Item | Value |
---|---|
geneid | 83548 |
ensemblid | ENSG00000136152.15 |
hgncid | 18619 |
symbol | COG3 |
name | component of oligomeric golgi complex 3 |
refseq_nuc | NM_031431.4 |
refseq_prot | NP_113619.3 |
ensembl_nuc | ENST00000349995.10 |
ensembl_prot | ENSP00000258654.8 |
mane_status | MANE Select |
chr | chr13 |
start | 45464939 |
end | 45536701 |
strand | + |
ver | v1.2 |
region | chr13:45464939-45536701 |
region5000 | chr13:45459939-45541701 |
regionname0 | COG3_chr13_45464939_45536701 |
regionname5000 | COG3_chr13_45459939_45541701 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 828 | 209 | 37 | 47 | 100 | 4 | 21 | 79 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0002 | 1/0 | 828 | 119 | 41 | 19 | 42 | 4 | 12 | 26 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0003 | 0/0 | 828 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0004 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0005 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0006 | 0/0 | 828 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0007 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
a0008 | 0/1 | 828 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | MAEAA others(823): Show |
chr13 | 45459939 | 45541701 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2484 | 104 | 9 | 20 | 59 | 2 | 14 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0001c0002 | 0/0 | 2484 | 99 | 27 | 26 | 40 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0001c0008 | 0/0 | 2484 | 2 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0001c0010 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0001c0011 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0001c0014 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0001c0015 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0002c0003 | 0/0 | 2484 | 64 | 21 | 10 | 24 | 2 | 7 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0002c0004 | 1/0 | 2484 | 30 | 2 | 5 | 16 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0002c0005 | 0/0 | 2484 | 16 | 10 | 3 | 2 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0002c0007 | 0/0 | 2484 | 7 | 6 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0002c0012 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0002c0016 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0003c0006 | 0/0 | 2484 | 8 | 8 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0004c0009 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0005c0019 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0006c0018 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0007c0017 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 | ||
a0008c0013 | 0/1 | 2484 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | ATGGC others(2479): Show |
chr13 | 45459939 | 45541701 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4555 | 100 | 9 | 18 | 57 | 2 | 14 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0001t0005 | 0/0 | 4555 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0001t0006 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0001t0008 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0002t0001 | 0/0 | 4555 | 97 | 26 | 25 | 40 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0002t0007 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0002t0009 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0008t0001 | 0/0 | 4555 | 2 | 0 | 1 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0010t0001 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0011t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0014t0004 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0001c0015t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0003t0002 | 0/0 | 4555 | 64 | 21 | 10 | 24 | 2 | 7 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0004t0001 | 1/0 | 4555 | 29 | 2 | 5 | 15 | 2 | 4 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0004t0010 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0005t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0005t0003 | 0/0 | 4553 | 11 | 7 | 2 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4548): Show |
chr13 | 45459939 | 45541701 |
a0002c0005t0011 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0005t0012 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0005t0013 | 0/0 | 4553 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4548): Show |
chr13 | 45459939 | 45541701 |
a0002c0005t0014 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0007t0002 | 0/0 | 4555 | 7 | 6 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0012t0001 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0002c0016t0003 | 0/0 | 4553 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4548): Show |
chr13 | 45459939 | 45541701 |
a0003c0006t0004 | 0/0 | 4555 | 7 | 7 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0003c0006t0015 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0004c0009t0001 | 0/0 | 4555 | 2 | 2 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0005c0019t0001 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0006c0018t0001 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0007c0017t0001 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
a0008c0013t0001 | 0/1 | 4555 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | GCAGT others(4550): Show |
chr13 | 45459939 | 45541701 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0007g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0002t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0008t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0010t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0011t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0014t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0001c0015t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0004t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0013g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0005t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0007t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0012t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0002c0016t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0003c0006t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0004c0009t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0004c0009t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0005c0019t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0006c0018t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0007c0017t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
a0008c0013t0001g0316 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0273 | EUR | GBR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00280 | hp1 | a0002 | c0004 | t0001 | g0028 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00280 | hp2 | a0002 | c0003 | t0002 | g0171 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0144 | EUR | FIN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00408 | hp1 | a0002 | c0005 | t0003 | g0158 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00423 | hp1 | a0002 | c0003 | t0002 | g0162 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00597 | hp1 | a0002 | c0004 | t0010 | g0027 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00597 | hp2 | a0002 | c0003 | t0002 | g0190 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00609 | hp1 | a0002 | c0003 | t0002 | g0173 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00621 | hp1 | a0002 | c0003 | t0002 | g0169 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00639 | hp1 | a0002 | c0005 | t0003 | g0004 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00642 | hp1 | a0002 | c0004 | t0001 | g0019 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00738 | hp1 | a0001 | c0002 | t0007 | g0304 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00738 | hp2 | a0001 | c0008 | t0001 | g0120 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01069 | hp1 | a0002 | c0003 | t0002 | g0007 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01070 | hp2 | a0002 | c0003 | t0002 | g0178 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0007 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0235 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0207 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01109 | hp2 | a0002 | c0003 | t0002 | g0208 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01192 | hp1 | a0002 | c0007 | t0002 | g0224 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01243 | hp1 | a0002 | c0005 | t0003 | g0004 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01256 | hp1 | a0002 | c0004 | t0001 | g0021 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0329 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0030 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0061 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01258 | hp1 | a0002 | c0004 | t0001 | g0022 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0060 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01261 | hp1 | a0002 | c0004 | t0001 | g0034 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0218 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01496 | hp1 | a0002 | c0003 | t0002 | g0187 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01496 | hp2 | a0002 | c0003 | t0002 | g0216 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01516 | hp1 | a0002 | c0004 | t0001 | g0014 | EUR | IBS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0242 | EUR | IBS | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0165 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01934 | hp2 | a0002 | c0003 | t0002 | g0217 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01975 | hp1 | a0002 | c0005 | t0013 | g0154 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0318 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | PEL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02015 | hp1 | a0002 | c0005 | t0003 | g0159 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02015 | hp2 | a0002 | c0004 | t0001 | g0012 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02040 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02055 | hp2 | a0002 | c0003 | t0002 | g0161 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02056 | hp2 | a0002 | c0003 | t0002 | g0181 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02074 | hp1 | a0002 | c0004 | t0001 | g0026 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02129 | hp1 | a0005 | c0019 | t0001 | g0070 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02129 | hp2 | a0002 | c0004 | t0001 | g0015 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02132 | hp1 | a0002 | c0003 | t0002 | g0167 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02145 | hp1 | a0002 | c0003 | t0002 | g0211 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02165 | hp1 | a0002 | c0004 | t0001 | g0025 | EAS | CDX | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02257 | hp1 | a0002 | c0007 | t0002 | g0226 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02280 | hp1 | a0002 | c0003 | t0002 | g0164 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02280 | hp2 | a0002 | c0003 | t0002 | g0214 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02523 | hp1 | a0002 | c0003 | t0002 | g0186 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02572 | hp1 | a0002 | c0005 | t0003 | g0153 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02572 | hp2 | a0002 | c0007 | t0002 | g0223 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0188 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02615 | hp1 | a0002 | c0005 | t0003 | g0152 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02615 | hp2 | a0004 | c0009 | t0001 | g0023 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02622 | hp1 | a0002 | c0003 | t0002 | g0234 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02630 | hp2 | a0003 | c0006 | t0015 | g0200 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0231 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02647 | hp2 | a0002 | c0003 | t0002 | g0212 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02683 | hp2 | a0002 | c0003 | t0002 | g0176 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02698 | hp2 | a0002 | c0005 | t0001 | g0312 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02717 | hp1 | a0003 | c0006 | t0004 | g0197 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02717 | hp2 | a0002 | c0003 | t0002 | g0215 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02723 | hp1 | a0002 | c0005 | t0003 | g0192 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0253 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02818 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02895 | hp2 | a0003 | c0006 | t0004 | g0196 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02896 | hp2 | a0002 | c0007 | t0002 | g0228 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02897 | hp1 | a0003 | c0006 | t0004 | g0195 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02922 | hp1 | a0002 | c0016 | t0003 | g0156 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02965 | hp2 | a0002 | c0005 | t0003 | g0155 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02976 | hp2 | a0002 | c0003 | t0002 | g0219 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03041 | hp1 | a0002 | c0007 | t0002 | g0232 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03041 | hp2 | a0002 | c0003 | t0002 | g0233 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03098 | hp1 | a0003 | c0006 | t0004 | g0198 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03098 | hp2 | a0002 | c0005 | t0003 | g0157 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03139 | hp1 | a0002 | c0005 | t0012 | g0148 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03139 | hp2 | a0001 | c0014 | t0004 | g0194 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03209 | hp2 | a0002 | c0003 | t0002 | g0222 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03225 | hp1 | a0002 | c0005 | t0014 | g0206 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03225 | hp2 | a0002 | c0007 | t0002 | g0227 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03239 | hp1 | a0001 | c0008 | t0001 | g0042 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03453 | hp1 | a0002 | c0007 | t0002 | g0225 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03453 | hp2 | a0002 | c0003 | t0002 | g0210 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03486 | hp1 | a0002 | c0003 | t0002 | g0209 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03486 | hp2 | a0003 | c0006 | t0004 | g0193 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03491 | hp1 | a0002 | c0003 | t0002 | g0174 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0175 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03516 | hp1 | a0002 | c0004 | t0001 | g0038 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | ESN | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03540 | hp1 | a0002 | c0003 | t0002 | g0202 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0236 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03669 | hp1 | a0002 | c0004 | t0001 | g0011 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03831 | hp1 | a0002 | c0003 | t0002 | g0238 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03942 | hp2 | a0002 | c0004 | t0001 | g0031 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04184 | hp2 | a0006 | c0018 | t0001 | g0308 | SAS | BEB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04199 | hp1 | a0002 | c0004 | t0001 | g0016 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04204 | hp2 | a0001 | c0015 | t0001 | g0261 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04228 | hp1 | a0001 | c0011 | t0001 | g0246 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG04228 | hp2 | a0002 | c0004 | t0001 | g0029 | SAS | STU | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18522 | hp2 | a0002 | c0005 | t0011 | g0150 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18612 | hp1 | a0002 | c0003 | t0002 | g0172 | EAS | CHB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18906 | hp1 | a0002 | c0003 | t0002 | g0237 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18939 | hp2 | a0002 | c0003 | t0002 | g0184 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18945 | hp1 | a0001 | c0010 | t0001 | g0128 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18945 | hp2 | a0002 | c0003 | t0002 | g0177 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18949 | hp1 | a0002 | c0003 | t0002 | g0166 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18950 | hp1 | a0002 | c0004 | t0001 | g0020 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0160 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18971 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18979 | hp1 | a0002 | c0004 | t0001 | g0033 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18982 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18984 | hp1 | a0007 | c0017 | t0001 | g0298 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18991 | hp2 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18994 | hp1 | a0002 | c0003 | t0002 | g0182 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18997 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18998 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18999 | hp1 | a0002 | c0004 | t0001 | g0032 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19001 | hp1 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19002 | hp2 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19010 | hp2 | a0002 | c0004 | t0001 | g0017 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19011 | hp2 | a0002 | c0003 | t0002 | g0189 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19012 | hp2 | a0002 | c0003 | t0002 | g0180 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0324 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19043 | hp2 | a0002 | c0003 | t0002 | g0240 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19066 | hp2 | a0002 | c0003 | t0002 | g0183 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19077 | hp1 | a0002 | c0003 | t0002 | g0006 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19082 | hp1 | a0002 | c0003 | t0002 | g0170 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19085 | hp2 | a0002 | c0003 | t0002 | g0185 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19087 | hp1 | a0002 | c0004 | t0001 | g0018 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19089 | hp2 | a0002 | c0003 | t0002 | g0191 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA19240 | hp2 | a0002 | c0003 | t0002 | g0213 | AFR | YRI | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA20129 | hp1 | a0002 | c0003 | t0002 | g0163 | AFR | ASW | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA20905 | hp1 | a0002 | c0003 | t0002 | g0179 | SAS | GIH | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | GIH | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | CLM | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02109 | hp1 | a0004 | c0009 | t0001 | g0024 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG02559 | hp2 | a0003 | c0006 | t0004 | g0199 | AFR | ACB | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03471 | hp1 | a0001 | c0002 | t0009 | g0291 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG03471 | hp2 | a0002 | c0005 | t0003 | g0010 | AFR | MSL | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG06807 | hp1 | a0002 | c0003 | t0002 | g0221 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
HG06807 | hp2 | a0002 | c0012 | t0001 | g0102 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18955 | hp1 | a0002 | c0003 | t0002 | g0168 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA20300 | hp1 | a0002 | c0005 | t0003 | g0151 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | USA | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA21309 | hp1 | a0003 | c0006 | t0004 | g0201 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
NA21309 | hp2 | a0002 | c0003 | t0002 | g0220 | AFR | LWK | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
homoSapiens | chm13v2 | a0008 | c0013 | t0001 | g0316 | REF | REF | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
homoSapiens | grch38p0 | a0002 | c0004 | t0001 | g0039 | REF | REF | COG3_chr13_45459939_45541701 | COG3 | chr13 | 45459939 | 45541701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:45465143 | C | G | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.107C>G | p.Thr36Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/23 | 205/4555 | 107/2487 | 36/828 | chr13 | 45465143 | |||
chr13:45476207 | A | T | 1 | a0006 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.181A>T | p.Ile61Phe | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/23 | 279/4555 | 181/2487 | 61/828 | chr13 | 45476207 | |||
chr13:45480223 | A | G | 1 | a0004 | 2 | HG02109.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.482A>G | p.Gln161Arg | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/23 | 580/4555 | 482/2487 | 161/828 | chr13 | 45480223 | |||
chr13:45486564 | C | G | 1 | a0007 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.913C>G | p.Pro305Ala | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/23 | 1011/4555 | 913/2487 | 305/828 | chr13 | 45486564 | |||
chr13:45529800 | A | G | 5 | a0001 a0003 a0005 others(2): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
missense_variant | MODERATE | c.2240A>G | p.Asn747Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/23 | 2338/4555 | 2240/2487 | 747/828 | chr13 | 45529800 | |||
chr13:45534721 | T | C | 1 | a0003 | 8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.2477T>C | p.Val826Ala | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 2575/4555 | 2477/2487 | 826/828 | chr13 | 45534721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:45481232 | G | A | 1 | a0001c0010 | 1 | NA18945.hp1 | splice_region_variant&synonymous_variant | LOW | c.552G>A | p.Ser184Ser | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/23 | 650/4555 | 552/2487 | 184/828 | chr13 | 45481232 | |||
chr13:45493417 | T | C | 1 | a0001c0011 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1258T>C | p.Leu420Leu | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/23 | 1356/4555 | 1258/2487 | 420/828 | chr13 | 45493417 | |||
chr13:45493458 | G | A | 5 | a0001c0001 a0001c0008 a0001c0010 others(2): Show |
109 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
synonymous_variant | LOW | c.1299G>A | p.Glu433Glu | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/23 | 1397/4555 | 1299/2487 | 433/828 | chr13 | 45493458 | |||
chr13:45496234 | C | T | 1 | a0002c0016 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1410C>T | p.Ile470Ile | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/23 | 1508/4555 | 1410/2487 | 470/828 | chr13 | 45496234 | |||
chr13:45503246 | G | A | 16 | a0001c0001 a0001c0002 a0001c0008 others(13): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
splice_region_variant&synonymous_variant | LOW | c.1491G>A | p.Gln497Gln | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/23 | 1589/4555 | 1491/2487 | 497/828 | chr13 | 45503246 | |||
chr13:45529891 | C | T | 1 | a0001c0015 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.2331C>T | p.Thr777Thr | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/23 | 2429/4555 | 2331/2487 | 777/828 | chr13 | 45529891 | |||
chr13:45530714 | C | T | 2 | a0001c0008 a0002c0007 |
9 | HG00738.hp2 HG01192.hp1 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.2391C>T | p.His797His | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/23 | 2489/4555 | 2391/2487 | 797/828 | chr13 | 45530714 | |||
chr13:45534719 | G | A | 11 | a0001c0001 a0001c0002 a0001c0008 others(8): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
synonymous_variant | LOW | c.2475G>A | p.Leu825Leu | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 2573/4555 | 2475/2487 | 825/828 | chr13 | 45534719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:45464993 | T | C | 1 | a0001c0001t0006 | 1 | NA18974.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/23 | 44 | chr13 | 45464993 | ||||||
chr13:45534829 | G | A | 1 | a0001c0002t0007 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 98 | chr13 | 45534829 | ||||||
chr13:45534891 | T | A | 2 | a0002c0003t0002 a0002c0007t0002 |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 160 | chr13 | 45534891 | ||||||
chr13:45534899 | G | T | 1 | a0003c0006t0015 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 168 | chr13 | 45534899 | ||||||
chr13:45535057 | T | G | 1 | a0001c0001t0005 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 326 | chr13 | 45535057 | ||||||
chr13:45535237 | T | C | 1 | a0001c0001t0008 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*506T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 506 | chr13 | 45535237 | ||||||
chr13:45535308 | T | C | 1 | a0001c0002t0009 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 577 | chr13 | 45535308 | ||||||
chr13:45535532 | G | A | 1 | a0002c0004t0010 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*801G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 801 | chr13 | 45535532 | ||||||
chr13:45535546 | T | C | 2 | a0002c0005t0011 a0002c0005t0012 |
2 | HG03139.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*815T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 815 | chr13 | 45535546 | ||||||
chr13:45536023 | C | A | 1 | a0002c0005t0013 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1292 | chr13 | 45536023 | ||||||
chr13:45536105 | ACT | A | 3 | a0002c0005t0003 a0002c0005t0013 a0002c0016t0003 |
13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1379_*1380delCT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1379 | INFO_REALIGN_3_PRIME | chr13 | 45536105 | |||||
chr13:45536241 | G | T | 1 | a0002c0005t0012 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1510G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1510 | chr13 | 45536241 | ||||||
chr13:45536249 | T | C | 3 | a0001c0014t0004 a0003c0006t0004 a0003c0006t0015 |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1518T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1518 | chr13 | 45536249 | ||||||
chr13:45536487 | A | T | 1 | a0002c0005t0014 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 23/23 | 1756 | chr13 | 45536487 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:45465272 | G | T | 92 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0241 others(89): Show |
94 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.174+62G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465272 | |||||||
chr13:45465363 | C | T | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.174+153C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465363 | |||||||
chr13:45465412 | C | A | 1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.174+202C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465412 | |||||||
chr13:45465651 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.174+441C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465651 | |||||||
chr13:45465674 | G | T | 1 | a0002c0003t0002g0238 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174+464G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465674 | |||||||
chr13:45465726 | G | C | 30 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(27): Show |
34 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+516G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465726 | |||||||
chr13:45465814 | A | G | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+604A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45465814 | |||||||
chr13:45466024 | C | A | 1 | a0001c0002t0001g0241 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.174+814C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466024 | |||||||
chr13:45466072 | C | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+862C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466072 | |||||||
chr13:45466109 | C | T | 1 | a0001c0002t0001g0205 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.174+899C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466109 | |||||||
chr13:45466222 | A | G | 6 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(3): Show |
6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+1012A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466222 | |||||||
chr13:45466256 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+1046C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466256 | |||||||
chr13:45466328 | C | T | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.174+1118C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466328 | |||||||
chr13:45466528 | G | T | 1 | a0002c0007t0002g0232 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.174+1318G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466528 | |||||||
chr13:45466687 | A | G | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.174+1477A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466687 | |||||||
chr13:45466760 | C | T | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.174+1550C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45466760 | |||||||
chr13:45467160 | C | T | 218 | a0001c0001t0001g0149 a0001c0002t0001g0008 a0001c0002t0001g0009 others(215): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.174+1950C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467160 | |||||||
chr13:45467217 | G | A | 1 | a0002c0004t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.174+2007G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467217 | |||||||
chr13:45467221 | A | G | 218 | a0001c0001t0001g0149 a0001c0002t0001g0008 a0001c0002t0001g0009 others(215): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.174+2011A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467221 | |||||||
