Item | Value |
---|---|
geneid | 5654 |
ensemblid | ENSG00000166033.13 |
hgncid | 9476 |
symbol | HTRA1 |
name | HtrA serine peptidase 1 |
refseq_nuc | NM_002775.5 |
refseq_prot | NP_002766.1 |
ensembl_nuc | ENST00000368984.8 |
ensembl_prot | ENSP00000357980.3 |
mane_status | MANE Select |
chr | chr10 |
start | 122461553 |
end | 122514907 |
strand | + |
ver | v1.2 |
region | chr10:122461553-122514907 |
region5000 | chr10:122456553-122519907 |
regionname0 | HTRA1_chr10_122461553_122514907 |
regionname5000 | HTRA1_chr10_122456553_122519907 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 480 | 314 | 85 | 70 | 110 | 16 | 31 | 79 | HTRA1_chr10_122456553_122519907 | HTRA1 | MQIPR others(475): Show |
chr10 | 122456553 | 122519907 |
a0002 | 0/0 | 480 | 43 | 0 | 1 | 36 | 0 | 6 | 29 | HTRA1_chr10_122456553_122519907 | HTRA1 | MQIPR others(475): Show |
chr10 | 122456553 | 122519907 |
a0003 | 0/0 | 480 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | MQIPR others(475): Show |
chr10 | 122456553 | 122519907 |
a0004 | 0/0 | 480 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | MQIPR others(475): Show |
chr10 | 122456553 | 122519907 |
a0005 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | MQIPR others(475): Show |
chr10 | 122456553 | 122519907 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1440 | 185 | 57 | 49 | 49 | 8 | 21 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0002 | 0/1 | 1440 | 101 | 22 | 16 | 54 | 4 | 4 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0004 | 0/0 | 1440 | 10 | 1 | 4 | 0 | 4 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0005 | 0/0 | 1440 | 9 | 3 | 1 | 0 | 0 | 5 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0007 | 0/0 | 1440 | 3 | 0 | 0 | 3 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0008 | 0/0 | 1440 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0009 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0011 | 0/0 | 1440 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0013 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0001c0014 | 0/0 | 1440 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0002c0003 | 0/0 | 1440 | 43 | 0 | 1 | 36 | 0 | 6 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0003c0006 | 0/0 | 1440 | 3 | 2 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0004c0012 | 0/0 | 1440 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 | ||
a0005c0010 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ATGCA others(1435): Show |
chr10 | 122456553 | 122519907 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2091 | 176 | 54 | 46 | 47 | 8 | 20 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0001t0002 | 0/0 | 2091 | 4 | 1 | 3 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0001t0003 | 0/0 | 2091 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0001t0004 | 0/0 | 2091 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0001t0005 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0001t0006 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0002t0001 | 0/1 | 2091 | 101 | 22 | 16 | 54 | 4 | 4 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0004t0001 | 0/0 | 2091 | 10 | 1 | 4 | 0 | 4 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0005t0001 | 0/0 | 2091 | 9 | 3 | 1 | 0 | 0 | 5 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0007t0001 | 0/0 | 2091 | 3 | 0 | 0 | 3 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0008t0001 | 0/0 | 2091 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0009t0001 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0011t0001 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0013t0001 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0001c0014t0001 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0002c0003t0001 | 0/0 | 2091 | 43 | 0 | 1 | 36 | 0 | 6 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0003c0006t0001 | 0/0 | 2091 | 3 | 2 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0004c0012t0001 | 0/0 | 2091 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
a0005c0010t0001 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | ACTCG others(2086): Show |
chr10 | 122456553 | 122519907 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0007t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0007t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0008t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0008t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0009t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0011t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0013t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0001c0014t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0003c0006t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0003c0006t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0003c0006t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0004c0012t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
a0005c0010t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0311 | EUR | GBR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0285 | EUR | GBR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | FIN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0308 | EUR | FIN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00408 | hp2 | a0001 | c0008 | t0001 | g0139 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0076 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0052 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00673 | hp1 | a0001 | c0007 | t0001 | g0180 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | CHS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0065 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01167 | hp1 | a0001 | c0004 | t0001 | g0310 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01168 | hp2 | a0004 | c0012 | t0001 | g0132 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01243 | hp2 | a0001 | c0004 | t0001 | g0309 | AMR | PUR | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0319 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0312 | EUR | IBS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0314 | EUR | IBS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0313 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0306 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01975 | hp1 | a0001 | c0005 | t0001 | g0002 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02071 | hp1 | a0002 | c0003 | t0001 | g0075 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | CDX | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | CDX | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0165 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0078 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02602 | hp2 | a0001 | c0005 | t0001 | g0334 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02886 | hp2 | a0001 | c0009 | t0001 | g0093 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02976 | hp1 | a0001 | c0005 | t0001 | g0201 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0023 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03239 | hp1 | a0001 | c0005 | t0001 | g0329 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03490 | hp1 | a0002 | c0003 | t0001 | g0079 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03490 | hp2 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0006 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0006 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03492 | hp2 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0116 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03834 | hp1 | a0002 | c0003 | t0001 | g0081 | SAS | BEB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0061 | SAS | BEB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG03927 | hp2 | a0001 | c0005 | t0001 | g0133 | SAS | BEB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04115 | hp2 | a0003 | c0006 | t0001 | g0316 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | CHB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | CHB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18940 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18942 | hp2 | a0001 | c0008 | t0001 | g0033 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18945 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18961 | hp2 | a0001 | c0007 | t0001 | g0191 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18965 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18969 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0069 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18973 | hp2 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18975 | hp2 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18977 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18978 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18983 | hp1 | a0001 | c0014 | t0001 | g0017 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18993 | hp2 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19010 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19011 | hp1 | a0001 | c0011 | t0001 | g0200 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19030 | hp1 | a0005 | c0010 | t0001 | g0304 | AFR | LWK | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | LWK | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19043 | hp2 | a0003 | c0006 | t0001 | g0317 | AFR | LWK | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19063 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19064 | hp1 | a0001 | c0007 | t0001 | g0193 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19068 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19070 | hp1 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19240 | hp1 | a0003 | c0006 | t0001 | g0318 | AFR | YRI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | TSI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0286 | EUR | TSI | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0307 | SAS | GIH | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | GIH | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0160 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA18955 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
NA21309 | hp2 | a0001 | c0013 | t0001 | g0170 | AFR | LWK | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0100 | REF | REF | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0153 | REF | REF | HTRA1_chr10_122456553_122519907 | HTRA1 | chr10 | 122456553 | 122519907 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:122461711 | C | T | 1 | a0002 | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
missense_variant | MODERATE | c.59C>T | p.Ala20Val | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 159/2091 | 59/1443 | 20/480 | chr10 | 122461711 | |||
chr10:122461729 | G | A | 1 | a0003 | 3 | HG04115.hp2 NA19043.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.77G>A | p.Arg26Gln | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 177/2091 | 77/1443 | 26/480 | chr10 | 122461729 | |||
chr10:122461779 | C | T | 1 | a0004 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.127C>T | p.Pro43Ser | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 227/2091 | 127/1443 | 43/480 | chr10 | 122461779 | |||
chr10:122514330 | A | T | 1 | a0005 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.1414A>T | p.Thr472Ser | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 9/9 | 1514/2091 | 1414/1443 | 472/480 | chr10 | 122514330 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:122461686 | C | T | 1 | a0001c0014 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.34C>T | p.Leu12Leu | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 134/2091 | 34/1443 | 12/480 | chr10 | 122461686 | |||
chr10:122461754 | C | T | 2 | a0001c0002 a0001c0013 |
101 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
synonymous_variant | LOW | c.102C>T | p.Ala34Ala | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 202/2091 | 102/1443 | 34/480 | chr10 | 122461754 | |||
chr10:122461760 | G | C | 1 | a0001c0004 | 10 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(7): Show |
synonymous_variant | LOW | c.108G>C | p.Gly36Gly | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 208/2091 | 108/1443 | 36/480 | chr10 | 122461760 | |||
chr10:122461760 | G | T | 1 | a0001c0002 | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
synonymous_variant | LOW | c.108G>T | p.Gly36Gly | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 208/2091 | 108/1443 | 36/480 | chr10 | 122461760 | |||
chr10:122461853 | G | A | 1 | a0001c0009 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.201G>A | p.Val67Val | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 301/2091 | 201/1443 | 67/480 | chr10 | 122461853 | |||
chr10:122489602 | C | T | 1 | a0001c0005 | 9 | HG01975.hp1 HG02109.hp2 HG02602.hp2 others(6): Show |
synonymous_variant | LOW | c.753C>T | p.Ile251Ile | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/9 | 853/2091 | 753/1443 | 251/480 | chr10 | 122489602 | |||
chr10:122506747 | C | T | 1 | a0001c0008 | 2 | HG00408.hp2 NA18942.hp2 |
synonymous_variant | LOW | c.834C>T | p.Phe278Phe | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/9 | 934/2091 | 834/1443 | 278/480 | chr10 | 122506747 | |||
chr10:122506756 | C | T | 1 | a0001c0011 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.843C>T | p.Ala281Ala | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/9 | 943/2091 | 843/1443 | 281/480 | chr10 | 122506756 | |||
chr10:122512012 | C | T | 1 | a0001c0007 | 3 | HG00673.hp1 NA18961.hp2 NA19064.hp1 |
synonymous_variant | LOW | c.1221C>T | p.Asp407Asp | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/9 | 1321/2091 | 1221/1443 | 407/480 | chr10 | 122512012 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:122461596 | C | A | 1 | a0001c0001t0002 | 4 | HG01256.hp2 HG01258.hp2 HG01346.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-57C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/9 | 57 | chr10 | 122461596 | ||||||
chr10:122514429 | G | C | 1 | a0001c0001t0004 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 9/9 | 70 | chr10 | 122514429 | ||||||
chr10:122514550 | G | A | 1 | a0001c0001t0005 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 9/9 | 191 | chr10 | 122514550 | ||||||
chr10:122514655 | C | G | 1 | a0001c0001t0003 | 2 | NA18966.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 9/9 | 296 | chr10 | 122514655 | ||||||
chr10:122514859 | G | A | 1 | a0001c0001t0006 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*500G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 9/9 | 500 | chr10 | 122514859 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:122462130 | C | A | 1 | a0001c0014t0001g0017 | 1 | NA18983.hp1 | splice_region_variant&intron_variant | LOW | c.472+6C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462130 | |||||||
chr10:122462589 | G | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(32): Show |
36 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.472+465G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462589 | |||||||
chr10:122462628 | T | A | 1 | a0001c0001t0002g0004 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.472+504T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462628 | |||||||
chr10:122462695 | C | A | 1 | a0002c0003t0001g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.472+571C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462695 | |||||||
chr10:122462712 | C | T | 10 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
10 | HG01175.hp1 HG02886.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.472+588C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462712 | |||||||
chr10:122462757 | C | G | 1 | a0001c0002t0001g0337 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.472+633C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462757 | |||||||
chr10:122462776 | G | C | 41 | a0002c0003t0001g0005 a0002c0003t0001g0006 a0002c0003t0001g0052 others(38): Show |
43 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.472+652G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122462776 | |||||||
chr10:122463017 | A | G | 43 | a0001c0001t0001g0335 a0001c0002t0001g0336 a0002c0003t0001g0005 others(40): Show |
45 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.472+893A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122463017 | |||||||
chr10:122463063 | G | C | 9 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(6): Show |
9 | HG01192.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.472+939G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122463063 | |||||||
chr10:122463164 | G | A | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(22): Show |
25 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.472+1040G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122463164 | |||||||
chr10:122463355 | TAG | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0320 a0001c0001t0001g0321 others(13): Show |
17 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.472+1236_472+1237d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122463355 | ||||||
chr10:122463500 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.472+1376C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122463500 | |||||||
chr10:122463559 | G | T | 1 | a0001c0004t0001g0319 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.472+1435G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122463559 | |||||||
chr10:122464212 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.472+2088T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464212 | |||||||
chr10:122464258 | T | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.472+2134T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464258 | |||||||
chr10:122464344 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.472+2220G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464344 | |||||||
chr10:122464428 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(185): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.472+2304C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464428 | |||||||
chr10:122464514 | C | T | 3 | a0003c0006t0001g0316 a0003c0006t0001g0317 a0003c0006t0001g0318 |
3 | HG04115.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.472+2390C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464514 | |||||||
chr10:122464571 | C | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(22): Show |
