Item | Value |
---|---|
geneid | 1495 |
ensemblid | ENSG00000044115.21 |
hgncid | 2509 |
symbol | CTNNA1 |
name | catenin alpha 1 |
refseq_nuc | NM_001903.5 |
refseq_prot | NP_001894.2 |
ensembl_nuc | ENST00000302763.12 |
ensembl_prot | ENSP00000304669.7 |
mane_status | MANE Select |
chr | chr5 |
start | 138753425 |
end | 138935034 |
strand | + |
ver | v1.2 |
region | chr5:138753425-138935034 |
region5000 | chr5:138748425-138940034 |
regionname0 | CTNNA1_chr5_138753425_138935034 |
regionname5000 | CTNNA1_chr5_138748425_138940034 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 906 | 175 | 68 | 42 | 29 | 10 | 24 | 20 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | MTAVH others(901): Show |
chr5 | 138748425 | 138940034 |
a0002 | 0/0 | 906 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | MTAVH others(901): Show |
chr5 | 138748425 | 138940034 |
a0003 | 0/0 | 906 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | MTAVH others(901): Show |
chr5 | 138748425 | 138940034 |
a0004 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | MTAVH others(901): Show |
chr5 | 138748425 | 138940034 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2718 | 106 | 40 | 21 | 28 | 4 | 12 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0002 | 0/1 | 2718 | 51 | 19 | 18 | 1 | 3 | 9 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0003 | 0/0 | 2718 | 6 | 1 | 2 | 0 | 1 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0004 | 0/0 | 2718 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0005 | 0/0 | 2718 | 3 | 0 | 1 | 0 | 1 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0008 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0009 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0011 | 0/0 | 2718 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0012 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0013 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0001c0014 | 0/0 | 2718 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0002c0007 | 0/0 | 2718 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0003c0006 | 0/0 | 2718 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 | ||
a0004c0010 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | ATGAC others(2713): Show |
chr5 | 138748425 | 138940034 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3754 | 102 | 38 | 19 | 28 | 4 | 12 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0001c0001t0006 | 0/0 | 3754 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0001c0001t0007 | 0/0 | 3754 | 2 | 0 | 2 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0001c0002t0002 | 0/1 | 3753 | 30 | 3 | 13 | 1 | 3 | 9 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3748): Show |
chr5 | 138748425 | 138940034 |
a0001c0002t0003 | 0/0 | 3750 | 17 | 12 | 5 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0002t0005 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3748): Show |
chr5 | 138748425 | 138940034 |
a0001c0002t0008 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCC others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0003t0002 | 0/0 | 3753 | 6 | 1 | 2 | 0 | 1 | 2 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3748): Show |
chr5 | 138748425 | 138940034 |
a0001c0004t0004 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0005t0001 | 0/0 | 3754 | 3 | 0 | 1 | 0 | 1 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0001c0008t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0009t0004 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0011t0001 | 0/0 | 3754 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0001c0012t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0013t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3745): Show |
chr5 | 138748425 | 138940034 |
a0001c0014t0001 | 0/0 | 3754 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0002c0007t0001 | 0/0 | 3754 | 2 | 2 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0003c0006t0001 | 0/0 | 3754 | 2 | 0 | 0 | 2 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
a0004c0010t0001 | 0/0 | 3754 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | CTCCT others(3749): Show |
chr5 | 138748425 | 138940034 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0002t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0004t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0004t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0005t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0008t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0009t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0011t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0012t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0013t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0001c0014t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0002c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0002c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0003c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0003c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
a0004c0010t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0001 | g0167 | EUR | GBR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | FIN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00423 | hp2 | a0004 | c0010 | t0001 | g0169 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0055 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG00741 | hp2 | a0001 | c0005 | t0001 | g0156 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0111 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0024 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01167 | hp2 | a0001 | c0002 | t0003 | g0048 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01168 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0044 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0064 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0052 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01516 | hp1 | a0001 | c0003 | t0002 | g0062 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0021 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02280 | hp1 | a0001 | c0012 | t0003 | g0019 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02630 | hp2 | a0001 | c0008 | t0003 | g0030 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02647 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02738 | hp1 | a0001 | c0003 | t0002 | g0076 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02809 | hp1 | a0001 | c0004 | t0004 | g0180 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02818 | hp1 | a0001 | c0013 | t0003 | g0031 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0050 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0034 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0049 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02965 | hp2 | a0002 | c0007 | t0001 | g0100 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03139 | hp1 | a0001 | c0014 | t0001 | g0145 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03225 | hp2 | a0001 | c0004 | t0004 | g0005 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0077 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03453 | hp2 | a0001 | c0002 | t0005 | g0026 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03540 | hp2 | a0001 | c0004 | t0004 | g0007 | AFR | GWD | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03579 | hp1 | a0002 | c0007 | t0001 | g0099 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03654 | hp2 | a0001 | c0005 | t0001 | g0168 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0070 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | BEB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18906 | hp2 | a0001 | c0002 | t0008 | g0028 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0022 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19057 | hp2 | a0003 | c0006 | t0001 | g0095 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19060 | hp1 | a0003 | c0006 | t0001 | g0090 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0025 | AFR | YRI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | ASW | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA20805 | hp1 | a0001 | c0011 | t0001 | g0107 | EUR | TSI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0079 | EUR | TSI | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0078 | SAS | GIH | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02486 | hp2 | a0001 | c0009 | t0004 | g0006 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | USA | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0063 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | LWK | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0065 | REF | REF | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0053 | REF | REF | CTNNA1_chr5_138748425_138940034 | CTNNA1 | chr5 | 138748425 | 138940034 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:138824596 | C | T | 1 | a0002 | 2 | HG02965.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.655C>T | p.Pro219Ser | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/18 | 743/3754 | 655/2721 | 219/906 | chr5 | 138824596 | |||
chr5:138824711 | A | G | 1 | a0003 | 2 | NA19057.hp2 NA19060.hp1 |
missense_variant | MODERATE | c.770A>G | p.Asn257Ser | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/18 | 858/3754 | 770/2721 | 257/906 | chr5 | 138824711 | |||
chr5:138925306 | T | A | 1 | a0004 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1798T>A | p.Ser600Thr | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/18 | 1886/3754 | 1798/2721 | 600/906 | chr5 | 138925306 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:138812254 | A | C | 1 | a0001c0003 | 6 | HG00642.hp1 HG01346.hp2 HG01516.hp1 others(3): Show |
synonymous_variant | LOW | c.540A>C | p.Leu180Leu | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/18 | 628/3754 | 540/2721 | 180/906 | chr5 | 138812254 | |||
chr5:138812260 | T | G | 3 | a0001c0004 a0001c0008 a0001c0009 |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.546T>G | p.Pro182Pro | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/18 | 634/3754 | 546/2721 | 182/906 | chr5 | 138812260 | |||
chr5:138917757 | C | T | 2 | a0001c0004 a0001c0009 |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.1405C>T | p.Leu469Leu | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/18 | 1493/3754 | 1405/2721 | 469/906 | chr5 | 138917757 | |||
chr5:138930475 | G | A | 1 | a0001c0011 | 1 | NA20805.hp1 | splice_region_variant&synonymous_variant | LOW | c.2013G>A | p.Ala671Ala | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 15/18 | 2101/3754 | 2013/2721 | 671/906 | chr5 | 138930475 | |||
chr5:138930857 | G | A | 7 | a0001c0002 a0001c0003 a0001c0004 others(4): Show |
63 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
synonymous_variant | LOW | c.2220G>A | p.Ser740Ser | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/18 | 2308/3754 | 2220/2721 | 740/906 | chr5 | 138930857 | |||
chr5:138930863 | C | G | 1 | a0001c0005 | 3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
synonymous_variant | LOW | c.2226C>G | p.Val742Val | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/18 | 2314/3754 | 2226/2721 | 742/906 | chr5 | 138930863 | |||
chr5:138932622 | A | G | 1 | a0001c0014 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.2343A>G | p.Gln781Gln | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/18 | 2431/3754 | 2343/2721 | 781/906 | chr5 | 138932622 | |||
chr5:138933822 | G | A | 1 | a0001c0012 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2454G>A | p.Leu818Leu | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 2542/3754 | 2454/2721 | 818/906 | chr5 | 138933822 | |||
chr5:138933882 | C | T | 1 | a0001c0009 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2514C>T | p.Val838Val | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 2602/3754 | 2514/2721 | 838/906 | chr5 | 138933882 | |||
chr5:138933900 | A | G | 1 | a0001c0013 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2532A>G | p.Gln844Gln | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 2620/3754 | 2532/2721 | 844/906 | chr5 | 138933900 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:138753429 | T | C | 1 | a0001c0002t0008 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/18 | 28496 | chr5 | 138753429 | ||||||
chr5:138934469 | C | T | 1 | a0001c0002t0005 | 3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*380C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 380 | chr5 | 138934469 | ||||||
chr5:138934602 | T | TATC | 3 | a0001c0002t0002 a0001c0002t0005 a0001c0003t0002 |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*516_*518dupCAT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 519 | INFO_REALIGN_3_PRIME | chr5 | 138934602 | |||||
chr5:138934749 | T | C | 1 | a0001c0001t0006 | 2 | NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*660T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 660 | chr5 | 138934749 | ||||||
chr5:138934799 | A | G | 1 | a0001c0001t0007 | 2 | HG01099.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 710 | chr5 | 138934799 | ||||||
chr5:138934853 | T | A | 5 | a0001c0002t0002 a0001c0002t0005 a0001c0003t0002 others(2): Show |
42 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*764T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 764 | chr5 | 138934853 | ||||||
chr5:138934902 | GTGAT | G | 10 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0005 others(7): Show |
63 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*827_*830delGATT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 18/18 | 827 | INFO_REALIGN_3_PRIME | chr5 | 138934902 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:138753535 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-3+25G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753535 | |||||||
chr5:138753541 | G | C | 2 | a0001c0002t0002g0002 a0001c0002t0002g0003 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-3+31G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753541 | |||||||
chr5:138753598 | G | A | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+88G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753598 | |||||||
chr5:138753610 | C | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-3+100C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753610 | |||||||
chr5:138753726 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+216G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138753726 | |||||||
chr5:138754014 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-3+504A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754014 | |||||||
chr5:138754059 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-3+549A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754059 | |||||||
chr5:138754231 | G | GT | 95 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+736dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138754231 | ||||||
chr5:138754241 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+731T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754241 | |||||||
chr5:138754821 | G | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+1311G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754821 | |||||||
chr5:138754880 | C | T | 1 | a0001c0002t0002g0085 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-3+1370C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138754880 | |||||||
chr5:138755002 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-3+1492C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755002 | |||||||
chr5:138755040 | G | A | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+1530G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755040 | |||||||
chr5:138755141 | G | GGT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+1634_-3+1635dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755141 | ||||||
chr5:138755332 | G | A | 7 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(4): Show |
7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+1822G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755332 | |||||||
chr5:138755845 | C | CT | 11 | a0001c0002t0002g0003 a0001c0002t0002g0078 a0001c0002t0002g0079 others(8): Show |
11 | HG00735.hp1 HG01070.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+2370dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTT | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0017 others(4): Show |
7 | HG02074.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+2367_-3+2370del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG00438.hp2 HG01243.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+2366_-3+2370del others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0179 |
3 | HG01361.hp1 HG02129.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-3+2361_-3+2370del others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(4): Show |
C | 75 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(72): Show |
75 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-3+2360_-3+2370del others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 others(13): Show |
16 | HG01243.hp2 HG01516.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3+2359_-3+2370del others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18946.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-3+2358_-3+2370del others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(8): Show |
C | 6 | a0001c0002t0003g0033 a0001c0002t0003g0034 a0001c0004t0004g0005 others(3): Show |
6 | HG00741.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+2356_-3+2370del others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(9): Show |
C | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+2355_-3+2370del others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(12): Show |
C | 12 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0002t0003g0021 others(9): Show |
12 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+2352_-3+2370del others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(13): Show |
C | 2 | a0001c0002t0003g0020 a0001c0002t0003g0027 |
2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-3+2351_-3+2370del others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755845 | CTTTTTTT others(15): Show |
C | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3+2349_-3+2370del others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138755845 | ||||||
chr5:138755934 | C | T | 2 | a0001c0001t0001g0087 a0004c0010t0001g0169 |
2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-3+2424C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138755934 | |||||||
chr5:138756008 | T | G | 7 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
7 | HG00423.hp1 HG02132.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+2498T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756008 | |||||||
chr5:138756027 | C | CTTAT | 2 | a0001c0002t0003g0029 a0001c0002t0008g0028 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-3+2544_-3+2547dup others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138756027 | ||||||
chr5:138756027 | CTTAT | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
113 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3+2544_-3+2547del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138756027 | ||||||
chr5:138756382 | G | C | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+2872G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756382 | |||||||
chr5:138756607 | G | T | 2 | a0001c0005t0001g0167 a0001c0005t0001g0168 |
2 | HG00099.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-3+3097G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756607 | |||||||
chr5:138756783 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-3+3273G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756783 | |||||||
chr5:138756795 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+3285G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756795 | |||||||
chr5:138756978 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-3+3468C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138756978 | |||||||
chr5:138757028 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-3+3518G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757028 | |||||||
chr5:138757194 | TCAAA | T | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-3+3689_-3+3692del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138757194 | ||||||
chr5:138757327 | A | G | 3 | a0001c0002t0002g0074 a0001c0002t0002g0075 a0001c0002t0002g0084 |
3 | HG01070.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-3+3817A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757327 | |||||||
chr5:138757420 | G | C | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+3910G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757420 | |||||||
chr5:138757494 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-3+3984T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757494 | |||||||
chr5:138757625 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+4115G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757625 | |||||||
chr5:138757732 | AGTTCTTG others(5): Show |
A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+4225_-3+4236del others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138757732 | ||||||
chr5:138757837 | A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+4327A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757837 | |||||||
chr5:138757969 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-3+4459C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138757969 | |||||||