chr13:45467267 | C | T | 36 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(33): Show |
37 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+2057C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467267 | |||||||
chr13:45467362 | C | A | 50 | a0001c0001t0001g0149 a0002c0003t0002g0005 a0002c0003t0002g0006 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.174+2152C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467362 | |||||||
chr13:45467366 | A | C | 39 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(36): Show |
40 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.174+2156A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467366 | |||||||
chr13:45467516 | C | T | 220 | a0001c0001t0001g0149 a0001c0002t0001g0008 a0001c0002t0001g0009 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.174+2306C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467516 | |||||||
chr13:45467517 | A | G | 220 | a0001c0001t0001g0149 a0001c0002t0001g0008 a0001c0002t0001g0009 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.174+2307A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467517 | |||||||
chr13:45467519 | A | G | 220 | a0001c0001t0001g0149 a0001c0002t0001g0008 a0001c0002t0001g0009 others(217): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.174+2309A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467519 | |||||||
chr13:45467556 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+2346C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467556 | |||||||
chr13:45467597 | A | AAAAAG | 36 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(33): Show |
37 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+2389_174+2390i others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45467597 | ||||||
chr13:45467647 | A | G | 50 | a0001c0001t0001g0149 a0002c0003t0002g0005 a0002c0003t0002g0006 others(47): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.174+2437A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467647 | |||||||
chr13:45467755 | C | T | 30 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(27): Show |
34 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+2545C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45467755 | |||||||
chr13:45468071 | G | T | 43 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0160 others(40): Show |
46 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.174+2861G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468071 | |||||||
chr13:45468349 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.174+3139C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468349 | |||||||
chr13:45468686 | GA | G | 30 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(27): Show |
34 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+3478delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45468686 | ||||||
chr13:45468863 | C | T | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.174+3653C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468863 | |||||||
chr13:45468894 | A | G | 1 | a0002c0003t0002g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.174+3684A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45468894 | |||||||
chr13:45469004 | T | C | 3 | a0001c0002t0001g0008 a0001c0002t0001g0242 a0001c0002t0001g0243 |
4 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+3794T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469004 | |||||||
chr13:45469232 | C | G | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.174+4022C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469232 | |||||||
chr13:45469245 | CAT | C | 3 | a0001c0002t0001g0204 a0001c0002t0001g0329 a0001c0002t0001g0330 |
3 | HG01256.hp2 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.174+4038_174+4039d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45469245 | ||||||
chr13:45469250 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02071.hp1 NA18977.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+4040C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469250 | |||||||
chr13:45469332 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.174+4122G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469332 | |||||||
chr13:45469372 | T | C | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+4162T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469372 | |||||||
chr13:45469459 | A | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.174+4249A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469459 | |||||||
chr13:45469961 | T | C | 1 | a0001c0002t0001g0244 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.174+4751T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45469961 | |||||||
chr13:45470067 | C | G | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.174+4857C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470067 | |||||||
chr13:45470215 | A | G | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.174+5005A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470215 | |||||||
chr13:45470703 | A | G | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+5493A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470703 | |||||||
chr13:45470739 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-5462G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470739 | |||||||
chr13:45470817 | T | G | 1 | a0001c0002t0001g0035 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.175-5384T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470817 | |||||||
chr13:45470869 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175-5332A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470869 | |||||||
chr13:45470926 | C | T | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.175-5275C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470926 | |||||||
chr13:45470952 | C | T | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.175-5249C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470952 | |||||||
chr13:45470996 | A | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-5205A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45470996 | |||||||
chr13:45471123 | G | T | 2 | a0001c0002t0001g0327 a0001c0002t0001g0328 |
2 | HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.175-5078G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471123 | |||||||
chr13:45471242 | GA | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.175-4949delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45471242 | ||||||
chr13:45471246 | A | T | 40 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(37): Show |
42 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.175-4955A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471246 | |||||||
chr13:45471683 | T | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.175-4518T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471683 | |||||||
chr13:45471687 | TGTA | T | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0231 |
3 | HG02647.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.175-4510_175-4508d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45471687 | ||||||
chr13:45471720 | A | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.175-4481A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471720 | |||||||
chr13:45471727 | G | GT | 188 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(185): Show |
193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.175-4464dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45471727 | ||||||
chr13:45471754 | C | T | 1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.175-4447C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471754 | |||||||
chr13:45471881 | C | T | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-4320C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471881 | |||||||
chr13:45471930 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.175-4271G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471930 | |||||||
chr13:45471946 | T | G | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.175-4255T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471946 | |||||||
chr13:45471991 | C | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-4210C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45471991 | |||||||
chr13:45472105 | T | C | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-4096T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472105 | |||||||
chr13:45472106 | G | T | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-4095G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472106 | |||||||
chr13:45472107 | A | T | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-4094A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472107 | |||||||
chr13:45472148 | A | G | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175-4053A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472148 | |||||||
chr13:45472498 | A | G | 1 | a0002c0003t0002g0191 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.175-3703A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472498 | |||||||
chr13:45472705 | C | T | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 |
4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-3496C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472705 | |||||||
chr13:45472746 | C | T | 30 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(27): Show |
30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.175-3455C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472746 | |||||||
chr13:45472893 | G | A | 1 | a0001c0011t0001g0246 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175-3308G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45472893 | |||||||
chr13:45473015 | G | A | 5 | a0001c0002t0001g0247 a0001c0002t0001g0248 a0001c0002t0001g0249 others(2): Show |
5 | HG01069.hp2 HG01081.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-3186G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473015 | |||||||
chr13:45473026 | C | T | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.175-3175C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473026 | |||||||
chr13:45473114 | C | T | 1 | a0002c0003t0002g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.175-3087C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473114 | |||||||
chr13:45473314 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.175-2887A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473314 | |||||||
chr13:45473364 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.175-2837A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473364 | |||||||
chr13:45473408 | C | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-2793C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473408 | |||||||
chr13:45473949 | G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.175-2252G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473949 | |||||||
chr13:45473965 | A | G | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175-2236A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45473965 | |||||||
chr13:45474151 | C | CT | 9 | a0002c0003t0002g0233 a0002c0004t0001g0032 a0002c0004t0001g0033 others(6): Show |
9 | HG01261.hp1 HG02257.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-2026dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | ||||||
chr13:45474151 | C | CTCT | 9 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(6): Show |
9 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-2049_175-2048i others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | ||||||
chr13:45474151 | C | CTT | 8 | a0001c0002t0001g0229 a0002c0003t0002g0163 a0002c0003t0002g0164 others(5): Show |
8 | HG01074.hp2 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-2027_175-2026d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | ||||||
chr13:45474151 | C | CTTT | 51 | a0001c0002t0001g0230 a0002c0003t0002g0005 a0002c0003t0002g0006 others(48): Show |
54 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.175-2028_175-2026d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | ||||||
chr13:45474151 | CTTTTT | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.175-2030_175-2026d others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | ||||||
chr13:45474151 | CTTTTTT | C | 6 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(3): Show |
6 | HG01167.hp1 HG01256.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-2031_175-2026d others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474151 | ||||||
chr13:45474188 | C | T | 2 | a0002c0004t0001g0031 a0002c0004t0001g0034 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.175-2013C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474188 | |||||||
chr13:45474220 | C | T | 5 | a0001c0002t0001g0324 a0002c0005t0003g0157 a0002c0005t0003g0158 others(2): Show |
5 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-1981C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474220 | |||||||
chr13:45474286 | T | G | 1 | a0001c0002t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.175-1915T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474286 | |||||||
chr13:45474332 | T | G | 7 | a0001c0001t0001g0043 a0001c0002t0001g0205 a0001c0002t0001g0257 others(4): Show |
7 | NA18906.hp1 NA18942.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-1869T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474332 | |||||||
chr13:45474361 | A | G | 2 | a0002c0005t0003g0158 a0002c0005t0003g0159 |
2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.175-1840A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474361 | |||||||
chr13:45474414 | A | G | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.175-1787A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474414 | |||||||
chr13:45474433 | A | T | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.175-1768A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474433 | |||||||
chr13:45474437 | C | T | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.175-1764C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474437 | |||||||
chr13:45474478 | A | G | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.175-1723A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474478 | |||||||
chr13:45474484 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.175-1717A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474484 | |||||||
chr13:45474576 | A | G | 2 | a0002c0003t0002g0189 a0002c0003t0002g0190 |
2 | HG00597.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.175-1625A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474576 | |||||||
chr13:45474784 | A | AC | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.175-1416dupC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474784 | ||||||
chr13:45474825 | T | A | 4 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-1376T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474825 | |||||||
chr13:45474864 | T | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(202): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.175-1337T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45474864 | |||||||
chr13:45474946 | A | AGTCT | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.175-1252_175-1249d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45474946 | ||||||
chr13:45475003 | G | A | 4 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1198G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475003 | |||||||
chr13:45475232 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.175-969C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475232 | |||||||
chr13:45475280 | C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175-921C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475280 | |||||||
chr13:45475402 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.175-799C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475402 | |||||||
chr13:45475483 | C | T | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.175-718C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475483 | |||||||
chr13:45475492 | C | T | 1 | a0001c0002t0001g0326 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175-709C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475492 | |||||||
chr13:45475505 | T | C | 1 | a0002c0003t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.175-696T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475505 | |||||||
chr13:45475575 | A | G | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.175-626A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | chr13 | 45475575 | |||||||
chr13:45475964 | CA | C | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.175-222delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr13 | 45475964 | ||||||
chr13:45476384 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.321+37T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476384 | |||||||
chr13:45476523 | A | G | 46 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(43): Show |
49 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.321+176A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476523 | |||||||
chr13:45476610 | T | C | 40 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(37): Show |
42 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.321+263T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476610 | |||||||
chr13:45476711 | T | TA | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.321+370dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 45476711 | ||||||
chr13:45476712 | A | T | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.321+365A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476712 | |||||||
chr13:45476748 | A | G | 1 | a0001c0002t0001g0322 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.321+401A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476748 | |||||||
chr13:45476916 | G | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.321+569G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45476916 | |||||||
chr13:45477144 | C | T | 2 | a0002c0003t0002g0006 a0002c0003t0002g0162 |
3 | HG00423.hp1 NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.321+797C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477144 | |||||||
chr13:45477152 | C | T | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.321+805C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477152 | |||||||
chr13:45477238 | T | C | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.321+891T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477238 | |||||||
chr13:45477259 | G | C | 1 | a0001c0002t0001g0322 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.321+912G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477259 | |||||||
chr13:45477453 | T | C | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.321+1106T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477453 | |||||||
chr13:45477619 | A | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG00558.hp1 NA18949.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.321+1272A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477619 | |||||||
chr13:45477631 | C | CT | 84 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(81): Show |
88 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.321+1298dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 45477631 | ||||||
chr13:45477632 | T | A | 1 | a0001c0015t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.321+1285T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477632 | |||||||
chr13:45477906 | G | A | 1 | a0001c0002t0001g0331 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.322-1099G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477906 | |||||||
chr13:45477916 | A | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.322-1089A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477916 | |||||||
chr13:45477955 | A | C | 4 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-1050A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477955 | |||||||
chr13:45477999 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.322-1006G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45477999 | |||||||
chr13:45478196 | CT | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.322-796delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | 45478196 | ||||||
chr13:45478214 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.322-791C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478214 | |||||||
chr13:45478261 | G | A | 21 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(18): Show |
21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.322-744G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478261 | |||||||
chr13:45478303 | C | T | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-702C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478303 | |||||||
chr13:45478402 | A | G | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.322-603A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478402 | |||||||
chr13:45478470 | C | T | 1 | a0002c0003t0002g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.322-535C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478470 | |||||||
chr13:45478479 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.322-526T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478479 | |||||||
chr13:45478546 | C | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.322-459C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478546 | |||||||
chr13:45478551 | T | G | 1 | a0001c0002t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322-454T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478551 | |||||||
chr13:45478592 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.322-413A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478592 | |||||||
chr13:45478645 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.322-360C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478645 | |||||||
chr13:45478649 | T | C | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.322-356T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478649 | |||||||
chr13:45478732 | G | A | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.322-273G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478732 | |||||||
chr13:45478749 | A | G | 1 | a0002c0004t0001g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-256A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478749 | |||||||
chr13:45478797 | G | A | 21 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(18): Show |
21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.322-208G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 2/22 | chr13 | 45478797 | |||||||
chr13:45479385 | A | AGGAGAAA others(25): Show |
1 | a0001c0002t0001g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.383+320_383+351dup others(32): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr13 | 45479385 | ||||||
chr13:45479409 | T | G | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.383+343T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479409 | |||||||
chr13:45479414 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.383+348A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479414 | |||||||
chr13:45479458 | C | T | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.383+392C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479458 | |||||||
chr13:45479603 | G | A | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.384-522G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 3/22 | chr13 | 45479603 | |||||||
chr13:45480489 | G | A | 1 | a0002c0004t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.549+199G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480489 | |||||||
chr13:45480534 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.549+244A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480534 | |||||||
chr13:45480668 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0145 |
2 | HG02165.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.549+378C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480668 | |||||||
chr13:45480765 | C | T | 3 | a0001c0002t0001g0318 a0001c0002t0001g0319 a0001c0002t0001g0320 |
3 | HG01123.hp2 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.550-465C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480765 | |||||||
chr13:45480918 | A | C | 1 | a0001c0010t0001g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.550-312A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45480918 | |||||||
chr13:45481068 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.550-162T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45481068 | |||||||
chr13:45481090 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG00544.hp2 HG00621.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.550-140G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 4/22 | chr13 | 45481090 | |||||||
chr13:45481342 | T | A | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.624+38T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481342 | |||||||
chr13:45481660 | T | C | 44 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(41): Show |
47 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.624+356T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481660 | |||||||
chr13:45481798 | A | G | 1 | a0001c0002t0001g0317 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.624+494A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481798 | |||||||
chr13:45481837 | AG | A | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.624+534delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45481837 | |||||||
chr13:45482125 | A | G | 1 | a0001c0002t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.625-256A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482125 | |||||||
chr13:45482213 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.625-168C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482213 | |||||||
chr13:45482245 | A | G | 1 | a0002c0003t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.625-136A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482245 | |||||||
chr13:45482348 | A | G | 4 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-33A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 5/22 | chr13 | 45482348 | |||||||
chr13:45482674 | T | A | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.717+201T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482674 | |||||||
chr13:45482778 | C | T | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.717+305C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482778 | |||||||
chr13:45482816 | T | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.717+343T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482816 | |||||||
chr13:45482852 | A | G | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 |
4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-378A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45482852 | |||||||
chr13:45483020 | G | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.718-210G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45483020 | |||||||
chr13:45483071 | T | C | 1 | a0001c0002t0001g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.718-159T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45483071 | |||||||
chr13:45483151 | G | A | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.718-79G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 6/22 | chr13 | 45483151 | |||||||
chr13:45483374 | A | G | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+19A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483374 | |||||||
chr13:45483422 | A | C | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.843+67A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483422 | |||||||
chr13:45483522 | A | G | 6 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(3): Show |
6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+167A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483522 | |||||||
chr13:45483584 | C | T | 53 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.843+229C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483584 | |||||||
chr13:45483633 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.843+278A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483633 | |||||||
chr13:45483637 | C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843+282C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483637 | |||||||
chr13:45483876 | A | C | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.843+521A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45483876 | |||||||
chr13:45484176 | T | G | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.843+821T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484176 | |||||||
chr13:45484234 | T | A | 9 | a0001c0002t0001g0264 a0002c0003t0002g0216 a0002c0007t0002g0223 others(6): Show |
9 | HG01192.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.843+879T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484234 | |||||||
chr13:45484371 | GAGGGATG others(7): Show |
G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.843+1017_843+1030d others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484371 | |||||||
chr13:45484460 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843+1105A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484460 | |||||||
chr13:45484513 | A | G | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843+1158A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484513 | |||||||
chr13:45484574 | TTGCTTAT others(3): Show |
T | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.843+1221_843+1230d others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45484574 | ||||||
chr13:45484577 | CTTAT | C | 18 | a0001c0001t0001g0095 a0001c0001t0001g0125 a0001c0001t0001g0142 others(15): Show |
19 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.843+1257_843+1260d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45484577 | ||||||
chr13:45484577 | CTTATTTA others(1): Show |
C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.843+1253_843+1260d others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45484577 | ||||||