25 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.472+2447C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464571 | |||||||
chr10:122464624 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.472+2500G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122464624 | |||||||
chr10:122465081 | A | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0101 others(51): Show |
59 | HG00140.hp1 HG00642.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.472+2957A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465081 | |||||||
chr10:122465111 | G | A | 3 | a0001c0002t0001g0222 a0001c0002t0001g0223 a0001c0002t0001g0224 |
3 | HG02109.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.472+2987G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465111 | |||||||
chr10:122465191 | T | C | 40 | a0001c0002t0001g0336 a0002c0003t0001g0005 a0002c0003t0001g0006 others(37): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.472+3067T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465191 | |||||||
chr10:122465388 | A | G | 16 | a0001c0001t0001g0016 a0001c0001t0001g0320 a0001c0001t0001g0321 others(13): Show |
17 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.472+3264A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465388 | |||||||
chr10:122465400 | G | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(109): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.472+3276G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465400 | |||||||
chr10:122465626 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.472+3502A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465626 | |||||||
chr10:122465841 | G | A | 3 | a0001c0002t0001g0225 a0001c0002t0001g0226 a0001c0002t0001g0227 |
3 | HG02630.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.472+3717G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465841 | |||||||
chr10:122465848 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.472+3724C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465848 | |||||||
chr10:122465971 | T | A | 24 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(21): Show |
24 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.472+3847T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122465971 | |||||||
chr10:122466043 | T | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG02895.hp2 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.472+3919T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466043 | |||||||
chr10:122466126 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.472+4002A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466126 | |||||||
chr10:122466174 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.472+4050T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466174 | |||||||
chr10:122466322 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.472+4198C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466322 | |||||||
chr10:122466332 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.472+4208A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466332 | |||||||
chr10:122466625 | T | C | 13 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(10): Show |
13 | HG01192.hp2 HG01243.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.472+4501T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466625 | |||||||
chr10:122466651 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.472+4527A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466651 | |||||||
chr10:122466683 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(29): Show |
33 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.472+4559G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466683 | |||||||
chr10:122466699 | A | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.472+4575A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466699 | |||||||
chr10:122466719 | T | A | 23 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(20): Show |
23 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.472+4595T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466719 | |||||||
chr10:122466946 | TAAC | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.472+4825_472+4827d others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122466946 | ||||||
chr10:122466976 | A | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
12 | HG01192.hp1 HG01361.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.472+4852A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122466976 | |||||||
chr10:122467069 | T | C | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.472+4945T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467069 | |||||||
chr10:122467090 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472+4966C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467090 | |||||||
chr10:122467114 | G | T | 97 | a0001c0001t0001g0031 a0001c0001t0001g0338 a0001c0001t0003g0210 others(94): Show |
103 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.472+4990G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467114 | |||||||
chr10:122467270 | C | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | NA18964.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.472+5146C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467270 | |||||||
chr10:122467275 | G | A | 1 | a0005c0010t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472+5151G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467275 | |||||||
chr10:122467277 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.472+5153G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467277 | |||||||
chr10:122467772 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.472+5648G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467772 | |||||||
chr10:122467831 | C | T | 2 | a0001c0001t0001g0305 a0005c0010t0001g0304 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+5707C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122467831 | |||||||
chr10:122468063 | T | C | 2 | a0001c0001t0001g0305 a0001c0001t0005g0020 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.472+5939T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468063 | |||||||
chr10:122468108 | C | T | 131 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(128): Show |
138 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.472+5984C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468108 | |||||||
chr10:122468159 | G | A | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.472+6035G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468159 | |||||||
chr10:122468232 | T | C | 39 | a0001c0002t0001g0336 a0002c0003t0001g0005 a0002c0003t0001g0052 others(36): Show |
40 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.472+6108T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468232 | |||||||
chr10:122468402 | G | GTCA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0091 a0001c0001t0001g0111 others(4): Show |
8 | HG00639.hp2 HG01257.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+6317_472+6319d others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122468402 | ||||||
chr10:122468402 | GTCA | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0303 a0001c0001t0001g0305 others(2): Show |
5 | HG03139.hp1 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+6317_472+6319d others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122468402 | ||||||
chr10:122468402 | GTCATCA | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.472+6314_472+6319d others(8): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122468402 | ||||||
chr10:122468402 | GTCATCAT others(2): Show |
G | 86 | a0001c0001t0001g0031 a0001c0001t0001g0164 a0001c0001t0001g0206 others(83): Show |
92 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.472+6311_472+6319d others(11): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122468402 | ||||||
chr10:122468411 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.472+6287A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468411 | |||||||
chr10:122468471 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.472+6347G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468471 | |||||||
chr10:122468574 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0109 others(4): Show |
7 | HG02630.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.472+6450G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468574 | |||||||
chr10:122468686 | T | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.472+6562T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468686 | |||||||
chr10:122468925 | T | C | 2 | a0001c0002t0001g0232 a0001c0002t0001g0233 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.472+6801T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122468925 | |||||||
chr10:122469042 | C | T | 1 | a0001c0002t0001g0302 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.472+6918C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469042 | |||||||
chr10:122469063 | T | C | 1 | a0005c0010t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472+6939T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469063 | |||||||
chr10:122469106 | A | C | 2 | a0001c0001t0001g0161 a0001c0005t0001g0160 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.472+6982A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469106 | |||||||
chr10:122469231 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.472+7107T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469231 | |||||||
chr10:122469408 | G | T | 3 | a0001c0001t0001g0305 a0001c0001t0005g0020 a0005c0010t0001g0304 |
3 | HG03139.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+7284G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469408 | |||||||
chr10:122469529 | C | T | 1 | a0003c0006t0001g0318 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.472+7405C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469529 | |||||||
chr10:122469545 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0005g0020 a0005c0010t0001g0304 |
3 | HG03139.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+7421G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469545 | |||||||
chr10:122469672 | A | T | 1 | a0002c0003t0001g0087 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.472+7548A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469672 | |||||||
chr10:122469687 | C | T | 130 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(127): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.472+7563C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469687 | |||||||
chr10:122469972 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0173 a0001c0001t0002g0174 |
4 | HG01256.hp2 HG01258.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+7848G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469972 | |||||||
chr10:122469985 | G | A | 2 | a0001c0001t0001g0031 a0001c0002t0001g0227 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.472+7861G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122469985 | |||||||
chr10:122470087 | C | G | 1 | a0001c0002t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.472+7963C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470087 | |||||||
chr10:122470312 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.472+8188G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470312 | |||||||
chr10:122470388 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472+8264C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470388 | |||||||
chr10:122470508 | A | C | 105 | a0001c0001t0001g0031 a0001c0001t0001g0161 a0001c0001t0001g0164 others(102): Show |
112 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.472+8384A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470508 | |||||||
chr10:122470563 | C | A | 2 | a0001c0001t0001g0305 a0001c0001t0005g0020 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.472+8439C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470563 | |||||||
chr10:122470583 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.472+8459A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470583 | |||||||
chr10:122470881 | A | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0325 a0001c0001t0001g0326 others(7): Show |
11 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.472+8757A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470881 | |||||||
chr10:122470965 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.472+8841G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470965 | |||||||
chr10:122470997 | G | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(45): Show |
49 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.472+8873G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122470997 | |||||||
chr10:122471096 | C | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
17 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.472+8972C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471096 | |||||||
chr10:122471234 | G | T | 113 | a0001c0001t0001g0031 a0001c0001t0001g0164 a0001c0001t0001g0206 others(110): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.472+9110G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471234 | |||||||
chr10:122471364 | A | G | 1 | a0001c0001t0001g0338 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.472+9240A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471364 | |||||||
chr10:122471420 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.472+9296G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471420 | |||||||
chr10:122471425 | T | C | 40 | a0001c0001t0001g0335 a0001c0002t0001g0336 a0002c0003t0001g0005 others(37): Show |
41 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.472+9301T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471425 | |||||||
chr10:122471763 | T | A | 1 | a0001c0002t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.472+9639T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471763 | |||||||
chr10:122471787 | T | A | 2 | a0001c0002t0001g0239 a0001c0002t0001g0240 |
2 | NA18965.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.472+9663T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471787 | |||||||
chr10:122471798 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0315 |
2 | HG01099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.472+9674G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471798 | |||||||
chr10:122471943 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0339 a0001c0001t0001g0340 others(5): Show |
8 | HG02602.hp2 NA18945.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.472+9819C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471943 | |||||||
chr10:122471948 | G | A | 104 | a0001c0001t0001g0031 a0001c0001t0001g0164 a0001c0001t0001g0206 others(101): Show |
111 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.472+9824G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122471948 | |||||||
chr10:122472044 | A | C | 7 | a0001c0002t0001g0239 a0001c0002t0001g0240 a0001c0002t0001g0297 others(4): Show |
7 | HG00544.hp2 NA18955.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.472+9920A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472044 | |||||||
chr10:122472115 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.472+9991T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472115 | |||||||
chr10:122472195 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.472+10071T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472195 | |||||||
chr10:122472229 | A | G | 1 | a0003c0006t0001g0318 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.472+10105A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472229 | |||||||
chr10:122472290 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01175.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.472+10166T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472290 | |||||||
chr10:122472321 | A | G | 27 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(24): Show |
27 | HG01175.hp1 HG01891.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.472+10197A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472321 | |||||||
chr10:122472369 | C | CTAT | 28 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(25): Show |
28 | HG01081.hp2 HG01175.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.472+10286_472+1028 others(7): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | C | CTATTAT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
21 | HG00140.hp1 HG00642.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.472+10283_472+1028 others(10): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTAT | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
40 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.472+10286_472+1028 others(7): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTATTAT | C | 16 | a0001c0001t0001g0031 a0001c0001t0001g0103 a0001c0001t0001g0205 others(13): Show |
16 | HG00323.hp2 HG00621.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+10283_472+1028 others(10): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTATTATT others(2): Show |
C | 112 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0161 others(109): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.472+10280_472+1028 others(13): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTATTATT others(5): Show |
C | 16 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(13): Show |
16 | HG01192.hp2 HG01243.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+10277_472+1028 others(16): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTATTATT others(14): Show |
C | 39 | a0001c0001t0001g0335 a0001c0002t0001g0336 a0002c0003t0001g0005 others(36): Show |
40 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.472+10268_472+1028 others(25): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTATTATT others(20): Show |
C | 1 | a0002c0003t0001g0054 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.472+10262_472+1028 others(31): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472369 | CTATTATT others(26): Show |
C | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.472+10256_472+1028 others(37): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122472369 | ||||||
chr10:122472715 | C | G | 3 | a0001c0001t0001g0305 a0001c0001t0005g0020 a0005c0010t0001g0304 |
3 | HG03139.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+10591C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472715 | |||||||
