Item | Value |
---|---|
geneid | 2653 |
ensemblid | ENSG00000140905.11 |
hgncid | 4208 |
symbol | GCSH |
name | glycine cleavage system protein H |
refseq_nuc | NM_004483.5 |
refseq_prot | NP_004474.2 |
ensembl_nuc | ENST00000315467.9 |
ensembl_prot | ENSP00000319531.3 |
mane_status | MANE Select |
chr | chr16 |
start | 81081945 |
end | 81096395 |
strand | - |
ver | v1.2 |
region | chr16:81081945-81096395 |
region5000 | chr16:81076945-81101395 |
regionname0 | GCSH_chr16_81081945_81096395 |
regionname5000 | GCSH_chr16_81076945_81101395 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 173 | 227 | 42 | 48 | 98 | 13 | 25 | 75 | GCSH_chr16_81076945_81101395 | GCSH | MALRV others(168): Show |
chr16 | 81076945 | 81101395 |
a0002 | 1/0 | 173 | 106 | 33 | 11 | 52 | 1 | 8 | 42 | GCSH_chr16_81076945_81101395 | GCSH | MALRV others(168): Show |
chr16 | 81076945 | 81101395 |
a0003 | 0/0 | 173 | 18 | 12 | 0 | 6 | 0 | 0 | 5 | GCSH_chr16_81076945_81101395 | GCSH | MALRV others(168): Show |
chr16 | 81076945 | 81101395 |
a0004 | 0/0 | 173 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | MALRV others(168): Show |
chr16 | 81076945 | 81101395 |
a0005 | 0/0 | 173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | MALRV others(168): Show |
chr16 | 81076945 | 81101395 |
a0006 | 0/0 | 173 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | MALRV others(168): Show |
chr16 | 81076945 | 81101395 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 519 | 227 | 42 | 48 | 98 | 13 | 25 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0002c0002 | 1/0 | 519 | 93 | 26 | 6 | 52 | 0 | 8 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0002c0004 | 0/0 | 519 | 11 | 6 | 4 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0002c0005 | 0/0 | 519 | 2 | 1 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0003c0003 | 0/0 | 519 | 18 | 12 | 0 | 6 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0004c0007 | 0/0 | 519 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0005c0006 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 | ||
a0006c0008 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | ATGGC others(514): Show |
chr16 | 81076945 | 81101395 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1560 | 194 | 35 | 44 | 81 | 11 | 22 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0002 | 0/0 | 1557 | 4 | 0 | 0 | 3 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0003 | 0/0 | 1560 | 21 | 4 | 3 | 10 | 2 | 2 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0005 | 0/0 | 1561 | 4 | 2 | 1 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1556): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0011 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0012 | 0/0 | 1568 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1563): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0015 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0001c0001t0016 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACTGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0001 | 1/0 | 1560 | 41 | 24 | 2 | 12 | 0 | 2 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0002 | 0/0 | 1557 | 44 | 1 | 3 | 34 | 0 | 6 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0005 | 0/0 | 1561 | 2 | 1 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1556): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0007 | 0/0 | 1560 | 3 | 0 | 0 | 3 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0009 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0010 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0002c0002t0014 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0002c0004t0002 | 0/0 | 1557 | 11 | 6 | 4 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0002c0005t0008 | 0/0 | 1557 | 2 | 1 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0003c0003t0004 | 0/0 | 1557 | 12 | 6 | 0 | 6 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0003c0003t0006 | 0/0 | 1557 | 6 | 6 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0004c0007t0001 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
a0005c0006t0013 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1552): Show |
chr16 | 81076945 | 81101395 |
a0006c0008t0001 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | ACCGC others(1555): Show |
chr16 | 81076945 | 81101395 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 69 | 20 | 13 | 24 | 6 | 6 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0003 | 0/0 | 20 | 1 | 3 | 15 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0005 | 0/0 | 8 | 1 | 4 | 0 | 1 | 2 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0006 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0003g0004 | 0/0 | 19 | 4 | 3 | 8 | 2 | 2 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0005g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0012g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0015g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0001c0001t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0002 | 0/0 | 30 | 1 | 2 | 22 | 0 | 5 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0002t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0004t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0004t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0004t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0004t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0005t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0002c0005t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0006g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0003c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0004c0007t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0005c0006t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
a0006c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00323 | hp1 | a0002 | c0004 | t0002 | g0028 | EUR | FIN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00558 | hp2 | a0002 | c0002 | t0007 | g0053 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00639 | hp2 | a0002 | c0002 | t0005 | g0044 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00735 | hp2 | a0002 | c0004 | t0002 | g0031 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01070 | hp2 | a0002 | c0004 | t0002 | g0030 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01081 | hp1 | a0002 | c0004 | t0002 | g0028 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01192 | hp1 | a0004 | c0007 | t0001 | g0144 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01346 | hp1 | a0002 | c0004 | t0002 | g0030 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01433 | hp2 | a0002 | c0005 | t0008 | g0069 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01884 | hp1 | a0003 | c0003 | t0006 | g0021 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02055 | hp2 | a0005 | c0006 | t0013 | g0095 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02074 | hp1 | a0002 | c0002 | t0007 | g0049 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0109 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | CDX | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0153 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02258 | hp2 | a0002 | c0004 | t0002 | g0015 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02523 | hp2 | a0003 | c0003 | t0004 | g0149 | EAS | KHV | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02572 | hp1 | a0002 | c0002 | t0005 | g0043 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02572 | hp2 | a0002 | c0004 | t0002 | g0083 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02615 | hp2 | a0002 | c0004 | t0002 | g0015 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0080 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02809 | hp2 | a0002 | c0004 | t0002 | g0082 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02886 | hp2 | a0003 | c0003 | t0006 | g0151 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02970 | hp2 | a0003 | c0003 | t0006 | g0150 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0022 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03098 | hp2 | a0003 | c0003 | t0004 | g0041 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0022 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03453 | hp1 | a0003 | c0003 | t0004 | g0148 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03486 | hp2 | a0003 | c0003 | t0006 | g0021 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG04204 | hp2 | a0006 | c0008 | t0001 | g0145 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18522 | hp1 | a0003 | c0003 | t0004 | g0041 | AFR | YRI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18948 | hp2 | a0003 | c0003 | t0004 | g0039 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18959 | hp2 | a0001 | c0001 | t0015 | g0146 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18965 | hp2 | a0003 | c0003 | t0004 | g0039 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18977 | hp1 | a0003 | c0003 | t0004 | g0147 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18978 | hp2 | a0002 | c0002 | t0009 | g0042 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18987 | hp1 | a0003 | c0003 | t0004 | g0040 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18987 | hp2 | a0002 | c0002 | t0010 | g0076 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19005 | hp2 | a0002 | c0002 | t0007 | g0051 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0022 | AFR | LWK | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | LWK | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | LWK | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19063 | hp1 | a0001 | c0001 | t0012 | g0087 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19081 | hp2 | a0002 | c0002 | t0014 | g0070 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19091 | hp1 | a0003 | c0003 | t0004 | g0040 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | YRI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02109 | hp1 | a0002 | c0004 | t0002 | g0015 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG02559 | hp2 | a0003 | c0003 | t0006 | g0021 | AFR | ACB | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG03471 | hp2 | a0002 | c0004 | t0002 | g0031 | AFR | MSL | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | USA | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA21309 | hp1 | a0003 | c0003 | t0006 | g0152 | AFR | LWK | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
