 3293 | 4 | 2 | 2 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0002t0012 | 0/0 | 3293 | 2 | 1 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0002t0020 | 0/0 | 3293 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0002t0021 | 0/0 | 3293 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0004t0006 | 0/0 | 3298 | 5 | 5 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0005t0010 | 0/0 | 3293 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0006t0003 | 0/0 | 3293 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0006t0022 | 0/0 | 3293 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GTATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0007t0001 | 0/0 | 3298 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0007t0002 | 0/0 | 3298 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0011t0010 | 0/0 | 3293 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0001c0015t0002 | 0/0 | 3298 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0001c0016t0001 | 0/0 | 3298 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0002c0003t0003 | 0/0 | 3293 | 7 | 0 | 4 | 1 | 0 | 2 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3288): Show |
chr5 | 10245280 | 10271389 |
a0003c0010t0002 | 0/0 | 3298 | 2 | 1 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0004c0008t0001 | 0/0 | 3298 | 2 | 0 | 0 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0005c0009t0001 | 0/0 | 3298 | 2 | 0 | 2 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0006c0012t0005 | 0/0 | 3298 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0007c0014t0002 | 0/0 | 3298 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
a0008c0013t0001 | 0/0 | 3298 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | GCATT others(3293): Show |
chr5 | 10245280 | 10271389 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 53 | 0 | 11 | 34 | 4 | 4 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0005 | 0/0 | 22 | 0 | 0 | 22 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0006 | 0/0 | 17 | 3 | 1 | 8 | 1 | 4 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0016 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0002 | 0/0 | 39 | 2 | 12 | 8 | 7 | 10 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0005g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0007g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0009g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0013g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0014g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0015g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0018g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0001t0019g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0004 | 0/0 | 18 | 11 | 5 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0003 | 1/0 | 25 | 0 | 0 | 21 | 1 | 2 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0008 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0010 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0008g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0008g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0012g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0020g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0002t0021g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0004t0006g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0004t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0005t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0006t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0006t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0007t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0007t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0011t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0015t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0001c0016t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0002c0003t0003g0004 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0002c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0003c0010t0002g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0004c0008t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0005c0009t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0006c0012t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0007c0014t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
a0008c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00558 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00609 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00673 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00738 | hp2 | a0001 | c0001 | t0013 | g0020 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00741 | hp1 | a0003 | c0010 | t0002 | g0034 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0063 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01069 | hp1 | a0001 | c0002 | t0012 | g0025 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01069 | hp2 | a0002 | c0003 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01071 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01167 | hp2 | a0001 | c0002 | t0004 | g0008 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0008 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01243 | hp1 | a0001 | c0002 | t0008 | g0024 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0012 | AMR | PUR | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01255 | hp2 | a0001 | c0002 | t0008 | g0052 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01346 | hp2 | a0001 | c0002 | t0004 | g0039 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0042 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01361 | hp2 | a0001 | c0001 | t0015 | g0120 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01433 | hp1 | a0002 | c0003 | t0003 | g0004 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01496 | hp1 | a0001 | c0002 | t0020 | g0048 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01516 | hp2 | a0001 | c0002 | t0004 | g0003 | EUR | IBS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0057 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01943 | hp2 | a0001 | c0002 | t0004 | g0008 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01952 | hp2 | a0001 | c0007 | t0002 | g0108 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01975 | hp1 | a0001 | c0002 | t0004 | g0008 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0047 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01981 | hp1 | a0001 | c0001 | t0016 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01981 | hp2 | a0002 | c0003 | t0003 | g0004 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02004 | hp1 | a0001 | c0002 | t0004 | g0043 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02015 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02040 | hp1 | a0004 | c0008 | t0001 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02055 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02071 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02135 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02145 | hp1 | a0001 | c0004 | t0006 | g0017 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02148 | hp1 | a0001 | c0002 | t0004 | g0008 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02258 | hp1 | a0001 | c0002 | t0008 | g0024 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0059 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02273 | hp1 | a0005 | c0009 | t0001 | g0029 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02293 | hp1 | a0005 | c0009 | t0001 | g0029 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0008 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02300 | hp1 | a0001 | c0001 | t0018 | g0001 