chr10:122472904 | G | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0320 a0001c0001t0001g0321 others(12): Show |
16 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+10780G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122472904 | |||||||
chr10:122473091 | G | T | 1 | a0001c0002t0001g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.472+10967G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473091 | |||||||
chr10:122473092 | G | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.472+10968G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473092 | |||||||
chr10:122473244 | G | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.472+11120G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473244 | |||||||
chr10:122473325 | C | T | 2 | a0001c0002t0001g0295 a0001c0002t0001g0296 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.472+11201C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473325 | |||||||
chr10:122473399 | C | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(19): Show |
23 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.472+11275C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473399 | |||||||
chr10:122473557 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18973.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.472+11433G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473557 | |||||||
chr10:122473665 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG00639.hp1 HG01517.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.472+11541C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473665 | |||||||
chr10:122473986 | G | C | 35 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(32): Show |
35 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.472+11862G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122473986 | |||||||
chr10:122474071 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0320 a0001c0001t0001g0321 others(12): Show |
16 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+11947C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474071 | |||||||
chr10:122474359 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.472+12235G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474359 | |||||||
chr10:122474416 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472+12292T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474416 | |||||||
chr10:122474521 | G | C | 104 | a0001c0001t0001g0031 a0001c0001t0001g0164 a0001c0001t0001g0206 others(101): Show |
111 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.472+12397G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474521 | |||||||
chr10:122474564 | C | T | 3 | a0001c0001t0001g0021 a0002c0003t0001g0085 a0002c0003t0001g0086 |
3 | HG02055.hp1 NA18998.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.472+12440C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474564 | |||||||
chr10:122474626 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.472+12502A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474626 | |||||||
chr10:122474656 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.472+12532C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474656 | |||||||
chr10:122474697 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.472+12573A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474697 | |||||||
chr10:122474709 | C | T | 1 | a0001c0002t0001g0234 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.472+12585C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474709 | |||||||
chr10:122474713 | G | A | 15 | a0001c0002t0001g0246 a0001c0002t0001g0255 a0001c0002t0001g0256 others(12): Show |
15 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.472+12589G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474713 | |||||||
chr10:122474768 | A | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.472+12644A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474768 | |||||||
chr10:122474804 | G | A | 66 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(63): Show |
68 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.472+12680G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474804 | |||||||
chr10:122474883 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.472+12759C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122474883 | |||||||
chr10:122475088 | A | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(43): Show |
47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.472+12964A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475088 | |||||||
chr10:122475153 | C | T | 2 | a0001c0001t0001g0099 a0001c0002t0001g0228 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.472+13029C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475153 | |||||||
chr10:122475277 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG00423.hp1 HG01175.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.472+13153C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475277 | |||||||
chr10:122475364 | C | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(92): Show |
98 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.472+13240C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475364 | |||||||
chr10:122475369 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG01175.hp1 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.472+13245C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475369 | |||||||
chr10:122475383 | C | T | 38 | a0001c0002t0001g0336 a0002c0003t0001g0005 a0002c0003t0001g0052 others(35): Show |
39 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.472+13259C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475383 | |||||||
chr10:122475472 | G | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(219): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.472+13348G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475472 | |||||||
chr10:122475543 | G | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0184 a0001c0001t0001g0322 others(9): Show |
13 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.473-13359G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475543 | |||||||
chr10:122475671 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0184 a0001c0001t0001g0320 others(11): Show |
15 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.473-13231G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475671 | |||||||
chr10:122475710 | T | G | 20 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(17): Show |
21 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.473-13192T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475710 | |||||||
chr10:122475780 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.473-13122T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475780 | |||||||
chr10:122475839 | G | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(218): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.473-13063G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475839 | |||||||
chr10:122475913 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.473-12989G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475913 | |||||||
chr10:122475921 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG01175.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.473-12981G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475921 | |||||||
chr10:122475994 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.473-12908G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122475994 | |||||||
chr10:122476078 | C | T | 1 | a0001c0002t0001g0293 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.473-12824C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476078 | |||||||
chr10:122476214 | G | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0184 |
2 | HG02273.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.473-12688G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476214 | |||||||
chr10:122476285 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.473-12617T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476285 | |||||||
chr10:122476386 | C | T | 1 | a0001c0001t0001g0340 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.473-12516C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476386 | |||||||
chr10:122476523 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.473-12379A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476523 | |||||||
chr10:122476630 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.473-12272C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476630 | |||||||
chr10:122476641 | A | G | 1 | a0001c0002t0001g0270 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.473-12261A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476641 | |||||||
chr10:122476703 | TG | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0112 others(13): Show |
17 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.473-12192delG | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122476703 | ||||||
chr10:122476815 | G | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.473-12087G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476815 | |||||||
chr10:122476819 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473-12083G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476819 | |||||||
chr10:122476958 | T | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0002c0003t0001g0057 |
3 | NA18979.hp1 NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.473-11944T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122476958 | |||||||
chr10:122476964 | CT | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(164): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.473-11917delT | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122476964 | ||||||
chr10:122476964 | CTT | C | 8 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0001g0171 others(5): Show |
8 | HG00639.hp2 HG02040.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-11918_473-1191 others(6): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122476964 | ||||||
chr10:122477007 | A | G | 1 | a0001c0002t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.473-11895A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477007 | |||||||
chr10:122477068 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0101 others(48): Show |
54 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.473-11834C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477068 | |||||||
chr10:122477114 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.473-11788C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477114 | |||||||
chr10:122477157 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.473-11745C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477157 | |||||||
chr10:122477158 | T | A | 2 | a0002c0003t0001g0085 a0002c0003t0001g0086 |
2 | NA18998.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.473-11744T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477158 | |||||||
chr10:122477158 | T | G | 9 | a0001c0001t0001g0111 a0001c0001t0001g0161 a0001c0002t0001g0165 others(6): Show |
9 | HG00438.hp1 HG00597.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.473-11744T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477158 | |||||||
chr10:122477168 | T | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
19 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.473-11734T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477168 | |||||||
chr10:122477174 | A | G | 1 | a0002c0003t0001g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.473-11728A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477174 | |||||||
chr10:122477182 | C | T | 9 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0144 others(6): Show |
10 | HG02040.hp1 HG02109.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.473-11720C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477182 | |||||||
chr10:122477203 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): Show |
118 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.473-11699A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477203 | |||||||
chr10:122477240 | T | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(60): Show |
66 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.473-11662T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477240 | |||||||
chr10:122477258 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.473-11644T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477258 | |||||||
chr10:122477318 | A | G | 2 | a0001c0001t0001g0151 a0001c0002t0001g0015 |
3 | HG00735.hp1 HG02273.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.473-11584A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477318 | |||||||
chr10:122477340 | C | T | 3 | a0001c0005t0001g0002 a0001c0005t0001g0133 a0004c0012t0001g0132 |
5 | HG01168.hp2 HG01975.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-11562C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477340 | |||||||
chr10:122477459 | G | A | 1 | a0001c0001t0003g0210 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.473-11443G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477459 | |||||||
chr10:122477475 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.473-11427C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477475 | |||||||
chr10:122477625 | T | G | 40 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0041 others(37): Show |
42 | HG00408.hp1 HG01099.hp2 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.473-11277T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477625 | |||||||
chr10:122477662 | G | A | 11 | a0001c0001t0001g0175 a0001c0001t0001g0325 a0001c0001t0001g0326 others(8): Show |
11 | HG00733.hp1 HG01433.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.473-11240G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477662 | |||||||
chr10:122477727 | G | A | 2 | a0001c0001t0001g0047 a0003c0006t0001g0317 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.473-11175G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477727 | |||||||
chr10:122477798 | C | CT | 40 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0041 others(37): Show |
42 | HG00408.hp1 HG01099.hp2 HG01358.hp1 others(39): Show |
intron_variant | MODIFIER | c.473-11102dupT | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122477798 | ||||||
chr10:122477822 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-11080A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477822 | |||||||
chr10:122477884 | C | G | 1 | a0002c0003t0001g0054 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.473-11018C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477884 | |||||||
chr10:122477912 | AC | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(287): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.473-10986delC | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122477912 | ||||||
chr10:122477982 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-10920A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122477982 | |||||||
chr10:122478076 | C | G | 1 | a0001c0002t0001g0289 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.473-10826C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478076 | |||||||
chr10:122478096 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-10806A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478096 | |||||||
chr10:122478239 | G | T | 3 | a0001c0001t0001g0161 a0001c0005t0001g0023 a0001c0005t0001g0160 |
3 | HG02109.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.473-10663G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478239 | |||||||
chr10:122478263 | C | T | 1 | a0001c0002t0001g0288 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.473-10639C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478263 | |||||||
chr10:122478392 | A | AT | 34 | a0001c0001t0001g0043 a0001c0001t0001g0103 a0001c0001t0001g0150 others(31): Show |
35 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.473-10492dupT | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122478392 | ||||||
chr10:122478392 | A | ATT | 23 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0138 others(20): Show |
24 | HG00438.hp1 HG00741.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.473-10493_473-1049 others(6): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122478392 | ||||||
chr10:122478392 | A | ATTT | 133 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(130): Show |
140 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.473-10494_473-1049 others(7): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122478392 | ||||||
chr10:122478392 | A | ATTTT | 8 | a0001c0001t0001g0145 a0001c0001t0001g0324 a0001c0001t0001g0328 others(5): Show |
8 | HG01975.hp2 HG02300.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-10495_473-1049 others(8): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122478392 | ||||||
chr10:122478392 | A | ATTTTT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(100): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.473-10496_473-1049 others(9): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122478392 | ||||||
chr10:122478392 | A | ATTTTTT | 23 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0091 others(20): Show |
23 | HG00438.hp2 HG00544.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.473-10497_473-1049 others(10): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122478392 | ||||||
chr10:122478416 | G | A | 1 | a0002c0003t0001g0061 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.473-10486G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478416 | |||||||
chr10:122478423 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.473-10479C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478423 | |||||||
chr10:122478431 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-10471T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478431 | |||||||
chr10:122478541 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-10361T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478541 | |||||||
chr10:122478637 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0034 others(88): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.473-10265C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478637 | |||||||
chr10:122478643 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-10259T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478643 | |||||||