NA21309 | hp2 | a0002 | c0005 | t0008 | g0068 | AFR | LWK | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0130 | REF | REF | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0008 | REF | REF | GCSH_chr16_81076945_81101395 | GCSH | chr16 | 81076945 | 81101395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:81090611 | T | C | 2 | a0003 a0005 |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
missense_variant | MODERATE | c.218A>G | p.Asn73Ser | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/5 | 335/1560 | 218/522 | 73/173 | chr16 | 81090611 | |||
chr16:81096217 | G | A | 4 | a0001 a0004 a0005 others(1): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
missense_variant | MODERATE | c.62C>T | p.Ser21Leu | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 179/1560 | 62/522 | 21/173 | chr16 | 81096217 | |||
chr16:81096226 | G | A | 1 | a0004 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.53C>T | p.Ala18Val | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 170/1560 | 53/522 | 18/173 | chr16 | 81096226 | |||
chr16:81096257 | T | C | 1 | a0006 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.22A>G | p.Ser8Gly | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 139/1560 | 22/522 | 8/173 | chr16 | 81096257 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:81087632 | G | C | 3 | a0002c0005 a0003c0003 a0005c0006 |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
synonymous_variant | LOW | c.261C>G | p.Leu87Leu | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/5 | 378/1560 | 261/522 | 87/173 | chr16 | 81087632 | |||
chr16:81087641 | A | G | 3 | a0002c0005 a0003c0003 a0005c0006 |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
synonymous_variant | LOW | c.252T>C | p.Tyr84Tyr | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/5 | 369/1560 | 252/522 | 84/173 | chr16 | 81087641 | |||
chr16:81090670 | G | A | 1 | a0002c0004 | 11 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(8): Show |
synonymous_variant | LOW | c.159C>T | p.Phe53Phe | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/5 | 276/1560 | 159/522 | 53/173 | chr16 | 81090670 | |||
chr16:81096189 | G | C | 1 | a0003c0003 | 18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
synonymous_variant | LOW | c.90C>G | p.Pro30Pro | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 207/1560 | 90/522 | 30/173 | chr16 | 81096189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:81081968 | C | T | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*898G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 898 | chr16 | 81081968 | ||||||
chr16:81082016 | TAAC | T | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*847_*849delGTT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 847 | chr16 | 81082016 | ||||||
chr16:81082082 | T | C | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*784A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 784 | chr16 | 81082082 | ||||||
chr16:81082152 | T | C | 2 | a0003c0003t0006 a0005c0006t0013 |
7 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*714A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 714 | chr16 | 81082152 | ||||||
chr16:81082218 | G | C | 1 | a0002c0002t0007 | 3 | HG00558.hp2 HG02074.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*648C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 648 | chr16 | 81082218 | ||||||
chr16:81082228 | T | G | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*638A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 638 | chr16 | 81082228 | ||||||
chr16:81082237 | A | G | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*629T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 629 | chr16 | 81082237 | ||||||
chr16:81082250 | G | A | 1 | a0001c0001t0011 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*616C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 616 | chr16 | 81082250 | ||||||
chr16:81082252 | A | G | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*614T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 614 | chr16 | 81082252 | ||||||
chr16:81082405 | G | A | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*461C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 461 | chr16 | 81082405 | ||||||
chr16:81082464 | C | CTTCCAGT others(4): Show |
1 | a0001c0001t0012 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*401dupAATAAC others(5): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 401 | chr16 | 81082464 | ||||||
chr16:81082513 | C | T | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 353 | chr16 | 81082513 | ||||||
chr16:81082675 | G | A | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*191C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 191 | chr16 | 81082675 | ||||||
chr16:81082702 | G | C | 1 | a0001c0001t0003 | 21 | HG00099.hp1 HG00140.hp1 HG01167.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*164C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 164 | chr16 | 81082702 | ||||||
chr16:81082763 | G | A | 1 | a0002c0002t0010 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 103 | chr16 | 81082763 | ||||||
chr16:81082767 | T | C | 1 | a0002c0002t0014 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*99A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 99 | chr16 | 81082767 | ||||||
chr16:81082778 | T | G | 10 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(7): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*88A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 88 | chr16 | 81082778 | ||||||
chr16:81082784 | C | T | 1 | a0002c0002t0010 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 82 | chr16 | 81082784 | ||||||
chr16:81082804 | T | C | 1 | a0002c0005t0008 | 2 | HG01433.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 5/5 | 62 | chr16 | 81082804 | ||||||
chr16:81096292 | C | CG | 2 | a0001c0001t0005 a0002c0002t0005 |
6 | HG00639.hp2 HG01361.hp2 HG02080.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-15dupC | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 15 | chr16 | 81096292 | ||||||
chr16:81096292 | C | G | 1 | a0002c0002t0009 | 1 | NA18978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 14 | chr16 | 81096292 | ||||||
chr16:81096299 | C | A | 1 | a0001c0001t0015 | 1 | NA18959.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 21 | chr16 | 81096299 | ||||||
chr16:81096315 | G | A | 2 | a0003c0003t0004 a0003c0003t0006 |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | chr16 | 81096315 | |||||||
chr16:81096343 | G | A | 1 | a0002c0002t0009 | 1 | NA18978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 65 | chr16 | 81096343 | ||||||
chr16:81096344 | A | G | 1 | a0002c0002t0009 | 1 | NA18978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | 66 | chr16 | 81096344 | ||||||
chr16:81096393 | G | A | 1 | a0001c0001t0016 | 1 | HG02257.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-115C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/5 | chr16 | 81096393 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:81083078 | A | G | 1 | a0002c0002t0002g0013 | 3 | NA18967.hp2 NA19064.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.425-115T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083078 | |||||||
chr16:81083085 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.425-122A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083085 | |||||||
chr16:81083175 | TAATA | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.425-216_425-213del others(4): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083175 | |||||||
chr16:81083180 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.425-217T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083180 | |||||||
chr16:81083290 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-327T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083290 | |||||||
chr16:81083306 | C | T | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.425-343G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083306 | |||||||
chr16:81083315 | C | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-352G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083315 | |||||||
chr16:81083317 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.425-354T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083317 | |||||||
chr16:81083334 | A | G | 2 | a0002c0005t0008g0068 a0002c0005t0008g0069 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.425-371T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083334 | |||||||
chr16:81083343 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.425-380G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083343 | |||||||
chr16:81083365 | A | G | 1 | a0002c0002t0001g0012 | 3 | HG02717.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-402T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083365 | |||||||
chr16:81083387 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-424T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083387 | |||||||
chr16:81083395 | T | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-432A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083395 | |||||||