chr13:45484608 | A | T | 1 | a0002c0004t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.843+1253A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484608 | |||||||
chr13:45484683 | G | A | 40 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(37): Show |
42 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.843+1328G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484683 | |||||||
chr13:45484807 | C | G | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+1452C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484807 | |||||||
chr13:45484856 | C | A | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.843+1501C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484856 | |||||||
chr13:45484873 | C | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.843+1518C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45484873 | |||||||
chr13:45485001 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.844-1494C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485001 | |||||||
chr13:45485005 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.844-1490C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485005 | |||||||
chr13:45485013 | C | T | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844-1482C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485013 | |||||||
chr13:45485076 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.844-1419T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485076 | |||||||
chr13:45485158 | C | T | 2 | a0002c0005t0003g0158 a0002c0005t0003g0159 |
2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.844-1337C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485158 | |||||||
chr13:45485176 | G | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.844-1319G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485176 | |||||||
chr13:45485178 | C | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.844-1317C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485178 | |||||||
chr13:45485191 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.844-1304C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485191 | |||||||
chr13:45485224 | A | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1271A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485224 | |||||||
chr13:45485224 | A | G | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-1271A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485224 | |||||||
chr13:45485228 | G | A | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.844-1267G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485228 | |||||||
chr13:45485242 | C | G | 47 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(44): Show |
50 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.844-1253C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485242 | |||||||
chr13:45485257 | T | C | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1238T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485257 | |||||||
chr13:45485270 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1225C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485270 | |||||||
chr13:45485284 | A | AC | 33 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(30): Show |
34 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-1211_844-1210i others(3): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485284 | |||||||
chr13:45485285 | A | C | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1210A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485285 | |||||||
chr13:45485307 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.844-1188A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485307 | |||||||
chr13:45485311 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1184C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485311 | |||||||
chr13:45485312 | A | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.844-1183A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485312 | |||||||
chr13:45485319 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(143): Show |
148 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.844-1176T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485319 | |||||||
chr13:45485381 | G | A | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1114G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485381 | |||||||
chr13:45485384 | C | CGGGGCGG others(772): Show |
1 | a0002c0004t0001g0033 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485384 | ||||||
chr13:45485384 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1111C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485384 | |||||||
chr13:45485389 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1106C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485389 | |||||||
chr13:45485401 | C | G | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1094C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485401 | |||||||
chr13:45485402 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1093G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485402 | |||||||
chr13:45485402 | G | GGAGGGCT others(365): Show |
1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(365): Show |
1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(365): Show |
24 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(21): Show |
25 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(365): Show |
3 | a0002c0003t0002g0218 a0002c0003t0002g0219 a0002c0003t0002g0220 |
3 | HG01361.hp2 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.844-1092_844-1091i others(374): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(316): Show |
2 | a0002c0003t0002g0213 a0002c0003t0002g0214 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.844-1092_844-1091i others(325): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(366): Show |
1 | a0002c0003t0002g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.844-1092_844-1091i others(375): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(368): Show |
1 | a0002c0003t0002g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.844-1092_844-1091i others(377): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(368): Show |
1 | a0002c0007t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(377): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGAGGGCT others(369): Show |
1 | a0002c0003t0002g0238 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.844-1092_844-1091i others(378): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(770): Show |
2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(770): Show |
1 | a0002c0004t0001g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(770): Show |
20 | a0002c0004t0001g0001 a0002c0004t0001g0002 a0002c0004t0001g0011 others(17): Show |
24 | HG00280.hp1 HG00642.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(770): Show |
1 | a0001c0002t0001g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(779): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(771): Show |
1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(771): Show |
1 | a0002c0004t0001g0025 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGC others(771): Show |
1 | a0002c0004t0001g0026 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.844-1075_844-1074i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGG others(772): Show |
1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.844-1087_844-1086i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGG others(826): Show |
1 | a0001c0002t0001g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.844-1087_844-1086i others(835): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485402 | G | GGGGGGGG others(776): Show |
1 | a0002c0004t0010g0027 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.844-1087_844-1086i others(785): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485402 | ||||||
chr13:45485403 | G | T | 1 | a0001c0002t0001g0315 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.844-1092G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485403 | |||||||
chr13:45485412 | A | AC | 14 | a0001c0001t0001g0086 a0001c0002t0001g0229 a0001c0002t0001g0230 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.844-1075dupC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACACCCCC others(593): Show |
1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.844-1082_844-1081i others(602): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACC | 17 | a0002c0003t0002g0210 a0002c0003t0002g0211 a0002c0003t0002g0212 others(14): Show |
17 | HG01074.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.844-1076_844-1075d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0002c0004t0001g0034 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0005t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
2 | a0002c0005t0003g0158 a0002c0005t0003g0159 |
2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
2 | a0002c0005t0003g0157 a0002c0016t0003g0156 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
21 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(18): Show |
23 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0002c0003t0002g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(826): Show |
1 | a0002c0003t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(835): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(771): Show |
4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(780): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
2 | a0002c0003t0002g0180 a0002c0003t0002g0181 |
2 | HG02056.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0182 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0002c0003t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
9 | a0001c0014t0004g0194 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
1 | a0002c0003t0002g0184 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0002c0003t0002g0185 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(823): Show |
1 | a0002c0003t0002g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
2 | a0002c0003t0002g0187 a0002c0003t0002g0191 |
2 | HG01496.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(823): Show |
1 | a0002c0003t0002g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(772): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | NA18944.hp2 NA18969.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(674): Show |
1 | a0001c0001t0001g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(683): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
3 | a0001c0002t0001g0266 a0001c0002t0001g0267 a0001c0002t0001g0322 |
3 | HG02965.hp1 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0055 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
72 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0204 others(69): Show |
74 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
2 | a0001c0002t0001g0265 a0001c0002t0001g0305 |
2 | HG02074.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(873): Show |
1 | a0001c0002t0001g0306 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(882): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(772): Show |
65 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0043 others(62): Show |
66 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
5 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG02622.hp2 HG03831.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0139 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0116 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0135 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(772): Show |
1 | a0001c0001t0001g0117 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(781): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(823): Show |
1 | a0001c0002t0001g0260 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(826): Show |
1 | a0006c0018t0001g0308 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(835): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0118 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(775): Show |
1 | a0001c0001t0001g0080 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(784): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
3 | a0001c0002t0001g0262 a0001c0002t0001g0309 a0001c0002t0001g0310 |
3 | HG01175.hp1 HG01993.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(824): Show |
1 | a0001c0002t0001g0255 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(833): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(674): Show |
1 | a0001c0008t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(683): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(675): Show |
1 | a0001c0008t0001g0120 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(684): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(698): Show |
1 | a0001c0015t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(707): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
1 | a0001c0002t0001g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0121 |
2 | HG01099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0132 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(821): Show |
2 | a0001c0002t0001g0327 a0001c0002t0001g0328 |
2 | HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(830): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
2 | a0001c0002t0001g0245 a0002c0005t0001g0312 |
2 | HG02630.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(822): Show |
2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.844-1075_844-1074i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(773): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0123 |
2 | HG04204.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.844-1075_844-1074i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(774): Show |
1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.844-1075_844-1074i others(783): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(823): Show |
1 | a0001c0002t0001g0313 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.844-1075_844-1074i others(832): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(778): Show |
1 | a0001c0001t0001g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.844-1075_844-1074i others(787): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485412 | A | ACCCCCCC others(780): Show |
1 | a0001c0001t0001g0125 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.844-1075_844-1074i others(789): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485412 | ||||||
chr13:45485414 | C | CCCCCCCA others(822): Show |
2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.844-1056_844-1055i others(831): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485414 | ||||||
chr13:45485414 | C | CCCCCCCA others(816): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(825): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485414 | ||||||
chr13:45485414 | C | CCCCCCCA others(820): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(829): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485414 | ||||||
chr13:45485435 | C | CGGGGCGG others(773): Show |
1 | a0001c0001t0001g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485435 | ||||||
chr13:45485439 | G | GCGGCTGG others(773): Show |
1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.844-1056_844-1055i others(782): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485439 | |||||||
chr13:45485440 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.844-1055T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485440 | |||||||
chr13:45485457 | C | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-1038C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485457 | |||||||
chr13:45485516 | G | A | 8 | a0002c0005t0014g0206 a0002c0007t0002g0223 a0002c0007t0002g0224 others(5): Show |
8 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-979G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485516 | |||||||
chr13:45485527 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.844-968C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485527 | |||||||
chr13:45485586 | C | T | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.844-909C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485586 | |||||||
chr13:45485614 | C | T | 1 | a0002c0003t0002g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.844-881C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485614 | |||||||
chr13:45485632 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-863C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485632 | |||||||
chr13:45485636 | G | A | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.844-859G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485636 | |||||||
chr13:45485648 | CAGA | C | 9 | a0001c0014t0004g0194 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-846_844-844del others(3): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485648 | |||||||
chr13:45485654 | C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844-841C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485654 | |||||||
chr13:45485729 | ACGCTCCT others(33): Show |
A | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.844-745_844-706del others(40): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485729 | ||||||
chr13:45485818 | A | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(107): Show |
111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.844-677A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485818 | |||||||
chr13:45485851 | C | T | 30 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(27): Show |
30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.844-644C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485851 | |||||||
chr13:45485865 | T | C | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-630T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485865 | |||||||
chr13:45485894 | A | G | 1 | a0001c0002t0001g0255 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.844-601A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485894 | |||||||
chr13:45485904 | C | CG | 8 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0126 others(5): Show |
8 | HG01099.hp1 HG01192.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-587dupG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45485904 | ||||||
chr13:45485982 | G | T | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-513G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485982 | |||||||
chr13:45485989 | G | A | 2 | a0001c0002t0001g0327 a0001c0002t0001g0328 |
2 | HG01169.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.844-506G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45485989 | |||||||
chr13:45486060 | G | A | 23 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(20): Show |
23 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.844-435G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486060 | |||||||
chr13:45486067 | C | A | 1 | a0001c0002t0001g0305 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.844-428C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486067 | |||||||
chr13:45486068 | G | C | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.844-427G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486068 | |||||||
chr13:45486084 | C | T | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.844-411C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486084 | |||||||
chr13:45486093 | C | T | 9 | a0002c0005t0012g0148 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-402C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486093 | |||||||
chr13:45486106 | T | C | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.844-389T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486106 | |||||||
chr13:45486133 | A | G | 48 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(45): Show |
51 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.844-362A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486133 | |||||||
chr13:45486138 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.844-357C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486138 | |||||||
chr13:45486161 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.844-334C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486161 | |||||||
chr13:45486238 | C | T | 4 | a0001c0002t0001g0203 a0001c0002t0001g0331 a0001c0011t0001g0246 others(1): Show |
4 | HG02080.hp2 HG02698.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-257C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486238 | |||||||
chr13:45486265 | C | A | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.844-230C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486265 | |||||||
chr13:45486265 | C | T | 1 | a0002c0003t0002g0189 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.844-230C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486265 | |||||||
chr13:45486271 | G | C | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-224G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486271 | |||||||
chr13:45486289 | T | TCGGGAGA | 5 | a0002c0004t0001g0011 a0002c0004t0001g0029 a0002c0004t0001g0030 others(2): Show |
5 | HG01257.hp1 HG01261.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-156_844-150dup others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | ||||||
chr13:45486289 | T | TCGGGAGA others(14): Show |
1 | a0002c0004t0001g0012 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.844-170_844-150dup others(21): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | ||||||
chr13:45486289 | TCGGGAGA | T | 10 | a0001c0001t0005g0060 a0001c0001t0005g0061 a0002c0004t0001g0019 others(7): Show |
10 | HG00597.hp1 HG00642.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.844-156_844-150del others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | ||||||
chr13:45486289 | TCGGGAGA others(7): Show |
T | 27 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0054 others(24): Show |
28 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.844-163_844-150del others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | ||||||
chr13:45486289 | TCGGGAGA others(14): Show |
T | 52 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(49): Show |
54 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.844-170_844-150del others(21): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486289 | ||||||
chr13:45486290 | C | G | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-205C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486290 | |||||||
chr13:45486297 | CG | C | 12 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(9): Show |
12 | HG01074.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-195delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | ||||||
chr13:45486297 | CGGGAGAC others(1): Show |
C | 17 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(14): Show |
17 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.844-195_844-188del others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | ||||||
chr13:45486297 | CGGGAGAC others(8): Show |
C | 5 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.844-195_844-181del others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | ||||||
chr13:45486297 | CGGGAGAC others(15): Show |
C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-195_844-174del others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486297 | ||||||
chr13:45486303 | AC | A | 12 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(9): Show |
12 | HG01074.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-191delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486303 | |||||||
chr13:45486308 | A | G | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-187A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486308 | |||||||
chr13:45486310 | AC | A | 29 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(26): Show |
29 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.844-184delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486310 | |||||||
chr13:45486315 | A | G | 13 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(10): Show |
13 | HG01074.hp2 HG01192.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-180A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486315 | |||||||
chr13:45486317 | AC | A | 33 | a0001c0001t0001g0076 a0001c0002t0001g0229 a0001c0002t0001g0230 others(30): Show |
34 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-177delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486317 | |||||||
chr13:45486318 | C | G | 2 | a0002c0007t0002g0224 a0002c0007t0002g0232 |
2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-177C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486318 | |||||||
chr13:45486318 | C | T | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.844-177C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486318 | |||||||
chr13:45486322 | A | G | 29 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(26): Show |
29 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.844-173A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486322 | |||||||
chr13:45486323 | G | A | 2 | a0002c0007t0002g0224 a0002c0007t0002g0232 |
2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-172G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486323 | |||||||
chr13:45486324 | A | G | 2 | a0002c0007t0002g0224 a0002c0007t0002g0232 |
2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-171A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486324 | |||||||
chr13:45486324 | AC | A | 34 | a0001c0001t0001g0076 a0001c0001t0001g0114 a0001c0002t0001g0229 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-170delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486324 | |||||||
chr13:45486325 | C | CGGGAGAC others(6): Show |
1 | a0002c0004t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.844-169_844-157dup others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486325 | ||||||
chr13:45486325 | C | G | 3 | a0002c0003t0002g0208 a0002c0007t0002g0224 a0002c0007t0002g0232 |
3 | HG01109.hp2 HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-170C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486325 | |||||||
chr13:45486325 | CGGGAGAC others(1): Show |
C | 3 | a0001c0002t0001g0264 a0001c0002t0001g0283 a0001c0015t0001g0261 |
3 | HG01891.hp1 HG03209.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.844-167_844-160del others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486325 | ||||||
chr13:45486329 | A | G | 33 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(30): Show |
34 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.844-166A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486329 | |||||||
chr13:45486331 | A | G | 2 | a0002c0007t0002g0224 a0002c0007t0002g0232 |
2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.844-164A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486331 | |||||||
chr13:45486331 | AC | A | 34 | a0001c0001t0001g0076 a0001c0001t0001g0114 a0001c0002t0001g0229 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-163delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486331 | |||||||
chr13:45486332 | C | G | 3 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0232 |
3 | HG01192.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.844-163C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486332 | |||||||
chr13:45486332 | CG | C | 63 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(60): Show |
65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.844-160delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486332 | ||||||
chr13:45486332 | CGGGAGAC others(6): Show |
C | 5 | a0003c0006t0004g0195 a0003c0006t0004g0196 a0003c0006t0004g0197 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-156_844-144del others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486332 | ||||||
chr13:45486336 | A | G | 35 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(32): Show |
36 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-159A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486336 | |||||||
chr13:45486337 | G | A | 1 | a0002c0007t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-158G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486337 | |||||||
chr13:45486338 | A | AGGGAG | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0056 others(6): Show |
9 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | AGGGAGAG others(4): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(25): Show |
29 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | AGGGAGAG others(10): Show |
14 | a0001c0001t0001g0052 a0001c0001t0001g0069 a0001c0001t0001g0075 others(11): Show |
14 | HG00099.hp1 HG01981.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | AGGGAGAG others(16): Show |
7 | a0001c0001t0001g0076 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(23): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | AGGGAGAG others(22): Show |
9 | a0001c0001t0001g0041 a0001c0001t0001g0071 a0001c0001t0001g0072 others(6): Show |
9 | HG00438.hp1 HG01106.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-157_844-156ins others(29): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | AGGGAGAG others(28): Show |
3 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0134 |
3 | HG00558.hp1 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.844-157_844-156ins others(35): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | AGGGAGAG others(34): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0114 |
2 | NA18939.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.844-157_844-156ins others(41): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | A | G | 3 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0232 |
3 | HG01192.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.844-157A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486338 | AC | A | 110 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0063 others(107): Show |
113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.844-156delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486338 | |||||||