chr10:122478672 | T | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.473-10230T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478672 | |||||||
chr10:122478681 | T | TG | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(288): Show |
309 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.473-10221_473-1022 others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478681 | |||||||
chr10:122478682 | C | T | 3 | a0002c0003t0001g0055 a0002c0003t0001g0066 a0002c0003t0001g0087 |
3 | NA18943.hp2 NA18977.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.473-10220C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478682 | |||||||
chr10:122478686 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0031 others(2): Show |
5 | HG02572.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-10216C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478686 | |||||||
chr10:122478823 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.473-10079A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122478823 | |||||||
chr10:122479193 | A | G | 4 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-9709A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479193 | |||||||
chr10:122479194 | T | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(192): Show |
205 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.473-9708T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479194 | |||||||
chr10:122479254 | G | A | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.473-9648G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479254 | |||||||
chr10:122479255 | T | A | 4 | a0001c0002t0001g0336 a0002c0003t0001g0074 a0002c0003t0001g0075 others(1): Show |
4 | HG00438.hp1 HG00597.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-9647T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479255 | |||||||
chr10:122479356 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.473-9546C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479356 | |||||||
chr10:122479433 | G | A | 198 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.473-9469G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479433 | |||||||
chr10:122479467 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(279): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.473-9435G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479467 | |||||||
chr10:122479481 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.473-9421T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479481 | |||||||
chr10:122479548 | A | T | 4 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 others(1): Show |
4 | HG02717.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-9354A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479548 | |||||||
chr10:122479557 | A | G | 3 | a0001c0001t0001g0161 a0001c0005t0001g0023 a0001c0005t0001g0160 |
3 | HG02109.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.473-9345A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479557 | |||||||
chr10:122479633 | G | A | 9 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0190 others(6): Show |
9 | HG01361.hp2 HG01433.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.473-9269G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479633 | |||||||
chr10:122479642 | A | G | 1 | a0002c0003t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.473-9260A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479642 | |||||||
chr10:122479682 | G | C | 3 | a0001c0001t0001g0161 a0001c0005t0001g0023 a0001c0005t0001g0160 |
3 | HG02109.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.473-9220G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479682 | |||||||
chr10:122479728 | G | A | 1 | a0001c0001t0005g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.473-9174G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479728 | |||||||
chr10:122479784 | G | A | 1 | a0001c0002t0001g0298 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.473-9118G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479784 | |||||||
chr10:122479785 | A | AGGAGAT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0022 others(120): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.473-9114_473-9109d others(8): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122479785 | ||||||
chr10:122479794 | C | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(183): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.473-9108C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479794 | |||||||
chr10:122479921 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(168): Show |
183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.473-8981G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479921 | |||||||
chr10:122479963 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.473-8939G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122479963 | |||||||
chr10:122480198 | AGGCATTA others(3148): Show |
A | 5 | a0001c0001t0001g0186 a0001c0001t0001g0321 a0002c0003t0001g0078 others(2): Show |
5 | HG02602.hp1 HG02735.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-8700_473-5546d others(2): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122480198 | ||||||
chr10:122480261 | G | A | 1 | a0005c0010t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.473-8641G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480261 | |||||||
chr10:122480340 | CG | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
104 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.473-8559delG | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122480340 | ||||||
chr10:122480483 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.473-8419C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480483 | |||||||
chr10:122480780 | C | G | 1 | a0002c0003t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.473-8122C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480780 | |||||||
chr10:122480794 | T | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
107 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.473-8108T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480794 | |||||||
chr10:122480823 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473-8079A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480823 | |||||||
chr10:122480920 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
107 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.473-7982G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480920 | |||||||
chr10:122480949 | T | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0002c0003t0001g0084 others(2): Show |
5 | HG02129.hp1 HG02129.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-7953T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480949 | |||||||
chr10:122480951 | A | T | 1 | a0001c0002t0001g0281 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.473-7951A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122480951 | |||||||
chr10:122481146 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
107 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.473-7756G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481146 | |||||||
chr10:122481206 | T | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
107 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.473-7696T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481206 | |||||||
chr10:122481269 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
101 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.473-7633C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481269 | |||||||
chr10:122481293 | C | CA | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
107 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.473-7609_473-7608i others(3): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481293 | |||||||
chr10:122481307 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
101 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.473-7595C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481307 | |||||||
chr10:122481336 | T | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
107 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.473-7566T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481336 | |||||||
chr10:122481576 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.473-7326A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481576 | |||||||
chr10:122481613 | A | T | 2 | a0001c0001t0001g0220 a0001c0002t0001g0227 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.473-7289A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481613 | |||||||
chr10:122481771 | C | T | 1 | a0001c0004t0001g0308 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.473-7131C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481771 | |||||||
chr10:122481772 | G | T | 1 | a0002c0003t0001g0069 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.473-7130G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481772 | |||||||
chr10:122481801 | C | T | 29 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(26): Show |
30 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.473-7101C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122481801 | |||||||
chr10:122482041 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0034 others(83): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.473-6861A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482041 | |||||||
chr10:122482208 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0034 others(83): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.473-6694C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482208 | |||||||
chr10:122482331 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(97): Show |
106 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.473-6571C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482331 | |||||||
chr10:122482373 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473-6529A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482373 | |||||||
chr10:122482578 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473-6324G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482578 | |||||||
chr10:122482647 | C | T | 2 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
2 | NA18985.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.473-6255C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482647 | |||||||
chr10:122482648 | G | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
101 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.473-6254G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482648 | |||||||
chr10:122482751 | CTACTAAA others(2): Show |
C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(91): Show |
100 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.473-6147_473-6139d others(11): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122482751 | ||||||
chr10:122482917 | C | CA | 81 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(78): Show |
84 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.473-5961dupA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122482917 | ||||||
chr10:122482917 | CA | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0043 others(117): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.473-5961delA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122482917 | ||||||
chr10:122482917 | CAA | C | 17 | a0001c0001t0001g0031 a0001c0001t0001g0148 a0001c0001t0001g0161 others(14): Show |
17 | HG00733.hp1 HG01928.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.473-5962_473-5961d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122482917 | ||||||
chr10:122482917 | CAAA | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(77): Show |
86 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.473-5963_473-5961d others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122482917 | ||||||
chr10:122482917 | CAAAA | C | 6 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(3): Show |
6 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.473-5964_473-5961d others(6): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122482917 | ||||||
chr10:122482946 | A | G | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(1): Show |
4 | HG01074.hp2 HG01109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.473-5956A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482946 | |||||||
chr10:122482949 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473-5953T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482949 | |||||||
chr10:122482979 | C | T | 1 | a0001c0004t0001g0308 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.473-5923C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482979 | |||||||
chr10:122482994 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0137 a0001c0002t0001g0239 others(8): Show |
11 | HG00544.hp2 HG02015.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.473-5908A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122482994 | |||||||
chr10:122483192 | A | C | 1 | a0001c0002t0001g0285 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.473-5710A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483192 | |||||||
chr10:122483301 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
138 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.473-5601G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483301 | |||||||
chr10:122483504 | G | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0101 others(2): Show |
5 | HG00099.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-5398G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483504 | |||||||
chr10:122483638 | G | A | 29 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(26): Show |
30 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.473-5264G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483638 | |||||||
chr10:122483673 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
102 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.473-5229T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483673 | |||||||
chr10:122483941 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0034 others(83): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.473-4961A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483941 | |||||||
chr10:122483947 | G | A | 1 | a0002c0003t0001g0077 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.473-4955G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122483947 | |||||||
chr10:122483979 | C | CAT | 29 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(26): Show |
30 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.473-4916_473-4915d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122483979 | ||||||
chr10:122484071 | A | G | 3 | a0001c0001t0001g0187 a0001c0004t0001g0307 a0001c0004t0001g0319 |
3 | HG01175.hp2 HG01358.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.473-4831A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122484071 | |||||||
chr10:122484144 | CA | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0040 others(26): Show |
31 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.473-4757delA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122484144 | |||||||
chr10:122484268 | G | A | 1 | a0002c0003t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.473-4634G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122484268 | |||||||
chr10:122484467 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.473-4435G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122484467 | |||||||
chr10:122484641 | G | A | 8 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0118 others(5): Show |
8 | HG02258.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-4261G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122484641 | |||||||
chr10:122484878 | C | T | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-4024C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122484878 | |||||||
chr10:122485068 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.473-3834T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485068 | |||||||
chr10:122485176 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG00597.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.473-3726T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485176 | |||||||
chr10:122485267 | G | C | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.473-3635G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485267 | |||||||
chr10:122485380 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.473-3522C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485380 | |||||||
chr10:122485388 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.473-3514C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485388 | |||||||
chr10:122485453 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
108 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.473-3449T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485453 | |||||||
chr10:122485902 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.473-3000C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485902 | |||||||
chr10:122485967 | G | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
103 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.473-2935G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122485967 | |||||||
chr10:122486311 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.473-2591T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486311 | |||||||
chr10:122486351 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
108 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.473-2551T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486351 | |||||||
chr10:122486486 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
108 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.473-2416A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486486 | |||||||
chr10:122486487 | C | T | 2 | a0001c0001t0001g0196 a0001c0002t0001g0238 |
2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.473-2415C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486487 | |||||||
chr10:122486611 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.473-2291G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486611 | |||||||
chr10:122486739 | C | CGT | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(91): Show |
100 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.473-2146_473-2145d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122486739 | ||||||
chr10:122486739 | C | CGTGT | 3 | a0001c0001t0001g0143 a0001c0001t0001g0212 a0001c0001t0006g0032 |