chr16:81083396 | T | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-433A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083396 | |||||||
chr16:81083496 | G | A | 23 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(20): Show |
62 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.425-533C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083496 | |||||||
chr16:81083664 | C | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.425-701G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083664 | |||||||
chr16:81083789 | G | A | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.424+674C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083789 | |||||||
chr16:81083856 | A | AT | 25 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(22): Show |
64 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.424+606dupA | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083856 | |||||||
chr16:81083862 | G | A | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.424+601C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083862 | |||||||
chr16:81083899 | T | C | 1 | a0003c0003t0004g0022 | 3 | HG03041.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+564A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083899 | |||||||
chr16:81083941 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.424+522T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81083941 | |||||||
chr16:81084184 | G | GC | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.424+278dupG | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81084184 | |||||||
chr16:81084191 | C | G | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.424+272G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81084191 | |||||||
chr16:81084201 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.424+262T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81084201 | |||||||
chr16:81084227 | C | A | 4 | a0002c0004t0002g0028 a0002c0004t0002g0030 a0002c0004t0002g0031 others(1): Show |
7 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+236G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81084227 | |||||||
chr16:81084301 | A | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.424+162T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 4/4 | chr16 | 81084301 | |||||||
chr16:81084602 | G | GA | 4 | a0003c0003t0006g0021 a0003c0003t0006g0150 a0003c0003t0006g0151 others(1): Show |
6 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-9dupT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084602 | |||||||
chr16:81084661 | C | T | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-67G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084661 | |||||||
chr16:81084662 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0081 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.293-68C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084662 | |||||||
chr16:81084684 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.293-90G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084684 | |||||||
chr16:81084711 | CT | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(41): Show |
130 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.293-118delA | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084711 | |||||||
chr16:81084711 | CTT | C | 39 | a0001c0001t0001g0110 a0001c0001t0002g0091 a0001c0001t0002g0116 others(36): Show |
85 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.293-119_293-118del others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084711 | |||||||
chr16:81084770 | C | G | 5 | a0003c0003t0006g0021 a0003c0003t0006g0150 a0003c0003t0006g0151 others(2): Show |
7 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-176G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084770 | |||||||
chr16:81084771 | G | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-177C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084771 | |||||||
chr16:81084853 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-259T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084853 | |||||||
chr16:81084856 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-262G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084856 | |||||||
chr16:81084856 | C | T | 16 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(13): Show |
20 | HG00408.hp2 HG01168.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-262G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084856 | |||||||
chr16:81084861 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-267T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084861 | |||||||
chr16:81084864 | T | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-270A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084864 | |||||||
chr16:81084887 | T | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-293A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084887 | |||||||
chr16:81084916 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.293-322A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084916 | |||||||
chr16:81084918 | T | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-324A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084918 | |||||||
chr16:81084949 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.293-355G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084949 | |||||||
chr16:81084962 | G | A | 1 | a0002c0002t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293-368C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084962 | |||||||
chr16:81084966 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.293-372G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084966 | |||||||
chr16:81084994 | C | A | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-400G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084994 | |||||||
chr16:81084995 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-401T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81084995 | |||||||
chr16:81085006 | C | T | 3 | a0001c0001t0001g0086 a0002c0002t0001g0029 a0002c0002t0001g0081 |
4 | HG02818.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-412G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085006 | |||||||
chr16:81085007 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-413T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085007 | |||||||
chr16:81085015 | C | CT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.293-422dupA | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085015 | |||||||
chr16:81085015 | C | CTT | 35 | a0001c0001t0001g0017 a0001c0001t0001g0084 a0001c0001t0001g0086 others(32): Show |
79 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.293-423_293-422dup others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085015 | |||||||
chr16:81085055 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-461T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085055 | |||||||
chr16:81085075 | T | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-481A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085075 | |||||||
chr16:81085122 | C | A | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-528G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085122 | |||||||
chr16:81085160 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.293-566C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085160 | |||||||
chr16:81085164 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-570T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085164 | |||||||
chr16:81085280 | T | C | 36 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(33): Show |
82 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.293-686A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085280 | |||||||
chr16:81085303 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.293-709C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085303 | |||||||
chr16:81085315 | C | A | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-721G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085315 | |||||||
chr16:81085340 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.293-746T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085340 | |||||||
chr16:81085425 | A | G | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-831T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085425 | |||||||
chr16:81085449 | A | C | 37 | a0001c0001t0002g0091 a0001c0001t0002g0116 a0001c0001t0002g0133 others(34): Show |
83 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.293-855T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085449 | |||||||
chr16:81085451 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.293-857A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085451 | |||||||
chr16:81085591 | A | G | 38 | a0001c0001t0001g0009 a0001c0001t0002g0091 a0001c0001t0002g0116 others(35): Show |
87 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.293-997T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085591 | |||||||
chr16:81085618 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.293-1024G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085618 | |||||||
chr16:81085626 | T | G | 17 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(14): Show |
21 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-1032A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085626 | |||||||
chr16:81085721 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.293-1127C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085721 | |||||||
chr16:81085766 | A | G | 1 | a0002c0002t0001g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-1172T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085766 | |||||||
chr16:81085770 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.293-1176C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085770 | |||||||