chr13:45486339 | C | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0045 others(71): Show |
75 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.844-156C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486339 | |||||||
chr13:45486339 | C | CGGAGA | 16 | a0001c0002t0001g0241 a0001c0002t0001g0256 a0001c0002t0001g0262 others(13): Show |
16 | HG00642.hp2 HG01074.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.844-154_844-153ins others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGA | 38 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0002c0003t0002g0005 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.844-131_844-126dup others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAC others(5): Show |
8 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0255 others(5): Show |
8 | HG00099.hp2 HG00733.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-150_844-149ins others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAC others(12): Show |
2 | a0001c0002t0001g0277 a0001c0002t0001g0317 |
2 | HG00558.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.844-150_844-149ins others(19): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAG others(5): Show |
9 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0014t0004g0194 others(6): Show |
9 | HG01891.hp2 HG01943.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-137_844-126dup others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAG others(11): Show |
9 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0058 others(6): Show |
9 | HG01123.hp1 HG02071.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-143_844-126dup others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAG others(17): Show |
9 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0093 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-149_844-126dup others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAG others(23): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0092 a0001c0001t0001g0130 |
3 | HG01099.hp2 HG01261.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.844-155_844-126dup others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAG others(29): Show |
2 | a0001c0001t0001g0095 a0001c0001t0001g0239 |
2 | HG03491.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.844-126_844-125ins others(36): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | CGGGAGAG others(41): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | HG02056.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.844-126_844-125ins others(48): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr13 | 45486339 | ||||||
chr13:45486339 | C | G | 1 | a0002c0007t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-156C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486339 | |||||||
chr13:45486343 | A | G | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-152A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486343 | |||||||
chr13:45486344 | G | C | 1 | a0001c0001t0001g0059 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.844-151G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486344 | |||||||
chr13:45486345 | A | G | 1 | a0002c0007t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.844-150A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486345 | |||||||
chr13:45486349 | A | G | 34 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(31): Show |
35 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.844-146A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486349 | |||||||
chr13:45486355 | A | G | 28 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(25): Show |
29 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.844-140A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486355 | |||||||
chr13:45486361 | A | G | 21 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(18): Show |
21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.844-134A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 7/22 | chr13 | 45486361 | |||||||
chr13:45486950 | A | T | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.924+375A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45486950 | |||||||
chr13:45486964 | A | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.924+389A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45486964 | |||||||
chr13:45486979 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.924+404T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45486979 | |||||||
chr13:45487021 | A | G | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.924+446A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487021 | |||||||
chr13:45487258 | A | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.924+683A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487258 | |||||||
chr13:45487412 | T | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.924+837T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487412 | |||||||
chr13:45487695 | C | T | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0231 |
3 | HG02647.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.924+1120C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487695 | |||||||
chr13:45487756 | C | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.924+1181C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487756 | |||||||
chr13:45487861 | C | T | 295 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.924+1286C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487861 | |||||||
chr13:45487949 | G | A | 1 | a0002c0003t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.924+1374G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45487949 | |||||||
chr13:45488024 | A | T | 50 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(47): Show |
53 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.924+1449A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488024 | |||||||
chr13:45488034 | A | G | 14 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(11): Show |
14 | HG00558.hp1 HG02080.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.924+1459A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488034 | |||||||
chr13:45488155 | G | A | 109 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(106): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.924+1580G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488155 | |||||||
chr13:45488255 | G | C | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.924+1680G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488255 | |||||||
chr13:45488306 | AG | A | 17 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(14): Show |
17 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.924+1732delG | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488306 | |||||||
chr13:45488334 | C | T | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.924+1759C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488334 | |||||||
chr13:45488359 | C | T | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.924+1784C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488359 | |||||||
chr13:45488370 | G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.924+1795G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488370 | |||||||
chr13:45488394 | G | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.924+1819G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488394 | |||||||
chr13:45488428 | A | C | 49 | a0001c0014t0004g0194 a0002c0003t0002g0005 a0002c0003t0002g0006 others(46): Show |
52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.924+1853A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488428 | |||||||
chr13:45488460 | C | T | 25 | a0002c0004t0001g0001 a0002c0004t0001g0002 a0002c0004t0001g0011 others(22): Show |
29 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.924+1885C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488460 | |||||||
chr13:45488734 | G | C | 48 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(45): Show |
51 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.924+2159G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488734 | |||||||
chr13:45488981 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0081 |
2 | HG01943.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.925-1934A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488981 | |||||||
chr13:45488982 | G | A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0085 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-1933G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45488982 | |||||||
chr13:45489009 | G | A | 1 | a0002c0005t0001g0312 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.925-1906G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489009 | |||||||
chr13:45489055 | G | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.925-1860G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489055 | |||||||
chr13:45489100 | C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.925-1815C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489100 | |||||||
chr13:45489140 | T | C | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.925-1775T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489140 | |||||||
chr13:45489186 | C | CAA | 6 | a0001c0001t0001g0121 a0003c0006t0004g0193 a0003c0006t0004g0195 others(3): Show |
6 | HG01981.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.925-1704_925-1703d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | ||||||
chr13:45489186 | CA | C | 117 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0072 others(114): Show |
119 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.925-1703delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | ||||||
chr13:45489186 | CAA | C | 6 | a0001c0001t0001g0073 a0001c0002t0001g0244 a0001c0002t0001g0256 others(3): Show |
6 | HG01074.hp2 HG02040.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.925-1704_925-1703d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | ||||||
chr13:45489186 | CAAAAAA | C | 70 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(67): Show |
77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.925-1708_925-1703d others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | ||||||
chr13:45489186 | CAAAAAAA | C | 9 | a0002c0003t0002g0179 a0002c0005t0003g0004 a0002c0005t0003g0010 others(6): Show |
10 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.925-1709_925-1703d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489186 | ||||||
chr13:45489213 | G | C | 8 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0155 others(5): Show |
9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.925-1702G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489213 | |||||||
chr13:45489223 | G | A | 49 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0204 others(46): Show |
51 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.925-1692G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489223 | |||||||
chr13:45489262 | C | CAAA | 33 | a0002c0004t0001g0001 a0002c0004t0001g0002 a0002c0004t0001g0011 others(30): Show |
38 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.925-1637_925-1635d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAA | 7 | a0002c0005t0003g0010 a0002c0005t0003g0157 a0002c0005t0003g0158 others(4): Show |
7 | HG00408.hp1 HG02015.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.925-1638_925-1635d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAA | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.925-1639_925-1635d others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAA | 20 | a0002c0003t0002g0007 a0002c0003t0002g0166 a0002c0003t0002g0180 others(17): Show |
21 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.925-1640_925-1635d others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAAA | 12 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(9): Show |
12 | HG01109.hp2 HG01192.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.925-1641_925-1635d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0072 others(8): Show |
11 | HG00099.hp1 HG01167.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.925-1643_925-1635d others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAAA others(3): Show |
132 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(129): Show |
133 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.925-1644_925-1635d others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAAA others(4): Show |
51 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0067 others(48): Show |
52 | HG00544.hp1 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.925-1645_925-1635d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAAA others(5): Show |
18 | a0001c0002t0001g0008 a0001c0002t0001g0242 a0001c0002t0001g0253 others(15): Show |
19 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.925-1646_925-1635d others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489262 | C | CAAAAAAA others(6): Show |
2 | a0001c0002t0001g0271 a0001c0002t0001g0321 |
2 | HG01106.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.925-1647_925-1635d others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489262 | ||||||
chr13:45489362 | A | G | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.925-1553A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489362 | |||||||
chr13:45489819 | A | AT | 40 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(37): Show |
42 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.925-1080dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | ||||||
chr13:45489819 | AT | A | 11 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0211 others(8): Show |
11 | HG01074.hp2 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.925-1080delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | ||||||
chr13:45489819 | ATT | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0119 others(14): Show |
18 | HG01975.hp1 HG01978.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.925-1081_925-1080d others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | ||||||
chr13:45489819 | ATTT | A | 207 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.925-1082_925-1080d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | ||||||
chr13:45489819 | ATTTT | A | 8 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0155 others(5): Show |
9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.925-1083_925-1080d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45489819 | ||||||
chr13:45489882 | A | G | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.925-1033A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489882 | |||||||
chr13:45489947 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.925-968G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45489947 | |||||||
chr13:45490053 | A | G | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.925-862A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490053 | |||||||
chr13:45490209 | G | A | 1 | a0001c0008t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925-706G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490209 | |||||||
chr13:45490337 | A | G | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.925-578A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490337 | |||||||
chr13:45490357 | A | G | 2 | a0001c0002t0001g0299 a0001c0002t0001g0300 |
2 | NA18951.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.925-558A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490357 | |||||||
chr13:45490540 | A | T | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.925-375A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490540 | |||||||
chr13:45490655 | AAAC | A | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.925-258_925-256del others(3): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr13 | 45490655 | ||||||
chr13:45490689 | A | G | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.925-226A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490689 | |||||||
chr13:45490750 | TA | T | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.925-164delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 8/22 | chr13 | 45490750 | |||||||
chr13:45491061 | G | C | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.968+103G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491061 | |||||||
chr13:45491100 | G | A | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.968+142G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491100 | |||||||
chr13:45491108 | C | G | 30 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(27): Show |
30 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.968+150C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491108 | |||||||
chr13:45491132 | T | G | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 |
4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.968+174T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491132 | |||||||
chr13:45491169 | A | T | 1 | a0005c0019t0001g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.968+211A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 9/22 | chr13 | 45491169 | |||||||
chr13:45491583 | A | G | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1095+45A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45491583 | |||||||
chr13:45491699 | C | G | 1 | a0002c0004t0001g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1095+161C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45491699 | |||||||
chr13:45491878 | TA | T | 14 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(11): Show |
15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-275delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr13 | 45491878 | ||||||
chr13:45492028 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1096-131T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45492028 | |||||||
chr13:45492057 | G | A | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1096-102G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 10/22 | chr13 | 45492057 | |||||||
chr13:45492414 | AGTTATTT others(8): Show |
A | 4 | a0002c0005t0003g0157 a0002c0005t0003g0158 a0002c0005t0003g0159 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187+167_1187+181d others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 45492414 | ||||||
chr13:45492438 | TA | T | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1187+190delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr13 | 45492438 | ||||||
chr13:45492464 | G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1187+214G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492464 | |||||||
chr13:45492601 | G | T | 1 | a0001c0002t0001g0325 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1187+351G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492601 | |||||||
chr13:45492691 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1187+441A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492691 | |||||||
chr13:45492707 | A | G | 2 | a0001c0008t0001g0042 a0001c0008t0001g0120 |
2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1187+457A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492707 | |||||||
chr13:45492719 | A | T | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1187+469A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492719 | |||||||
chr13:45492964 | G | T | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188-383G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492964 | |||||||
chr13:45492987 | G | A | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1188-360G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45492987 | |||||||
chr13:45493051 | G | A | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1188-296G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493051 | |||||||
chr13:45493054 | A | G | 1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1188-293A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493054 | |||||||
chr13:45493067 | T | C | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1188-280T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493067 | |||||||
chr13:45493147 | G | A | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1188-200G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493147 | |||||||
chr13:45493192 | G | A | 1 | a0001c0002t0001g0247 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1188-155G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 11/22 | chr13 | 45493192 | |||||||
chr13:45493569 | C | CAGGGAA | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+83_1327+84ins others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493569 | |||||||
chr13:45493570 | C | T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+84C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493570 | |||||||
chr13:45493572 | C | T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+86C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493572 | |||||||
chr13:45493866 | G | GT | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1327+384dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45493866 | ||||||
chr13:45493875 | A | G | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1327+389A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493875 | |||||||
chr13:45493909 | A | G | 4 | a0002c0005t0003g0157 a0002c0005t0003g0158 a0002c0005t0003g0159 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327+423A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493909 | |||||||
chr13:45493961 | C | G | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1327+475C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45493961 | |||||||
chr13:45494018 | A | G | 3 | a0001c0002t0001g0253 a0001c0002t0001g0271 a0001c0002t0001g0273 |
3 | HG00099.hp2 HG01106.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1327+532A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494018 | |||||||
chr13:45494036 | C | G | 1 | a0002c0004t0001g0012 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1327+550C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494036 | |||||||
chr13:45494215 | C | T | 2 | a0001c0002t0001g0279 a0007c0017t0001g0298 |
2 | NA18973.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1327+729C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494215 | |||||||
chr13:45494268 | T | C | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 |
4 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1327+782T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494268 | |||||||
chr13:45494281 | C | T | 37 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(34): Show |
39 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1327+795C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494281 | |||||||
chr13:45494325 | T | TA | 17 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0085 others(14): Show |
17 | HG00738.hp2 HG01978.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1327+858dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494325 | ||||||
chr13:45494325 | TA | T | 16 | a0001c0001t0001g0068 a0002c0003t0002g0219 a0002c0003t0002g0231 others(13): Show |
17 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1327+858delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494325 | ||||||
chr13:45494341 | A | C | 1 | a0002c0003t0002g0178 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1327+855A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494341 | |||||||
chr13:45494348 | C | A | 37 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(34): Show |
39 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1327+862C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494348 | |||||||
chr13:45494462 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1327+976C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494462 | |||||||
chr13:45494616 | C | G | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1327+1130C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494616 | |||||||
chr13:45494765 | G | C | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1327+1279G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494765 | |||||||
chr13:45494864 | C | CT | 207 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1328-1274dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494864 | ||||||
chr13:45494864 | CT | C | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1328-1274delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45494864 | ||||||
chr13:45494871 | T | C | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1328-1281T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494871 | |||||||
chr13:45494914 | C | T | 4 | a0002c0005t0003g0157 a0002c0005t0003g0158 a0002c0005t0003g0159 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328-1238C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494914 | |||||||
chr13:45494915 | G | A | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1328-1237G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494915 | |||||||
chr13:45494980 | G | A | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1328-1172G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494980 | |||||||
chr13:45494997 | C | T | 1 | a0001c0002t0001g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1328-1155C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45494997 | |||||||
chr13:45495063 | C | G | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1328-1089C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495063 | |||||||
chr13:45495068 | T | C | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1328-1084T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495068 | |||||||
chr13:45495122 | C | G | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1328-1030C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495122 | |||||||
chr13:45495145 | CT | C | 287 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(284): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.1328-986delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45495145 | ||||||
chr13:45495145 | CTTTTTTT others(4): Show |
C | 1 | a0002c0005t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1328-996_1328-986d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr13 | 45495145 | ||||||
chr13:45495180 | G | A | 1 | a0002c0003t0002g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1328-972G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495180 | |||||||
chr13:45495241 | G | A | 2 | a0002c0003t0002g0184 a0002c0003t0002g0185 |
2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1328-911G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495241 | |||||||
chr13:45495256 | G | A | 5 | a0003c0006t0004g0195 a0003c0006t0004g0196 a0003c0006t0004g0197 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1328-896G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495256 | |||||||
chr13:45495660 | G | A | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328-492G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495660 | |||||||
chr13:45495769 | C | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1328-383C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495769 | |||||||
chr13:45495786 | A | T | 8 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0155 others(5): Show |
9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1328-366A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 12/22 | chr13 | 45495786 | |||||||
chr13:45496354 | C | T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1488+42C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496354 | |||||||
chr13:45496374 | T | C | 5 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1488+62T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496374 | |||||||
chr13:45496375 | A | AT | 4 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488+70dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45496375 | ||||||
chr13:45496404 | G | A | 3 | a0001c0002t0001g0204 a0001c0002t0001g0329 a0001c0002t0001g0330 |
3 | HG01256.hp2 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1488+92G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496404 | |||||||
chr13:45496653 | T | G | 1 | a0002c0004t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1488+341T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496653 | |||||||
chr13:45496773 | G | A | 4 | a0002c0005t0003g0157 a0002c0005t0003g0158 a0002c0005t0003g0159 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+461G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496773 | |||||||
chr13:45496775 | G | A | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1488+463G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496775 | |||||||
chr13:45496796 | C | T | 2 | a0002c0003t0002g0184 a0002c0003t0002g0185 |
2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1488+484C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496796 | |||||||
chr13:45496814 | C | T | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1488+502C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496814 | |||||||
chr13:45496915 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1488+603C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496915 | |||||||
chr13:45496920 | G | A | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1488+608G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496920 | |||||||
chr13:45496920 | G | C | 1 | a0002c0004t0001g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1488+608G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496920 | |||||||
chr13:45496921 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1488+609C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45496921 | |||||||
chr13:45497034 | G | A | 229 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1488+722G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497034 | |||||||
chr13:45497041 | A | G | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1488+729A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497041 | |||||||