3 | HG02148.hp1 HG02293.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.473-2148_473-2145d others(6): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122486739 | ||||||
chr10:122486825 | A | G | 2 | a0001c0002t0001g0258 a0001c0002t0001g0263 |
2 | HG02015.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.473-2077A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486825 | |||||||
chr10:122486852 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02896.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.473-2050A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486852 | |||||||
chr10:122486864 | G | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0040 others(29): Show |
34 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.473-2038G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122486864 | |||||||
chr10:122487222 | C | T | 1 | a0002c0003t0001g0072 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.473-1680C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122487222 | |||||||
chr10:122487275 | G | A | 1 | a0005c0010t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.473-1627G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122487275 | |||||||
chr10:122487346 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0040 others(28): Show |
33 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.473-1556C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122487346 | |||||||
chr10:122487407 | C | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(49): Show |
55 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.473-1495C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122487407 | |||||||
chr10:122487462 | C | G | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.473-1440C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122487462 | |||||||
chr10:122487575 | C | A | 1 | a0001c0002t0001g0238 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.473-1327C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122487575 | |||||||
chr10:122488112 | G | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0157 others(2): Show |
5 | HG00408.hp2 NA18942.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-790G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488112 | |||||||
chr10:122488122 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.473-780G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488122 | |||||||
chr10:122488169 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.473-733C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488169 | |||||||
chr10:122488247 | C | T | 1 | a0002c0003t0001g0084 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.473-655C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488247 | |||||||
chr10:122488395 | C | CG | 3 | a0001c0001t0001g0124 a0001c0001t0001g0205 a0001c0002t0001g0267 |
3 | NA18972.hp1 NA18978.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.473-505dupG | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 122488395 | ||||||
chr10:122488485 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.473-417C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488485 | |||||||
chr10:122488575 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(48): Show |
54 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.473-327A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488575 | |||||||
chr10:122488726 | C | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.473-176C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488726 | |||||||
chr10:122488864 | A | G | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-38A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488864 | |||||||
chr10:122488894 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | splice_region_variant&intron_variant | LOW | c.473-8G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 1/8 | chr10 | 122488894 | |||||||
chr10:122489021 | T | C | 7 | a0002c0003t0001g0054 a0002c0003t0001g0055 a0002c0003t0001g0062 others(4): Show |
7 | NA18943.hp2 NA18945.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.572+20T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 2/8 | chr10 | 122489021 | |||||||
chr10:122489101 | C | T | 2 | a0002c0003t0001g0064 a0002c0003t0001g0068 |
2 | NA18953.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.572+100C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 2/8 | chr10 | 122489101 | |||||||
chr10:122489263 | C | CA | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-153dupA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 122489263 | ||||||
chr10:122489318 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.573-104C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 2/8 | chr10 | 122489318 | |||||||
chr10:122489669 | C | T | 1 | a0002c0003t0001g0061 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.777+43C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122489669 | |||||||
chr10:122489719 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.777+93C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122489719 | |||||||
chr10:122489793 | G | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.777+167G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122489793 | |||||||
chr10:122489883 | G | A | 1 | a0001c0009t0001g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.777+257G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122489883 | |||||||
chr10:122489936 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.777+310C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122489936 | |||||||
chr10:122490478 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.777+852C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122490478 | |||||||
chr10:122490500 | T | C | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+874T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122490500 | |||||||
chr10:122490577 | G | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(53): Show |
59 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.777+951G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122490577 | |||||||
chr10:122490719 | A | G | 3 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0229 |
3 | HG02258.hp2 HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.777+1093A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122490719 | |||||||
chr10:122490808 | G | A | 1 | a0002c0003t0001g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.777+1182G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122490808 | |||||||
chr10:122490868 | G | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(87): Show |
94 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.777+1242G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122490868 | |||||||
chr10:122491087 | G | C | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+1461G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491087 | |||||||
chr10:122491125 | G | A | 1 | a0001c0001t0006g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.777+1499G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491125 | |||||||
chr10:122491347 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.777+1721G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491347 | |||||||
chr10:122491514 | G | A | 11 | a0001c0001t0001g0144 a0001c0001t0001g0177 a0001c0002t0001g0255 others(8): Show |
12 | HG02735.hp2 NA18940.hp1 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.777+1888G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491514 | |||||||
chr10:122491519 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.777+1893G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491519 | |||||||
chr10:122491530 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.777+1904C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491530 | |||||||
chr10:122491532 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.777+1906C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491532 | |||||||
chr10:122491538 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+1912C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491538 | |||||||
chr10:122491544 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
97 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.777+1918C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491544 | |||||||
chr10:122491574 | A | G | 58 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(55): Show |
60 | HG00099.hp1 HG00280.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.777+1948A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491574 | |||||||
chr10:122491578 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.777+1952C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491578 | |||||||
chr10:122491582 | C | A | 1 | a0001c0002t0001g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.777+1956C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491582 | |||||||
chr10:122491582 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(46): Show |
52 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.777+1956C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491582 | |||||||
chr10:122491710 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0148 others(3): Show |
6 | HG02572.hp1 HG02970.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+2084T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491710 | |||||||
chr10:122491723 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.777+2097C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122491723 | |||||||
chr10:122492140 | C | G | 1 | a0002c0003t0001g0090 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.777+2514C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492140 | |||||||
chr10:122492181 | T | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(89): Show |
96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.777+2555T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492181 | |||||||
chr10:122492220 | G | A | 1 | a0001c0005t0001g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.777+2594G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492220 | |||||||
chr10:122492447 | C | T | 1 | a0001c0002t0001g0269 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.777+2821C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492447 | |||||||
chr10:122492627 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.777+3001C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492627 | |||||||
chr10:122492631 | G | A | 1 | a0001c0009t0001g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.777+3005G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492631 | |||||||
chr10:122492674 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.777+3048T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492674 | |||||||
chr10:122492763 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(46): Show |
52 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.777+3137G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492763 | |||||||
chr10:122492769 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(46): Show |
52 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.777+3143C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492769 | |||||||
chr10:122492917 | G | A | 1 | a0001c0002t0001g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.777+3291G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122492917 | |||||||
chr10:122493107 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+3481C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493107 | |||||||
chr10:122493161 | G | A | 1 | a0001c0007t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.777+3535G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493161 | |||||||
chr10:122493227 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.777+3601C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493227 | |||||||
chr10:122493247 | T | C | 1 | a0001c0001t0005g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.777+3621T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493247 | |||||||
chr10:122493379 | G | C | 1 | a0001c0002t0001g0290 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.777+3753G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493379 | |||||||
chr10:122493503 | G | T | 3 | a0001c0007t0001g0180 a0001c0007t0001g0191 a0001c0007t0001g0193 |
3 | HG00673.hp1 NA18961.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.777+3877G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493503 | |||||||
chr10:122493917 | CT | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0099 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+4292delT | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122493917 | |||||||
chr10:122494039 | C | T | 1 | a0001c0002t0001g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.777+4413C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494039 | |||||||
chr10:122494120 | T | G | 3 | a0001c0001t0001g0213 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG00741.hp1 HG01928.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.777+4494T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494120 | |||||||
chr10:122494218 | C | T | 5 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0157 others(2): Show |
5 | HG00408.hp2 NA18942.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+4592C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494218 | |||||||
chr10:122494326 | C | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.777+4700C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494326 | |||||||
chr10:122494330 | A | T | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.777+4704A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494330 | |||||||
chr10:122494545 | C | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(88): Show |
95 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.777+4919C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494545 | |||||||
chr10:122494564 | C | T | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.777+4938C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494564 | |||||||
chr10:122494565 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.777+4939G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494565 | |||||||
chr10:122494662 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.777+5036C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494662 | |||||||
chr10:122494664 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.777+5038G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494664 | |||||||
chr10:122494827 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(97): Show |
104 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.777+5201C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494827 | |||||||
chr10:122494844 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(238): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.777+5218G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494844 | |||||||
chr10:122494871 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.777+5245C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494871 | |||||||
chr10:122494936 | T | C | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.777+5310T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494936 | |||||||
chr10:122494961 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.777+5335G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494961 | |||||||
chr10:122494972 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.777+5346C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122494972 | |||||||
chr10:122495085 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0185 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.777+5459C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122495085 | |||||||
chr10:122495095 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.777+5469C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122495095 | |||||||
chr10:122495792 | G | A | 1 | a0002c0003t0001g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.777+6166G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122495792 | |||||||
chr10:122495824 | T | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(57): Show |
63 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.777+6198T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122495824 | |||||||
chr10:122496062 | C | G | 29 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(26): Show |
30 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.777+6436C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496062 | |||||||
chr10:122496098 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0205 a0001c0002t0001g0272 |
3 | NA18961.hp1 NA18972.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.777+6472C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496098 | |||||||
chr10:122496145 | C | T | 3 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0229 |
3 | HG02258.hp2 HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.777+6519C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496145 | |||||||
chr10:122496170 | G | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(69): Show |
75 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.777+6544G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496170 | |||||||
chr10:122496176 | A | G | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+6550A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496176 | |||||||
chr10:122496224 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.777+6598G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | G | GTTTTTT | 9 | a0001c0001t0001g0048 a0001c0001t0001g0206 a0001c0001t0001g0207 others(6): Show |
9 | HG02129.hp1 HG02135.hp2 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.777+6598_777+6599i others(8): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | G | GTTTTTTT | 8 | a0001c0001t0001g0041 a0001c0001t0001g0152 a0001c0001t0001g0205 others(5): Show |
8 | HG01099.hp2 HG01358.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+6598_777+6599i others(9): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | G | GTTTTTTT others(3): Show |
2 | a0002c0003t0001g0063 a0002c0003t0001g0066 |
2 | NA18943.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.777+6598_777+6599i others(12): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | G | GTTTTTTT others(4): Show |
2 | a0002c0003t0001g0055 a0002c0003t0001g0087 |