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0058 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0062 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0060 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02683 | hp1 | a0001 | c0015 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02698 | hp1 | a0001 | c0002 | t0004 | g0045 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02809 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02818 | hp2 | a0001 | c0002 | t0021 | g0065 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02895 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02896 | hp1 | a0001 | c0004 | t0006 | g0017 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02897 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02897 | hp2 | a0001 | c0004 | t0006 | g0017 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0036 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02970 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03098 | hp2 | a0001 | c0006 | t0022 | g0050 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03130 | hp1 | a0001 | c0005 | t0010 | g0021 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03130 | hp2 | a0001 | c0006 | t0003 | g0023 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03139 | hp2 | a0001 | c0005 | t0010 | g0021 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03209 | hp2 | a0001 | c0002 | t0012 | g0025 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0067 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0049 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03490 | hp2 | a0001 | c0002 | t0004 | g0010 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03491 | hp1 | a0001 | c0002 | t0004 | g0028 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03491 | hp2 | a0001 | c0002 | t0004 | g0053 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03492 | hp1 | a0001 | c0002 | t0004 | g0028 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0119 | AFR | ESN | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03540 | hp1 | a0001 | c0004 | t0006 | g0017 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0064 | AFR | GWD | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0010 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03669 | hp2 | a0001 | c0002 | t0004 | g0003 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03688 | hp1 | a0001 | c0002 | t0004 | g0003 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0010 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03710 | hp1 | a0002 | c0003 | t0003 | g0066 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04184 | hp1 | a0001 | c0002 | t0004 | g0046 | SAS | BEB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04184 | hp2 | a0001 | c0002 | t0004 | g0056 | SAS | BEB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04199 | hp1 | a0002 | c0003 | t0003 | g0041 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04204 | hp1 | a0001 | c0002 | t0004 | g0044 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04204 | hp2 | a0001 | c0002 | t0004 | g0010 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0054 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG04228 | hp2 | a0001 | c0002 | t0004 | g0055 | SAS | STU | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | YRI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | YRI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18906 | hp2 | a0001 | c0004 | t0006 | g0123 | AFR | YRI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18944 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18947 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18954 | hp1 | a0001 | c0007 | t0001 | g0121 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18962 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18969 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18974 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18975 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18984 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18985 | hp1 | a0001 | c0016 | t0001 | g0087 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18987 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18997 | hp1 | a0007 | c0014 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | LWK | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0051 | AFR | LWK | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | LWK | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | LWK | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19055 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19057 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19058 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19064 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19066 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19080 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19086 | hp2 | a0004 | c0008 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19087 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19088 | hp1 | a0008 | c0013 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | YRI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20752 | hp2 | a0001 | c0001 | t0009 | g0020 | EUR | TSI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | TSI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0105 | EUR | TSI | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02109 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0068 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG03471 | hp2 | a0006 | c0012 | t0005 | g0009 | AFR | MSL | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG06807 | hp1 | a0001 | c0011 | t0010 | g0021 | AFR | USA | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
HG06807 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | USA | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA18955 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | USA | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA21309 | hp1 | a0003 | c0010 | t0002 | g0034 | AFR | LWK | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0003 | REF | REF | CCT5_chr5_10245280_10271389 | CCT5 | chr5 | 10245280 | 10271389 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:10256060 | A | T | 1 | a0002 | 7 | HG01069.hp2 HG01071.hp1 HG01433.hp1 others(4): Show |
missense_variant | MODERATE | c.437A>T | p.Glu146Val | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/11 | 498/3293 | 437/1626 | 146/541 | chr5 | 10256060 | |||
chr5:10256063 | A | G | 1 | a0003 | 2 | HG00741.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.440A>G | p.His147Arg | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/11 | 501/3293 | 440/1626 | 147/541 | chr5 | 10256063 | |||
chr5:10256110 | G | A | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.487G>A | p.Glu163Lys | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/11 | 548/3293 | 487/1626 | 163/541 | chr5 | 10256110 | |||
chr5:10261636 | G | A | 1 | a0004 | 2 | HG02040.hp1 NA19086.hp2 |
missense_variant | MODERATE | c.1070G>A | p.Gly357Asp | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/11 | 1131/3293 | 1070/1626 | 357/541 | chr5 | 10261636 | |||
chr5:10261641 | G | A | 1 | a0008 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.1075G>A | p.Val359Ile | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/11 | 1136/3293 | 1075/1626 | 359/541 | chr5 | 10261641 | |||
chr5:10261652 | C | G | 1 | a0005 | 2 | HG02273.hp1 HG02293.hp1 |
missense_variant | MODERATE | c.1086C>G | p.Ile362Met | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/11 | 1147/3293 | 1086/1626 | 362/541 | chr5 | 10261652 | |||