chr5:138758294 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+4784C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758294 | |||||||
chr5:138758318 | C | T | 1 | a0001c0002t0002g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-3+4808C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758318 | |||||||
chr5:138758347 | G | A | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+4837G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758347 | |||||||
chr5:138758524 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+5014A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758524 | |||||||
chr5:138758534 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+5024G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758534 | |||||||
chr5:138758749 | A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-3+5239A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758749 | |||||||
chr5:138758960 | C | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5450C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138758960 | |||||||
chr5:138759147 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3+5637G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759147 | |||||||
chr5:138759516 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-3+6006C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759516 | |||||||
chr5:138759517 | A | G | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+6007A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759517 | |||||||
chr5:138759863 | T | A | 2 | a0001c0003t0002g0076 a0001c0003t0002g0077 |
2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-3+6353T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759863 | |||||||
chr5:138759923 | T | G | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-3+6413T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759923 | |||||||
chr5:138759954 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-3+6444T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138759954 | |||||||
chr5:138759980 | C | CT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0098 others(11): Show |
14 | HG00323.hp1 HG00735.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+6499dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | ||||||
chr5:138759980 | CT | C | 69 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3+6499delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | ||||||
chr5:138759980 | CTT | C | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+6498_-3+6499del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | ||||||
chr5:138759980 | CTTT | C | 8 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0002t0003g0021 others(5): Show |
8 | HG01099.hp2 HG01109.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+6497_-3+6499del others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138759980 | ||||||
chr5:138760241 | G | A | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-3+6731G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760241 | |||||||
chr5:138760371 | C | CT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.-3+6871dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138760371 | ||||||
chr5:138760413 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+6903G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760413 | |||||||
chr5:138760417 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+6907G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760417 | |||||||
chr5:138760462 | CA | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-3+6956delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138760462 | ||||||
chr5:138760624 | G | A | 2 | a0002c0007t0001g0099 a0002c0007t0001g0100 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-3+7114G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760624 | |||||||
chr5:138760658 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-3+7148G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760658 | |||||||
chr5:138760894 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0166 a0001c0001t0001g0170 |
3 | HG00323.hp2 HG02129.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-3+7384G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138760894 | |||||||
chr5:138761127 | A | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-3+7617A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761127 | |||||||
chr5:138761273 | C | T | 2 | a0001c0001t0001g0087 a0004c0010t0001g0169 |
2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-3+7763C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761273 | |||||||
chr5:138761315 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+7805A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761315 | |||||||
chr5:138761322 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-3+7812C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761322 | |||||||
chr5:138761479 | C | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+7969C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761479 | |||||||
chr5:138761480 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3+7970G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761480 | |||||||
chr5:138761486 | C | T | 9 | a0001c0001t0001g0103 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
9 | HG00639.hp2 HG01070.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+7976C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761486 | |||||||
chr5:138761595 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+8085T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138761595 | |||||||
chr5:138761603 | T | TA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+8100dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138761603 | ||||||
chr5:138762035 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+8525C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762035 | |||||||
chr5:138762093 | A | G | 2 | a0001c0002t0002g0075 a0001c0002t0002g0084 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-3+8583A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762093 | |||||||
chr5:138762247 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+8737C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762247 | |||||||
chr5:138762375 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3+8865C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762375 | |||||||
chr5:138762487 | G | GT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+8986dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138762487 | ||||||
chr5:138762733 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+9223C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762733 | |||||||
chr5:138762741 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+9231C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762741 | |||||||
chr5:138762789 | CTG | C | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-3+9281_-3+9282del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138762789 | ||||||
chr5:138762827 | G | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+9317G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762827 | |||||||
chr5:138762862 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-3+9352T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762862 | |||||||
chr5:138762993 | A | G | 83 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-3+9483A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138762993 | |||||||
chr5:138763083 | A | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+9573A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763083 | |||||||
chr5:138763099 | G | GT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-3+9598dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138763099 | ||||||
chr5:138763332 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+9822C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763332 | |||||||
chr5:138763408 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+9898A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763408 | |||||||
chr5:138763496 | C | T | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+9986C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763496 | |||||||
chr5:138763583 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+10073A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763583 | |||||||
chr5:138763727 | G | C | 1 | a0001c0002t0002g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-3+10217G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763727 | |||||||
chr5:138763816 | TGTC | T | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+10307_-3+10309d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763816 | |||||||
chr5:138763882 | AGT | A | 83 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-3+10377_-3+10378d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138763882 | ||||||
chr5:138763908 | A | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+10398A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138763908 | |||||||
chr5:138764145 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10635A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764145 | |||||||
chr5:138764171 | C | T | 2 | a0001c0002t0002g0066 a0001c0002t0002g0083 |
2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-3+10661C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764171 | |||||||
chr5:138764185 | AAAAAAAC | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10696_-3+10702d others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764185 | ||||||
chr5:138764304 | T | C | 3 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0034 |
3 | HG00741.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-3+10794T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764304 | |||||||
chr5:138764320 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10810C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764320 | |||||||
chr5:138764353 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+10843T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764353 | |||||||
chr5:138764483 | T | A | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+10973T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764483 | |||||||
chr5:138764623 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-3+11113C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764623 | |||||||
chr5:138764766 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-3+11256T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764766 | |||||||
chr5:138764776 | A | G | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-3+11266A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764776 | |||||||
chr5:138764868 | C | CT | 30 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0091 others(27): Show |
30 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-3+11380dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | ||||||
chr5:138764868 | C | CTT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-3+11379_-3+11380d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | ||||||
chr5:138764868 | C | CTTT | 25 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0088 others(22): Show |
25 | HG00423.hp1 HG00735.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+11378_-3+11380d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | ||||||
chr5:138764868 | CT | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+11380delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138764868 | ||||||
chr5:138764869 | T | TC | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11359_-3+11360i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764869 | |||||||
chr5:138764906 | C | T | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+11396C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138764906 | |||||||
chr5:138765186 | AC | A | 10 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0051 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+11679delC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765186 | ||||||
chr5:138765197 | C | T | 1 | a0001c0002t0002g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-3+11687C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765197 | |||||||
chr5:138765309 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+11799A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765309 | |||||||
chr5:138765331 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-3+11821G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765331 | |||||||
chr5:138765333 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01099.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+11823G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765333 | |||||||
chr5:138765348 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+11838A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765348 | |||||||
chr5:138765409 | T | C | 11 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0117 others(8): Show |
11 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+11899T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765409 | |||||||
chr5:138765779 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-3+12269T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765779 | |||||||
chr5:138765839 | C | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+12329C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765839 | |||||||
chr5:138765897 | C | T | 31 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-3+12387C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765897 | |||||||
chr5:138765947 | C | CA | 17 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(14): Show |
17 | HG00423.hp1 HG00642.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3+12461dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765947 | ||||||
chr5:138765947 | CA | C | 37 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0040 others(34): Show |
37 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3+12461delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765947 | ||||||
chr5:138765947 | CAA | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(4): Show |
7 | HG00423.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+12460_-3+12461d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138765947 | ||||||
chr5:138765971 | A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-3+12461A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138765971 | |||||||
chr5:138766137 | C | CACAT | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+12631_-3+12634d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138766137 | ||||||
chr5:138766229 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+12719C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766229 | |||||||
chr5:138766451 | G | GT | 105 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-3+12956dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138766451 | ||||||
chr5:138766451 | G | T | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+12941G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766451 | |||||||
chr5:138766456 | T | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+12946T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766456 | |||||||
chr5:138766489 | A | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+12979A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766489 | |||||||
chr5:138766761 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-3+13251A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766761 | |||||||
chr5:138766800 | T | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+13290T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766800 | |||||||
chr5:138766861 | G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-3+13351G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766861 | |||||||
chr5:138766974 | A | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+13464A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138766974 | |||||||
chr5:138767031 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-3+13521A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767031 | |||||||
chr5:138767033 | T | TTTTC | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-3+13535_-3+13538d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138767033 | ||||||
chr5:138767053 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-3+13543T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767053 | |||||||
chr5:138767071 | C | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+13561C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767071 | |||||||
chr5:138767283 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-3+13773A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767283 | |||||||
chr5:138767577 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-3+14067A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767577 | |||||||
chr5:138767647 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-3+14137T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767647 | |||||||
chr5:138767949 | A | C | 4 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-13974A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138767949 | |||||||
chr5:138768198 | A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-13725A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768198 | |||||||
chr5:138768322 | C | G | 2 | a0001c0002t0002g0070 a0001c0002t0002g0079 |
2 | HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-2-13601C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768322 | |||||||
chr5:138768338 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-2-13585C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768338 | |||||||
chr5:138768558 | G | GT | 8 | a0001c0001t0001g0018 a0001c0001t0006g0174 a0001c0001t0006g0175 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13341dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | ||||||
chr5:138768558 | G | GTT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(5): Show |
8 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13342_-2-13341d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | ||||||
chr5:138768558 | GT | G | 79 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0086 others(76): Show |
79 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-2-13341delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | ||||||
chr5:138768558 | GTT | G | 26 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(23): Show |
26 | HG00323.hp2 HG00438.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-13342_-2-13341d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138768558 | ||||||
chr5:138768568 | T | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-13355T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768568 | |||||||
chr5:138768654 | A | C | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-13269A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768654 | |||||||
chr5:138768924 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-12999C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138768924 | |||||||
chr5:138769009 | A | G | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12914A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769009 | |||||||
chr5:138769081 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-2-12842T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769081 | |||||||
chr5:138769144 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-12779T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769144 | |||||||
chr5:138769210 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-2-12713C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769210 | |||||||
chr5:138769336 | C | G | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-12587C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769336 | |||||||
chr5:138769379 | G | GTTA | 6 | a0001c0002t0002g0057 a0001c0002t0002g0058 a0001c0002t0002g0066 others(3): Show |
6 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-12523_-2-12521d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138769379 | ||||||
chr5:138769667 | C | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-12256C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769667 | |||||||
chr5:138769787 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-12136C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769787 | |||||||
chr5:138769794 | A | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0002c0007t0001g0099 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12129A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769794 | |||||||
chr5:138769826 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2-12097C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769826 | |||||||
chr5:138769915 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-12008C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138769915 | |||||||
chr5:138770124 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-2-11799C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770124 | |||||||
chr5:138770145 | T | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11778T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770145 | |||||||
chr5:138770269 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11654G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770269 | |||||||
chr5:138770637 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-11286T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770637 | |||||||
chr5:138770641 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-11282C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770641 | |||||||