chr16:81085775 | A | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-1181T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085775 | |||||||
chr16:81085797 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.293-1203A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085797 | |||||||
chr16:81085808 | C | T | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-1214G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085808 | |||||||
chr16:81085820 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.293-1226T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085820 | |||||||
chr16:81085844 | T | C | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.293-1250A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085844 | |||||||
chr16:81085854 | C | G | 1 | a0002c0002t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.293-1260G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085854 | |||||||
chr16:81085859 | CAAAAACA others(346): Show |
C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.292+1389_293-1266d others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81085859 | |||||||
chr16:81086162 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+1427_292+1438d others(14): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086162 | |||||||
chr16:81086162 | CAAAAAAA others(8): Show |
C | 1 | a0002c0002t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292+1424_292+1438d others(17): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086162 | |||||||
chr16:81086210 | A | C | 1 | a0002c0002t0001g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292+1391T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086210 | |||||||
chr16:81086260 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292+1341G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086260 | |||||||
chr16:81086261 | G | A | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1340C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086261 | |||||||
chr16:81086263 | C | T | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1338G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086263 | |||||||
chr16:81086270 | T | C | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1331A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086270 | |||||||
chr16:81086273 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.292+1328A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086273 | |||||||
chr16:81086275 | G | A | 1 | a0001c0001t0003g0115 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.292+1326C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086275 | |||||||
chr16:81086324 | C | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1277G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086324 | |||||||
chr16:81086324 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.292+1277G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086324 | |||||||
chr16:81086379 | G | A | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1222C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086379 | |||||||
chr16:81086392 | T | A | 1 | a0002c0002t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292+1209A>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086392 | |||||||
chr16:81086401 | T | A | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1200A>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086401 | |||||||
chr16:81086429 | T | C | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1172A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086429 | |||||||
chr16:81086437 | C | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1164G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086437 | |||||||
chr16:81086441 | C | T | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1160G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086441 | |||||||
chr16:81086442 | A | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1159T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086442 | |||||||
chr16:81086467 | G | A | 6 | a0003c0003t0004g0022 a0003c0003t0006g0021 a0003c0003t0006g0150 others(3): Show |
10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+1134C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086467 | |||||||
chr16:81086470 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.292+1131A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086470 | |||||||
chr16:81086508 | T | C | 1 | a0002c0002t0002g0073 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.292+1093A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086508 | |||||||
chr16:81086509 | G | A | 14 | a0001c0001t0001g0032 a0002c0005t0008g0068 a0002c0005t0008g0069 others(11): Show |
21 | HG01070.hp1 HG01071.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1092C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086509 | |||||||
chr16:81086528 | G | C | 13 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(10): Show |
19 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+1073C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086528 | |||||||
chr16:81086535 | C | A | 13 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(10): Show |
19 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+1066G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086535 | |||||||
chr16:81086564 | T | TAAG | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+1034_292+1036d others(5): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086564 | |||||||
chr16:81086571 | A | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.292+1030T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086571 | |||||||
chr16:81086595 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.292+1006T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086595 | |||||||
chr16:81086608 | AAC | A | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+991_292+992del others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086608 | |||||||
chr16:81086673 | G | GGAAAAAG others(15): Show |
27 | a0001c0001t0001g0093 a0001c0001t0002g0091 a0001c0001t0002g0116 others(24): Show |
66 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.292+927_292+928ins others(22): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086673 | |||||||
chr16:81086738 | C | CGAAAAAA others(8): Show |
27 | a0001c0001t0001g0093 a0001c0001t0002g0091 a0001c0001t0002g0116 others(24): Show |
66 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.292+862_292+863ins others(15): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086738 | |||||||
chr16:81086796 | C | T | 16 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(13): Show |
20 | HG00408.hp2 HG01168.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.292+805G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086796 | |||||||
chr16:81086809 | G | GTTAGGGT others(30): Show |
26 | a0001c0001t0001g0093 a0001c0001t0002g0091 a0001c0001t0002g0116 others(23): Show |
65 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.292+791_292+792ins others(37): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086809 | |||||||
chr16:81086811 | G | A | 26 | a0001c0001t0001g0093 a0001c0001t0002g0091 a0001c0001t0002g0116 others(23): Show |
65 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.292+790C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086811 | |||||||
chr16:81086887 | A | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+714T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086887 | |||||||
chr16:81086992 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.292+609G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81086992 | |||||||
chr16:81087029 | T | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0079 a0002c0002t0001g0080 |
4 | HG02280.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+572A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087029 | |||||||
chr16:81087070 | T | C | 2 | a0002c0005t0008g0068 a0002c0005t0008g0069 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.292+531A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087070 | |||||||
chr16:81087115 | G | A | 1 | a0002c0002t0001g0026 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+486C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087115 | |||||||
chr16:81087154 | C | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0079 a0002c0002t0001g0080 |
4 | HG02280.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+447G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087154 | |||||||
chr16:81087195 | G | T | 2 | a0002c0005t0008g0068 a0002c0005t0008g0069 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.292+406C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087195 | |||||||
chr16:81087207 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(140): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.292+394T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087207 | |||||||
chr16:81087309 | C | T | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+292G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087309 | |||||||
chr16:81087311 | A | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+290T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087311 | |||||||
chr16:81087328 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.292+273G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087328 | |||||||
chr16:81087335 | T | G | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+266A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087335 | |||||||
chr16:81087377 | C | T | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+224G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087377 | |||||||
chr16:81087392 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.292+209G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087392 | |||||||