chr5:10262584 | C | G | 1 | a0007 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.1283C>G | p.Ser428Cys | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/11 | 1344/3293 | 1283/1626 | 428/541 | chr5 | 10262584 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:10254705 | A | G | 11 | a0001c0001 a0001c0004 a0001c0007 others(8): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
synonymous_variant | LOW | c.198A>G | p.Gly66Gly | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/11 | 259/3293 | 198/1626 | 66/541 | chr5 | 10254705 | |||
chr5:10254735 | C | T | 1 | a0001c0016 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.228C>T | p.Thr76Thr | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/11 | 289/3293 | 228/1626 | 76/541 | chr5 | 10254735 | |||
chr5:10256049 | T | C | 13 | a0001c0001 a0001c0004 a0001c0005 others(10): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
synonymous_variant | LOW | c.426T>C | p.Arg142Arg | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/11 | 487/3293 | 426/1626 | 142/541 | chr5 | 10256049 | |||
chr5:10256082 | T | C | 1 | a0001c0011 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.459T>C | p.Asp153Asp | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/11 | 520/3293 | 459/1626 | 153/541 | chr5 | 10256082 | |||
chr5:10258261 | C | T | 1 | a0001c0015 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.681C>T | p.Gly227Gly | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 5/11 | 742/3293 | 681/1626 | 227/541 | chr5 | 10258261 | |||
chr5:10258400 | G | A | 1 | a0001c0007 | 2 | HG01952.hp2 NA18954.hp1 |
synonymous_variant | LOW | c.738G>A | p.Ala246Ala | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/11 | 799/3293 | 738/1626 | 246/541 | chr5 | 10258400 | |||
chr5:10262495 | G | A | 1 | a0001c0004 | 5 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.1194G>A | p.Ala398Ala | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/11 | 1255/3293 | 1194/1626 | 398/541 | chr5 | 10262495 | |||
chr5:10263166 | G | A | 1 | a0001c0006 | 2 | HG03098.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.1350G>A | p.Ala450Ala | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/11 | 1411/3293 | 1350/1626 | 450/541 | chr5 | 10263166 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:10250281 | C | T | 1 | a0001c0006t0022 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/11 | 60 | chr5 | 10250281 | ||||||
chr5:10250318 | G | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
5_prime_UTR_variant | MODIFIER | c.-23G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/11 | 23 | chr5 | 10250318 | ||||||
chr5:10250331 | T | C | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/11 | chr5 | 10250331 | |||||||
chr5:10264848 | G | C | 1 | a0001c0001t0013 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*65G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 65 | chr5 | 10264848 | ||||||
chr5:10264850 | A | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*67A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 67 | chr5 | 10264850 | ||||||
chr5:10264964 | C | T | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*181C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 181 | chr5 | 10264964 | ||||||
chr5:10265075 | A | G | 1 | a0001c0001t0019 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 292 | chr5 | 10265075 | ||||||
chr5:10265103 | T | C | 1 | a0001c0002t0020 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 320 | chr5 | 10265103 | ||||||
chr5:10265165 | C | T | 11 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(8): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*382C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 382 | chr5 | 10265165 | ||||||
chr5:10265166 | A | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*383A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 383 | chr5 | 10265166 | ||||||
chr5:10265270 | C | T | 1 | a0001c0001t0011 | 2 | HG02818.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*487C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 487 | chr5 | 10265270 | ||||||
chr5:10265295 | C | T | 1 | a0001c0001t0018 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 512 | chr5 | 10265295 | ||||||
chr5:10265296 | G | C | 2 | a0001c0001t0009 a0001c0001t0013 |
4 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 513 | chr5 | 10265296 | ||||||
chr5:10265350 | G | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*567G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 567 | chr5 | 10265350 | ||||||
chr5:10265376 | A | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(22): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*593A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 593 | chr5 | 10265376 | ||||||
chr5:10265453 | T | A | 1 | a0001c0002t0012 | 2 | HG01069.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*670T>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 670 | chr5 | 10265453 | ||||||
chr5:10265538 | A | G | 1 | a0001c0001t0017 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*755A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 755 | chr5 | 10265538 | ||||||
chr5:10265559 | T | C | 1 | a0001c0001t0014 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 776 | chr5 | 10265559 | ||||||
chr5:10265607 | C | G | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(17): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*824C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 824 | chr5 | 10265607 | ||||||
chr5:10265612 | G | A | 1 | a0001c0002t0021 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*829G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 829 | chr5 | 10265612 | ||||||
chr5:10265639 | A | C | 2 | a0001c0001t0009 a0001c0001t0013 |
4 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*856A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 856 | chr5 | 10265639 | ||||||
chr5:10265648 | C | T | 1 | a0001c0001t0016 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 865 | chr5 | 10265648 | ||||||
chr5:10265649 | A | C | 2 | a0001c0001t0005 a0006c0012t0005 |
9 | HG01358.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*866A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 866 | chr5 | 10265649 | ||||||
chr5:10265774 | C | CTCTAT | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(21): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*994_*995insATTCT | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 995 | INFO_REALIGN_3_PRIME | chr5 | 10265774 | |||||
chr5:10265778 | G | A | 1 | a0001c0001t0007 | 4 | HG01192.hp2 HG02895.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*995G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 995 | chr5 | 10265778 | ||||||
chr5:10265781 | A | C | 1 | a0001c0001t0007 | 4 | HG01192.hp2 HG02895.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*998A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 998 | chr5 | 10265781 | ||||||
chr5:10265782 | T | TG | 1 | a0001c0001t0007 | 4 | HG01192.hp2 HG02895.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*999_*1000insG | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1000 | chr5 | 10265782 | ||||||
chr5:10265785 | G | A | 1 | a0001c0001t0007 | 4 | HG01192.hp2 HG02895.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1002G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1002 | chr5 | 10265785 | ||||||
chr5:10265786 | C | T | 1 | a0001c0001t0007 | 4 | HG01192.hp2 HG02895.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1003C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1003 | chr5 | 10265786 | ||||||
chr5:10265870 | A | T | 1 | a0001c0001t0015 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1087 | chr5 | 10265870 | ||||||