chr5:138770671 | C | T | 3 | a0001c0002t0002g0051 a0001c0002t0002g0071 a0001c0002t0002g0078 |
3 | HG01081.hp2 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-2-11252C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770671 | |||||||
chr5:138770695 | T | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-2-11228T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770695 | |||||||
chr5:138770747 | G | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-2-11176G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770747 | |||||||
chr5:138770808 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-11115C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770808 | |||||||
chr5:138770896 | G | A | 2 | a0001c0002t0003g0029 a0001c0002t0008g0028 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-11027G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138770896 | |||||||
chr5:138770950 | CA | C | 86 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-2-10958delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138770950 | ||||||
chr5:138771153 | A | G | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-2-10770A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771153 | |||||||
chr5:138771172 | C | T | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-10751C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771172 | |||||||
chr5:138771210 | A | AT | 5 | a0001c0002t0002g0002 a0001c0004t0004g0005 a0001c0004t0004g0007 others(2): Show |
5 | HG01981.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-10701dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138771210 | ||||||
chr5:138771301 | C | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-10622C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771301 | |||||||
chr5:138771740 | A | C | 1 | a0001c0002t0003g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-2-10183A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771740 | |||||||
chr5:138771762 | A | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-10161A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771762 | |||||||
chr5:138771865 | A | G | 1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-2-10058A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771865 | |||||||
chr5:138771926 | T | TA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(16): Show |
19 | HG01109.hp2 HG01993.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-2-9987dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138771926 | ||||||
chr5:138771948 | T | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-9975T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138771948 | |||||||
chr5:138772035 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-9888T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138772035 | |||||||
chr5:138772203 | A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-9720A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138772203 | |||||||
chr5:138772237 | T | C | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-9686T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138772237 | |||||||
chr5:138773014 | T | C | 10 | a0001c0001t0001g0088 a0001c0001t0001g0102 a0001c0001t0001g0114 others(7): Show |
10 | HG02132.hp1 HG02602.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-8909T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773014 | |||||||
chr5:138773254 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-2-8669G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773254 | |||||||
chr5:138773261 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-8662C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773261 | |||||||
chr5:138773335 | C | T | 5 | a0001c0001t0001g0106 a0001c0004t0004g0005 a0001c0004t0004g0007 others(2): Show |
5 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8588C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773335 | |||||||
chr5:138773559 | T | C | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2-8364T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773559 | |||||||
chr5:138773652 | T | TAG | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-2-8268_-2-8267dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138773652 | ||||||
chr5:138773680 | AG | A | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-8242delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773680 | |||||||
chr5:138773696 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-8227C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773696 | |||||||
chr5:138773850 | A | G | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-8073A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138773850 | |||||||
chr5:138774151 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-7772G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774151 | |||||||
chr5:138774383 | T | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-7540T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774383 | |||||||
chr5:138774402 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-2-7521T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774402 | |||||||
chr5:138774484 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-2-7439C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774484 | |||||||
chr5:138774832 | A | ATC | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-7088_-2-7087dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138774832 | ||||||
chr5:138774851 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-2-7072C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774851 | |||||||
chr5:138774905 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-2-7018G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138774905 | |||||||
chr5:138775013 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-6910A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775013 | |||||||
chr5:138775209 | A | T | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-6714A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775209 | |||||||
chr5:138775261 | A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2-6662A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775261 | |||||||
chr5:138775430 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-6493A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775430 | |||||||
chr5:138775502 | C | T | 3 | a0001c0002t0002g0051 a0001c0002t0002g0071 a0001c0002t0002g0078 |
3 | HG01081.hp2 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-2-6421C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775502 | |||||||
chr5:138775714 | C | CT | 44 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0088 others(41): Show |
44 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-2-6184dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138775714 | ||||||
chr5:138775714 | CT | C | 28 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2-6184delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138775714 | ||||||
chr5:138775714 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-6191_-2-6184del others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138775714 | ||||||
chr5:138775762 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-2-6161G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775762 | |||||||
chr5:138775773 | A | C | 1 | a0001c0002t0003g0047 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-2-6150A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775773 | |||||||
chr5:138775803 | A | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-6120A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775803 | |||||||
chr5:138775917 | G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-6006G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775917 | |||||||
chr5:138775963 | T | C | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-5960T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138775963 | |||||||
chr5:138776037 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-5886T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776037 | |||||||
chr5:138776039 | C | CT | 90 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-2-5860dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776039 | ||||||
chr5:138776039 | C | CTT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(26): Show |
29 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-5861_-2-5860dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776039 | ||||||
chr5:138776039 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-5884C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776039 | |||||||
chr5:138776039 | CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0002g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2-5872_-2-5860del others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776039 | ||||||
chr5:138776159 | GTCTCTGG others(182): Show |
G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0045 others(1): Show |
4 | HG00438.hp2 HG02074.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5763_-2-5575del | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776159 | |||||||
chr5:138776330 | C | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-5593C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776330 | |||||||
chr5:138776349 | C | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0045 others(1): Show |
4 | HG00438.hp2 HG02074.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5574C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776349 | |||||||
chr5:138776350 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0045 others(1): Show |
4 | HG00438.hp2 HG02074.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-5573A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776350 | |||||||
chr5:138776379 | G | A | 1 | a0003c0006t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-2-5544G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776379 | |||||||
chr5:138776458 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0149 others(2): Show |
5 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-5465C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776458 | |||||||
chr5:138776475 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-2-5448A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776475 | |||||||
chr5:138776586 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2-5337G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776586 | |||||||
chr5:138776632 | C | T | 1 | a0001c0002t0005g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-5291C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776632 | |||||||
chr5:138776657 | G | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-2-5266G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776657 | |||||||
chr5:138776679 | C | A | 2 | a0001c0002t0003g0029 a0001c0002t0008g0028 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-5244C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776679 | |||||||
chr5:138776804 | A | AC | 14 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-5112dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776804 | ||||||
chr5:138776826 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-5097C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776826 | |||||||
chr5:138776843 | CG | C | 125 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-2-5073delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776843 | ||||||
chr5:138776856 | T | TCCCCCAC others(42): Show |
1 | a0001c0002t0002g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-2-5048_-2-5000dup others(49): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776856 | ||||||
chr5:138776867 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-5056C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776867 | |||||||
chr5:138776875 | GCGGGGCG others(42): Show |
G | 1 | a0001c0002t0002g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-2-5029_-2-4981del others(49): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776875 | ||||||
chr5:138776894 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-5029A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776894 | |||||||
chr5:138776905 | CCCCCCAC others(42): Show |
C | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2-4984_-2-4936del others(49): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138776905 | ||||||
chr5:138776924 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0164 |
2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-2-4999A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776924 | |||||||
chr5:138776931 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-4992G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776931 | |||||||
chr5:138776938 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-4985C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776938 | |||||||
chr5:138776975 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-4948G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776975 | |||||||
chr5:138776978 | G | T | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-4945G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776978 | |||||||
chr5:138776979 | C | T | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-4944C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776979 | |||||||
chr5:138776996 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-2-4927G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138776996 | |||||||
chr5:138777077 | C | T | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2-4846C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777077 | |||||||
chr5:138777141 | C | T | 1 | a0001c0003t0002g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2-4782C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777141 | |||||||
chr5:138777178 | C | CG | 4 | a0001c0001t0001g0013 a0001c0001t0001g0117 a0001c0002t0002g0082 others(1): Show |
4 | HG01109.hp2 HG02602.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4741dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777178 | ||||||
chr5:138777181 | G | A | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-4742G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777181 | |||||||
chr5:138777194 | T | C | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-4729T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777194 | |||||||
chr5:138777201 | G | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-4722G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777201 | |||||||
chr5:138777215 | A | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-4708A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777215 | |||||||
chr5:138777260 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2-4663G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777260 | |||||||
chr5:138777277 | G | A | 2 | a0001c0002t0003g0029 a0001c0002t0008g0028 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-4646G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777277 | |||||||
chr5:138777303 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-4620G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777303 | |||||||
chr5:138777342 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0043 a0001c0002t0003g0044 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-4581C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777342 | |||||||
chr5:138777450 | C | CG | 14 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0120 others(11): Show |
14 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-4469dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777450 | ||||||
chr5:138777506 | C | T | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(7): Show |
10 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-4417C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777506 | |||||||
chr5:138777530 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-4393G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777530 | |||||||
chr5:138777552 | C | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-4371C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777552 | |||||||
chr5:138777577 | T | C | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-4346T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777577 | |||||||
chr5:138777665 | G | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-4258G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777665 | |||||||
chr5:138777719 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-2-4204A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777719 | |||||||
chr5:138777876 | A | AGAGGGAG others(8): Show |
1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2-4020_-2-4006dup others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777876 | ||||||
chr5:138777876 | AGAGGGAG others(8): Show |
A | 7 | a0001c0001t0001g0166 a0001c0001t0001g0170 a0001c0002t0002g0071 others(4): Show |
7 | HG00741.hp2 HG02129.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-4020_-2-4006del others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777876 | ||||||
chr5:138777888 | A | AGAGGAGG others(8): Show |
4 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0103 others(1): Show |
4 | HG01243.hp2 HG01516.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4021_-2-4020ins others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777888 | ||||||
chr5:138777888 | A | AGAGGAGG others(83): Show |
1 | a0001c0001t0006g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2-4021_-2-4020ins others(90): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777888 | ||||||
chr5:138777888 | A | AGAGGAGG others(98): Show |
1 | a0001c0001t0006g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-2-4021_-2-4020ins others(105): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777888 | ||||||
chr5:138777903 | A | AGAGGAGG others(8): Show |
14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG01884.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-3970_-2-3956dup others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | ||||||
chr5:138777903 | A | AGAGGAGG others(23): Show |
5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0002t0003g0032 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-3985_-2-3956dup others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | ||||||
chr5:138777903 | A | AGAGGAGG others(38): Show |
2 | a0001c0002t0003g0034 a0001c0002t0005g0050 |
2 | HG02895.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-2-4000_-2-3956dup others(45): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | ||||||
chr5:138777903 | A | AGAGGAGG others(83): Show |
1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-2-3956_-2-3955ins others(90): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777903 | ||||||
chr5:138777903 | A | G | 102 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2-4020A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777903 | |||||||
chr5:138777913 | GA | G | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4009delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138777913 | |||||||
chr5:138777929 | A | AGGGGGAG others(24): Show |
1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-2-3989_-2-3959dup others(31): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777929 | ||||||
chr5:138777937 | G | GAGGGAGA others(23): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-3957_-2-3956ins others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777937 | ||||||
chr5:138777988 | C | CT | 8 | a0001c0002t0002g0054 a0001c0002t0002g0070 a0001c0002t0002g0075 others(5): Show |
8 | HG01071.hp1 HG01361.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-3912dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138777988 | C | CTT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG02622.hp1 HG02970.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-3913_-2-3912dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138777988 | C | CTTT | 6 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG01099.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-3914_-2-3912dup others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138777988 | C | CTTTT | 56 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(53): Show |
56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-2-3915_-2-3912dup others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138777988 | C | CTTTTT | 36 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0097 others(33): Show |
36 | HG00423.hp2 HG00438.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-2-3916_-2-3912dup others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138777988 | CT | C | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(12): Show |
15 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-3912delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138777988 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-2-3922_-2-3912del others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138777988 | ||||||
chr5:138778155 | G | A | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3768G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778155 | |||||||
chr5:138778160 | A | AT | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-2-3757dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138778160 | ||||||
chr5:138778344 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-3579G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778344 | |||||||
chr5:138778400 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-3523A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778400 | |||||||