2 | NA18977.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.777+6598_777+6599i others(13): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0340 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.777+6598_777+6599i others(14): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | GGTTCTTT others(5): Show |
G | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.777+6599_777+6610d others(14): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496224 | GGTTCTTT others(9): Show |
G | 1 | a0002c0003t0001g0006 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.777+6599_777+6614d others(18): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496224 | |||||||
chr10:122496225 | G | GT | 17 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0125 others(14): Show |
18 | HG00639.hp2 HG00642.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.777+6601dupT | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTT | 20 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0211 others(17): Show |
22 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.777+6600_777+6601d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTT | 26 | a0001c0001t0001g0016 a0001c0001t0001g0111 a0001c0001t0001g0114 others(23): Show |
30 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTT | 7 | a0001c0001t0001g0045 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00639.hp1 HG02071.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(6): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTT | 6 | a0001c0001t0001g0158 a0001c0001t0005g0020 a0001c0002t0001g0234 others(3): Show |
6 | HG01074.hp2 HG01081.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(8): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT | 12 | a0001c0001t0001g0027 a0001c0001t0001g0096 a0001c0001t0001g0120 others(9): Show |
12 | HG00544.hp2 HG01099.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(9): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(1): Show |
16 | a0001c0001t0001g0097 a0001c0001t0001g0113 a0001c0001t0001g0137 others(13): Show |
16 | HG00597.hp2 HG00741.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(10): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(2): Show |
14 | a0001c0001t0001g0028 a0001c0001t0001g0092 a0001c0001t0001g0105 others(11): Show |
14 | HG00438.hp1 HG02071.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(11): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(3): Show |
13 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0104 others(10): Show |
14 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(12): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(4): Show |
17 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0046 others(14): Show |
17 | HG00099.hp2 HG01071.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(13): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(5): Show |
9 | a0001c0001t0001g0026 a0001c0001t0001g0154 a0001c0001t0001g0156 others(6): Show |
9 | HG00733.hp2 HG01358.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(14): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(6): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0150 a0001c0002t0001g0166 others(1): Show |
4 | HG01891.hp1 HG02165.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(15): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(7): Show |
5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0025 others(2): Show |
5 | HG01168.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+6601_777+6602i others(16): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(8): Show |
1 | a0001c0004t0001g0307 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.777+6601_777+6602i others(17): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | GTTTTTTT others(12): Show |
1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.777+6601_777+6602i others(21): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | G | T | 25 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(22): Show |
25 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.777+6599G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496225 | |||||||
chr10:122496225 | GTTCTTTT others(3): Show |
G | 6 | a0001c0001t0001g0219 a0001c0001t0003g0195 a0001c0001t0003g0210 others(3): Show |
6 | HG02300.hp2 NA18966.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+6602_777+6611d others(12): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | GTTCTTTT others(4): Show |
G | 9 | a0001c0001t0001g0127 a0001c0001t0001g0218 a0001c0001t0001g0333 others(6): Show |
9 | HG01361.hp1 HG01361.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+6602_777+6612d others(13): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | GTTCTTTT others(5): Show |
G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0102 others(29): Show |
36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.777+6602_777+6613d others(14): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | GTTCTTTT others(6): Show |
G | 10 | a0001c0001t0001g0038 a0001c0001t0001g0122 a0001c0001t0001g0171 others(7): Show |
10 | HG01081.hp2 HG03453.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.777+6602_777+6614d others(15): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | GTTCTTTT others(7): Show |
G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(44): Show |
50 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.777+6602_777+6615d others(16): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | GTTCTTTT others(8): Show |
G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0183 a0001c0001t0001g0203 others(2): Show |
5 | HG00642.hp2 HG01106.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.777+6602_777+6616d others(17): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496225 | GTTCTTTT others(9): Show |
G | 2 | a0001c0001t0001g0303 a0001c0002t0001g0222 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.777+6602_777+6617d others(18): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496225 | ||||||
chr10:122496227 | TC | T | 3 | a0001c0005t0001g0002 a0001c0005t0001g0023 a0001c0005t0001g0334 |
4 | HG01975.hp1 HG02602.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+6602delC | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496227 | |||||||
chr10:122496228 | C | T | 204 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(201): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.777+6602C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496228 | |||||||
chr10:122496258 | T | TTTTTTTT others(7): Show |
2 | a0001c0001t0001g0110 a0001c0002t0001g0165 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.777+6633_777+6634i others(16): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122496258 | ||||||
chr10:122496307 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.777+6681T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496307 | |||||||
chr10:122496341 | G | A | 29 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(26): Show |
30 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.777+6715G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496341 | |||||||
chr10:122496533 | G | A | 1 | a0001c0002t0001g0011 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.777+6907G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496533 | |||||||
chr10:122496783 | C | G | 1 | a0001c0001t0005g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.777+7157C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496783 | |||||||
chr10:122496829 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0043 others(89): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.777+7203G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122496829 | |||||||
chr10:122497137 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.777+7511C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497137 | |||||||
chr10:122497189 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.777+7563C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497189 | |||||||
chr10:122497189 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.777+7563C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497189 | |||||||
chr10:122497270 | T | G | 1 | a0001c0001t0006g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.777+7644T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497270 | |||||||
chr10:122497279 | A | G | 1 | a0003c0006t0001g0316 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+7653A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497279 | |||||||
chr10:122497321 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0148 others(3): Show |
6 | HG02572.hp1 HG02970.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+7695A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497321 | |||||||
chr10:122497425 | T | A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.777+7799T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497425 | |||||||
chr10:122497704 | G | A | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.777+8078G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497704 | |||||||
chr10:122497810 | G | T | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.777+8184G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497810 | |||||||
chr10:122497868 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.777+8242G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497868 | |||||||
chr10:122497902 | G | A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.777+8276G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497902 | |||||||
chr10:122497936 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.777+8310C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497936 | |||||||
chr10:122497973 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.777+8347C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122497973 | |||||||
chr10:122498135 | GCT | G | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.777+8516_777+8517d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122498135 | ||||||
chr10:122498251 | C | T | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-8440C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498251 | |||||||
chr10:122498353 | T | G | 1 | a0002c0003t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.778-8338T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498353 | |||||||
chr10:122498430 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.778-8261C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498430 | |||||||
chr10:122498480 | A | G | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-8211A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498480 | |||||||
chr10:122498565 | C | T | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-8126C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498565 | |||||||
chr10:122498587 | A | G | 4 | a0001c0002t0001g0014 a0001c0002t0001g0242 a0001c0002t0001g0273 others(1): Show |
5 | HG00621.hp2 NA18984.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-8104A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498587 | |||||||
chr10:122498592 | C | G | 1 | a0001c0005t0001g0329 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.778-8099C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498592 | |||||||
chr10:122498603 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.778-8088G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498603 | |||||||
chr10:122498620 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(268): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.778-8071C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498620 | |||||||
chr10:122498746 | C | G | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0113 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-7945C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498746 | |||||||
chr10:122498813 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-7878A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498813 | |||||||
chr10:122498814 | G | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-7877G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498814 | |||||||
chr10:122498861 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(235): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.778-7830C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498861 | |||||||
chr10:122498870 | T | G | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-7821T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498870 | |||||||
chr10:122498902 | C | T | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-7789C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498902 | |||||||
chr10:122498981 | A | G | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-7710A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122498981 | |||||||
chr10:122499020 | C | T | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-7671C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499020 | |||||||
chr10:122499131 | G | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0148 others(3): Show |
6 | HG02572.hp1 HG02970.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-7560G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499131 | |||||||
chr10:122499242 | A | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(236): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.778-7449A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499242 | |||||||
chr10:122499245 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.778-7446G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499245 | |||||||
chr10:122499296 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.778-7395C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499296 | |||||||
chr10:122499546 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(236): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.778-7145G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499546 | |||||||
chr10:122499614 | G | A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-7077G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499614 | |||||||
chr10:122499710 | A | G | 34 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(31): Show |
35 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(32): Show |
intron_variant | MODIFIER | c.778-6981A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499710 | |||||||
chr10:122499723 | G | A | 33 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0108 others(30): Show |
34 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-6968G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499723 | |||||||
chr10:122499804 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.778-6887G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499804 | |||||||
chr10:122499926 | G | T | 1 | a0001c0011t0001g0200 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.778-6765G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499926 | |||||||
chr10:122499994 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.778-6697G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122499994 | |||||||
chr10:122500061 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0214 others(3): Show |
9 | HG01192.hp1 HG01361.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-6630T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500061 | |||||||
chr10:122500083 | C | T | 2 | a0001c0001t0001g0145 a0001c0002t0001g0250 |
2 | NA18962.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.778-6608C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500083 | |||||||
chr10:122500190 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.778-6501A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500190 | |||||||
chr10:122500234 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-6457C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500234 | |||||||
chr10:122500242 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.778-6449C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500242 | |||||||
chr10:122500315 | G | A | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(297): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.778-6376G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500315 | |||||||
chr10:122500334 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.778-6357T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500334 | |||||||
chr10:122500643 | C | T | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-6048C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500643 | |||||||
chr10:122500998 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.778-5693G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122500998 | |||||||
chr10:122501009 | G | A | 328 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(325): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.778-5682G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501009 | |||||||
chr10:122501048 | C | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(57): Show |
63 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.778-5643C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501048 | |||||||
chr10:122501085 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.778-5606C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501085 | |||||||
chr10:122501150 | C | T | 1 | a0004c0012t0001g0132 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.778-5541C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501150 | |||||||
chr10:122501223 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-5468C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501223 | |||||||
chr10:122501249 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.778-5442C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501249 | |||||||
chr10:122501363 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(333): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.778-5328T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501363 | |||||||
chr10:122501446 | T | C | 1 | a0002c0003t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.778-5245T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501446 | |||||||
chr10:122501454 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.778-5237T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501454 | |||||||
chr10:122501691 | G | A | 3 | a0001c0005t0001g0002 a0001c0005t0001g0133 a0001c0005t0001g0334 |
5 | HG01975.hp1 HG02602.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.778-5000G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501691 | |||||||