chr13:45497079 | T | C | 8 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0155 others(5): Show |
9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488+767T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497079 | |||||||
chr13:45497085 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1488+773T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497085 | |||||||
chr13:45497191 | C | T | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1488+879C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497191 | |||||||
chr13:45497192 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1488+880G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497192 | |||||||
chr13:45497479 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1488+1167G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497479 | |||||||
chr13:45497591 | C | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1488+1279C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497591 | |||||||
chr13:45497764 | T | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1488+1452T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497764 | |||||||
chr13:45497784 | T | TCAA | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1488+1506_1488+150 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAA | 5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0081 others(2): Show |
5 | HG01943.hp2 HG03225.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1488+1503_1488+150 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAAC others(2): Show |
117 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0045 others(114): Show |
119 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1488+1500_1488+150 others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAAC others(5): Show |
118 | a0001c0001t0001g0041 a0001c0001t0001g0073 a0001c0001t0001g0076 others(115): Show |
120 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1488+1497_1488+150 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAAC others(8): Show |
27 | a0001c0001t0001g0040 a0001c0002t0001g0260 a0001c0002t0001g0287 others(24): Show |
28 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1488+1494_1488+150 others(19): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAAC others(11): Show |
9 | a0002c0003t0002g0005 a0002c0003t0002g0160 a0002c0003t0002g0166 others(6): Show |
10 | HG02040.hp1 HG02132.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1488+1491_1488+150 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAAC others(14): Show |
1 | a0002c0003t0002g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1488+1488_1488+150 others(25): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497784 | T | TCAACAAC others(17): Show |
1 | a0002c0003t0002g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1488+1485_1488+150 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497784 | ||||||
chr13:45497812 | CAACAACA | C | 10 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0005t0003g0004 others(7): Show |
11 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1488+1503_1488+150 others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497812 | ||||||
chr13:45497815 | CAACA | C | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+1506_1488+150 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45497815 | ||||||
chr13:45497845 | G | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1488+1533G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45497845 | |||||||
chr13:45498191 | A | G | 1 | a0002c0007t0002g0228 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1488+1879A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498191 | |||||||
chr13:45498228 | C | T | 7 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1488+1916C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498228 | |||||||
chr13:45498234 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1488+1922A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498234 | |||||||
chr13:45498251 | A | C | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1488+1939A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498251 | |||||||
chr13:45498298 | C | T | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1488+1986C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498298 | |||||||
chr13:45498356 | C | CT | 85 | a0001c0001t0001g0076 a0001c0002t0001g0008 a0001c0002t0001g0009 others(82): Show |
87 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1488+2064dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | ||||||
chr13:45498356 | C | CTT | 10 | a0001c0002t0001g0262 a0001c0002t0001g0274 a0001c0002t0001g0275 others(7): Show |
10 | HG00438.hp2 HG00642.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488+2063_1488+206 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | ||||||
chr13:45498356 | CT | C | 53 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0097 others(50): Show |
56 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1488+2064delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | ||||||
chr13:45498356 | CTT | C | 32 | a0001c0002t0001g0230 a0002c0003t0002g0007 a0002c0003t0002g0167 others(29): Show |
33 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1488+2063_1488+206 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | ||||||
chr13:45498356 | CTTT | C | 7 | a0001c0002t0001g0229 a0002c0003t0002g0233 a0002c0003t0002g0234 others(4): Show |
7 | HG01074.hp2 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1488+2062_1488+206 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498356 | ||||||
chr13:45498385 | G | GTT | 3 | a0002c0004t0001g0019 a0002c0004t0001g0028 a0002c0004t0001g0030 |
3 | HG00280.hp1 HG00642.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1488+2075_1488+207 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45498385 | ||||||
chr13:45498420 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1488+2108C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498420 | |||||||
chr13:45498431 | C | G | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1488+2119C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498431 | |||||||
chr13:45498464 | A | C | 8 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0155 others(5): Show |
9 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488+2152A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498464 | |||||||
chr13:45498711 | G | C | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+2399G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498711 | |||||||
chr13:45498717 | G | A | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1488+2405G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498717 | |||||||
chr13:45498798 | T | TTCC | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+2486_1488+248 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498798 | |||||||
chr13:45498798 | T | TTTC | 59 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(56): Show |
62 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1488+2486_1488+248 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498798 | |||||||
chr13:45498814 | A | G | 24 | a0002c0003t0002g0007 a0002c0003t0002g0202 a0002c0003t0002g0208 others(21): Show |
25 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1488+2502A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45498814 | |||||||
chr13:45499214 | A | G | 1 | a0002c0003t0002g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1488+2902A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499214 | |||||||
chr13:45499325 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1488+3013C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499325 | |||||||
chr13:45499402 | G | A | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1488+3090G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499402 | |||||||
chr13:45499666 | A | G | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1488+3354A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499666 | |||||||
chr13:45499759 | C | T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1488+3447C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499759 | |||||||
chr13:45499760 | G | A | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1488+3448G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499760 | |||||||
chr13:45499851 | A | G | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1489-3393A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499851 | |||||||
chr13:45499885 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1489-3359G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45499885 | |||||||
chr13:45500017 | TAA | T | 10 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(7): Show |
11 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1489-3219_1489-321 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500017 | ||||||
chr13:45500023 | AAAATAT | A | 14 | a0002c0003t0002g0208 a0002c0003t0002g0210 a0002c0003t0002g0213 others(11): Show |
14 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1489-3219_1489-321 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500023 | ||||||
chr13:45500025 | A | T | 275 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1489-3219A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500025 | |||||||
chr13:45500027 | T | C | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3217T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500027 | |||||||
chr13:45500034 | ATATGTAT others(1): Show |
A | 25 | a0002c0003t0002g0144 a0002c0003t0002g0160 a0002c0003t0002g0161 others(22): Show |
25 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1489-3208_1489-320 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500034 | ||||||
chr13:45500036 | A | G | 22 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0163 others(19): Show |
24 | HG00280.hp2 HG00597.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1489-3208A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500036 | |||||||
chr13:45500038 | G | A | 14 | a0002c0003t0002g0208 a0002c0003t0002g0210 a0002c0003t0002g0213 others(11): Show |
14 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1489-3206G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500038 | |||||||
chr13:45500038 | GTA | G | 4 | a0002c0003t0002g0209 a0002c0003t0002g0211 a0002c0003t0002g0212 others(1): Show |
4 | HG02145.hp1 HG02647.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3204_1489-320 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500038 | ||||||
chr13:45500040 | A | G | 29 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0001c0002t0001g0284 others(26): Show |
32 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1489-3204A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500040 | |||||||
chr13:45500040 | ATGTG | A | 4 | a0002c0004t0001g0018 a0002c0004t0001g0033 a0002c0005t0011g0150 others(1): Show |
4 | HG03139.hp1 NA18522.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3181_1489-317 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500040 | ||||||
chr13:45500055 | T | A | 1 | a0001c0002t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1489-3189T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500055 | |||||||
chr13:45500057 | T | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1489-3187T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500057 | |||||||
chr13:45500059 | T | A | 11 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0163 others(8): Show |
13 | HG00280.hp2 HG00597.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489-3185T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500059 | |||||||
chr13:45500061 | T | A | 14 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0007 others(11): Show |
15 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1489-3183T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500061 | |||||||
chr13:45500061 | TGTGTGA | T | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-3177_1489-317 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500061 | ||||||
chr13:45500063 | T | A | 5 | a0002c0003t0002g0217 a0002c0005t0003g0004 a0002c0005t0003g0010 others(2): Show |
6 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1489-3181T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500063 | |||||||
chr13:45500065 | T | A | 5 | a0002c0003t0002g0202 a0002c0005t0003g0157 a0002c0005t0003g0158 others(2): Show |
5 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-3179T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500065 | |||||||
chr13:45500065 | TGA | T | 3 | a0001c0002t0001g0263 a0002c0005t0003g0010 a0002c0005t0003g0192 |
3 | HG02723.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1489-3177_1489-317 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500065 | ||||||
chr13:45500067 | A | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1489-3177A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500067 | |||||||
chr13:45500069 | T | A | 5 | a0002c0004t0001g0030 a0002c0005t0003g0151 a0002c0005t0003g0152 others(2): Show |
5 | HG01257.hp1 HG01975.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-3175T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500069 | |||||||
chr13:45500086 | GTGTGTGT others(5): Show |
G | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1489-3156_1489-314 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500086 | ||||||
chr13:45500088 | GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1489-3154_1489-313 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500088 | ||||||
chr13:45500088 | GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1489-3154_1489-313 others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500088 | ||||||
chr13:45500090 | GTGTGTAT others(11): Show |
G | 2 | a0001c0001t0001g0137 a0002c0012t0001g0102 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1489-3152_1489-313 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500090 | ||||||
chr13:45500092 | G | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1489-3152G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500092 | |||||||
chr13:45500092 | GTGTATAT others(9): Show |
G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0043 others(78): Show |
82 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1489-3150_1489-313 others(20): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500092 | ||||||
chr13:45500092 | GTGTATAT others(11): Show |
G | 1 | a0001c0002t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1489-3150_1489-313 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500092 | ||||||
chr13:45500094 | G | A | 5 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(2): Show |
5 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-3150G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500094 | |||||||
chr13:45500094 | G | GTGTGTGT others(3): Show |
2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1489-3149_1489-314 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTA | G | 26 | a0002c0003t0002g0240 a0002c0004t0001g0001 a0002c0004t0001g0002 others(23): Show |
30 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1489-3129_1489-312 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATA | G | 3 | a0002c0003t0002g0236 a0002c0003t0002g0238 a0002c0005t0012g0148 |
3 | HG03139.hp1 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1489-3131_1489-312 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATATA | G | 15 | a0001c0001t0001g0082 a0001c0002t0001g0205 a0001c0002t0001g0301 others(12): Show |
17 | HG00408.hp1 HG00597.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1489-3133_1489-312 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATATAT others(1): Show |
G | 27 | a0001c0002t0001g0244 a0001c0002t0001g0253 a0001c0002t0001g0264 others(24): Show |
27 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1489-3135_1489-312 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATATAT others(3): Show |
G | 53 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0035 others(50): Show |
55 | HG00280.hp2 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1489-3137_1489-312 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATATAT others(5): Show |
G | 24 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(21): Show |
24 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1489-3139_1489-312 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATATAT others(7): Show |
G | 17 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0054 others(14): Show |
17 | HG00408.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1489-3141_1489-312 others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500094 | GTATATAT others(9): Show |
G | 18 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0002t0001g0252 others(15): Show |
18 | HG01106.hp1 HG02040.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1489-3143_1489-312 others(20): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr13 | 45500094 | ||||||
chr13:45500096 | A | G | 48 | a0001c0002t0001g0263 a0002c0003t0002g0144 a0002c0003t0002g0160 others(45): Show |
48 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1489-3148A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500096 | |||||||
chr13:45500098 | A | G | 49 | a0001c0002t0001g0263 a0002c0003t0002g0144 a0002c0003t0002g0160 others(46): Show |
49 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1489-3146A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500098 | |||||||
chr13:45500100 | A | G | 50 | a0001c0002t0001g0263 a0002c0003t0002g0144 a0002c0003t0002g0160 others(47): Show |
50 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1489-3144A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500100 | |||||||
chr13:45500102 | A | G | 59 | a0001c0001t0001g0082 a0001c0002t0001g0205 a0001c0002t0001g0263 others(56): Show |
61 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1489-3142A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500102 | |||||||
chr13:45500104 | A | G | 66 | a0001c0001t0001g0082 a0001c0002t0001g0205 a0001c0002t0001g0244 others(63): Show |
68 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1489-3140A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500104 | |||||||
chr13:45500106 | A | G | 75 | a0001c0001t0001g0082 a0001c0002t0001g0008 a0001c0002t0001g0009 others(72): Show |
77 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1489-3138A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500106 | |||||||
chr13:45500108 | A | G | 96 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(93): Show |
98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1489-3136A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500108 | |||||||
chr13:45500110 | A | G | 83 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0035 others(80): Show |
85 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1489-3134A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500110 | |||||||
chr13:45500112 | A | G | 3 | a0001c0002t0001g0299 a0001c0002t0001g0300 a0001c0002t0001g0324 |
3 | NA18951.hp1 NA18962.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1489-3132A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500112 | |||||||
chr13:45500117 | A | T | 2 | a0002c0005t0013g0154 a0002c0005t0014g0206 |
2 | HG01975.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1489-3127A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500117 | |||||||
chr13:45500306 | A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1489-2938A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500306 | |||||||
chr13:45500697 | G | A | 16 | a0001c0002t0001g0252 a0001c0002t0001g0255 a0001c0002t0001g0256 others(13): Show |
16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1489-2547G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500697 | |||||||
chr13:45500822 | G | C | 1 | a0001c0002t0001g0294 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1489-2422G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500822 | |||||||
chr13:45500864 | C | T | 14 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(11): Show |
15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1489-2380C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500864 | |||||||
chr13:45500933 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1489-2311C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45500933 | |||||||
chr13:45501158 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1489-2086A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501158 | |||||||
chr13:45501245 | G | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1489-1999G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501245 | |||||||
chr13:45501252 | C | T | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1489-1992C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501252 | |||||||
chr13:45501289 | C | G | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1489-1955C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501289 | |||||||
chr13:45501292 | G | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1489-1952G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501292 | |||||||
chr13:45501389 | G | A | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1489-1855G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501389 | |||||||
chr13:45501390 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1489-1854G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501390 | |||||||
chr13:45501493 | A | G | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1489-1751A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501493 | |||||||
chr13:45501529 | T | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1489-1715T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501529 | |||||||
chr13:45501603 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1489-1641C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45501603 | |||||||
chr13:45502467 | A | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1489-777A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45502467 | |||||||
chr13:45502523 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1489-721G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45502523 | |||||||
chr13:45502960 | C | A | 2 | a0002c0003t0002g0166 a0002c0003t0002g0172 |
2 | NA18612.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1489-284C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45502960 | |||||||
chr13:45503165 | T | C | 1 | a0002c0004t0001g0015 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1489-79T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45503165 | |||||||
chr13:45503166 | G | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1489-78G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 13/22 | chr13 | 45503166 | |||||||
chr13:45503621 | G | A | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1594+272G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45503621 | |||||||
chr13:45503958 | A | G | 2 | a0004c0009t0001g0023 a0004c0009t0001g0024 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1594+609A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45503958 | |||||||
chr13:45503986 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1594+637T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45503986 | |||||||
chr13:45504106 | G | A | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1594+757G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504106 | |||||||
chr13:45504124 | A | G | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+775A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504124 | |||||||
chr13:45504175 | C | T | 1 | a0001c0002t0001g0320 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1594+826C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504175 | |||||||
chr13:45504252 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1594+903T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504252 | |||||||
chr13:45504285 | G | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1594+936G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504285 | |||||||
chr13:45504357 | C | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1594+1008C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504357 | |||||||
chr13:45504408 | C | T | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1594+1059C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504408 | |||||||
chr13:45504419 | C | T | 4 | a0001c0002t0001g0009 a0001c0002t0001g0288 a0001c0002t0001g0313 others(1): Show |
5 | HG01978.hp1 NA18971.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1594+1070C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504419 | |||||||
chr13:45504565 | T | C | 21 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(18): Show |
21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1594+1216T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504565 | |||||||
chr13:45504642 | G | T | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+1293G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504642 | |||||||
chr13:45504788 | G | A | 1 | a0002c0004t0001g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1594+1439G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504788 | |||||||
chr13:45504861 | C | T | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1594+1512C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45504861 | |||||||
chr13:45505167 | A | G | 2 | a0002c0005t0003g0158 a0002c0005t0003g0159 |
2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1594+1818A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505167 | |||||||
chr13:45505206 | G | A | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1594+1857G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505206 | |||||||
chr13:45505305 | C | CT | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1594+1968dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45505305 | ||||||
chr13:45505309 | T | G | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1594+1960T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505309 | |||||||
chr13:45505394 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0117 |
2 | NA18966.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1594+2045C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505394 | |||||||
chr13:45505403 | G | A | 2 | a0002c0003t0002g0189 a0002c0003t0002g0190 |
2 | HG00597.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1594+2054G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505403 | |||||||
chr13:45505459 | G | A | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1594+2110G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505459 | |||||||
chr13:45505493 | G | A | 1 | a0002c0004t0001g0013 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1594+2144G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505493 | |||||||
chr13:45505589 | G | GCCACTGC others(7): Show |
2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1594+2242_1594+225 others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45505589 | ||||||
chr13:45505601 | G | A | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1594+2252G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505601 | |||||||
chr13:45505656 | G | A | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1594+2307G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505656 | |||||||
chr13:45505689 | G | A | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594+2340G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505689 | |||||||
chr13:45505784 | G | A | 1 | a0002c0003t0002g0007 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1594+2435G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505784 | |||||||
chr13:45505790 | C | T | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0005t0014g0206 |
3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1594+2441C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505790 | |||||||
chr13:45505800 | C | T | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1594+2451C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505800 | |||||||
chr13:45505942 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1594+2593A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45505942 | |||||||
chr13:45506014 | A | G | 71 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0005 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1594+2665A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506014 | |||||||
chr13:45506072 | CT | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1594+2729delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45506072 | ||||||
chr13:45506152 | G | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1594+2803G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506152 | |||||||
chr13:45506285 | C | T | 1 | a0002c0005t0003g0157 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1594+2936C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506285 | |||||||
chr13:45506314 | A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1594+2965A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506314 | |||||||
chr13:45506317 | C | G | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1594+2968C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506317 | |||||||
chr13:45506370 | G | A | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1594+3021G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506370 | |||||||
chr13:45506374 | T | C | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1594+3025T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506374 | |||||||
chr13:45506489 | A | T | 1 | a0002c0004t0001g0017 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1594+3140A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506489 | |||||||
chr13:45506497 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1594+3148C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506497 | |||||||
chr13:45506510 | G | A | 1 | a0002c0003t0002g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1594+3161G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506510 | |||||||