chr5:138778544 | C | T | 5 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-3379C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778544 | |||||||
chr5:138778868 | G | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0043 a0001c0002t0003g0044 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-3055G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778868 | |||||||
chr5:138778886 | G | GT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-3027dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138778886 | ||||||
chr5:138778947 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-2-2976C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138778947 | |||||||
chr5:138779032 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-2891C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779032 | |||||||
chr5:138779530 | T | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-2393T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779530 | |||||||
chr5:138779536 | A | T | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2-2387A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779536 | |||||||
chr5:138779666 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-2-2257G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779666 | |||||||
chr5:138779717 | G | GT | 8 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(5): Show |
8 | HG01243.hp1 HG02074.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-2201dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138779717 | ||||||
chr5:138779717 | G | GTT | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0003g0032 others(3): Show |
6 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-2202_-2-2201dup others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138779717 | ||||||
chr5:138779717 | G | T | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-2206G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779717 | |||||||
chr5:138779721 | TTG | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-2-2200_-2-2199del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138779721 | ||||||
chr5:138779722 | TG | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-2200delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779722 | |||||||
chr5:138779723 | G | T | 27 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(24): Show |
27 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-2-2200G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779723 | |||||||
chr5:138779724 | T | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2-2199T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138779724 | |||||||
chr5:138780242 | C | A | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-1681C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780242 | |||||||
chr5:138780276 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2-1647G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780276 | |||||||
chr5:138780346 | C | G | 83 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-2-1577C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780346 | |||||||
chr5:138780352 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-1571G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780352 | |||||||
chr5:138780439 | C | T | 3 | a0001c0005t0001g0156 a0001c0005t0001g0167 a0001c0005t0001g0168 |
3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-2-1484C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780439 | |||||||
chr5:138780472 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0002c0007t0001g0099 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1451C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780472 | |||||||
chr5:138780520 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-1403T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780520 | |||||||
chr5:138780641 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-1282C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780641 | |||||||
chr5:138780674 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(2): Show |
5 | NA18946.hp1 NA18948.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-1249G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780674 | |||||||
chr5:138780735 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1188C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780735 | |||||||
chr5:138780810 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1113C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780810 | |||||||
chr5:138780948 | CTG | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-2-973_-2-972delGT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138780948 | ||||||
chr5:138780988 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-2-935G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138780988 | |||||||
chr5:138781152 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-771C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138781152 | |||||||
chr5:138781236 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-687G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138781236 | |||||||
chr5:138781285 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-638T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | chr5 | 138781285 | |||||||
chr5:138781554 | CA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
137 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-2-352delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 138781554 | ||||||
chr5:138782070 | A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.105+41A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782070 | |||||||
chr5:138782166 | T | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+137T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782166 | |||||||
chr5:138782188 | G | A | 1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.105+159G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782188 | |||||||
chr5:138782245 | G | A | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.105+216G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782245 | |||||||
chr5:138782249 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.105+220A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782249 | |||||||
chr5:138782602 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+573C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782602 | |||||||
chr5:138782646 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.106-531A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782646 | |||||||
chr5:138782649 | G | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.106-528G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 2/17 | chr5 | 138782649 | |||||||
chr5:138783709 | A | G | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+337A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138783709 | |||||||
chr5:138783711 | A | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.301+339A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138783711 | |||||||
chr5:138784366 | A | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.301+994A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784366 | |||||||
chr5:138784424 | A | C | 6 | a0001c0003t0002g0055 a0001c0003t0002g0062 a0001c0003t0002g0063 others(3): Show |
6 | HG00642.hp1 HG01346.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1052A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784424 | |||||||
chr5:138784665 | C | G | 11 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0117 others(8): Show |
11 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.301+1293C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784665 | |||||||
chr5:138784675 | T | C | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.301+1303T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784675 | |||||||
chr5:138784838 | T | C | 1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.301+1466T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784838 | |||||||
chr5:138784909 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.301+1537G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784909 | |||||||
chr5:138784916 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301+1544C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138784916 | |||||||
chr5:138785064 | A | AT | 126 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.301+1707dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138785064 | ||||||
chr5:138785064 | A | ATT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.301+1706_301+1707d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138785064 | ||||||
chr5:138785086 | G | A | 6 | a0001c0003t0002g0055 a0001c0003t0002g0062 a0001c0003t0002g0063 others(3): Show |
6 | HG00642.hp1 HG01346.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1714G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785086 | |||||||
chr5:138785088 | G | A | 1 | a0001c0002t0002g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.301+1716G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785088 | |||||||
chr5:138785139 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+1767T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785139 | |||||||
chr5:138785144 | C | A | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.301+1772C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785144 | |||||||
chr5:138785154 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+1782C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785154 | |||||||
chr5:138785162 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301+1790C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785162 | |||||||
chr5:138785262 | T | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+1890T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785262 | |||||||
chr5:138785330 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 |
3 | HG02451.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.301+1958G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785330 | |||||||
chr5:138785349 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.301+1977T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785349 | |||||||
chr5:138785623 | C | T | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.301+2251C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785623 | |||||||
chr5:138785646 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.301+2274C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785646 | |||||||
chr5:138785671 | C | G | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+2299C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785671 | |||||||
chr5:138785717 | C | A | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+2345C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785717 | |||||||
chr5:138785763 | T | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+2391T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785763 | |||||||
chr5:138785841 | G | A | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+2469G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785841 | |||||||
chr5:138785888 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.301+2516C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785888 | |||||||
chr5:138785892 | C | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+2520C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138785892 | |||||||
chr5:138786246 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.301+2874T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786246 | |||||||
chr5:138786430 | C | T | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.301+3058C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786430 | |||||||
chr5:138786504 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.301+3132C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786504 | |||||||
chr5:138786639 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.301+3267G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786639 | |||||||
chr5:138786704 | T | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+3332T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138786704 | |||||||
chr5:138787440 | T | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.301+4068T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787440 | |||||||
chr5:138787485 | A | G | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4113A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787485 | |||||||
chr5:138787538 | T | G | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4166T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787538 | |||||||
chr5:138787575 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.301+4203A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787575 | |||||||
chr5:138787664 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.301+4292A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787664 | |||||||
chr5:138787698 | T | C | 4 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4326T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787698 | |||||||
chr5:138787869 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.301+4497G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787869 | |||||||
chr5:138787957 | A | G | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.301+4585A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787957 | |||||||
chr5:138787983 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+4611G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138787983 | |||||||
chr5:138788013 | T | A | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+4641T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788013 | |||||||
chr5:138788266 | C | T | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.301+4894C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788266 | |||||||
chr5:138788305 | T | G | 82 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.301+4933T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788305 | |||||||
chr5:138788309 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+4937C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788309 | |||||||
chr5:138788382 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301+5010G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788382 | |||||||
chr5:138788437 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.301+5065T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788437 | |||||||
chr5:138788587 | C | A | 1 | a0001c0002t0002g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.301+5215C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788587 | |||||||
chr5:138788620 | G | A | 2 | a0001c0002t0002g0075 a0001c0002t0002g0084 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.301+5248G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788620 | |||||||
chr5:138788701 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+5329C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788701 | |||||||
chr5:138788765 | A | G | 7 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(4): Show |
7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+5393A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788765 | |||||||
chr5:138788787 | T | C | 2 | a0001c0002t0003g0029 a0001c0002t0008g0028 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+5415T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788787 | |||||||
chr5:138788810 | T | C | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5438T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788810 | |||||||
chr5:138788845 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.301+5473A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788845 | |||||||
chr5:138788921 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.301+5549C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138788921 | |||||||
chr5:138789022 | C | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+5650C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789022 | |||||||
chr5:138789050 | G | A | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5678G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789050 | |||||||
chr5:138789183 | GT | G | 13 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0105 others(10): Show |
13 | HG00423.hp1 HG01433.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+5816delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138789183 | ||||||
chr5:138789183 | GTT | G | 9 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 others(6): Show |
9 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5815_301+5816d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138789183 | ||||||
chr5:138789188 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+5816T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789188 | |||||||
chr5:138789188 | TC | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.301+5826delC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138789188 | ||||||
chr5:138789190 | C | T | 14 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(11): Show |
14 | HG00423.hp2 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.301+5818C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789190 | |||||||
chr5:138789193 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.301+5821C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789193 | |||||||
chr5:138789196 | C | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+5824C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789196 | |||||||
chr5:138789196 | C | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.301+5824C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789196 | |||||||
chr5:138789223 | C | T | 1 | a0003c0006t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.301+5851C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789223 | |||||||
chr5:138789400 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+6028G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789400 | |||||||
chr5:138789497 | G | A | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.301+6125G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789497 | |||||||
chr5:138789735 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.301+6363C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789735 | |||||||
chr5:138789988 | C | T | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.301+6616C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138789988 | |||||||
chr5:138790237 | G | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+6865G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138790237 | |||||||
chr5:138790250 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.301+6878G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138790250 | |||||||
chr5:138791230 | G | A | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+7858G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138791230 | |||||||
chr5:138791288 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+7916G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138791288 | |||||||
chr5:138791615 | C | CA | 29 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(26): Show |
29 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.301+8270dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791615 | C | CAA | 15 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0097 others(12): Show |
15 | HG00741.hp1 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+8269_301+8270d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791615 | C | CAAA | 38 | a0001c0001t0001g0038 a0001c0001t0001g0087 a0001c0001t0001g0098 others(35): Show |
38 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.301+8268_301+8270d others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791615 | C | CAAAA | 29 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0106 others(26): Show |
29 | HG00438.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.301+8267_301+8270d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791615 | C | CAAAAA | 13 | a0001c0001t0001g0036 a0001c0001t0001g0128 a0001c0001t0001g0131 others(10): Show |
13 | HG01071.hp2 HG01081.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+8266_301+8270d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791615 | C | CAAAAAAA | 7 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(4): Show |
7 | HG02451.hp2 HG03453.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.301+8264_301+8270d others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791615 | CAAAAAAA others(4): Show |
C | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+8260_301+8270d others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791615 | ||||||
chr5:138791691 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.301+8319C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138791691 | |||||||
chr5:138791787 | C | CT | 117 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.301+8435dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791787 | ||||||
chr5:138791787 | C | CTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG00438.hp1 HG01109.hp2 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.301+8434_301+8435d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791787 | ||||||
chr5:138791787 | CTTTTTTT others(3): Show |
C | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.301+8426_301+8435d others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138791787 | ||||||
chr5:138792038 | G | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+8666G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792038 | |||||||
chr5:138792079 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.301+8707A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792079 | |||||||