chr16:81087495 | C | CAA | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+105_292+106ins others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087495 | |||||||
chr16:81087496 | C | A | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+105G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087496 | |||||||
chr16:81087540 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.292+61A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087540 | |||||||
chr16:81087578 | T | C | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.292+23A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087578 | |||||||
chr16:81087591 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.292+10C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087591 | |||||||
chr16:81087592 | A | C | 3 | a0002c0002t0001g0057 a0002c0002t0001g0059 a0002c0002t0001g0062 |
3 | HG01891.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.292+9T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 3/4 | chr16 | 81087592 | |||||||
chr16:81087744 | G | A | 3 | a0001c0001t0001g0086 a0002c0002t0001g0029 a0002c0002t0001g0081 |
4 | HG02818.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-80C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087744 | |||||||
chr16:81087748 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0093 others(2): Show |
13 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.229-84G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087748 | |||||||
chr16:81087783 | G | A | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.229-119C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087783 | |||||||
chr16:81087801 | A | G | 1 | a0002c0002t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.229-137T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087801 | |||||||
chr16:81087862 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0034 |
5 | HG01168.hp1 HG01169.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.229-198C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087862 | |||||||
chr16:81087866 | G | A | 1 | a0002c0002t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.229-202C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087866 | |||||||
chr16:81087932 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229-268G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81087932 | |||||||
chr16:81088052 | G | A | 1 | a0003c0003t0004g0022 | 3 | HG03041.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.229-388C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088052 | |||||||
chr16:81088086 | T | G | 1 | a0002c0002t0001g0012 | 3 | HG02717.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.229-422A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088086 | |||||||
chr16:81088152 | G | A | 3 | a0001c0001t0001g0086 a0002c0002t0001g0029 a0002c0002t0001g0081 |
4 | HG02818.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-488C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088152 | |||||||
chr16:81088303 | TCA | T | 14 | a0002c0005t0008g0068 a0002c0005t0008g0069 a0003c0003t0004g0022 others(11): Show |
21 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.229-641_229-640del others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088303 | |||||||
chr16:81088341 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.229-677G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088341 | |||||||
chr16:81088395 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.229-731G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088395 | |||||||
chr16:81088468 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.229-804T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088468 | |||||||
chr16:81088484 | T | C | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.229-820A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088484 | |||||||
chr16:81088485 | G | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.229-821C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088485 | |||||||
chr16:81088489 | C | T | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.229-825G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088489 | |||||||
chr16:81088501 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.229-837G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088501 | |||||||
chr16:81088643 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.229-979T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088643 | |||||||
chr16:81088653 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.229-989C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088653 | |||||||
chr16:81088655 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.229-991G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088655 | |||||||
chr16:81088692 | C | T | 6 | a0002c0002t0001g0079 a0003c0003t0004g0039 a0003c0003t0004g0040 others(3): Show |
8 | HG02523.hp2 HG03453.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-1028G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088692 | |||||||
chr16:81088698 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG00673.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.229-1034C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088698 | |||||||
chr16:81088765 | C | T | 1 | a0002c0002t0001g0026 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.229-1101G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088765 | |||||||
chr16:81088829 | A | T | 4 | a0003c0003t0006g0021 a0003c0003t0006g0150 a0003c0003t0006g0151 others(1): Show |
6 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-1165T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088829 | |||||||
chr16:81088850 | C | T | 13 | a0001c0001t0001g0138 a0003c0003t0004g0022 a0003c0003t0004g0039 others(10): Show |
20 | HG01884.hp1 HG02027.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.229-1186G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81088850 | |||||||
chr16:81089001 | A | G | 1 | a0002c0002t0001g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.229-1337T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089001 | |||||||
chr16:81089032 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.229-1368T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089032 | |||||||
chr16:81089149 | C | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+1452G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089149 | |||||||
chr16:81089156 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.228+1445G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089156 | |||||||
chr16:81089172 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0134 |
5 | HG01069.hp1 HG01071.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+1429G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089172 | |||||||
chr16:81089224 | G | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(5): Show |
22 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.228+1377C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089224 | |||||||
chr16:81089256 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.228+1345G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089256 | |||||||
chr16:81089296 | C | G | 20 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(17): Show |
24 | HG00408.hp2 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.228+1305G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089296 | |||||||
chr16:81089299 | G | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+1302C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089299 | |||||||
chr16:81089316 | A | G | 1 | a0002c0002t0001g0026 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.228+1285T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089316 | |||||||
chr16:81089333 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.228+1268C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089333 | |||||||
chr16:81089429 | G | T | 1 | a0002c0002t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.228+1172C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089429 | |||||||
chr16:81089439 | GC | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+1161delG | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089439 | |||||||
chr16:81089472 | T | C | 1 | a0003c0003t0006g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.228+1129A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089472 | |||||||
chr16:81089551 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(81): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.228+1050T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089551 | |||||||
chr16:81089566 | AG | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+1034delC | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089566 | |||||||
chr16:81089600 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.228+1001G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089600 | |||||||
chr16:81089627 | G | C | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+974C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089627 | |||||||
chr16:81089646 | C | CAT | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+954_228+955ins others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089646 | |||||||
chr16:81089668 | C | T | 1 | a0003c0003t0004g0041 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.228+933G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089668 | |||||||
chr16:81089669 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+932T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089669 | |||||||
chr16:81089704 | C | G | 1 | a0003c0003t0004g0147 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.228+897G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089704 | |||||||