chr5:10265955 | G | T | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(31): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*1172G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1172 | chr5 | 10265955 | ||||||
chr5:10266160 | C | G | 3 | a0001c0002t0008 a0001c0002t0012 a0001c0006t0022 |
7 | HG01069.hp1 HG01243.hp1 HG01255.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1377C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1377 | chr5 | 10266160 | ||||||
chr5:10266183 | A | G | 2 | a0001c0005t0010 a0001c0011t0010 |
3 | HG03130.hp1 HG03139.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1400A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 11/11 | 1400 | chr5 | 10266183 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:10250527 | C | T | 1 | a0001c0004t0006g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.105+82C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250527 | |||||||
chr5:10250604 | G | A | 4 | a0001c0002t0003g0023 a0001c0002t0003g0036 a0001c0002t0003g0037 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+159G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250604 | |||||||
chr5:10250612 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.105+167G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250612 | |||||||
chr5:10250616 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.105+171C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250616 | |||||||
chr5:10250649 | G | A | 1 | a0005c0009t0001g0029 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.105+204G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250649 | |||||||
chr5:10250696 | G | C | 1 | a0001c0002t0004g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.105+251G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250696 | |||||||
chr5:10250722 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.105+277A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250722 | |||||||
chr5:10250912 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.105+467G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250912 | |||||||
chr5:10250982 | A | G | 1 | a0001c0007t0001g0121 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.105+537A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250982 | |||||||
chr5:10250998 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.105+553G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10250998 | |||||||
chr5:10251257 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.105+812G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251257 | |||||||
chr5:10251311 | A | G | 1 | a0001c0001t0015g0120 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.105+866A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251311 | |||||||
chr5:10251404 | T | G | 1 | a0001c0001t0005g0071 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.105+959T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251404 | |||||||
chr5:10251454 | G | A | 1 | a0001c0002t0004g0040 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.105+1009G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251454 | |||||||
chr5:10251475 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.105+1030G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251475 | |||||||
chr5:10251493 | A | G | 1 | a0001c0002t0003g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.105+1048A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251493 | |||||||
chr5:10251533 | C | T | 1 | a0001c0001t0014g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.105+1088C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251533 | |||||||
chr5:10251563 | C | G | 10 | a0001c0001t0002g0035 a0001c0001t0002g0118 a0001c0001t0005g0009 others(7): Show |
18 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.105+1118C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251563 | |||||||
chr5:10251587 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.105+1142T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251587 | |||||||
chr5:10251740 | T | C | 10 | a0001c0001t0002g0035 a0001c0001t0002g0118 a0001c0001t0005g0009 others(7): Show |
18 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.105+1295T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251740 | |||||||
chr5:10251902 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.105+1457A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10251902 | |||||||
chr5:10252007 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.105+1562G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252007 | |||||||
chr5:10252044 | G | A | 1 | a0002c0003t0003g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.105+1599G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252044 | |||||||
chr5:10252066 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.105+1621G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252066 | |||||||
chr5:10252094 | T | C | 1 | a0001c0002t0003g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.105+1649T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252094 | |||||||
chr5:10252119 | C | T | 1 | a0001c0002t0004g0028 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.105+1674C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252119 | |||||||
chr5:10252151 | T | G | 2 | a0001c0005t0010g0021 a0001c0011t0010g0021 |
3 | HG03130.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.105+1706T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252151 | |||||||
chr5:10252166 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.105+1721C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252166 | |||||||
chr5:10252330 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0114 |
5 | NA18980.hp2 NA18986.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-1815G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252330 | |||||||
chr5:10252364 | C | T | 1 | a0001c0002t0003g0067 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.106-1781C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252364 | |||||||
chr5:10252466 | TTGAC | T | 25 | a0001c0002t0003g0004 a0001c0002t0003g0011 a0001c0002t0003g0014 others(22): Show |
58 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.106-1676_106-1673d others(6): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 10252466 | ||||||
chr5:10252471 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.106-1674T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252471 | |||||||
chr5:10252533 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.106-1612G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252533 | |||||||
chr5:10252575 | A | G | 1 | a0002c0003t0003g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.106-1570A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252575 | |||||||
chr5:10252610 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.106-1535G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252610 | |||||||
chr5:10252614 | C | CA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.106-1514dupA | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 10252614 | ||||||
chr5:10252614 | C | CAA | 12 | a0001c0001t0001g0030 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
20 | HG00733.hp1 HG01358.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.106-1515_106-1514d others(4): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 10252614 | ||||||
chr5:10252635 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | HG01070.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.106-1510G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252635 | |||||||
chr5:10252735 | T | C | 1 | a0001c0002t0003g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.106-1410T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252735 | |||||||