chr5:138792256 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0097 |
2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.301+8884A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792256 | |||||||
chr5:138792390 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+9018C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792390 | |||||||
chr5:138792414 | T | C | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.301+9042T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792414 | |||||||
chr5:138792845 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.301+9473T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792845 | |||||||
chr5:138792856 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+9484C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792856 | |||||||
chr5:138792937 | A | G | 1 | a0003c0006t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.301+9565A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792937 | |||||||
chr5:138792998 | G | A | 3 | a0001c0005t0001g0156 a0001c0005t0001g0167 a0001c0005t0001g0168 |
3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.301+9626G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138792998 | |||||||
chr5:138793012 | A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.301+9640A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793012 | |||||||
chr5:138793219 | G | A | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.301+9847G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793219 | |||||||
chr5:138793299 | G | A | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+9927G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793299 | |||||||
chr5:138793439 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.301+10067C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793439 | |||||||
chr5:138793845 | T | A | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.301+10473T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138793845 | |||||||
chr5:138794012 | A | AT | 6 | a0001c0001t0001g0088 a0001c0001t0006g0174 a0001c0001t0006g0175 others(3): Show |
6 | HG00741.hp2 HG02723.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+10663dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | ||||||
chr5:138794012 | A | ATT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.301+10662_301+1066 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | ||||||
chr5:138794012 | AT | A | 78 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(75): Show |
78 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.301+10663delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | ||||||
chr5:138794012 | ATT | A | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(10): Show |
13 | HG01243.hp2 HG01515.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.301+10662_301+1066 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138794012 | ||||||
chr5:138794056 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+10684C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794056 | |||||||
chr5:138794336 | A | G | 1 | a0001c0002t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.301+10964A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794336 | |||||||
chr5:138794362 | A | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+10990A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794362 | |||||||
chr5:138794577 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.301+11205T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794577 | |||||||
chr5:138794811 | G | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.301+11439G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138794811 | |||||||
chr5:138795138 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.301+11766G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795138 | |||||||
chr5:138795151 | C | CA | 11 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0002t0002g0070 others(8): Show |
11 | HG00438.hp2 HG01109.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.301+11802dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | ||||||
chr5:138795151 | CAA | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01099.hp2 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+11801_301+1180 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | ||||||
chr5:138795151 | CAAA | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.301+11800_301+1180 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | ||||||
chr5:138795151 | CAAAA | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0091 others(6): Show |
9 | HG01361.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+11799_301+1180 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138795151 | ||||||
chr5:138795288 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.301+11916C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795288 | |||||||
chr5:138795442 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+12070C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795442 | |||||||
chr5:138795659 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+12287T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795659 | |||||||
chr5:138795680 | A | G | 6 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(3): Show |
6 | NA18946.hp1 NA18948.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+12308A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795680 | |||||||
chr5:138795703 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+12331C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795703 | |||||||
chr5:138795749 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.301+12377C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795749 | |||||||
chr5:138795923 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0045 |
2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.301+12551C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138795923 | |||||||
chr5:138796200 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.301+12828A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796200 | |||||||
chr5:138796332 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.301+12960G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796332 | |||||||
chr5:138796370 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+12998C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796370 | |||||||
chr5:138796388 | CA | C | 82 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.301+13022delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138796388 | ||||||
chr5:138796468 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+13096C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796468 | |||||||
chr5:138796538 | C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.301+13166C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796538 | |||||||
chr5:138796558 | A | AGT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.301+13186_301+1318 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796558 | |||||||
chr5:138796566 | G | GTAT | 4 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 others(1): Show |
4 | HG01099.hp2 HG02630.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+13194_301+1319 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796566 | |||||||
chr5:138796566 | G | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.301+13194G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138796566 | |||||||
chr5:138796969 | AT | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-13065delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138796969 | ||||||
chr5:138797030 | T | C | 1 | a0001c0002t0005g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.302-13008T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797030 | |||||||
chr5:138797238 | T | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0148 |
3 | HG02280.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.302-12800T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797238 | |||||||
chr5:138797261 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-12777G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797261 | |||||||
chr5:138797771 | C | G | 1 | a0001c0002t0003g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.302-12267C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797771 | |||||||
chr5:138797885 | T | TA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-12143dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138797885 | ||||||
chr5:138797898 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-12140T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797898 | |||||||
chr5:138797994 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.302-12044A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138797994 | |||||||
chr5:138798180 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-11858A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798180 | |||||||
chr5:138798193 | CAG | C | 2 | a0001c0001t0001g0087 a0004c0010t0001g0169 |
2 | HG00423.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.302-11843_302-1184 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138798193 | ||||||
chr5:138798197 | AGTATTTG others(9): Show |
A | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.302-11839_302-1182 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138798197 | ||||||
chr5:138798218 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0138 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302-11820A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798218 | |||||||
chr5:138798571 | G | A | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.302-11467G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798571 | |||||||
chr5:138798606 | C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.302-11432C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798606 | |||||||
chr5:138798864 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-11174C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138798864 | |||||||
chr5:138799026 | T | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-11012T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799026 | |||||||
chr5:138799061 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.302-10977G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799061 | |||||||
chr5:138799120 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.302-10918C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799120 | |||||||
chr5:138799168 | TTTG | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-10867_302-1086 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799168 | ||||||
chr5:138799221 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(2): Show |
5 | NA18946.hp1 NA18948.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-10817C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799221 | |||||||
chr5:138799254 | G | A | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.302-10784G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799254 | |||||||
chr5:138799435 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.302-10603C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799435 | |||||||
chr5:138799514 | A | G | 1 | a0001c0002t0003g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.302-10524A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138799514 | |||||||
chr5:138799625 | A | AT | 11 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
11 | HG01071.hp2 HG01099.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.302-10399dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799625 | ||||||
chr5:138799625 | AT | A | 14 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(11): Show |
14 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.302-10399delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799625 | ||||||
chr5:138799857 | G | GATGGATG others(9): Show |
2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-10178_302-1017 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | ||||||
chr5:138799857 | G | GATGT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.302-10148_302-1014 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | ||||||
chr5:138799857 | G | GATGTATG others(1): Show |
85 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(82): Show |
85 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.302-10152_302-1014 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | ||||||
chr5:138799857 | G | GATGTATG others(5): Show |
12 | a0001c0001t0001g0103 a0001c0001t0001g0126 a0001c0001t0001g0130 others(9): Show |
12 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.302-10156_302-1014 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799857 | ||||||
chr5:138799878 | ATGTATGT others(9): Show |
A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-10156_302-1014 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799878 | ||||||
chr5:138799890 | A | ATGTATGT others(3): Show |
1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.302-10145_302-1014 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138799890 | ||||||
chr5:138800000 | G | A | 2 | a0002c0007t0001g0099 a0002c0007t0001g0100 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.302-10038G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800000 | |||||||
chr5:138800094 | G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302-9944G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800094 | |||||||
chr5:138800156 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.302-9882A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800156 | |||||||
chr5:138800232 | C | A | 78 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.302-9806C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800232 | |||||||
chr5:138800378 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-9660A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800378 | |||||||
chr5:138800494 | A | C | 1 | a0001c0002t0002g0081 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.302-9544A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800494 | |||||||
chr5:138800497 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.302-9541A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800497 | |||||||
chr5:138800593 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-9445G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800593 | |||||||
chr5:138800665 | T | C | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.302-9373T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800665 | |||||||
chr5:138800717 | C | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302-9321C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800717 | |||||||
chr5:138800727 | T | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.302-9311T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800727 | |||||||
chr5:138800734 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.302-9304C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800734 | |||||||
chr5:138800768 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.302-9270A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800768 | |||||||
chr5:138800896 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.302-9142G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800896 | |||||||
chr5:138800930 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-9108C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138800930 | |||||||
chr5:138801090 | G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302-8948G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801090 | |||||||
chr5:138801227 | T | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-8811T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801227 | |||||||
chr5:138801248 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.302-8790C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801248 | |||||||
chr5:138801265 | G | A | 10 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0136 others(7): Show |
10 | HG01071.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-8773G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801265 | |||||||
chr5:138801981 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-8057T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138801981 | |||||||
chr5:138802039 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-7999A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802039 | |||||||
chr5:138802268 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0138 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.302-7770A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802268 | |||||||
chr5:138802318 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.302-7720A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802318 | |||||||
chr5:138802759 | G | C | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-7279G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802759 | |||||||
chr5:138802968 | A | AT | 6 | a0001c0002t0003g0025 a0001c0004t0004g0005 a0001c0004t0004g0007 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-7058dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138802968 | ||||||
chr5:138802968 | AT | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-7058delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138802968 | ||||||
chr5:138802980 | T | A | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-7058T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138802980 | |||||||
chr5:138803158 | A | AT | 11 | a0001c0001t0001g0094 a0001c0001t0001g0116 a0001c0001t0001g0166 others(8): Show |
11 | HG00323.hp2 HG01109.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-6865dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138803158 | ||||||
chr5:138803427 | A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-6611A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803427 | |||||||
chr5:138803500 | T | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-6538T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803500 | |||||||
chr5:138803521 | T | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-6517T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803521 | |||||||
chr5:138803588 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-6450C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803588 | |||||||
chr5:138803618 | G | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-6420G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803618 | |||||||
chr5:138803989 | G | A | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.302-6049G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138803989 | |||||||
chr5:138804091 | T | G | 31 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.302-5947T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138804091 | |||||||
chr5:138804285 | G | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.302-5753G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138804285 | |||||||
chr5:138804375 | T | TC | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.302-5663_302-5662i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138804375 | |||||||
chr5:138804738 | C | CTG | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-5299_302-5298i others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138804738 | ||||||
chr5:138805006 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.302-5032A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805006 | |||||||
chr5:138805011 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0157 a0001c0001t0001g0173 |
3 | HG00735.hp2 NA18961.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.302-5027G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805011 | |||||||
chr5:138805063 | G | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4975G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805063 | |||||||
chr5:138805065 | G | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-4973G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805065 | |||||||
chr5:138805108 | A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.302-4930A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805108 | |||||||
chr5:138805196 | C | T | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-4842C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805196 | |||||||
chr5:138805428 | G | A | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-4610G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805428 | |||||||
chr5:138805797 | T | C | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-4241T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805797 | |||||||
chr5:138805863 | G | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-4175G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805863 | |||||||
chr5:138805900 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.302-4138G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138805900 | |||||||
chr5:138806601 | T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.302-3437T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138806601 | |||||||
chr5:138807008 | CT | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
23 | HG01109.hp2 HG01169.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.302-3010delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138807008 | ||||||
chr5:138807168 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.302-2870G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807168 | |||||||
chr5:138807613 | TTG | T | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-2421_302-2420d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138807613 | ||||||