chr13:45506540 | C | T | 1 | a0002c0003t0002g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1595-3152C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506540 | |||||||
chr13:45506544 | T | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0115 |
2 | HG00438.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1595-3148T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506544 | |||||||
chr13:45506549 | G | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1595-3143G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506549 | |||||||
chr13:45506728 | A | G | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595-2964A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506728 | |||||||
chr13:45506763 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1595-2929C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506763 | |||||||
chr13:45506931 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1595-2761G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506931 | |||||||
chr13:45506959 | G | T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1595-2733G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506959 | |||||||
chr13:45506973 | C | T | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-2719C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45506973 | |||||||
chr13:45507081 | G | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1595-2611G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507081 | |||||||
chr13:45507091 | C | T | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-2601C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507091 | |||||||
chr13:45507092 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1595-2600G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507092 | |||||||
chr13:45507237 | C | T | 1 | a0002c0003t0002g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1595-2455C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507237 | |||||||
chr13:45507272 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1595-2420A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507272 | |||||||
chr13:45507402 | T | TGA | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0005t0014g0206 |
3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1595-2279_1595-227 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45507402 | ||||||
chr13:45507493 | G | A | 1 | a0002c0005t0003g0158 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1595-2199G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507493 | |||||||
chr13:45507497 | G | A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1595-2195G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507497 | |||||||
chr13:45507644 | A | C | 31 | a0002c0003t0002g0007 a0002c0003t0002g0202 a0002c0003t0002g0208 others(28): Show |
32 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1595-2048A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507644 | |||||||
chr13:45507658 | G | A | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1595-2034G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507658 | |||||||
chr13:45507756 | C | G | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0005t0014g0206 |
3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1595-1936C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507756 | |||||||
chr13:45507774 | G | GA | 66 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(63): Show |
68 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1595-1905dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45507774 | ||||||
chr13:45507774 | GA | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1595-1905delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45507774 | ||||||
chr13:45507799 | G | A | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0005t0014g0206 |
3 | HG02922.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1595-1893G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507799 | |||||||
chr13:45507954 | A | T | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1595-1738A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507954 | |||||||
chr13:45507994 | A | G | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-1698A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45507994 | |||||||
chr13:45508023 | T | C | 294 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.1595-1669T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508023 | |||||||
chr13:45508028 | C | T | 1 | a0002c0004t0001g0002 | 3 | NA18964.hp1 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1595-1664C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508028 | |||||||
chr13:45508033 | C | T | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1595-1659C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508033 | |||||||
chr13:45508068 | T | TA | 20 | a0001c0001t0001g0080 a0001c0001t0001g0105 a0001c0001t0001g0117 others(17): Show |
21 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1595-1593dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0045 others(47): Show |
53 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1595-1594_1595-159 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAA | 32 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.1595-1595_1595-159 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAA | 8 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0116 others(5): Show |
8 | HG00738.hp2 HG02165.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1595-1596_1595-159 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAA | 9 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0092 others(6): Show |
9 | HG01106.hp1 HG01167.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1595-1597_1595-159 others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAA | 9 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0098 others(6): Show |
10 | HG00639.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1595-1598_1595-159 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAAA others(6): Show |
1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1595-1605_1595-159 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAAA others(11): Show |
1 | a0003c0006t0004g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1595-1610_1595-159 others(22): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAAA others(12): Show |
3 | a0003c0006t0004g0193 a0003c0006t0004g0199 a0003c0006t0015g0200 |
3 | HG02559.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1595-1611_1595-159 others(23): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAAA others(13): Show |
2 | a0003c0006t0004g0195 a0003c0006t0004g0196 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1595-1612_1595-159 others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAAA others(14): Show |
1 | a0003c0006t0004g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1595-1613_1595-159 others(25): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | T | TAAAAAAA others(37): Show |
1 | a0001c0002t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1595-1593_1595-159 others(48): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | TA | T | 86 | a0001c0001t0001g0113 a0001c0002t0001g0008 a0001c0002t0001g0037 others(83): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1595-1593delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | TAA | T | 18 | a0001c0002t0001g0241 a0002c0003t0002g0166 a0002c0003t0002g0172 others(15): Show |
18 | HG01074.hp1 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1595-1594_1595-159 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | TAAAAAAA others(3): Show |
T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1595-1602_1595-159 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0001g0296 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1595-1604_1595-159 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508068 | TAAAAAAA others(6): Show |
T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1595-1605_1595-159 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508068 | ||||||
chr13:45508281 | G | C | 6 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(3): Show |
6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1595-1411G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508281 | |||||||
chr13:45508333 | C | G | 9 | a0001c0014t0004g0194 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1595-1359C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508333 | |||||||
chr13:45508382 | ATT | A | 92 | a0001c0001t0001g0113 a0001c0002t0001g0008 a0001c0002t0001g0009 others(89): Show |
94 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1595-1306_1595-130 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508382 | ||||||
chr13:45508384 | T | TTA | 83 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(80): Show |
84 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1595-1307_1595-130 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508384 | ||||||
chr13:45508384 | T | TTATA | 4 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0008t0001g0042 others(1): Show |
4 | HG00738.hp2 HG03239.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595-1307_1595-130 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508384 | ||||||
chr13:45508384 | TTTTA | T | 44 | a0001c0002t0001g0265 a0001c0002t0001g0307 a0002c0003t0002g0005 others(41): Show |
46 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1595-1306_1595-130 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508384 | ||||||
chr13:45508386 | T | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1595-1306T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508386 | |||||||
chr13:45508399 | TATATACA others(5): Show |
T | 31 | a0002c0003t0002g0007 a0002c0003t0002g0202 a0002c0003t0002g0208 others(28): Show |
32 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1595-1291_1595-128 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508399 | ||||||
chr13:45508401 | T | TACACAC | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1595-1290_1595-128 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508401 | ||||||
chr13:45508403 | T | C | 4 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-1289T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508403 | |||||||
chr13:45508403 | T | TAC | 4 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG00741.hp2 HG01099.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1595-1267_1595-126 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508403 | ||||||
chr13:45508403 | T | TATATACA others(3): Show |
1 | a0001c0001t0001g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1595-1288_1595-128 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508403 | ||||||
chr13:45508403 | TAC | T | 3 | a0002c0004t0001g0012 a0002c0004t0010g0027 a0002c0005t0011g0150 |
3 | HG00597.hp1 HG02015.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1595-1267_1595-126 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508403 | ||||||
chr13:45508405 | C | T | 29 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0069 others(26): Show |
29 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1595-1287C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508405 | |||||||
chr13:45508407 | C | T | 7 | a0002c0005t0003g0010 a0002c0005t0003g0151 a0002c0005t0003g0152 others(4): Show |
7 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595-1285C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508407 | |||||||
chr13:45508409 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0003g0153 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1595-1283C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508409 | |||||||
chr13:45508419 | C | CACACATA others(61): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1595-1268_1595-126 others(72): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508419 | ||||||
chr13:45508419 | CACACACA others(1): Show |
C | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0160 others(33): Show |
39 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1595-1267_1595-126 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508419 | ||||||
chr13:45508421 | CACACAT | C | 6 | a0001c0014t0004g0194 a0002c0003t0002g0144 a0002c0003t0002g0207 others(3): Show |
6 | HG00323.hp2 HG01109.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595-1263_1595-125 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508421 | ||||||
chr13:45508423 | CACAT | C | 15 | a0001c0002t0001g0310 a0002c0005t0003g0153 a0002c0005t0003g0157 others(12): Show |
15 | HG00408.hp1 HG01175.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595-1265_1595-126 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508423 | ||||||
chr13:45508425 | CAT | C | 94 | a0001c0001t0001g0113 a0001c0002t0001g0008 a0001c0002t0001g0009 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1595-1265_1595-126 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45508425 | ||||||
chr13:45508427 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(145): Show |
150 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1595-1265T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508427 | |||||||
chr13:45508429 | C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1595-1263C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508429 | |||||||
chr13:45508431 | C | T | 2 | a0001c0002t0001g0205 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1595-1261C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508431 | |||||||
chr13:45508433 | T | C | 5 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595-1259T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508433 | |||||||
chr13:45508439 | T | C | 3 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 |
3 | HG02572.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1595-1253T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508439 | |||||||
chr13:45508500 | T | C | 69 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1595-1192T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508500 | |||||||
chr13:45508760 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1595-932T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508760 | |||||||
chr13:45508822 | A | T | 210 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1595-870A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45508822 | |||||||
chr13:45509042 | C | CT | 18 | a0001c0001t0001g0093 a0001c0001t0001g0109 a0001c0002t0001g0252 others(15): Show |
18 | HG02040.hp2 HG02071.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1595-635dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45509042 | ||||||
chr13:45509042 | CT | C | 63 | a0001c0001t0001g0071 a0002c0003t0002g0005 a0002c0003t0002g0006 others(60): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1595-635delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45509042 | ||||||
chr13:45509042 | CTTT | C | 6 | a0002c0003t0002g0144 a0002c0003t0002g0171 a0002c0003t0002g0174 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595-637_1595-635d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr13 | 45509042 | ||||||
chr13:45509337 | C | T | 1 | a0002c0003t0002g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1595-355C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45509337 | |||||||
chr13:45509412 | C | T | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1595-280C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45509412 | |||||||
chr13:45509495 | G | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1595-197G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 14/22 | chr13 | 45509495 | |||||||
chr13:45509837 | A | T | 1 | a0001c0002t0001g0276 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1719+21A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45509837 | |||||||
chr13:45509990 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1719+174G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45509990 | |||||||
chr13:45510148 | AGATG | A | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1719+333_1719+336d others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510148 | |||||||
chr13:45510419 | G | A | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1719+603G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510419 | |||||||
chr13:45510601 | A | G | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1719+785A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510601 | |||||||
chr13:45510972 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | NA18984.hp2 NA18999.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1720-793G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45510972 | |||||||
chr13:45511045 | T | G | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1720-720T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511045 | |||||||
chr13:45511158 | G | GT | 23 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(20): Show |
23 | HG00408.hp1 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1720-593dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr13 | 45511158 | ||||||
chr13:45511158 | GT | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1720-593delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr13 | 45511158 | ||||||
chr13:45511234 | A | G | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1720-531A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511234 | |||||||
chr13:45511266 | G | T | 1 | a0002c0003t0002g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1720-499G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511266 | |||||||
chr13:45511305 | G | A | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720-460G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511305 | |||||||
chr13:45511458 | G | A | 7 | a0002c0007t0002g0223 a0002c0007t0002g0224 a0002c0007t0002g0225 others(4): Show |
7 | HG01192.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1720-307G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511458 | |||||||
chr13:45511564 | G | A | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1720-201G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511564 | |||||||
chr13:45511611 | T | C | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1720-154T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511611 | |||||||
chr13:45511729 | A | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1720-36A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 15/22 | chr13 | 45511729 | |||||||
chr13:45511879 | C | G | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1809+25C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45511879 | |||||||
chr13:45511920 | A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1809+66A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45511920 | |||||||
chr13:45512004 | T | C | 1 | a0002c0003t0002g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1809+150T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512004 | |||||||
chr13:45512050 | A | T | 1 | a0002c0007t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1809+196A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512050 | |||||||
chr13:45512064 | C | T | 6 | a0002c0004t0001g0014 a0002c0004t0001g0016 a0002c0004t0001g0021 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1809+210C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512064 | |||||||
chr13:45512108 | CTTG | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0131 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+259_1809+261d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45512108 | ||||||
chr13:45512146 | T | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1809+292T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512146 | |||||||
chr13:45512171 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1809+317T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512171 | |||||||
chr13:45512330 | C | A | 1 | a0001c0008t0001g0120 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1809+476C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512330 | |||||||
chr13:45512452 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1809+598C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512452 | |||||||
chr13:45512494 | T | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1809+640T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512494 | |||||||
chr13:45512628 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1809+774T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512628 | |||||||
chr13:45512785 | T | G | 12 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(9): Show |
13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1809+931T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512785 | |||||||
chr13:45512848 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1809+994C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512848 | |||||||
chr13:45512913 | C | T | 1 | a0002c0007t0002g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1809+1059C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45512913 | |||||||
chr13:45512988 | A | AT | 284 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.1809+1146dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45512988 | ||||||
chr13:45513006 | G | C | 1 | a0001c0002t0001g0326 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1809+1152G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513006 | |||||||
chr13:45513183 | TTA | T | 21 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(18): Show |
21 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1809+1344_1809+134 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513183 | ||||||
chr13:45513185 | A | ATATATAT others(23): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1809+1344_1809+137 others(34): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513185 | ||||||
chr13:45513215 | TTA | T | 14 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0001c0002t0001g0257 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1809+1372_1809+137 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513215 | ||||||
chr13:45513217 | A | ATACATAT others(17): Show |
203 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1809+1365_1809+136 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | ||||||
chr13:45513217 | A | ATACATAT others(43): Show |
3 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0001c0002t0001g0244 |
3 | HG02451.hp2 HG02970.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1809+1365_1809+136 others(54): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | ||||||
chr13:45513217 | A | ATATATAT others(23): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1809+1373_1809+137 others(34): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | ||||||
chr13:45513217 | ATATATAT others(45): Show |
A | 2 | a0002c0005t0003g0158 a0002c0005t0003g0159 |
2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1809+1372_1809+142 others(56): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513217 | ||||||
chr13:45513220 | T | C | 4 | a0002c0005t0003g0010 a0002c0005t0003g0157 a0002c0005t0003g0192 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1809+1366T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513220 | |||||||
chr13:45513222 | T | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1809+1368T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513222 | |||||||
chr13:45513222 | T | TATAATAT others(17): Show |
1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1809+1371_1809+137 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513222 | ||||||
chr13:45513222 | TATATAAT others(145): Show |
T | 64 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(61): Show |
67 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1809+1424_1809+157 others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513222 | ||||||
chr13:45513224 | TATAATAT others(143): Show |
T | 3 | a0002c0003t0002g0217 a0002c0003t0002g0219 a0002c0003t0002g0240 |
3 | HG01934.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1809+1374_1809+152 others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513224 | ||||||
chr13:45513248 | CATATAAT others(17): Show |
C | 3 | a0002c0005t0003g0157 a0002c0007t0002g0224 a0002c0016t0003g0156 |
3 | HG01192.hp1 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1809+1420_1809+144 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513248 | ||||||
chr13:45513250 | T | G | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+1396T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513250 | |||||||
chr13:45513272 | T | C | 2 | a0002c0005t0003g0158 a0002c0005t0003g0159 |
2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1809+1418T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513272 | |||||||
chr13:45513272 | T | TAC | 13 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0001c0002t0001g0257 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1809+1419_1809+142 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513272 | ||||||
chr13:45513274 | T | C | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1809+1420T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513274 | |||||||
chr13:45513295 | A | ATATATAA others(15): Show |
1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1809+1443_1809+144 others(26): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513295 | ||||||
chr13:45513296 | TAC | T | 3 | a0001c0002t0001g0257 a0001c0015t0001g0261 a0002c0005t0003g0192 |
3 | HG02723.hp1 HG04204.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1809+1444_1809+144 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513296 | ||||||
chr13:45513298 | C | CATATAAT others(15): Show |
1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1809+1448_1809+146 others(26): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513298 | ||||||
chr13:45513298 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0014g0206 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1809+1444C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513298 | |||||||
chr13:45513298 | CAT | C | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1809+1448_1809+144 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513298 | ||||||
chr13:45513324 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0014g0206 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1809+1470C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513324 | |||||||
chr13:45513345 | T | TTATATAT others(19): Show |
1 | a0002c0005t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1809+1494_1809+151 others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513345 | ||||||
chr13:45513348 | T | TAC | 10 | a0001c0002t0001g0257 a0001c0015t0001g0261 a0003c0006t0004g0193 others(7): Show |
10 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1809+1495_1809+149 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513348 | ||||||
chr13:45513348 | T | TACATATA others(95): Show |
2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1809+1495_1809+149 others(106): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513348 | ||||||
chr13:45513348 | TATATAAT others(19): Show |
T | 9 | a0002c0004t0001g0002 a0002c0004t0001g0011 a0002c0004t0001g0012 others(6): Show |
11 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1809+1546_1809+157 others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513348 | ||||||
chr13:45513374 | C | CATATAAT others(17): Show |
2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1809+1522_1809+154 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513374 | ||||||
chr13:45513374 | C | CATATAAT others(45): Show |
8 | a0002c0004t0001g0001 a0002c0004t0001g0017 a0002c0004t0001g0018 others(5): Show |
10 | HG02074.hp1 HG02165.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1809+1545_1809+154 others(56): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513374 | ||||||
chr13:45513374 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1809+1520C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513374 | |||||||
chr13:45513395 | TTATACAT others(21): Show |
T | 3 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 |
3 | HG02572.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1809+1546_1809+157 others(32): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513395 | ||||||
chr13:45513395 | TTATACAT others(47): Show |
T | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1809+1546_1809+159 others(58): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513395 | ||||||
chr13:45513395 | TTATACAT others(99): Show |
T | 1 | a0002c0007t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1809+1546_1809+165 others(4): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513395 | ||||||
chr13:45513398 | TAC | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(112): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1809+1546_1809+154 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513398 | ||||||
chr13:45513400 | C | CATAATAT others(17): Show |
3 | a0001c0002t0001g0204 a0001c0002t0001g0294 a0001c0002t0001g0311 |
3 | HG02145.hp2 NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1809+1549_1809+155 others(28): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513400 | ||||||
chr13:45513400 | C | T | 27 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0002c0004t0001g0001 others(24): Show |
31 | HG00408.hp1 HG01256.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1809+1546C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513400 | |||||||
chr13:45513400 | CAT | C | 90 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(87): Show |
92 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1809+1550_1809+155 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513400 | ||||||
chr13:45513421 | TTA | T | 3 | a0001c0002t0001g0257 a0001c0015t0001g0261 a0002c0005t0014g0206 |
3 | HG03225.hp1 HG04204.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1809+1576_1809+157 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513421 | ||||||