chr5:10252789 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.106-1356A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252789 | |||||||
chr5:10252948 | A | G | 2 | a0001c0001t0014g0119 a0001c0002t0004g0047 |
2 | HG01978.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.106-1197A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10252948 | |||||||
chr5:10253052 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.106-1093G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253052 | |||||||
chr5:10253130 | A | T | 1 | a0001c0001t0002g0112 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.106-1015A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253130 | |||||||
chr5:10253140 | A | G | 2 | a0001c0001t0009g0020 a0001c0001t0013g0020 |
4 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-1005A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253140 | |||||||
chr5:10253155 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.106-990A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253155 | |||||||
chr5:10253201 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.106-944G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253201 | |||||||
chr5:10253231 | A | T | 1 | a0001c0002t0012g0025 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.106-914A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253231 | |||||||
chr5:10253328 | C | CA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.106-806dupA | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 10253328 | ||||||
chr5:10253374 | A | T | 1 | a0001c0001t0002g0110 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.106-771A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253374 | |||||||
chr5:10253425 | C | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.106-720C>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253425 | |||||||
chr5:10253671 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.106-474T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253671 | |||||||
chr5:10253807 | T | G | 7 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0026 others(4): Show |
14 | HG01074.hp2 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.106-338T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253807 | |||||||
chr5:10253878 | G | T | 3 | a0001c0001t0006g0111 a0001c0004t0006g0017 a0001c0004t0006g0123 |
6 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-267G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253878 | |||||||
chr5:10253914 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.106-231A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10253914 | |||||||
chr5:10254005 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.106-140C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 1/10 | chr5 | 10254005 | |||||||
chr5:10254224 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.166+19G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 2/10 | chr5 | 10254224 | |||||||
chr5:10254392 | C | CT | 8 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0004g0054 others(5): Show |
10 | HG00597.hp2 HG01069.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.166+204dupT | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 10254392 | ||||||
chr5:10254392 | CT | C | 30 | a0001c0001t0001g0078 a0001c0001t0001g0106 a0001c0001t0002g0002 others(27): Show |
77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.166+204delT | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 10254392 | ||||||
chr5:10254462 | A | G | 1 | a0001c0002t0003g0027 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.167-212A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 2/10 | chr5 | 10254462 | |||||||
chr5:10254646 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.167-28G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 2/10 | chr5 | 10254646 | |||||||
chr5:10254646 | G | T | 1 | a0001c0001t0014g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.167-28G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 2/10 | chr5 | 10254646 | |||||||
chr5:10254851 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.331+13A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10254851 | |||||||
chr5:10254852 | A | T | 1 | a0001c0007t0002g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.331+14A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10254852 | |||||||
chr5:10254909 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.331+71T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10254909 | |||||||
chr5:10254935 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.331+97A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10254935 | |||||||
chr5:10254971 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.331+133A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10254971 | |||||||
chr5:10254984 | C | CCT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.331+146_331+147ins others(2): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10254984 | |||||||
chr5:10255022 | A | G | 7 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0026 others(4): Show |
14 | HG01074.hp2 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+184A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255022 | |||||||
chr5:10255157 | A | C | 1 | a0001c0002t0003g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331+319A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255157 | |||||||
chr5:10255162 | C | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0118 |
3 | HG03471.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.331+324C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255162 | |||||||
chr5:10255186 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.331+348T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255186 | |||||||
chr5:10255337 | CTG | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.331+500_331+501del others(2): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255337 | |||||||
chr5:10255346 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.331+508G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255346 | |||||||
chr5:10255369 | T | C | 1 | a0001c0002t0021g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.331+531T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255369 | |||||||
chr5:10255370 | C | T | 7 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0026 others(4): Show |
14 | HG01074.hp2 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+532C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255370 | |||||||
chr5:10255603 | C | CAT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.332-352_332-351ins others(2): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255603 | |||||||
chr5:10255644 | C | G | 1 | a0001c0001t0002g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.332-311C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255644 | |||||||
chr5:10255709 | T | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0070 others(19): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.332-246T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255709 | |||||||
chr5:10255772 | C | T | 3 | a0001c0001t0006g0111 a0001c0004t0006g0017 a0001c0004t0006g0123 |
6 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-183C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255772 | |||||||
chr5:10255776 | C | T | 2 | a0001c0002t0003g0015 a0001c0002t0003g0060 |
5 | HG01361.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-179C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255776 | |||||||
chr5:10255891 | T | C | 4 | a0001c0002t0003g0014 a0001c0002t0003g0026 a0001c0002t0003g0061 others(1): Show |
8 | HG01074.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.332-64T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255891 | |||||||