chr5:138807684 | T | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.302-2354T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807684 | |||||||
chr5:138807992 | C | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-2046C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807992 | |||||||
chr5:138807993 | C | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.302-2045C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138807993 | |||||||
chr5:138808018 | T | TG | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(7): Show |
10 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-2017dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138808018 | ||||||
chr5:138808093 | G | T | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-1945G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808093 | |||||||
chr5:138808140 | G | C | 2 | a0001c0002t0003g0025 a0001c0012t0003g0019 |
2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.302-1898G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808140 | |||||||
chr5:138808263 | C | G | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-1775C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808263 | |||||||
chr5:138808685 | G | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302-1353G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808685 | |||||||
chr5:138808695 | T | TA | 94 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.302-1331dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138808695 | ||||||
chr5:138808695 | T | TAA | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
31 | HG00423.hp2 HG01099.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.302-1332_302-1331d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138808695 | ||||||
chr5:138808939 | A | C | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302-1099A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138808939 | |||||||
chr5:138809119 | A | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-919A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809119 | |||||||
chr5:138809256 | C | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-782C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809256 | |||||||
chr5:138809291 | C | T | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-747C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809291 | |||||||
chr5:138809440 | A | G | 1 | a0002c0007t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.302-598A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809440 | |||||||
chr5:138809574 | T | C | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.302-464T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809574 | |||||||
chr5:138809683 | T | G | 8 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0130 others(5): Show |
8 | HG00438.hp1 HG00735.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-355T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809683 | |||||||
chr5:138809742 | C | CT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.302-286dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 138809742 | ||||||
chr5:138809771 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.302-267C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809771 | |||||||
chr5:138809851 | A | G | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.302-187A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809851 | |||||||
chr5:138809955 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.302-83T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 3/17 | chr5 | 138809955 | |||||||
chr5:138810215 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.468+11A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810215 | |||||||
chr5:138810333 | T | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.468+129T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810333 | |||||||
chr5:138810534 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.468+330T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810534 | |||||||
chr5:138810725 | A | G | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.468+521A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810725 | |||||||
chr5:138810831 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.468+627G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810831 | |||||||
chr5:138810901 | C | T | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.468+697C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810901 | |||||||
chr5:138810914 | A | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.468+710A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810914 | |||||||
chr5:138810941 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.468+737C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810941 | |||||||
chr5:138810946 | G | A | 1 | a0001c0002t0003g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.468+742G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810946 | |||||||
chr5:138810963 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.468+759A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138810963 | |||||||
chr5:138811000 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.468+796G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811000 | |||||||
chr5:138811057 | G | A | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+853G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811057 | |||||||
chr5:138811200 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.469-983C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811200 | |||||||
chr5:138811237 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-946T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811237 | |||||||
chr5:138811278 | G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-905G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811278 | |||||||
chr5:138811314 | C | T | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-869C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811314 | |||||||
chr5:138811352 | G | A | 83 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.469-831G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811352 | |||||||
chr5:138811389 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-794C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811389 | |||||||
chr5:138811510 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-673C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811510 | |||||||
chr5:138811511 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.469-672A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811511 | |||||||
chr5:138811566 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.469-617T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811566 | |||||||
chr5:138811627 | T | C | 30 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(27): Show |
30 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.469-556T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811627 | |||||||
chr5:138811653 | C | T | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.469-530C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811653 | |||||||
chr5:138811673 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.469-510C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811673 | |||||||
chr5:138811674 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-509T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811674 | |||||||
chr5:138811681 | C | T | 83 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.469-502C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811681 | |||||||
chr5:138811702 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.469-481G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811702 | |||||||
chr5:138811737 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-446G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811737 | |||||||
chr5:138811829 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.469-354A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811829 | |||||||
chr5:138811892 | A | G | 1 | a0001c0002t0002g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.469-291A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 4/17 | chr5 | 138811892 | |||||||
chr5:138812304 | TAC | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 |
3 | HG02451.hp2 HG03486.hp2 HG03579.hp2 |
splice_region_variant&intron_variant | LOW | c.588+4_588+5delCA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138812304 | ||||||
chr5:138812339 | A | G | 1 | a0001c0002t0002g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.588+37A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812339 | |||||||
chr5:138812347 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.588+45A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812347 | |||||||
chr5:138812375 | T | C | 31 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.588+73T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812375 | |||||||
chr5:138812712 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588+410C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812712 | |||||||
chr5:138812759 | C | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+457C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812759 | |||||||
chr5:138812929 | C | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.588+627C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138812929 | |||||||
chr5:138813044 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0180 a0001c0008t0003g0030 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+742C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813044 | |||||||
chr5:138813161 | G | A | 2 | a0001c0002t0003g0020 a0001c0002t0003g0025 |
2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.588+859G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813161 | |||||||
chr5:138813316 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0017 |
2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.588+1014C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813316 | |||||||
chr5:138813341 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588+1039G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813341 | |||||||
chr5:138813596 | A | G | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.588+1294A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813596 | |||||||
chr5:138813650 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+1348A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813650 | |||||||
chr5:138813779 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+1477C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813779 | |||||||
chr5:138813843 | C | T | 1 | a0002c0007t0001g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.588+1541C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138813843 | |||||||
chr5:138814156 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+1854T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814156 | |||||||
chr5:138814158 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+1856T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814158 | |||||||
chr5:138814250 | C | CT | 29 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0041 others(26): Show |
29 | HG00438.hp2 HG00741.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.588+1963dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138814250 | ||||||
chr5:138814330 | C | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+2028C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814330 | |||||||
chr5:138814430 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.588+2128A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814430 | |||||||
chr5:138814721 | T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+2419T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814721 | |||||||
chr5:138814762 | G | GT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.588+2469dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138814762 | ||||||
chr5:138814763 | T | G | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+2461T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814763 | |||||||
chr5:138814834 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.588+2532A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814834 | |||||||
chr5:138814968 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.588+2666A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138814968 | |||||||
chr5:138815048 | T | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+2746T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815048 | |||||||
chr5:138815049 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.588+2747G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815049 | |||||||
chr5:138815179 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+2877A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815179 | |||||||
chr5:138815464 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.588+3162G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815464 | |||||||
chr5:138815502 | G | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+3200G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815502 | |||||||
chr5:138815584 | A | G | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.588+3282A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815584 | |||||||
chr5:138815636 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+3334G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815636 | |||||||
chr5:138815690 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.588+3388T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815690 | |||||||
chr5:138815992 | T | C | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+3690T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138815992 | |||||||
chr5:138816202 | T | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+3900T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816202 | |||||||
chr5:138816696 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.588+4394G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816696 | |||||||
chr5:138816759 | G | A | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.588+4457G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816759 | |||||||
chr5:138816769 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.588+4467C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816769 | |||||||
chr5:138816805 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.588+4503A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816805 | |||||||
chr5:138816937 | G | A | 10 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0136 others(7): Show |
10 | HG01071.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.588+4635G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816937 | |||||||
chr5:138816944 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.588+4642A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138816944 | |||||||
chr5:138817133 | C | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0002c0007t0001g0099 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+4831C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817133 | |||||||
chr5:138817253 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.588+4951A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817253 | |||||||
chr5:138817263 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.588+4961T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817263 | |||||||
chr5:138817503 | G | A | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.588+5201G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817503 | |||||||
chr5:138817655 | A | C | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.588+5353A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817655 | |||||||
chr5:138817731 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+5429C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817731 | |||||||
chr5:138817913 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.588+5611G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138817913 | |||||||
chr5:138818057 | T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.588+5755T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818057 | |||||||
chr5:138818134 | C | CT | 6 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(3): Show |
6 | HG00741.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+5845dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138818134 | ||||||
chr5:138818138 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.588+5836T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818138 | |||||||
chr5:138818147 | T | C | 1 | a0001c0003t0002g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.588+5845T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818147 | |||||||
chr5:138818267 | CT | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.588+5979delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138818267 | ||||||
chr5:138818281 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.588+5979T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818281 | |||||||
chr5:138818332 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.588+6030C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818332 | |||||||
chr5:138818414 | T | TA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.588+6113dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138818414 | ||||||
chr5:138818597 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.589-5933G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818597 | |||||||
chr5:138818841 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.589-5689C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818841 | |||||||
chr5:138818894 | C | T | 1 | a0001c0003t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.589-5636C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818894 | |||||||
chr5:138818926 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-5604C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138818926 | |||||||
chr5:138819023 | G | C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-5507G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819023 | |||||||
chr5:138819042 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.589-5488T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819042 | |||||||
chr5:138819065 | C | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.589-5465C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819065 | |||||||
chr5:138819069 | A | AC | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-5461_589-5460i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819069 | |||||||
chr5:138819208 | C | T | 2 | a0001c0001t0001g0170 a0001c0004t0004g0180 |
2 | HG02129.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.589-5322C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819208 | |||||||
chr5:138819213 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-5317G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819213 | |||||||
chr5:138819333 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-5197C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819333 | |||||||
chr5:138819424 | G | A | 4 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-5106G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819424 | |||||||
chr5:138819556 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-4974G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819556 | |||||||
chr5:138819689 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.589-4841C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819689 | |||||||
chr5:138819719 | C | G | 2 | a0002c0007t0001g0099 a0002c0007t0001g0100 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.589-4811C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819719 | |||||||
chr5:138819781 | C | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.589-4749C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819781 | |||||||
chr5:138819963 | C | G | 1 | a0001c0011t0001g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.589-4567C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138819963 | |||||||
chr5:138820236 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.589-4294A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820236 | |||||||
chr5:138820243 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.589-4287G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820243 | |||||||
chr5:138820270 | G | C | 78 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.589-4260G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820270 | |||||||
chr5:138820324 | A | G | 1 | a0001c0002t0003g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.589-4206A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820324 | |||||||
chr5:138820375 | G | T | 9 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(6): Show |
9 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.589-4155G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820375 | |||||||
chr5:138820493 | T | C | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-4037T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820493 | |||||||
chr5:138820531 | CT | C | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-3997delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138820531 | ||||||
chr5:138820748 | A | AG | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.589-3776dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138820748 | ||||||
chr5:138820818 | A | G | 1 | a0001c0014t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.589-3712A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820818 | |||||||