chr16:81089730 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(141): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.228+871C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089730 | |||||||
chr16:81089766 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+835T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089766 | |||||||
chr16:81089860 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.228+741C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089860 | |||||||
chr16:81089969 | T | C | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+632A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81089969 | |||||||
chr16:81090006 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.228+595A>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090006 | |||||||
chr16:81090008 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.228+593G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090008 | |||||||
chr16:81090096 | C | CT | 18 | a0001c0001t0002g0091 a0001c0001t0012g0087 a0002c0002t0001g0026 others(15): Show |
53 | HG00558.hp1 HG00621.hp2 HG01952.hp1 others(50): Show |
intron_variant | MODIFIER | c.228+504dupA | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090096 | |||||||
chr16:81090096 | C | CTTTT | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+501_228+504dup others(4): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090096 | |||||||
chr16:81090133 | C | G | 1 | a0002c0005t0008g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.228+468G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090133 | |||||||
chr16:81090142 | G | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+459C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090142 | |||||||
chr16:81090145 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.228+456A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090145 | |||||||
chr16:81090164 | T | C | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+437A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090164 | |||||||
chr16:81090374 | G | A | 2 | a0002c0002t0001g0025 a0002c0002t0001g0065 |
3 | HG02723.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.228+227C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090374 | |||||||
chr16:81090377 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+224T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090377 | |||||||
chr16:81090408 | G | C | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+193C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090408 | |||||||
chr16:81090452 | C | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.228+149G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090452 | |||||||
chr16:81090515 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.228+86G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090515 | |||||||
chr16:81090547 | A | G | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.228+54T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 2/4 | chr16 | 81090547 | |||||||
chr16:81090736 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0098 a0001c0001t0001g0124 |
5 | HG02165.hp2 NA18986.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-56G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81090736 | |||||||
chr16:81090777 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.149-97G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81090777 | |||||||
chr16:81090808 | G | A | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-128C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81090808 | |||||||
chr16:81090882 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.149-202T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81090882 | |||||||
chr16:81090889 | C | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-209G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81090889 | |||||||
chr16:81091045 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-365T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091045 | |||||||
chr16:81091104 | T | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0065 |
3 | HG02723.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.149-424A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091104 | |||||||
chr16:81091109 | T | TA | 6 | a0003c0003t0004g0039 a0003c0003t0004g0040 a0003c0003t0004g0147 others(3): Show |
8 | HG02523.hp2 HG03453.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-430dupT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091109 | |||||||
chr16:81091134 | C | T | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-454G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091134 | |||||||
chr16:81091296 | C | T | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-616G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091296 | |||||||
chr16:81091303 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-623T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091303 | |||||||
chr16:81091374 | A | G | 12 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(9): Show |
19 | HG01884.hp1 HG02055.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-694T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091374 | |||||||
chr16:81091389 | C | G | 1 | a0002c0002t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149-709G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091389 | |||||||
chr16:81091411 | C | T | 1 | a0002c0002t0001g0012 | 3 | HG02717.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.149-731G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091411 | |||||||
chr16:81091443 | G | A | 2 | a0002c0005t0008g0068 a0002c0005t0008g0069 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.149-763C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091443 | |||||||
chr16:81091450 | C | T | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-770G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091450 | |||||||
chr16:81091478 | G | A | 1 | a0002c0002t0001g0026 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.149-798C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091478 | |||||||
chr16:81091578 | C | G | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.149-898G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091578 | |||||||
chr16:81091578 | C | T | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-898G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091578 | |||||||
chr16:81091623 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.149-943C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091623 | |||||||
chr16:81091656 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.149-976A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091656 | |||||||
chr16:81091671 | T | C | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-991A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091671 | |||||||
chr16:81091706 | T | G | 2 | a0002c0005t0008g0068 a0002c0005t0008g0069 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.149-1026A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091706 | |||||||
chr16:81091725 | C | T | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-1045G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091725 | |||||||
chr16:81091758 | C | A | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1078G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091758 | |||||||
chr16:81091768 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0081 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.149-1088T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091768 | |||||||
chr16:81091801 | T | G | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1121A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091801 | |||||||
chr16:81091838 | C | G | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1158G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091838 | |||||||
chr16:81091855 | A | AAG | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1176_149-1175i others(4): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091855 | |||||||
chr16:81091878 | C | A | 20 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(17): Show |
24 | HG00408.hp2 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.149-1198G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091878 | |||||||
chr16:81091909 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0131 others(2): Show |
9 | HG02080.hp1 NA18944.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-1229G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81091909 | |||||||
chr16:81092131 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149-1451A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092131 | |||||||
chr16:81092213 | A | G | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1533T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092213 | |||||||
chr16:81092235 | G | A | 1 | a0002c0002t0005g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149-1555C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092235 | |||||||
chr16:81092242 | T | C | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1562A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092242 | |||||||
chr16:81092281 | A | G | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1601T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092281 | |||||||
chr16:81092294 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149-1614A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092294 | |||||||
chr16:81092302 | T | C | 5 | a0003c0003t0004g0039 a0003c0003t0004g0040 a0003c0003t0004g0147 others(2): Show |
7 | HG02523.hp2 HG03453.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-1622A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092302 | |||||||
chr16:81092323 | AC | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.149-1644delG | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092323 | |||||||