chr5:10255937 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.332-18C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 3/10 | chr5 | 10255937 | |||||||
chr5:10256253 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.530+100C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256253 | |||||||
chr5:10256297 | A | G | 1 | a0001c0002t0004g0056 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.530+144A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256297 | |||||||
chr5:10256312 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.530+159A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256312 | |||||||
chr5:10256498 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.530+345T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256498 | |||||||
chr5:10256499 | T | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.530+346T>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256499 | |||||||
chr5:10256595 | A | G | 1 | a0001c0002t0003g0014 | 4 | HG01074.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+442A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256595 | |||||||
chr5:10256610 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.530+457G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256610 | |||||||
chr5:10256660 | T | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.530+507T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256660 | |||||||
chr5:10256686 | C | CA | 5 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0002g0100 others(2): Show |
6 | HG01167.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+547dupA | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 10256686 | ||||||
chr5:10256686 | C | CAA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.530+546_530+547dup others(2): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 10256686 | ||||||
chr5:10256686 | C | CAAA | 7 | a0001c0001t0001g0079 a0001c0001t0005g0009 a0001c0001t0005g0071 others(4): Show |
11 | HG01358.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.530+545_530+547dup others(3): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 10256686 | ||||||
chr5:10256705 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0085 others(5): Show |
26 | HG00140.hp2 HG00597.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.530+552A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256705 | |||||||
chr5:10256781 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.530+628T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256781 | |||||||
chr5:10256791 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.530+638G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256791 | |||||||
chr5:10256818 | G | A | 17 | a0001c0002t0003g0004 a0001c0002t0003g0011 a0001c0002t0003g0023 others(14): Show |
43 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.530+665G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256818 | |||||||
chr5:10256857 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.530+704G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10256857 | |||||||
chr5:10257010 | A | G | 1 | a0001c0002t0003g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.530+857A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257010 | |||||||
chr5:10257092 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.530+939A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257092 | |||||||
chr5:10257190 | T | C | 1 | a0001c0002t0008g0049 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.531-921T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257190 | |||||||
chr5:10257194 | C | T | 5 | a0001c0001t0005g0009 a0001c0001t0005g0071 a0001c0001t0005g0116 others(2): Show |
9 | HG01358.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.531-917C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257194 | |||||||
chr5:10257348 | A | G | 7 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0026 others(4): Show |
14 | HG01074.hp2 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.531-763A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257348 | |||||||
chr5:10257433 | G | T | 1 | a0001c0002t0003g0027 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.531-678G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257433 | |||||||
chr5:10257446 | G | A | 2 | a0001c0001t0002g0102 a0001c0001t0002g0109 |
2 | NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.531-665G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257446 | |||||||
chr5:10257488 | C | T | 1 | a0001c0002t0003g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.531-623C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257488 | |||||||
chr5:10257546 | A | G | 2 | a0001c0005t0010g0021 a0001c0011t0010g0021 |
3 | HG03130.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.531-565A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257546 | |||||||
chr5:10257550 | T | A | 1 | a0001c0002t0004g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.531-561T>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257550 | |||||||
chr5:10257574 | CAT | C | 17 | a0001c0002t0003g0004 a0001c0002t0003g0011 a0001c0002t0003g0023 others(14): Show |
43 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.531-536_531-535del others(2): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257574 | |||||||
chr5:10257698 | G | A | 2 | a0001c0001t0005g0009 a0006c0012t0005g0009 |
6 | HG01358.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-413G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257698 | |||||||
chr5:10257711 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.531-400C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257711 | |||||||
chr5:10257798 | G | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.531-313G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10257798 | |||||||
chr5:10258001 | A | G | 1 | a0001c0002t0003g0015 | 4 | HG01361.hp1 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-110A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10258001 | |||||||
chr5:10258013 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.531-98G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 4/10 | chr5 | 10258013 | |||||||
chr5:10258555 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.873+20T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10258555 | |||||||
chr5:10258797 | A | G | 1 | a0001c0002t0012g0025 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.873+262A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10258797 | |||||||
chr5:10259049 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.873+514C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259049 | |||||||
chr5:10259071 | A | G | 1 | a0001c0016t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.873+536A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259071 | |||||||
chr5:10259261 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.873+726C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259261 | |||||||
chr5:10259262 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.873+727A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259262 | |||||||
chr5:10259285 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.873+750G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259285 | |||||||
chr5:10259315 | C | G | 1 | a0001c0002t0004g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.873+780C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259315 | |||||||
chr5:10259419 | T | C | 1 | a0001c0001t0014g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.873+884T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259419 | |||||||