chr10:122501812 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.778-4879C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501812 | |||||||
chr10:122501832 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-4859C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501832 | |||||||
chr10:122501860 | G | A | 1 | a0002c0003t0001g0075 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.778-4831G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501860 | |||||||
chr10:122501897 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(330): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.778-4794T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122501897 | |||||||
chr10:122501961 | GTTTTT | G | 27 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(24): Show |
27 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.778-4701_778-4697d others(7): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTT | G | 31 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0042 others(28): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.778-4702_778-4697d others(8): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT | G | 58 | a0001c0001t0001g0018 a0001c0001t0001g0096 a0001c0001t0001g0097 others(55): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.778-4703_778-4697d others(9): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(1): Show |
G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0156 a0001c0002t0001g0234 others(4): Show |
9 | HG01081.hp1 HG01109.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-4704_778-4697d others(10): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(2): Show |
G | 16 | a0001c0001t0001g0043 a0001c0001t0001g0108 a0001c0001t0001g0205 others(13): Show |
16 | HG00438.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.778-4705_778-4697d others(11): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(4): Show |
G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0022 others(24): Show |
29 | HG00597.hp1 HG00639.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-4707_778-4697d others(13): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(5): Show |
G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0030 others(44): Show |
49 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.778-4708_778-4697d others(14): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.778-4709_778-4697d others(15): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(7): Show |
G | 1 | a0001c0002t0001g0250 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.778-4710_778-4697d others(16): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122501961 | GTTTTTTT others(10): Show |
G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.778-4713_778-4697d others(19): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122501961 | ||||||
chr10:122502042 | T | C | 5 | a0001c0001t0001g0102 a0001c0001t0001g0331 a0001c0001t0001g0332 others(2): Show |
6 | HG00280.hp1 HG00735.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4649T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502042 | |||||||
chr10:122502075 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.778-4616C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502075 | |||||||
chr10:122502127 | G | T | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-4564G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502127 | |||||||
chr10:122502178 | A | G | 1 | a0002c0003t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.778-4513A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502178 | |||||||
chr10:122502187 | G | C | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-4504G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502187 | |||||||
chr10:122502338 | A | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0212 |
2 | HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.778-4353A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502338 | |||||||
chr10:122502596 | G | A | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-4095G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502596 | |||||||
chr10:122502637 | G | A | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-4054G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502637 | |||||||
chr10:122502638 | T | G | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-4053T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502638 | |||||||
chr10:122502642 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-4049C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502642 | |||||||
chr10:122502753 | A | G | 5 | a0001c0001t0001g0108 a0001c0002t0001g0223 a0001c0002t0001g0224 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-3938A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502753 | |||||||
chr10:122502885 | C | T | 2 | a0001c0001t0001g0152 a0001c0002t0001g0297 |
2 | NA18992.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.778-3806C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502885 | |||||||
chr10:122502903 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-3788A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502903 | |||||||
chr10:122502928 | G | A | 50 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0111 others(47): Show |
55 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.778-3763G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122502928 | |||||||
chr10:122503186 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.778-3505C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122503186 | |||||||
chr10:122503303 | C | T | 1 | a0005c0010t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.778-3388C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122503303 | |||||||
chr10:122503351 | C | T | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.778-3340C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122503351 | |||||||
chr10:122503359 | G | A | 1 | a0001c0002t0001g0259 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.778-3332G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122503359 | |||||||
chr10:122503458 | C | T | 1 | a0002c0003t0001g0057 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.778-3233C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122503458 | |||||||
chr10:122504019 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.778-2672C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504019 | |||||||
chr10:122504045 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.778-2646G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504045 | |||||||
chr10:122504083 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.778-2608G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504083 | |||||||
chr10:122504176 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(240): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.778-2515T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504176 | |||||||
chr10:122504200 | A | G | 1 | a0002c0003t0001g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.778-2491A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504200 | |||||||
chr10:122504357 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(57): Show |
63 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.778-2334C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504357 | |||||||
chr10:122504361 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-2330A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504361 | |||||||
chr10:122504409 | A | C | 1 | a0001c0002t0001g0293 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.778-2282A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504409 | |||||||
chr10:122504462 | A | G | 4 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0113 others(1): Show |
4 | HG01192.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-2229A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504462 | |||||||
chr10:122504465 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0043 others(90): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.778-2226C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504465 | |||||||
chr10:122504516 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.778-2175A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504516 | |||||||
chr10:122504579 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.778-2112C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504579 | |||||||
chr10:122504580 | G | A | 7 | a0001c0005t0001g0002 a0001c0005t0001g0023 a0001c0005t0001g0133 others(4): Show |
9 | HG01975.hp1 HG02109.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-2111G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504580 | |||||||
chr10:122504635 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.778-2056G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504635 | |||||||
chr10:122504667 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.778-2024C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504667 | |||||||
chr10:122504780 | C | T | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-1911C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122504780 | |||||||
chr10:122504841 | TG | T | 28 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(25): Show |
29 | HG01099.hp2 HG01358.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-1846delG | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122504841 | ||||||
chr10:122505060 | T | C | 1 | a0002c0003t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.778-1631T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505060 | |||||||
chr10:122505110 | C | T | 2 | a0002c0003t0001g0059 a0002c0003t0001g0060 |
2 | NA19068.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.778-1581C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505110 | |||||||
chr10:122505149 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0148 others(2): Show |
5 | HG02572.hp1 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-1542C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505149 | |||||||
chr10:122505206 | C | A | 1 | a0001c0004t0001g0313 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778-1485C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505206 | |||||||
chr10:122505300 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.778-1391C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505300 | |||||||
chr10:122505362 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0045 others(87): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.778-1329T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505362 | |||||||
chr10:122505512 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(88): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.778-1179A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505512 | |||||||
chr10:122505520 | C | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(88): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.778-1171C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505520 | |||||||
chr10:122505677 | G | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(177): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.778-1014G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505677 | |||||||
chr10:122505707 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.778-984C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505707 | |||||||
chr10:122505710 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-981G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505710 | |||||||
chr10:122505768 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-923G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505768 | |||||||
chr10:122505810 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(177): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.778-881C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505810 | |||||||
chr10:122505931 | C | G | 1 | a0001c0002t0001g0336 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.778-760C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122505931 | |||||||
chr10:122506096 | T | TCTTGCTG others(17): Show |
326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(323): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.778-586_778-585ins others(24): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122506096 | ||||||
chr10:122506096 | T | TCTTGTTG others(17): Show |
1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.778-591_778-590ins others(24): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 122506096 | ||||||
chr10:122506124 | C | G | 1 | a0001c0001t0001g0343 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.778-567C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122506124 | |||||||
chr10:122506188 | G | T | 1 | a0001c0001t0005g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.778-503G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122506188 | |||||||
chr10:122506220 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.778-471C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122506220 | |||||||
chr10:122506481 | C | T | 2 | a0001c0002t0001g0276 a0001c0002t0001g0278 |
2 | HG02486.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.778-210C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122506481 | |||||||
chr10:122506567 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.778-124C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122506567 | |||||||
chr10:122506671 | G | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
17 | HG02145.hp2 HG02257.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-20G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 3/8 | chr10 | 122506671 | |||||||
chr10:122506973 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.972+88G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122506973 | |||||||
chr10:122506984 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(93): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.972+99C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122506984 | |||||||
chr10:122507067 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.972+182C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122507067 | |||||||
chr10:122507100 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(176): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.972+215G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122507100 | |||||||
chr10:122507176 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.973-194G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122507176 | |||||||
chr10:122507220 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.973-150C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122507220 | |||||||
chr10:122507268 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.973-102C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122507268 | |||||||
chr10:122507294 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.973-76A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 4/8 | chr10 | 122507294 | |||||||
chr10:122507471 | G | C | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1005+69G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507471 | |||||||
chr10:122507475 | GTTGT | G | 123 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1005+84_1005+87del others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 122507475 | ||||||
chr10:122507571 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(93): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1005+169G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507571 | |||||||
chr10:122507591 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1005+189G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507591 | |||||||
chr10:122507657 | A | T | 7 | a0001c0005t0001g0002 a0001c0005t0001g0023 a0001c0005t0001g0133 others(4): Show |
9 | HG01975.hp1 HG02109.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1005+255A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507657 | |||||||
chr10:122507727 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0016 others(144): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1005+325T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507727 | |||||||
chr10:122507734 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(48): Show |
54 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1005+332G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507734 | |||||||
chr10:122507894 | T | C | 1 | a0001c0002t0001g0265 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1005+492T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507894 | |||||||
chr10:122507948 | C | CTAGAGGG others(18): Show |
51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(48): Show |
54 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1005+600_1005+624d others(27): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 122507948 | ||||||
chr10:122507958 | G | GCTCCGGG others(68): Show |
1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1005+559_1005+560i others(77): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 122507958 | ||||||
chr10:122507962 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1005+560T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122507962 | |||||||
chr10:122508004 | G | A | 27 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(24): Show |
28 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1005+602G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508004 | |||||||
chr10:122508067 | G | A | 2 | a0002c0003t0001g0085 a0002c0003t0001g0086 |
2 | NA18998.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1006-589G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508067 | |||||||
chr10:122508110 | G | A | 1 | a0001c0001t0006g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1006-546G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508110 | |||||||
chr10:122508114 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1006-542T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508114 | |||||||
chr10:122508235 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(19): Show |
24 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1006-421A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508235 | |||||||
chr10:122508581 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1006-75G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508581 | |||||||
chr10:122508609 | C | T | 1 | a0001c0002t0001g0245 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1006-47C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508609 | |||||||