chr16:81092332 | G | A | 1 | a0002c0002t0002g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.149-1652C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092332 | |||||||
chr16:81092395 | T | C | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-1715A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092395 | |||||||
chr16:81092455 | C | T | 1 | a0003c0003t0004g0041 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.149-1775G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092455 | |||||||
chr16:81092539 | G | C | 2 | a0002c0002t0001g0055 a0002c0002t0009g0042 |
2 | NA18978.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.149-1859C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092539 | |||||||
chr16:81092578 | T | TA | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-1899dupT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092578 | |||||||
chr16:81092718 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.149-2038T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092718 | |||||||
chr16:81092721 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.149-2041G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092721 | |||||||
chr16:81092747 | A | C | 9 | a0001c0001t0001g0139 a0002c0002t0001g0029 a0002c0002t0001g0081 others(6): Show |
15 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.149-2067T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092747 | |||||||
chr16:81092747 | AAAAC | A | 10 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(7): Show |
16 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-2071_149-2068d others(6): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092747 | |||||||
chr16:81092755 | C | A | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-2075G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092755 | |||||||
chr16:81092765 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149-2085G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092765 | |||||||
chr16:81092773 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149-2093C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092773 | |||||||
chr16:81092822 | A | T | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-2142T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092822 | |||||||
chr16:81092854 | G | A | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-2174C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092854 | |||||||
chr16:81092875 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.149-2195G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092875 | |||||||
chr16:81092903 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.149-2223T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092903 | |||||||
chr16:81092935 | C | A | 1 | a0002c0002t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.149-2255G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81092935 | |||||||
chr16:81093057 | G | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.149-2377C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093057 | |||||||
chr16:81093063 | C | T | 15 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(12): Show |
19 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-2383G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093063 | |||||||
chr16:81093068 | A | G | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-2388T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093068 | |||||||
chr16:81093102 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.149-2422G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093102 | |||||||
chr16:81093123 | C | CA | 6 | a0001c0001t0001g0126 a0002c0002t0001g0047 a0002c0002t0002g0027 others(3): Show |
7 | HG01433.hp2 HG02055.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-2444dupT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093123 | |||||||
chr16:81093123 | CA | C | 11 | a0001c0001t0001g0088 a0001c0001t0001g0131 a0001c0001t0012g0087 others(8): Show |
12 | HG01167.hp1 HG01981.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.149-2444delT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093123 | |||||||
chr16:81093153 | C | T | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-2473G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093153 | |||||||
chr16:81093193 | T | C | 4 | a0003c0003t0006g0021 a0003c0003t0006g0150 a0003c0003t0006g0151 others(1): Show |
6 | HG01884.hp1 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-2513A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093193 | |||||||
chr16:81093197 | T | C | 11 | a0003c0003t0004g0022 a0003c0003t0004g0039 a0003c0003t0004g0040 others(8): Show |
18 | HG01884.hp1 HG02523.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-2517A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093197 | |||||||
chr16:81093238 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149-2558G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093238 | |||||||
chr16:81093276 | T | G | 15 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(12): Show |
19 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.149-2596A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093276 | |||||||
chr16:81093355 | A | T | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.149-2675T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093355 | |||||||
chr16:81093378 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.149-2698A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093378 | |||||||
chr16:81093650 | G | A | 14 | a0002c0002t0001g0066 a0002c0002t0001g0072 a0002c0002t0002g0002 others(11): Show |
48 | HG00423.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.148+2481C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093650 | |||||||
chr16:81093734 | T | A | 1 | a0003c0003t0004g0041 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.148+2397A>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093734 | |||||||
chr16:81093734 | T | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.148+2397A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093734 | |||||||
chr16:81093828 | G | A | 1 | a0002c0002t0001g0012 | 3 | HG02717.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.148+2303C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093828 | |||||||
chr16:81093841 | G | A | 1 | a0003c0003t0004g0022 | 3 | HG03041.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.148+2290C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093841 | |||||||
chr16:81093866 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.148+2265A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093866 | |||||||
chr16:81093867 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.148+2264A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093867 | |||||||
chr16:81093965 | A | C | 2 | a0002c0002t0001g0064 a0002c0002t0005g0043 |
2 | HG01168.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.148+2166T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093965 | |||||||
chr16:81093967 | TCTAGGCT others(9): Show |
T | 1 | a0002c0004t0002g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.148+2148_148+2163d others(18): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093967 | |||||||
chr16:81093968 | C | A | 1 | a0003c0003t0004g0022 | 3 | HG03041.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.148+2163G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093968 | |||||||
chr16:81093976 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.148+2155C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81093976 | |||||||
chr16:81094042 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.148+2089C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094042 | |||||||
chr16:81094055 | C | G | 1 | a0002c0002t0001g0048 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.148+2076G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094055 | |||||||
chr16:81094061 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.148+2070T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094061 | |||||||
chr16:81094145 | C | G | 3 | a0003c0003t0006g0021 a0003c0003t0006g0150 a0003c0003t0006g0151 |
5 | HG01884.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1986G>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094145 | |||||||
chr16:81094146 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.148+1985G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094146 | |||||||
chr16:81094165 | G | A | 13 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(10): Show |
17 | HG00408.hp2 HG00558.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.148+1966C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094165 | |||||||
chr16:81094236 | T | C | 1 | a0002c0002t0001g0024 | 2 | NA18945.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.148+1895A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094236 | |||||||
chr16:81094262 | G | T | 1 | a0003c0003t0004g0022 | 3 | HG03041.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.148+1869C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094262 | |||||||
chr16:81094322 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.148+1809A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094322 | |||||||
chr16:81094353 | C | CT | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.148+1777dupA | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094353 | |||||||
chr16:81094362 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0128 |
3 | NA18963.hp2 NA18966.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.148+1769A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094362 | |||||||
chr16:81094409 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.148+1722C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094409 | |||||||