chr5:138820867 | G | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-3663G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138820867 | |||||||
chr5:138821123 | C | G | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.589-3407C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138821123 | |||||||
chr5:138822466 | G | A | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-2064G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138822466 | |||||||
chr5:138822530 | C | T | 1 | a0001c0013t0003g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.589-2000C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138822530 | |||||||
chr5:138822657 | A | T | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-1873A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138822657 | |||||||
chr5:138823589 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.589-941T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823589 | |||||||
chr5:138823606 | G | A | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.589-924G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823606 | |||||||
chr5:138823613 | A | C | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.589-917A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823613 | |||||||
chr5:138823630 | C | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-900C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823630 | |||||||
chr5:138823655 | T | C | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.589-875T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823655 | |||||||
chr5:138823728 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.589-802C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823728 | |||||||
chr5:138823813 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0176 |
2 | HG01099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.589-717C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138823813 | |||||||
chr5:138823956 | C | CAAAAAAA others(1): Show |
7 | a0001c0002t0002g0035 a0001c0002t0002g0057 a0001c0002t0002g0067 others(4): Show |
7 | HG00323.hp1 HG00642.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.589-551_589-544dup others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(2): Show |
6 | a0001c0002t0002g0061 a0001c0002t0002g0070 a0001c0002t0002g0071 others(3): Show |
6 | HG01361.hp2 HG02735.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-552_589-544dup others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0002g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.589-553_589-544dup others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(4): Show |
4 | a0001c0002t0002g0056 a0001c0002t0002g0060 a0001c0002t0002g0073 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-554_589-544dup others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(5): Show |
6 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0066 others(3): Show |
6 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-555_589-544dup others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0002g0083 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.589-556_589-544dup others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(7): Show |
1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.589-557_589-544dup others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(12): Show |
2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.589-562_589-544dup others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | C | CAAAAAAA others(14): Show |
1 | a0001c0002t0002g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.589-564_589-544dup others(21): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | CAA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01099.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-545_589-544del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | CAAA | C | 12 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0104 others(9): Show |
12 | HG00423.hp1 HG01891.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.589-546_589-544del others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | CAAAA | C | 76 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.589-547_589-544del others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | CAAAAA | C | 11 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0151 others(8): Show |
11 | HG00639.hp2 HG01070.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-548_589-544del others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138823956 | CAAAAAAA others(7): Show |
C | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.589-557_589-544del others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 138823956 | ||||||
chr5:138824111 | G | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-419G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824111 | |||||||
chr5:138824130 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.589-400C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824130 | |||||||
chr5:138824177 | A | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.589-353A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824177 | |||||||
chr5:138824282 | A | G | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.589-248A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824282 | |||||||
chr5:138824322 | G | C | 3 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0034 |
3 | HG00741.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.589-208G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824322 | |||||||
chr5:138824367 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.589-163A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 5/17 | chr5 | 138824367 | |||||||
chr5:138825062 | G | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.858+263G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825062 | |||||||
chr5:138825209 | G | A | 4 | a0001c0002t0002g0058 a0001c0002t0002g0066 a0001c0002t0002g0067 others(1): Show |
4 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+410G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825209 | |||||||
chr5:138825482 | G | GTTTTTT | 7 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(4): Show |
7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.858+694_858+699dup others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.858+690_858+699dup others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(5): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.858+688_858+699dup others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(6): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG02132.hp1 HG02602.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.858+687_858+699dup others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(7): Show |
16 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0102 others(13): Show |
16 | HG00639.hp2 HG01070.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.858+686_858+699dup others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(8): Show |
30 | a0001c0001t0001g0037 a0001c0001t0001g0087 a0001c0001t0001g0098 others(27): Show |
30 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.858+685_858+699dup others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(9): Show |
20 | a0001c0001t0001g0036 a0001c0001t0001g0106 a0001c0001t0001g0108 others(17): Show |
20 | HG00735.hp2 HG01109.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.858+684_858+699dup others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(10): Show |
16 | a0001c0001t0001g0038 a0001c0001t0001g0086 a0001c0001t0001g0089 others(13): Show |
16 | HG00423.hp2 HG01167.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(11): Show |
8 | a0001c0001t0001g0104 a0001c0001t0001g0142 a0001c0002t0003g0027 others(5): Show |
8 | HG00423.hp1 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(12): Show |
9 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0002t0003g0004 others(6): Show |
9 | HG00741.hp1 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(13): Show |
5 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0097 others(2): Show |
5 | HG01243.hp2 HG02129.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.858+699_858+700ins others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(16): Show |
1 | a0001c0001t0001g0046 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.858+699_858+700ins others(23): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(18): Show |
1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.858+699_858+700ins others(25): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825482 | G | GTTTTTTT others(22): Show |
1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.858+699_858+700ins others(29): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825482 | ||||||
chr5:138825529 | TA | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.858+744delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825529 | ||||||
chr5:138825529 | TAA | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.858+743_858+744del others(2): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138825529 | ||||||
chr5:138825775 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0097 |
2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.858+976A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825775 | |||||||
chr5:138825906 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.858+1107G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138825906 | |||||||
chr5:138826090 | T | G | 1 | a0001c0003t0002g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.858+1291T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826090 | |||||||
chr5:138826440 | T | C | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.859-1075T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826440 | |||||||
chr5:138826444 | G | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-1071G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826444 | |||||||
chr5:138826525 | AG | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.859-987delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138826525 | ||||||
chr5:138826536 | G | C | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.859-979G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826536 | |||||||
chr5:138826586 | G | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-929G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138826586 | |||||||
chr5:138827083 | G | A | 83 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.859-432G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138827083 | |||||||
chr5:138827158 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.859-357G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138827158 | |||||||
chr5:138827361 | G | GT | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-153dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 138827361 | ||||||
chr5:138827499 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.859-16A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 6/17 | chr5 | 138827499 | |||||||
chr5:138827887 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+169T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827887 | |||||||
chr5:138827970 | A | G | 1 | a0001c0002t0002g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1062+252A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827970 | |||||||
chr5:138827970 | A | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+252A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827970 | |||||||
chr5:138827987 | T | C | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+269T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138827987 | |||||||
chr5:138828026 | G | GT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+308_1062+309i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828026 | |||||||
chr5:138828027 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0164 |
2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1062+309G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828027 | |||||||
chr5:138828032 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+314T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828032 | |||||||
chr5:138828164 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+446A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828164 | |||||||
chr5:138828310 | A | G | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1062+592A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828310 | |||||||
chr5:138828370 | C | CT | 62 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(59): Show |
62 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1062+661dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138828370 | ||||||
chr5:138828398 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+680C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828398 | |||||||
chr5:138828428 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+710A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828428 | |||||||
chr5:138828618 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+900C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828618 | |||||||
chr5:138828767 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1062+1049C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138828767 | |||||||
chr5:138829037 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+1319G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829037 | |||||||
chr5:138829077 | G | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+1359G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829077 | |||||||
chr5:138829315 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+1597G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829315 | |||||||
chr5:138829378 | G | A | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1062+1660G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829378 | |||||||
chr5:138829528 | T | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+1810T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829528 | |||||||
chr5:138829562 | T | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+1844T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829562 | |||||||
chr5:138829897 | G | C | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+2179G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829897 | |||||||
chr5:138829962 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+2244A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138829962 | |||||||
chr5:138830166 | C | CA | 24 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(21): Show |
24 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1062+2461dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138830166 | ||||||
chr5:138830166 | CA | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1062+2461delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138830166 | ||||||
chr5:138830482 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0140 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+2764C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830482 | |||||||
chr5:138830683 | A | G | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062+2965A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830683 | |||||||
chr5:138830787 | AACAG | A | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3073_1062+307 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138830787 | ||||||
chr5:138830795 | A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+3077A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830795 | |||||||
chr5:138830818 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1062+3100G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830818 | |||||||
chr5:138830998 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3280A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138830998 | |||||||
chr5:138831072 | CATT | C | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3355_1062+335 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831072 | |||||||
chr5:138831081 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+3363A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831081 | |||||||
chr5:138831325 | C | T | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1062+3607C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831325 | |||||||
chr5:138831416 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+3698T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831416 | |||||||
chr5:138831581 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+3863T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831581 | |||||||
chr5:138831599 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1062+3881G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831599 | |||||||
chr5:138831808 | A | G | 78 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1062+4090A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831808 | |||||||
chr5:138831940 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+4222A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138831940 | |||||||
chr5:138832077 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1062+4359G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832077 | |||||||
chr5:138832351 | C | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062+4633C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832351 | |||||||
chr5:138832459 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1062+4741A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832459 | |||||||
chr5:138832727 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1062+5009T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832727 | |||||||
chr5:138832838 | A | G | 6 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG02132.hp1 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1062+5120A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138832838 | |||||||
chr5:138833095 | A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062+5377A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833095 | |||||||
chr5:138833243 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+5525C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833243 | |||||||
chr5:138833410 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1062+5692T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833410 | |||||||
chr5:138833534 | C | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+5816C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833534 | |||||||
chr5:138833581 | A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062+5863A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833581 | |||||||
chr5:138833597 | T | C | 1 | a0001c0001t0006g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1062+5879T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833597 | |||||||
chr5:138833839 | A | C | 1 | a0001c0002t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1062+6121A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833839 | |||||||
chr5:138833874 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+6156G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833874 | |||||||
chr5:138833990 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1062+6272T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138833990 | |||||||
chr5:138834104 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+6386A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834104 | |||||||
chr5:138834205 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+6487A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834205 | |||||||
chr5:138834241 | A | C | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1062+6523A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834241 | |||||||
chr5:138834770 | G | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+7052G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834770 | |||||||
chr5:138834793 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+7075T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138834793 | |||||||
chr5:138835338 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1062+7620C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835338 | |||||||
chr5:138835377 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+7659C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835377 | |||||||
chr5:138835513 | G | A | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+7795G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835513 | |||||||
chr5:138835718 | C | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+8000C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835718 | |||||||
chr5:138835734 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+8016T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835734 | |||||||
chr5:138835812 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+8094G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138835812 | |||||||
chr5:138836047 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+8329C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836047 | |||||||
chr5:138836203 | A | G | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+8485A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836203 | |||||||
chr5:138836307 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+8589A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836307 | |||||||
chr5:138836384 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1062+8666A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836384 | |||||||
chr5:138836531 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+8813C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836531 | |||||||