chr10:122508636 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1006-20G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 5/8 | chr10 | 122508636 | |||||||
chr10:122508881 | G | A | 27 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(24): Show |
28 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1120+111G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122508881 | |||||||
chr10:122508885 | C | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(96): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1120+115C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122508885 | |||||||
chr10:122508948 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1120+178A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122508948 | |||||||
chr10:122508968 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1120+198A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122508968 | |||||||
chr10:122508994 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1120+224A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122508994 | |||||||
chr10:122509009 | G | A | 3 | a0001c0001t0001g0331 a0001c0001t0001g0332 a0001c0001t0001g0333 |
3 | HG02683.hp1 HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1120+239G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509009 | |||||||
chr10:122509024 | G | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(326): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1120+254G>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509024 | |||||||
chr10:122509116 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1120+346G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509116 | |||||||
chr10:122509228 | C | T | 1 | a0001c0002t0001g0278 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1120+458C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509228 | |||||||
chr10:122509239 | T | C | 27 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(24): Show |
28 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1120+469T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509239 | |||||||
chr10:122509265 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1120+495C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509265 | |||||||
chr10:122509285 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1120+515A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509285 | |||||||
chr10:122509286 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1120+516C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509286 | |||||||
chr10:122509316 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1120+546C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509316 | |||||||
chr10:122509432 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0154 others(5): Show |
8 | HG00733.hp2 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120+662G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509432 | |||||||
chr10:122509565 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1121-531C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509565 | |||||||
chr10:122509586 | G | A | 2 | a0001c0002t0001g0274 a0001c0002t0001g0292 |
2 | NA18953.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1121-510G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509586 | |||||||
chr10:122509674 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1121-422G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509674 | |||||||
chr10:122509678 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121-418G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122509678 | |||||||
chr10:122510011 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1121-85G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 6/8 | chr10 | 122510011 | |||||||
chr10:122510276 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1178+123T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510276 | |||||||
chr10:122510302 | C | G | 27 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(24): Show |
28 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1178+149C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510302 | |||||||
chr10:122510440 | C | T | 1 | a0005c0010t0001g0304 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1178+287C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510440 | |||||||
chr10:122510499 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1178+346A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510499 | |||||||
chr10:122510508 | C | G | 1 | a0001c0002t0001g0290 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1178+355C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510508 | |||||||
chr10:122510578 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1178+425C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510578 | |||||||
chr10:122510579 | G | A | 2 | a0001c0001t0001g0152 a0001c0002t0001g0297 |
2 | NA18992.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1178+426G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510579 | |||||||
chr10:122510607 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1178+454C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510607 | |||||||
chr10:122510608 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1178+455G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510608 | |||||||
chr10:122510728 | A | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1178+575A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510728 | |||||||
chr10:122510940 | TAA | T | 27 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0152 others(24): Show |
28 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1178+789_1178+790d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122510940 | ||||||
chr10:122510993 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1178+840G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510993 | |||||||
chr10:122510998 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1178+845G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122510998 | |||||||
chr10:122511069 | T | G | 2 | a0001c0002t0001g0235 a0001c0013t0001g0170 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1179-901T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511069 | |||||||
chr10:122511133 | A | G | 231 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1179-837A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511133 | |||||||
chr10:122511199 | A | G | 2 | a0001c0001t0001g0110 a0001c0002t0001g0165 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1179-771A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511199 | |||||||
chr10:122511273 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1179-697A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511273 | |||||||
chr10:122511335 | C | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(176): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1179-635C>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511335 | |||||||
chr10:122511372 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1179-598G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511372 | |||||||
chr10:122511441 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1179-529C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511441 | |||||||
chr10:122511605 | C | T | 1 | a0001c0001t0001g0341 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1179-365C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511605 | |||||||
chr10:122511636 | G | A | 51 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0024 others(48): Show |
53 | HG00099.hp1 HG00280.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1179-334G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511636 | |||||||
chr10:122511696 | G | A | 3 | a0001c0005t0001g0002 a0001c0005t0001g0133 a0001c0005t0001g0334 |
5 | HG01975.hp1 HG02602.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179-274G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511696 | |||||||
chr10:122511732 | CA | C | 26 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0103 others(23): Show |
27 | HG00323.hp2 HG01358.hp1 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.1179-225delA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122511732 | ||||||
chr10:122511732 | CAA | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1179-226_1179-225d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122511732 | ||||||
chr10:122511736 | AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0001g0282 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1179-225_1179-212d others(16): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122511736 | ||||||
chr10:122511737 | AAAAAAAA others(6): Show |
A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(94): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1179-216_1179-204d others(15): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122511737 | ||||||
chr10:122511738 | AAAAAAAA others(5): Show |
A | 1 | a0001c0002t0001g0276 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1179-224_1179-213d others(14): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122511738 | ||||||
chr10:122511742 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1179-228A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511742 | |||||||
chr10:122511744 | A | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1179-226A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511744 | |||||||
chr10:122511746 | T | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0112 a0001c0001t0001g0123 others(17): Show |
22 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1179-224T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511746 | |||||||
chr10:122511750 | T | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0095 others(21): Show |
26 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1179-220T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511750 | |||||||
chr10:122511754 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1179-216A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511754 | |||||||
chr10:122511755 | A | T | 2 | a0001c0001t0001g0211 a0001c0002t0001g0270 |
2 | HG02129.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1179-215A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511755 | |||||||
chr10:122511759 | T | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0326 a0001c0001t0001g0327 others(4): Show |
7 | HG01433.hp2 HG01496.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1179-211T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511759 | |||||||
chr10:122511761 | AAT | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1179-207_1179-206d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 122511761 | ||||||
chr10:122511763 | T | A | 3 | a0001c0001t0001g0095 a0001c0001t0002g0173 a0001c0002t0001g0169 |
3 | HG03486.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1179-207T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511763 | |||||||
chr10:122511764 | A | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0112 others(18): Show |
23 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1179-206A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511764 | |||||||
chr10:122511818 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1179-152C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 7/8 | chr10 | 122511818 | |||||||
chr10:122512079 | G | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1274+14G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512079 | |||||||
chr10:122512194 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1274+129C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512194 | |||||||
chr10:122512470 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1274+405C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512470 | |||||||
chr10:122512512 | T | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0003c0006t0001g0317 |
3 | HG01175.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1274+447T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512512 | |||||||
chr10:122512593 | G | T | 231 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1274+528G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512593 | |||||||
chr10:122512618 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1274+553T>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512618 | |||||||
chr10:122512651 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1274+586A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512651 | |||||||
chr10:122512675 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1274+610G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512675 | |||||||
chr10:122512675 | G | T | 49 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(46): Show |
52 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.1274+610G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512675 | |||||||
chr10:122512914 | C | T | 25 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0205 others(22): Show |
26 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.1274+849C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512914 | |||||||
chr10:122512952 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1274+887T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512952 | |||||||
chr10:122512994 | A | C | 2 | a0001c0001t0001g0320 a0002c0003t0001g0089 |
2 | HG02083.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1274+929A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122512994 | |||||||
chr10:122513028 | T | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(46): Show |
52 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.1274+963T>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513028 | |||||||
chr10:122513101 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1274+1036A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513101 | |||||||
chr10:122513183 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1275-1008C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513183 | |||||||
chr10:122513192 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0178 a0002c0003t0001g0058 |
4 | NA18966.hp1 NA18989.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275-999G>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513192 | |||||||
chr10:122513199 | C | T | 1 | a0002c0003t0001g0071 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1275-992C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513199 | |||||||
chr10:122513321 | A | G | 1 | a0001c0001t0001g0342 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1275-870A>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513321 | |||||||
chr10:122513489 | G | A | 1 | a0002c0003t0001g0083 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1275-702G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513489 | |||||||
chr10:122513628 | CA | C | 21 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0035 others(18): Show |
23 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.1275-538delA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513628 | ||||||
chr10:122513628 | CAA | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(167): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1275-539_1275-538d others(4): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513628 | ||||||
chr10:122513628 | CAAA | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(89): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1275-540_1275-538d others(5): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513628 | ||||||
chr10:122513628 | CAAAA | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(45): Show |
51 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.1275-541_1275-538d others(6): Show |
HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513628 | ||||||
chr10:122513671 | C | T | 2 | a0001c0001t0003g0195 a0001c0001t0003g0210 |
2 | NA18966.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1275-520C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513671 | |||||||
chr10:122513677 | T | TA | 27 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0185 others(24): Show |
28 | HG01358.hp1 HG02129.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1275-503dupA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513677 | ||||||
chr10:122513677 | TA | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
79 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1275-503delA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513677 | ||||||
chr10:122513698 | G | A | 2 | a0001c0004t0001g0312 a0001c0004t0001g0314 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1275-493G>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513698 | |||||||
chr10:122513737 | TA | T | 3 | a0001c0001t0001g0213 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG00741.hp1 HG01928.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1275-453delA | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513737 | |||||||
chr10:122513750 | A | C | 1 | a0001c0001t0006g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1275-441A>C | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513750 | |||||||
chr10:122513842 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1275-349C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513842 | |||||||
chr10:122513893 | CT | C | 173 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(170): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1275-281delT | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 122513893 | ||||||
chr10:122513969 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1275-222C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122513969 | |||||||
chr10:122514076 | C | A | 1 | a0001c0002t0001g0234 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1275-115C>A | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122514076 | |||||||
chr10:122514077 | A | T | 1 | a0001c0002t0001g0234 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1275-114A>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122514077 | |||||||
chr10:122514096 | T | G | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1275-95T>G | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122514096 | |||||||
chr10:122514155 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
111 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.1275-36C>T | HTRA1 | ENSG00000166033.13 | transcript | ENST00000368984.8 | protein_coding | 8/8 | chr10 | 122514155 |