chr5:10259428 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.873+893G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259428 | |||||||
chr5:10259450 | C | G | 1 | a0001c0002t0008g0052 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.873+915C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259450 | |||||||
chr5:10259564 | G | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.873+1029G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259564 | |||||||
chr5:10259641 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.873+1106G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259641 | |||||||
chr5:10259750 | G | A | 5 | a0001c0002t0008g0024 a0001c0002t0008g0049 a0001c0002t0008g0052 others(2): Show |
7 | HG01069.hp1 HG01243.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.874-1042G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259750 | |||||||
chr5:10259761 | T | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-1031T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259761 | |||||||
chr5:10259764 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.874-1028C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259764 | |||||||
chr5:10259878 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-914A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259878 | |||||||
chr5:10259889 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-903T>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259889 | |||||||
chr5:10259890 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-902A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259890 | |||||||
chr5:10259891 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-901G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259891 | |||||||
chr5:10259946 | G | T | 1 | a0001c0002t0003g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.874-846G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10259946 | |||||||
chr5:10260039 | G | A | 1 | a0001c0001t0014g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.874-753G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260039 | |||||||
chr5:10260090 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.874-702A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260090 | |||||||
chr5:10260135 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.874-657A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260135 | |||||||
chr5:10260183 | G | A | 1 | a0001c0002t0012g0025 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.874-609G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260183 | |||||||
chr5:10260221 | C | G | 1 | a0001c0004t0006g0017 | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-571C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260221 | |||||||
chr5:10260235 | C | T | 5 | a0001c0002t0008g0024 a0001c0002t0008g0049 a0001c0002t0008g0052 others(2): Show |
7 | HG01069.hp1 HG01243.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.874-557C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260235 | |||||||
chr5:10260290 | C | T | 1 | a0001c0001t0001g0016 | 4 | HG01256.hp2 NA18949.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-502C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260290 | |||||||
chr5:10260348 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0082 |
2 | NA18982.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.874-444G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260348 | |||||||
chr5:10260372 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0073 |
4 | HG00408.hp1 NA18948.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-420C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260372 | |||||||
chr5:10260464 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-328A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260464 | |||||||
chr5:10260537 | G | A | 1 | a0001c0001t0014g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.874-255G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260537 | |||||||
chr5:10260544 | A | AT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.874-248_874-247ins others(1): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260544 | |||||||
chr5:10260776 | G | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0106 a0001c0001t0001g0113 |
6 | NA18939.hp2 NA18952.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-16G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 6/10 | chr5 | 10260776 | |||||||
chr5:10260953 | C | T | 9 | a0001c0002t0004g0008 a0001c0002t0004g0010 a0001c0002t0004g0039 others(6): Show |
18 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.993+42C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10260953 | |||||||
chr5:10261042 | A | G | 2 | a0001c0005t0010g0021 a0001c0011t0010g0021 |
3 | HG03130.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.993+131A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261042 | |||||||
chr5:10261087 | CTG | C | 2 | a0001c0005t0010g0021 a0001c0011t0010g0021 |
3 | HG03130.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.993+182_993+183del others(2): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 10261087 | ||||||
chr5:10261111 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0032 others(10): Show |
36 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.993+200C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261111 | |||||||
chr5:10261129 | C | T | 1 | a0001c0007t0002g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.993+218C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261129 | |||||||
chr5:10261138 | C | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.993+227C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261138 | |||||||
chr5:10261234 | A | G | 13 | a0001c0001t0005g0009 a0001c0001t0005g0071 a0001c0001t0005g0116 others(10): Show |
22 | HG01069.hp1 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.993+323A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261234 | |||||||
chr5:10261242 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.994-318G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261242 | |||||||
chr5:10261296 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.994-264T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261296 | |||||||
chr5:10261322 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.994-238G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261322 | |||||||
chr5:10261364 | A | G | 5 | a0001c0001t0005g0009 a0001c0001t0005g0071 a0001c0001t0005g0116 others(2): Show |
9 | HG01358.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.994-196A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261364 | |||||||
chr5:10261402 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0076 |
3 | NA18956.hp2 NA19012.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.994-158G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261402 | |||||||
chr5:10261430 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.994-130C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 7/10 | chr5 | 10261430 | |||||||
chr5:10261854 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1179+109G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10261854 | |||||||
chr5:10261871 | A | AG | 2 | a0001c0002t0003g0015 a0001c0002t0003g0060 |
5 | HG01361.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+126_1179+127i others(3): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10261871 | |||||||
chr5:10261873 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1179+128G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10261873 | |||||||
chr5:10261925 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1179+180G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10261925 | |||||||