chr13:45513422 | T | C | 96 | a0001c0001t0001g0112 a0001c0002t0001g0008 a0001c0002t0001g0009 others(93): Show |
98 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1809+1568T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513422 | |||||||
chr13:45513422 | T | TATATATA others(67): Show |
8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1809+1575_1809+157 others(78): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513422 | ||||||
chr13:45513422 | T | TATATATA others(93): Show |
1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1809+1575_1809+157 others(104): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513422 | ||||||
chr13:45513426 | T | C | 67 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1809+1572T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513426 | |||||||
chr13:45513428 | T | C | 2 | a0001c0002t0001g0257 a0001c0015t0001g0261 |
2 | HG04204.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1809+1574T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513428 | |||||||
chr13:45513447 | TTA | T | 67 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1809+1602_1809+160 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513447 | ||||||
chr13:45513448 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1809+1594T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513448 | |||||||
chr13:45513449 | A | ATATATAT others(13): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1809+1606_1809+160 others(24): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513449 | ||||||
chr13:45513473 | TTA | T | 3 | a0001c0002t0001g0294 a0001c0002t0001g0311 a0001c0014t0004g0194 |
3 | HG02145.hp2 HG03139.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1809+1628_1809+162 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513473 | ||||||
chr13:45513474 | T | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1809+1620T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513474 | |||||||
chr13:45513478 | T | C | 67 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1809+1624T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513478 | |||||||
chr13:45513493 | T | A | 3 | a0001c0002t0001g0009 a0001c0002t0001g0288 a0001c0002t0001g0313 |
4 | NA18971.hp2 NA18987.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+1639T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513493 | |||||||
chr13:45513498 | A | G | 1 | a0001c0002t0001g0284 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1809+1644A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513498 | |||||||
chr13:45513499 | TTA | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.1809+1654_1809+165 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45513499 | ||||||
chr13:45513500 | T | C | 1 | a0001c0015t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1809+1646T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513500 | |||||||
chr13:45513520 | A | G | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1809+1666A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513520 | |||||||
chr13:45513543 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0131 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809+1689C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513543 | |||||||
chr13:45513555 | A | G | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1809+1701A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513555 | |||||||
chr13:45513562 | A | ATATATAC others(19): Show |
2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1809+1708_1809+170 others(30): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513562 | |||||||
chr13:45513642 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1809+1788G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513642 | |||||||
chr13:45513646 | C | G | 9 | a0001c0014t0004g0194 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1809+1792C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513646 | |||||||
chr13:45513762 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0124 |
2 | HG02056.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1809+1908G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513762 | |||||||
chr13:45513865 | T | C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1809+2011T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513865 | |||||||
chr13:45513986 | T | C | 36 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1809+2132T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45513986 | |||||||
chr13:45514157 | C | CT | 49 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0072 others(46): Show |
52 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.1810-1965dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | ||||||
chr13:45514157 | C | CTT | 151 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(148): Show |
153 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1810-1966_1810-196 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | ||||||
chr13:45514157 | C | CTTT | 91 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0082 others(88): Show |
93 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1810-1967_1810-196 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | ||||||
chr13:45514157 | C | CTTTT | 8 | a0001c0002t0001g0268 a0001c0002t0001g0271 a0001c0002t0001g0280 others(5): Show |
8 | HG00741.hp1 HG01106.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1810-1968_1810-196 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr13 | 45514157 | ||||||
chr13:45514208 | T | C | 1 | a0002c0007t0002g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1810-1935T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514208 | |||||||
chr13:45514315 | C | T | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-1828C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514315 | |||||||
chr13:45514317 | C | T | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1810-1826C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514317 | |||||||
chr13:45514493 | G | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1810-1650G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514493 | |||||||
chr13:45514708 | C | G | 2 | a0002c0004t0001g0031 a0002c0004t0001g0034 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1810-1435C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514708 | |||||||
chr13:45514792 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1810-1351C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514792 | |||||||
chr13:45514867 | C | T | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1810-1276C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514867 | |||||||
chr13:45514903 | C | T | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1810-1240C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514903 | |||||||
chr13:45514928 | G | A | 1 | a0002c0004t0010g0027 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1810-1215G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514928 | |||||||
chr13:45514951 | C | T | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-1192C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45514951 | |||||||
chr13:45515058 | A | C | 2 | a0001c0002t0001g0277 a0001c0002t0001g0311 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1810-1085A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515058 | |||||||
chr13:45515062 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0145 |
3 | HG02080.hp1 HG02165.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1810-1081A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515062 | |||||||
chr13:45515126 | A | T | 288 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1810-1017A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515126 | |||||||
chr13:45515260 | T | C | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1810-883T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515260 | |||||||
chr13:45515299 | G | A | 4 | a0001c0002t0001g0008 a0001c0002t0001g0242 a0001c0002t0001g0243 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810-844G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515299 | |||||||
chr13:45515388 | A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1810-755A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515388 | |||||||
chr13:45515446 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1810-697C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515446 | |||||||
chr13:45515532 | C | T | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-611C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515532 | |||||||
chr13:45515545 | A | G | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1810-598A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515545 | |||||||
chr13:45515709 | A | G | 15 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(12): Show |
15 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1810-434A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515709 | |||||||
chr13:45515734 | C | G | 1 | a0001c0002t0001g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1810-409C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515734 | |||||||
chr13:45515774 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1810-369G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515774 | |||||||
chr13:45515782 | T | C | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1810-361T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515782 | |||||||
chr13:45515824 | A | T | 69 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1810-319A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45515824 | |||||||
chr13:45516098 | T | A | 1 | a0002c0003t0002g0202 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1810-45T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 16/22 | chr13 | 45516098 | |||||||
chr13:45516420 | C | T | 2 | a0002c0003t0002g0184 a0002c0003t0002g0185 |
2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1930+157C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516420 | |||||||
chr13:45516422 | A | G | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1930+159A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516422 | |||||||
chr13:45516551 | A | G | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1930+288A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516551 | |||||||
chr13:45516635 | G | A | 1 | a0002c0003t0002g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1930+372G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516635 | |||||||
chr13:45516684 | G | A | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1930+421G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516684 | |||||||
chr13:45516807 | T | G | 4 | a0002c0005t0003g0157 a0002c0005t0003g0158 a0002c0005t0003g0159 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930+544T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516807 | |||||||
chr13:45516893 | T | G | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1930+630T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45516893 | |||||||
chr13:45517033 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1930+770G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517033 | |||||||
chr13:45517228 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1930+965T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517228 | |||||||
chr13:45517232 | C | T | 23 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(20): Show |
23 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1930+969C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517232 | |||||||
chr13:45517250 | T | C | 4 | a0002c0005t0003g0157 a0002c0005t0003g0158 a0002c0005t0003g0159 others(1): Show |
4 | HG00408.hp1 HG02015.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930+987T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517250 | |||||||
chr13:45517385 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1930+1122T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517385 | |||||||
chr13:45517501 | A | T | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1930+1238A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517501 | |||||||
chr13:45517554 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1931-1208G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517554 | |||||||
chr13:45517557 | T | TTGGTTTG others(314): Show |
4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1931-1198_1931-119 others(325): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr13 | 45517557 | ||||||
chr13:45517587 | C | T | 234 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1931-1175C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517587 | |||||||
chr13:45517690 | G | C | 1 | a0002c0003t0002g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1931-1072G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517690 | |||||||
chr13:45517918 | T | A | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1931-844T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517918 | |||||||
chr13:45517987 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1931-775T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45517987 | |||||||
chr13:45518126 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1931-636A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518126 | |||||||
chr13:45518190 | A | G | 12 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(9): Show |
13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1931-572A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518190 | |||||||
chr13:45518285 | C | G | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1931-477C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518285 | |||||||
chr13:45518328 | C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1931-434C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518328 | |||||||
chr13:45518555 | C | T | 1 | a0001c0002t0001g0311 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1931-207C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518555 | |||||||
chr13:45518720 | G | A | 1 | a0002c0003t0002g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1931-42G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 17/22 | chr13 | 45518720 | |||||||
chr13:45518895 | T | A | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2019+45T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 18/22 | chr13 | 45518895 | |||||||
chr13:45519149 | C | G | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2154+55C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519149 | |||||||
chr13:45519304 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0078 |
2 | HG01106.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.2154+210G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519304 | |||||||
chr13:45519422 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(100): Show |
104 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2154+328A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519422 | |||||||
chr13:45519470 | G | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2154+376G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519470 | |||||||
chr13:45519592 | A | T | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154+498A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519592 | |||||||
chr13:45519637 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2154+543G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519637 | |||||||
chr13:45519694 | A | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.2154+600A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519694 | |||||||
chr13:45519736 | G | C | 1 | a0001c0002t0001g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2154+642G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45519736 | |||||||
chr13:45520108 | T | G | 4 | a0002c0005t0003g0151 a0002c0005t0003g0152 a0002c0005t0003g0153 others(1): Show |
4 | HG01975.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154+1014T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520108 | |||||||
chr13:45520131 | C | T | 88 | a0001c0001t0001g0110 a0001c0001t0001g0124 a0001c0002t0001g0263 others(85): Show |
91 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.2154+1037C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520131 | |||||||
chr13:45520145 | C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2154+1051C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520145 | |||||||
chr13:45520157 | C | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | NA18942.hp1 NA18944.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+1063C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520157 | |||||||
chr13:45520285 | C | CA | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2154+1201dupA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520285 | ||||||
chr13:45520285 | CA | C | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2154+1201delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520285 | ||||||
chr13:45520296 | T | A | 16 | a0001c0002t0001g0252 a0001c0002t0001g0255 a0001c0002t0001g0256 others(13): Show |
16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+1202T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520296 | |||||||
chr13:45520312 | AAT | A | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1220_2154+122 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520312 | ||||||
chr13:45520318 | A | G | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1224A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520318 | |||||||
chr13:45520320 | A | G | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1226A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520320 | |||||||
chr13:45520322 | G | A | 8 | a0003c0006t0004g0193 a0003c0006t0004g0195 a0003c0006t0004g0196 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154+1228G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520322 | |||||||
chr13:45520322 | G | GAGAA | 294 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(291): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.2154+1238_2154+124 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520322 | ||||||
chr13:45520527 | A | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2154+1433A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520527 | |||||||
chr13:45520678 | G | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(228): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.2154+1584G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520678 | |||||||
chr13:45520678 | G | C | 3 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0002c0003t0002g0240 |
3 | HG02922.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2154+1584G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520678 | |||||||
chr13:45520703 | A | AT | 220 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2154+1616dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45520703 | ||||||
chr13:45520971 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2154+1877A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45520971 | |||||||
chr13:45521054 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2154+1960C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521054 | |||||||
chr13:45521158 | A | AT | 38 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.2154+2074dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521158 | ||||||
chr13:45521371 | C | G | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2154+2277C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521371 | |||||||
chr13:45521419 | C | T | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2154+2325C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521419 | |||||||
chr13:45521424 | TC | T | 37 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(34): Show |
39 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.2154+2331delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521424 | |||||||
chr13:45521550 | G | A | 1 | a0001c0014t0004g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154+2456G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521550 | |||||||
chr13:45521577 | G | GCA | 5 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0143 others(2): Show |
5 | HG02071.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154+2507_2154+250 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCACA | 46 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(43): Show |
52 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.2154+2505_2154+250 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCACACA | 24 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0210 others(21): Show |
24 | HG01109.hp2 HG01192.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.2154+2503_2154+250 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCACACAC others(1): Show |
23 | a0002c0003t0002g0209 a0002c0003t0002g0233 a0002c0003t0002g0234 others(20): Show |
23 | HG00280.hp1 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2154+2501_2154+250 others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCACACAC others(3): Show |
5 | a0002c0003t0002g0007 a0002c0003t0002g0235 a0002c0005t0003g0152 others(2): Show |
6 | HG00408.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.2154+2499_2154+250 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCACACAC others(5): Show |
4 | a0002c0005t0003g0004 a0002c0005t0003g0151 a0002c0005t0003g0155 others(1): Show |
5 | HG00639.hp1 HG01243.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154+2497_2154+250 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCACACAC others(9): Show |
1 | a0002c0005t0003g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2154+2493_2154+250 others(20): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | G | GCGCACAC others(5): Show |
1 | a0002c0016t0003g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2154+2484_2154+248 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | GCA | G | 9 | a0002c0005t0014g0206 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2154+2507_2154+250 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521577 | GCACACAC others(5): Show |
G | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2154+2497_2154+250 others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521577 | ||||||
chr13:45521655 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2154+2561T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521655 | |||||||
chr13:45521717 | A | G | 1 | a0002c0004t0001g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2154+2623A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521717 | |||||||
chr13:45521802 | CTT | C | 69 | a0001c0001t0001g0140 a0002c0003t0002g0005 a0002c0003t0002g0006 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2154+2727_2154+272 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521802 | ||||||
chr13:45521802 | CTTT | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(211): Show |
217 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.2154+2726_2154+272 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45521802 | ||||||
chr13:45521845 | T | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(299): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.2154+2751T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521845 | |||||||
chr13:45521886 | T | C | 16 | a0001c0002t0001g0252 a0001c0002t0001g0255 a0001c0002t0001g0256 others(13): Show |
16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2154+2792T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521886 | |||||||
chr13:45521925 | C | T | 10 | a0002c0004t0001g0001 a0002c0004t0001g0002 a0002c0004t0001g0015 others(7): Show |
14 | HG02074.hp1 HG02129.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.2154+2831C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521925 | |||||||
chr13:45521958 | G | A | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2154+2864G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45521958 | |||||||
chr13:45522174 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2155-2802A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522174 | |||||||
chr13:45522218 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2155-2758C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522218 | |||||||
chr13:45522237 | G | A | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-2739G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522237 | |||||||
chr13:45522494 | A | T | 23 | a0002c0003t0002g0202 a0002c0003t0002g0208 a0002c0003t0002g0209 others(20): Show |
23 | HG01074.hp2 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2155-2482A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522494 | |||||||
chr13:45522572 | G | C | 69 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2155-2404G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522572 | |||||||
chr13:45522726 | G | A | 303 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(300): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.2155-2250G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522726 | |||||||
chr13:45522754 | C | T | 14 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(11): Show |
15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2155-2222C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522754 | |||||||
chr13:45522888 | G | A | 11 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(8): Show |
12 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2155-2088G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522888 | |||||||
chr13:45522940 | G | T | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2155-2036G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45522940 | |||||||
chr13:45523033 | G | T | 95 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.2155-1943G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523033 | |||||||
chr13:45523076 | G | T | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2155-1900G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523076 | |||||||
chr13:45523077 | C | G | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2155-1899C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523077 | |||||||
chr13:45523078 | T | C | 1 | a0001c0002t0001g0323 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2155-1898T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523078 | |||||||
chr13:45523149 | GT | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.2155-1813delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45523149 | ||||||
chr13:45523149 | GTT | G | 20 | a0001c0002t0001g0268 a0001c0002t0001g0285 a0001c0002t0001g0286 others(17): Show |
21 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.2155-1814_2155-181 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45523149 | ||||||
chr13:45523227 | A | T | 1 | a0002c0003t0002g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2155-1749A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523227 | |||||||
chr13:45523510 | TA | T | 5 | a0003c0006t0004g0195 a0003c0006t0004g0196 a0003c0006t0004g0197 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2155-1459delA | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45523510 | ||||||
chr13:45523748 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0149 |
3 | NA18939.hp1 NA18943.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2155-1228A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523748 | |||||||
chr13:45523976 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2155-1000G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45523976 | |||||||
chr13:45524057 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(179): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.2155-919A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524057 | |||||||
chr13:45524301 | CCCATAGC others(4): Show |
C | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2155-671_2155-661d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45524301 | ||||||
chr13:45524408 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0117 |
2 | NA18966.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2155-568A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524408 | |||||||
chr13:45524410 | G | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2155-566G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524410 | |||||||
chr13:45524540 | G | A | 1 | a0002c0003t0002g0160 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2155-436G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524540 | |||||||
chr13:45524593 | T | C | 31 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(28): Show |
33 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.2155-383T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524593 | |||||||
chr13:45524780 | T | C | 11 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(8): Show |
12 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2155-196T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524780 | |||||||
chr13:45524820 | AT | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(100): Show |
104 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2155-148delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr13 | 45524820 | ||||||
chr13:45524859 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.2155-117T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524859 | |||||||
chr13:45524966 | C | T | 1 | a0001c0002t0001g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2155-10C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524966 | |||||||
chr13:45524972 | T | C | 2 | a0002c0005t0003g0010 a0002c0005t0003g0192 |
2 | HG02723.hp1 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.2155-4T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 19/22 | chr13 | 45524972 | |||||||
chr13:45525108 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.2230+57A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525108 | |||||||
chr13:45525132 | G | A | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2230+81G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525132 | |||||||