chr16:81094418 | G | C | 28 | a0001c0001t0001g0129 a0002c0002t0001g0026 a0002c0002t0001g0066 others(25): Show |
70 | HG00423.hp1 HG00558.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.148+1713C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094418 | |||||||
chr16:81094418 | G | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(84): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.148+1713C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094418 | |||||||
chr16:81094434 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.148+1697T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094434 | |||||||
chr16:81094512 | A | G | 1 | a0002c0002t0014g0070 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.148+1619T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094512 | |||||||
chr16:81094526 | G | T | 1 | a0002c0002t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.148+1605C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094526 | |||||||
chr16:81094530 | G | C | 1 | a0003c0003t0004g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.148+1601C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094530 | |||||||
chr16:81094601 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.148+1530C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094601 | |||||||
chr16:81094625 | G | A | 31 | a0001c0001t0001g0086 a0001c0001t0005g0045 a0002c0002t0001g0007 others(28): Show |
41 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.148+1506C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094625 | |||||||
chr16:81094666 | A | G | 1 | a0002c0002t0001g0029 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.148+1465T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094666 | |||||||
chr16:81094686 | A | G | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.148+1445T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094686 | |||||||
chr16:81094694 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.148+1437A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094694 | |||||||
chr16:81094755 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.148+1376T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094755 | |||||||
chr16:81094764 | AAGCAGAG others(1): Show |
A | 10 | a0001c0001t0001g0086 a0001c0001t0005g0045 a0002c0002t0001g0029 others(7): Show |
16 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.148+1359_148+1366d others(10): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094764 | |||||||
chr16:81094779 | C | CA | 16 | a0002c0002t0001g0026 a0002c0002t0001g0066 a0002c0002t0001g0072 others(13): Show |
51 | HG00423.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.148+1351dupT | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094779 | |||||||
chr16:81094785 | A | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.148+1346T>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094785 | |||||||
chr16:81094790 | A | T | 10 | a0001c0001t0001g0086 a0001c0001t0005g0045 a0002c0002t0001g0029 others(7): Show |
16 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.148+1341T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094790 | |||||||
chr16:81094800 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.148+1331C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094800 | |||||||
chr16:81094839 | G | A | 5 | a0003c0003t0004g0039 a0003c0003t0004g0040 a0003c0003t0004g0147 others(2): Show |
7 | HG02523.hp2 HG03453.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+1292C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094839 | |||||||
chr16:81094869 | G | A | 1 | a0003c0003t0004g0022 | 3 | HG03041.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.148+1262C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094869 | |||||||
chr16:81094902 | G | T | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.148+1229C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094902 | |||||||
chr16:81094913 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+1218G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094913 | |||||||
chr16:81094986 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0131 others(9): Show |
18 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.148+1145C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81094986 | |||||||
chr16:81095008 | G | A | 1 | a0002c0002t0001g0056 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.148+1123C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095008 | |||||||
chr16:81095101 | GAA | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.148+1028_148+1029d others(4): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095101 | |||||||
chr16:81095164 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0002g0142 |
2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.148+967C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095164 | |||||||
chr16:81095370 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+761G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095370 | |||||||
chr16:81095377 | A | ATT | 4 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0063 others(1): Show |
6 | HG00408.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+752_148+753dup others(2): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095377 | |||||||
chr16:81095377 | A | ATTTT | 5 | a0002c0002t0001g0029 a0002c0002t0001g0081 a0002c0004t0002g0015 others(2): Show |
10 | HG00323.hp1 HG01070.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+750_148+753dup others(4): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095377 | |||||||
chr16:81095377 | A | ATTTTTT | 6 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
6 | HG01891.hp1 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.148+748_148+753dup others(6): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095377 | |||||||
chr16:81095377 | A | ATTTTTTT others(2): Show |
5 | a0002c0002t0001g0007 a0002c0002t0001g0054 a0002c0002t0001g0055 others(2): Show |
8 | HG00558.hp2 NA18950.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+745_148+753dup others(9): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095377 | |||||||
chr16:81095377 | A | ATTTTTTT others(3): Show |
7 | a0002c0002t0001g0048 a0002c0002t0001g0050 a0002c0002t0001g0052 others(4): Show |
7 | HG02074.hp1 HG02572.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+744_148+753dup others(10): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095377 | |||||||
chr16:81095377 | ATTTTTTT others(7): Show |
A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+740_148+753del others(14): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095377 | |||||||
chr16:81095438 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.148+693T>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095438 | |||||||
chr16:81095468 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+663A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095468 | |||||||
chr16:81095511 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+620A>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095511 | |||||||
chr16:81095559 | C | A | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.148+572G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095559 | |||||||
chr16:81095572 | T | C | 1 | a0002c0002t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.148+559A>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095572 | |||||||
chr16:81095584 | G | T | 1 | a0002c0002t0001g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.148+547C>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095584 | |||||||
chr16:81095603 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+528G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095603 | |||||||
chr16:81095629 | T | TCCTCGGC others(20): Show |
117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.148+501_148+502ins others(27): Show |
GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095629 | |||||||
chr16:81095649 | C | T | 1 | a0002c0004t0002g0028 | 2 | HG00323.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.148+482G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095649 | |||||||
chr16:81095806 | G | C | 1 | a0001c0001t0003g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.148+325C>G | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095806 | |||||||
chr16:81095811 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.148+320C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095811 | |||||||
chr16:81095890 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.148+241G>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095890 | |||||||
chr16:81095980 | T | TC | 8 | a0002c0002t0001g0029 a0002c0002t0001g0081 a0002c0004t0002g0015 others(5): Show |
14 | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.148+150dupG | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095980 | |||||||
chr16:81095985 | A | G | 21 | a0002c0002t0001g0007 a0002c0002t0001g0024 a0002c0002t0001g0048 others(18): Show |
25 | HG00408.hp2 HG00558.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.148+146T>C | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81095985 | |||||||
chr16:81096009 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.148+122G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81096009 | |||||||
chr16:81096021 | C | T | 1 | a0002c0002t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.148+110G>A | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81096021 | |||||||
chr16:81096044 | G | A | 5 | a0003c0003t0004g0022 a0003c0003t0004g0041 a0003c0003t0006g0150 others(2): Show |
8 | HG02886.hp2 HG02970.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.148+87C>T | GCSH | ENSG00000140905.11 | transcript | ENST00000315467.9 | protein_coding | 1/4 | chr16 | 81096044 |