chr5:10262046 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1179+301A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262046 | |||||||
chr5:10262148 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0118 |
3 | HG03471.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1180-333G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262148 | |||||||
chr5:10262175 | A | G | 1 | a0001c0001t0002g0013 | 5 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-306A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262175 | |||||||
chr5:10262235 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1180-246G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262235 | |||||||
chr5:10262254 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1180-227C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262254 | |||||||
chr5:10262293 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1180-188G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262293 | |||||||
chr5:10262426 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1180-55C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 8/10 | chr5 | 10262426 | |||||||
chr5:10262628 | C | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1317+10C>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10262628 | |||||||
chr5:10262658 | C | T | 7 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0026 others(4): Show |
14 | HG01074.hp2 HG01361.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1317+40C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10262658 | |||||||
chr5:10262906 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1318-228C>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10262906 | |||||||
chr5:10262929 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1318-205A>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10262929 | |||||||
chr5:10263033 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0118 |
3 | HG03471.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1318-101G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10263033 | |||||||
chr5:10263079 | C | T | 3 | a0001c0001t0002g0012 a0001c0001t0002g0115 a0001c0001t0019g0012 |
6 | HG01243.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1318-55C>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10263079 | |||||||
chr5:10263082 | T | G | 3 | a0001c0001t0006g0111 a0001c0004t0006g0017 a0001c0004t0006g0123 |
6 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1318-52T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 9/10 | chr5 | 10263082 | |||||||
chr5:10263339 | TGGAG | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1498+28_1498+31del others(4): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 10263339 | ||||||
chr5:10263341 | GA | G | 18 | a0001c0002t0003g0004 a0001c0002t0003g0011 a0001c0002t0003g0023 others(15): Show |
42 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1498+28delA | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263341 | |||||||
chr5:10263342 | A | G | 7 | a0001c0002t0003g0004 a0001c0002t0003g0015 a0001c0002t0003g0027 others(4): Show |
10 | HG00741.hp2 HG01168.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1498+28A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263342 | |||||||
chr5:10263342 | A | T | 1 | a0001c0002t0012g0025 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1498+28A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263342 | |||||||
chr5:10263348 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1498+34G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263348 | |||||||
chr5:10263350 | G | C | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1498+36G>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263350 | |||||||
chr5:10263352 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1498+38A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263352 | |||||||
chr5:10263416 | T | G | 1 | a0001c0002t0004g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1498+102T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263416 | |||||||
chr5:10263470 | G | A | 25 | a0001c0002t0003g0004 a0001c0002t0003g0011 a0001c0002t0003g0014 others(22): Show |
58 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1498+156G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263470 | |||||||
chr5:10263483 | A | G | 1 | a0001c0002t0004g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1498+169A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263483 | |||||||
chr5:10263505 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1498+191G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263505 | |||||||
chr5:10263580 | T | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1498+266T>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263580 | |||||||
chr5:10263613 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1498+299G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263613 | |||||||
chr5:10263635 | A | G | 1 | a0001c0002t0003g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1498+321A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263635 | |||||||
chr5:10263732 | G | A | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1498+418G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263732 | |||||||
chr5:10263751 | G | A | 4 | a0001c0001t0005g0009 a0001c0001t0005g0116 a0001c0001t0005g0117 others(1): Show |
8 | HG01358.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1498+437G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263751 | |||||||
chr5:10263769 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1498+455G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263769 | |||||||
chr5:10263996 | G | A | 1 | a0005c0009t0001g0029 | 2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1499-660G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10263996 | |||||||
chr5:10264009 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1499-647A>G | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264009 | |||||||
chr5:10264044 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1499-612G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264044 | |||||||
chr5:10264110 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1499-546A>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264110 | |||||||
chr5:10264118 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1499-534dupA | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 10264118 | ||||||
chr5:10264138 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1499-518C>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264138 | |||||||
chr5:10264168 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1499-488G>A | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264168 | |||||||
chr5:10264190 | G | T | 1 | a0001c0001t0014g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1499-466G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264190 | |||||||
chr5:10264253 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1499-403T>C | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264253 | |||||||
chr5:10264266 | C | CA | 34 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0013 others(31): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1499-380dupA | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 10264266 | ||||||
chr5:10264266 | C | CAA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1499-381_1499-380d others(4): Show |
CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 10264266 | ||||||
chr5:10264332 | G | T | 1 | a0001c0001t0002g0105 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1499-324G>T | CCT5 | ENSG00000150753.12 | transcript | ENST00000280326.9 | protein_coding | 10/10 | chr5 | 10264332 |