chr13:45525213 | G | A | 5 | a0002c0003t0002g0168 a0002c0003t0002g0170 a0002c0003t0002g0173 others(2): Show |
5 | HG00609.hp1 HG02056.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2230+162G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525213 | |||||||
chr13:45525401 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2230+350G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525401 | |||||||
chr13:45525471 | T | C | 1 | a0002c0004t0001g0012 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2230+420T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525471 | |||||||
chr13:45525481 | A | G | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2230+430A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525481 | |||||||
chr13:45525582 | C | CTTAAATG others(6): Show |
93 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(90): Show |
95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2230+531_2230+532i others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525582 | |||||||
chr13:45525583 | C | T | 93 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(90): Show |
95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2230+532C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525583 | |||||||
chr13:45525584 | C | A | 93 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(90): Show |
95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2230+533C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525584 | |||||||
chr13:45525633 | G | GTTTTTTT others(9): Show |
1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2230+582_2230+583i others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525633 | |||||||
chr13:45525634 | G | GT | 11 | a0002c0004t0001g0001 a0002c0004t0001g0002 a0002c0004t0001g0012 others(8): Show |
15 | HG00597.hp1 HG02015.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2230+601dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT | 8 | a0001c0002t0001g0249 a0001c0002t0007g0304 a0002c0003t0002g0217 others(5): Show |
8 | HG00738.hp1 HG01074.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2230+595_2230+601d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(1): Show |
105 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(102): Show |
109 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2230+594_2230+601d others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(2): Show |
54 | a0001c0002t0001g0229 a0001c0002t0001g0230 a0001c0002t0001g0245 others(51): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2230+593_2230+601d others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(3): Show |
20 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 others(17): Show |
20 | HG02056.hp2 HG02257.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2230+592_2230+601d others(12): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0121 a0002c0003t0002g0180 a0002c0016t0003g0156 |
3 | HG01981.hp1 HG02922.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2230+591_2230+601d others(13): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(5): Show |
77 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0043 others(74): Show |
78 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.2230+590_2230+601d others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(6): Show |
22 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0059 others(19): Show |
22 | HG00438.hp1 HG00639.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2230+589_2230+601d others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | GTTTTTTT others(7): Show |
8 | a0001c0001t0001g0067 a0001c0001t0001g0094 a0001c0001t0001g0113 others(5): Show |
8 | HG01261.hp2 HG02080.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2230+588_2230+601d others(16): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525634 | ||||||
chr13:45525634 | G | T | 2 | a0002c0005t0011g0150 a0002c0005t0012g0148 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2230+583G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525634 | |||||||
chr13:45525693 | T | A | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2230+642T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525693 | |||||||
chr13:45525695 | A | G | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2230+644A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525695 | |||||||
chr13:45525798 | T | TAGAG | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2230+749_2230+750i others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45525798 | ||||||
chr13:45525912 | G | T | 6 | a0002c0003t0002g0233 a0002c0003t0002g0234 a0002c0003t0002g0235 others(3): Show |
6 | HG01074.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2230+861G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45525912 | |||||||
chr13:45526076 | A | AT | 10 | a0002c0004t0001g0002 a0002c0004t0001g0013 a0002c0004t0001g0014 others(7): Show |
12 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2230+1055dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATT | 16 | a0001c0002t0001g0205 a0001c0002t0001g0229 a0001c0002t0001g0230 others(13): Show |
18 | HG00642.hp2 HG02074.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2230+1054_2230+105 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATTT | 23 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0097 others(20): Show |
24 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2230+1053_2230+105 others(7): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATTTT | 76 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0044 others(73): Show |
77 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.2230+1052_2230+105 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATTTTT | 78 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0052 others(75): Show |
78 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.2230+1051_2230+105 others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATTTTTT | 16 | a0001c0001t0001g0054 a0001c0001t0001g0076 a0001c0001t0001g0096 others(13): Show |
17 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2230+1050_2230+105 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATTTTTTT | 8 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0082 others(5): Show |
8 | HG00408.hp2 HG00438.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2230+1049_2230+105 others(11): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0116 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2230+1045_2230+105 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | AT | A | 6 | a0002c0004t0001g0038 a0002c0005t0003g0151 a0002c0005t0003g0152 others(3): Show |
6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2230+1055delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATT | A | 6 | a0001c0001t0001g0133 a0002c0005t0003g0004 a0002c0005t0003g0158 others(3): Show |
7 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2230+1054_2230+105 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATTTT | A | 32 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0144 others(29): Show |
34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.2230+1052_2230+105 others(8): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATTTTTT | A | 27 | a0002c0003t0002g0007 a0002c0003t0002g0202 a0002c0003t0002g0208 others(24): Show |
28 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2230+1050_2230+105 others(10): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2230+1046_2230+105 others(14): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2230+1045_2230+105 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATTTTTTT others(6): Show |
A | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2230+1043_2230+105 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526076 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0114 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2230+1042_2230+105 others(18): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45526076 | ||||||
chr13:45526114 | A | G | 1 | a0002c0003t0002g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2230+1063A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526114 | |||||||
chr13:45526158 | G | A | 67 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2230+1107G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526158 | |||||||
chr13:45526253 | T | C | 2 | a0001c0002t0001g0303 a0001c0002t0007g0304 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2230+1202T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526253 | |||||||
chr13:45526274 | C | T | 1 | a0002c0005t0014g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2230+1223C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526274 | |||||||
chr13:45526338 | G | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | NA18977.hp1 NA18985.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2230+1287G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526338 | |||||||
chr13:45526406 | T | C | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2230+1355T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526406 | |||||||
chr13:45526447 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2230+1396A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526447 | |||||||
chr13:45526637 | C | G | 93 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(90): Show |
95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2230+1586C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526637 | |||||||
chr13:45526878 | T | C | 14 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(11): Show |
15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2230+1827T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526878 | |||||||
chr13:45526879 | C | T | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2230+1828C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45526879 | |||||||
chr13:45527220 | A | T | 16 | a0001c0002t0001g0252 a0001c0002t0001g0255 a0001c0002t0001g0256 others(13): Show |
16 | HG02040.hp2 HG02071.hp2 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2230+2169A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527220 | |||||||
chr13:45527258 | T | C | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2230+2207T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527258 | |||||||
chr13:45527263 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0066 |
2 | HG00741.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.2230+2212G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527263 | |||||||
chr13:45527426 | G | A | 67 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2231-2365G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527426 | |||||||
chr13:45527429 | G | A | 67 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2231-2362G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527429 | |||||||
chr13:45527447 | A | G | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2231-2344A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527447 | |||||||
chr13:45527865 | T | A | 1 | a0002c0003t0002g0160 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2231-1926T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527865 | |||||||
chr13:45527925 | C | G | 1 | a0001c0002t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2231-1866C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45527925 | |||||||
chr13:45528018 | T | C | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2231-1773T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528018 | |||||||
chr13:45528097 | A | C | 69 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2231-1694A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528097 | |||||||
chr13:45528195 | A | G | 1 | a0002c0004t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2231-1596A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528195 | |||||||
chr13:45528223 | A | G | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2231-1568A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528223 | |||||||
chr13:45528293 | C | T | 14 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(11): Show |
15 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2231-1498C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528293 | |||||||
chr13:45528418 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(104): Show |
108 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.2231-1373C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528418 | |||||||
chr13:45528430 | G | A | 1 | a0002c0003t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2231-1361G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528430 | |||||||
chr13:45528465 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2231-1326A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528465 | |||||||
chr13:45528599 | T | C | 1 | a0002c0003t0002g0006 | 2 | NA19002.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2231-1192T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528599 | |||||||
chr13:45528955 | G | T | 1 | a0002c0005t0003g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2231-836G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45528955 | |||||||
chr13:45529002 | A | G | 12 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(9): Show |
13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2231-789A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529002 | |||||||
chr13:45529058 | C | G | 1 | a0001c0002t0001g0258 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2231-733C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529058 | |||||||
chr13:45529094 | C | G | 1 | a0002c0003t0002g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2231-697C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529094 | |||||||
chr13:45529138 | C | T | 1 | a0001c0002t0001g0258 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2231-653C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529138 | |||||||
chr13:45529207 | A | G | 69 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(66): Show |
72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2231-584A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529207 | |||||||
chr13:45529443 | A | ACTAGTGT | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2231-345_2231-339d others(9): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45529443 | ||||||
chr13:45529465 | CT | C | 70 | a0001c0001t0001g0062 a0002c0003t0002g0005 a0002c0003t0002g0006 others(67): Show |
73 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2231-314delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr13 | 45529465 | ||||||
chr13:45529722 | C | T | 1 | a0002c0003t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2231-69C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 20/22 | chr13 | 45529722 | |||||||
chr13:45529995 | G | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.2358+77G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45529995 | |||||||
chr13:45530189 | G | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2358+271G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530189 | |||||||
chr13:45530266 | G | A | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2358+348G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530266 | |||||||
chr13:45530281 | C | G | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2358+363C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530281 | |||||||
chr13:45530312 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2359-370C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530312 | |||||||
chr13:45530400 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2359-282T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530400 | |||||||
chr13:45530401 | G | A | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2359-281G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530401 | |||||||
chr13:45530458 | A | G | 9 | a0001c0014t0004g0194 a0003c0006t0004g0193 a0003c0006t0004g0195 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2359-224A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530458 | |||||||
chr13:45530528 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(282): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.2359-154C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 21/22 | chr13 | 45530528 | |||||||
chr13:45530886 | AT | A | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2457+107delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45530886 | |||||||
chr13:45531107 | TAAG | T | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2457+329_2457+331d others(5): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45531107 | ||||||
chr13:45531454 | A | G | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2457+674A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531454 | |||||||
chr13:45531504 | G | GT | 216 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(213): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.2457+729dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45531504 | ||||||
chr13:45531510 | G | T | 299 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.2457+730G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531510 | |||||||
chr13:45531543 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2457+763T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531543 | |||||||
chr13:45531548 | C | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2457+768C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531548 | |||||||
chr13:45531641 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2457+861A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531641 | |||||||
chr13:45531912 | C | T | 1 | a0002c0003t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2457+1132C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531912 | |||||||
chr13:45531936 | A | G | 48 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0204 others(45): Show |
50 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.2457+1156A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45531936 | |||||||
chr13:45532385 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2457+1605A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532385 | |||||||
chr13:45532393 | T | G | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2457+1613T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532393 | |||||||
chr13:45532462 | T | C | 12 | a0002c0005t0003g0004 a0002c0005t0003g0010 a0002c0005t0003g0151 others(9): Show |
13 | HG00408.hp1 HG00639.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2457+1682T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532462 | |||||||
chr13:45532486 | C | T | 15 | a0002c0003t0002g0208 a0002c0003t0002g0209 a0002c0003t0002g0210 others(12): Show |
15 | HG01109.hp2 HG01361.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.2457+1706C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532486 | |||||||
chr13:45532560 | G | GT | 7 | a0001c0001t0001g0140 a0002c0004t0001g0016 a0002c0004t0001g0026 others(4): Show |
8 | HG00639.hp1 HG01243.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2457+1807dupT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | ||||||
chr13:45532560 | GT | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0043 others(105): Show |
109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2457+1807delT | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | ||||||
chr13:45532560 | GTT | G | 61 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0072 others(58): Show |
64 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2457+1806_2457+180 others(6): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | ||||||
chr13:45532560 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0101 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2457+1797_2457+180 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | ||||||
chr13:45532560 | GTTTTTTT others(6): Show |
G | 94 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0203 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2457+1795_2457+180 others(17): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532560 | ||||||
chr13:45532575 | T | G | 1 | a0002c0003t0002g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2457+1795T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532575 | |||||||
chr13:45532601 | G | A | 1 | a0001c0002t0001g0325 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2457+1821G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532601 | |||||||
chr13:45532641 | C | T | 68 | a0002c0003t0002g0005 a0002c0003t0002g0006 a0002c0003t0002g0007 others(65): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2457+1861C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532641 | |||||||
chr13:45532652 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(106): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2457+1872C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532652 | |||||||
chr13:45532656 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2457+1876G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532656 | |||||||
chr13:45532791 | G | T | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2458-1911G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532791 | |||||||
chr13:45532803 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2458-1899C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45532803 | |||||||
chr13:45532813 | TC | T | 2 | a0002c0005t0003g0004 a0002c0005t0003g0155 |
3 | HG00639.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2458-1886delC | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45532813 | ||||||
chr13:45533012 | G | A | 1 | a0002c0003t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2458-1690G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533012 | |||||||
chr13:45533039 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1663G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533039 | |||||||
chr13:45533040 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1662G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533040 | |||||||
chr13:45533042 | C | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(213): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.2458-1660C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533042 | |||||||
chr13:45533043 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1659G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533043 | |||||||
chr13:45533044 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1658A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533044 | |||||||
chr13:45533045 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1657G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533045 | |||||||
chr13:45533047 | G | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0127 |
2 | HG01433.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2458-1655G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533047 | |||||||
chr13:45533048 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1654T>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533048 | |||||||
chr13:45533055 | ATGGATGG others(4): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1644_2458-163 others(15): Show |
COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr13 | 45533055 | ||||||
chr13:45533088 | T | C | 1 | a0002c0005t0013g0154 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2458-1614T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533088 | |||||||
chr13:45533090 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1612G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533090 | |||||||
chr13:45533091 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1611A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533091 | |||||||
chr13:45533095 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1607G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533095 | |||||||
chr13:45533110 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1592T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533110 | |||||||
chr13:45533111 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1591C>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533111 | |||||||
chr13:45533112 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2458-1590A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533112 | |||||||
chr13:45533112 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1590A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533112 | |||||||
chr13:45533114 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1588G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533114 | |||||||
chr13:45533115 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1587T>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533115 | |||||||
chr13:45533144 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1558C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533144 | |||||||
chr13:45533148 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1554G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533148 | |||||||
chr13:45533151 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1551A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533151 | |||||||
chr13:45533152 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1550G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533152 | |||||||
chr13:45533153 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1549G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533153 | |||||||
chr13:45533154 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1548G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533154 | |||||||
chr13:45533156 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1546G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533156 | |||||||
chr13:45533157 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1545G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533157 | |||||||
chr13:45533158 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1544A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533158 | |||||||
chr13:45533160 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1542A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533160 | |||||||
chr13:45533161 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1541C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533161 | |||||||
chr13:45533163 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1539G>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533163 | |||||||
chr13:45533181 | G | A | 1 | a0002c0003t0002g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2458-1521G>A | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533181 | |||||||
chr13:45533181 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1521G>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533181 | |||||||
chr13:45533203 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2458-1499A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533203 | |||||||
chr13:45533267 | A | C | 9 | a0001c0002t0001g0245 a0001c0002t0001g0263 a0001c0002t0001g0266 others(6): Show |
9 | HG02109.hp2 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2458-1435A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533267 | |||||||
chr13:45533270 | A | C | 1 | a0002c0005t0012g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2458-1432A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533270 | |||||||
chr13:45533615 | T | C | 1 | a0001c0002t0001g0314 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2458-1087T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533615 | |||||||
chr13:45533623 | A | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2458-1079A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533623 | |||||||
chr13:45533748 | A | G | 1 | a0007c0017t0001g0298 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2458-954A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533748 | |||||||
chr13:45533793 | C | T | 300 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.2458-909C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533793 | |||||||
chr13:45533803 | C | T | 1 | a0001c0002t0001g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2458-899C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45533803 | |||||||
chr13:45534093 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2458-609C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534093 | |||||||
chr13:45534166 | C | T | 2 | a0001c0002t0001g0229 a0001c0002t0001g0230 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2458-536C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534166 | |||||||
chr13:45534179 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2458-523C>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534179 | |||||||
chr13:45534508 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2458-194T>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534508 | |||||||
chr13:45534544 | A | G | 53 | a0001c0014t0004g0194 a0002c0003t0002g0005 a0002c0003t0002g0006 others(50): Show |
55 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2458-158A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534544 | |||||||
chr13:45534556 | A | C | 55 | a0001c0014t0004g0194 a0002c0003t0002g0005 a0002c0003t0002g0006 others(52): Show |
57 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.2458-146A>C | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534556 | |||||||
chr13:45534568 | A | T | 1 | a0002c0005t0011g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2458-134A>T | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534568 | |||||||
chr13:45534647 | C | G | 1 | a0001c0015t0001g0261 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2458-55C>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534647 | |||||||
chr13:45534666 | A | G | 3 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0037 |
3 | HG02257.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2458-36A>G | COG3 | ENSG00000136152.15 | transcript | ENST00000349995.10 | protein_coding | 22/22 | chr13 | 45534666 |