chr5:138836810 | C | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+9092C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138836810 | |||||||
chr5:138837463 | C | T | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1062+9745C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837463 | |||||||
chr5:138837537 | C | G | 2 | a0001c0002t0002g0075 a0001c0002t0002g0084 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1062+9819C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837537 | |||||||
chr5:138837693 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+9975C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837693 | |||||||
chr5:138837867 | G | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0160 a0001c0001t0001g0171 |
3 | HG00639.hp2 HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1062+10149G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837867 | |||||||
chr5:138837904 | G | A | 2 | a0003c0006t0001g0090 a0003c0006t0001g0095 |
2 | NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1062+10186G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138837904 | |||||||
chr5:138838101 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1062+10383A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838101 | |||||||
chr5:138838447 | T | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062+10729T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838447 | |||||||
chr5:138838530 | A | AT | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+10821dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138838530 | ||||||
chr5:138838789 | G | T | 12 | a0001c0002t0002g0056 a0001c0002t0002g0060 a0001c0002t0003g0020 others(9): Show |
12 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062+11071G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838789 | |||||||
chr5:138838831 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+11113G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838831 | |||||||
chr5:138838858 | T | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11140T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838858 | |||||||
chr5:138838911 | G | A | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+11193G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838911 | |||||||
chr5:138838932 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+11214A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138838932 | |||||||
chr5:138839070 | T | C | 31 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1062+11352T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839070 | |||||||
chr5:138839224 | A | AT | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11516dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138839224 | ||||||
chr5:138839538 | T | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11820T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839538 | |||||||
chr5:138839568 | A | G | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+11850A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839568 | |||||||
chr5:138839660 | T | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+11942T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839660 | |||||||
chr5:138839680 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+11962A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839680 | |||||||
chr5:138839753 | A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+12035A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138839753 | |||||||
chr5:138840137 | T | C | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1062+12419T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840137 | |||||||
chr5:138840184 | G | A | 1 | a0002c0007t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1062+12466G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840184 | |||||||
chr5:138840221 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+12503G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840221 | |||||||
chr5:138840715 | T | TAGAAATG others(46): Show |
1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+12997_1062+12 others(59): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840715 | |||||||
chr5:138840716 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+12998T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840716 | |||||||
chr5:138840717 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+12999T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840717 | |||||||
chr5:138840718 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1062+13000T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840718 | |||||||
chr5:138840769 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+13051G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138840769 | |||||||
chr5:138841000 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+13282C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841000 | |||||||
chr5:138841265 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+13547T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841265 | |||||||
chr5:138841432 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+13714G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841432 | |||||||
chr5:138841459 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1062+13741C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841459 | |||||||
chr5:138841572 | G | A | 31 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1062+13854G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841572 | |||||||
chr5:138841631 | CA | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+13917delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138841631 | ||||||
chr5:138841641 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0045 |
2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1062+13923A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841641 | |||||||
chr5:138841715 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+13997A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841715 | |||||||
chr5:138841757 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+14039G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841757 | |||||||
chr5:138841946 | A | G | 1 | a0001c0002t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1062+14228A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138841946 | |||||||
chr5:138842057 | T | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+14339T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842057 | |||||||
chr5:138842659 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+14941C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842659 | |||||||
chr5:138842697 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1062+14979C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842697 | |||||||
chr5:138842703 | A | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+14985A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842703 | |||||||
chr5:138842799 | A | G | 9 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(6): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1062+15081A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842799 | |||||||
chr5:138842913 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1062+15195C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138842913 | |||||||
chr5:138843482 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1062+15764C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843482 | |||||||
chr5:138843891 | A | G | 25 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
25 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1062+16173A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843891 | |||||||
chr5:138843950 | G | A | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+16232G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843950 | |||||||
chr5:138843968 | C | T | 1 | a0001c0003t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1062+16250C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138843968 | |||||||
chr5:138844049 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+16331A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844049 | |||||||
chr5:138844093 | T | TTA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+16375_1062+16 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844093 | |||||||
chr5:138844094 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+16376G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844094 | |||||||
chr5:138844204 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1062+16486C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844204 | |||||||
chr5:138844245 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1062+16527C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844245 | |||||||
chr5:138844627 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+16909G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138844627 | |||||||
chr5:138844769 | TTATG | T | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+17055_1062+17 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138844769 | ||||||
chr5:138845075 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1062+17357T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845075 | |||||||
chr5:138845518 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1062+17800A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845518 | |||||||
chr5:138845583 | G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062+17865G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845583 | |||||||
chr5:138845594 | C | CATTT | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+17877_1062+17 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138845594 | ||||||
chr5:138845729 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+18011A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845729 | |||||||
chr5:138845773 | T | G | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+18055T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845773 | |||||||
chr5:138845784 | T | A | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1062+18066T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845784 | |||||||
chr5:138845869 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1062+18151C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845869 | |||||||
chr5:138845874 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+18156A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845874 | |||||||
chr5:138845885 | G | A | 5 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(2): Show |
5 | HG01109.hp2 HG01993.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+18167G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845885 | |||||||
chr5:138845915 | TTTTTTTG others(8): Show |
T | 94 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1062+18213_1062+18 others(21): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138845915 | ||||||
chr5:138845916 | TTTTTTGT others(7): Show |
T | 1 | a0001c0001t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1062+18204_1062+18 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138845916 | ||||||
chr5:138845939 | T | C | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1062+18221T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138845939 | |||||||
chr5:138846013 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+18295G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846013 | |||||||
chr5:138846177 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+18459C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846177 | |||||||
chr5:138846213 | A | G | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+18495A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846213 | |||||||
chr5:138846216 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1062+18498T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846216 | |||||||
chr5:138846318 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+18600A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846318 | |||||||
chr5:138846542 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 |
3 | HG02257.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1062+18824A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846542 | |||||||
chr5:138846639 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+18921C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846639 | |||||||
chr5:138846768 | A | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1062+19050A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846768 | |||||||
chr5:138846769 | C | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1062+19051C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846769 | |||||||
chr5:138846841 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1062+19123C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138846841 | |||||||
chr5:138847122 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1062+19404A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847122 | |||||||
chr5:138847166 | A | G | 1 | a0001c0001t0006g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1062+19448A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847166 | |||||||
chr5:138847297 | T | TA | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+19580dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138847297 | ||||||
chr5:138847475 | A | C | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1062+19757A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847475 | |||||||
chr5:138847640 | G | A | 2 | a0001c0002t0002g0002 a0001c0002t0002g0003 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1062+19922G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138847640 | |||||||
chr5:138848101 | C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+20383C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848101 | |||||||
chr5:138848150 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+20432A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848150 | |||||||
chr5:138848168 | T | TG | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+20450_1062+20 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848168 | |||||||
chr5:138848399 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1062+20681G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848399 | |||||||
chr5:138848735 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1062+21017T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848735 | |||||||
chr5:138848985 | T | A | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+21267T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138848985 | |||||||
chr5:138849092 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1062+21374A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849092 | |||||||
chr5:138849228 | T | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0002c0007t0001g0099 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+21510T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849228 | |||||||
chr5:138849273 | A | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+21555A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849273 | |||||||
chr5:138849279 | A | T | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1062+21561A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849279 | |||||||
chr5:138849333 | A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+21615A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849333 | |||||||
chr5:138849456 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+21738A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849456 | |||||||
chr5:138849594 | G | A | 1 | a0001c0002t0003g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1062+21876G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849594 | |||||||
chr5:138849604 | C | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+21886C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849604 | |||||||
chr5:138849727 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1062+22009A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849727 | |||||||
chr5:138849815 | G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062+22097G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849815 | |||||||
chr5:138849937 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1062+22219T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138849937 | |||||||
chr5:138849989 | A | AAC | 3 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0150 |
3 | HG02630.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1062+22288_1062+22 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138849989 | ||||||
chr5:138849989 | A | AACAC | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062+22286_1062+22 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138849989 | ||||||
chr5:138849989 | A | AACACAC | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+22284_1062+22 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138849989 | ||||||
chr5:138850272 | CCTGGATG others(9): Show |
C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+22557_1062+22 others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138850272 | ||||||
chr5:138850353 | A | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+22635A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850353 | |||||||
chr5:138850618 | C | G | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1062+22900C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850618 | |||||||
chr5:138850667 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0017 |
2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1062+22949A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850667 | |||||||
chr5:138850784 | T | TC | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1062+23067dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138850784 | ||||||
chr5:138850895 | A | T | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1062+23177A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138850895 | |||||||
chr5:138851018 | G | T | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1062+23300G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138851018 | |||||||
chr5:138851075 | T | G | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+23357T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138851075 | |||||||
chr5:138852058 | G | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0083 |
2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1062+24340G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852058 | |||||||
chr5:138852202 | A | G | 1 | a0001c0002t0003g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1062+24484A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852202 | |||||||
chr5:138852351 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+24633C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852351 | |||||||
chr5:138852463 | T | TG | 14 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(11): Show |
14 | HG00423.hp2 HG01891.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+24753dupG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852463 | ||||||
chr5:138852565 | C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+24847C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852565 | |||||||
chr5:138852686 | A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+24968A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852686 | |||||||
chr5:138852723 | T | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1062+25005T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852723 | |||||||
chr5:138852772 | C | T | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25054C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852772 | |||||||
chr5:138852859 | T | TCGCGCGC others(20): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0016 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1062+25148_1062+25 others(33): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | ||||||
chr5:138852859 | T | TCGCGCGC others(17): Show |
1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+25150_1062+25 others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | ||||||
chr5:138852859 | T | TCGCGCGC others(17): Show |
4 | a0001c0001t0001g0139 a0001c0001t0006g0174 a0001c0001t0006g0175 others(1): Show |
4 | HG01884.hp2 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+25152_1062+25 others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | ||||||
chr5:138852859 | T | TCGCGCGC others(19): Show |
88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1062+25152_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | ||||||
chr5:138852859 | T | TCGCGCGC others(21): Show |
1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1062+25152_1062+25 others(34): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | ||||||
chr5:138852859 | T | TCGCGCGT others(19): Show |
12 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1062+25147_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852859 | ||||||
chr5:138852860 | C | T | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1062+25142C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852860 | |||||||
chr5:138852863 | G | GCGCGCGC others(19): Show |
3 | a0001c0005t0001g0156 a0001c0005t0001g0167 a0001c0005t0001g0168 |
3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1062+25152_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852863 | ||||||
chr5:138852868 | C | CGCACGCG others(19): Show |
1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1062+25152_1062+25 others(32): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852868 | ||||||
chr5:138852871 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1062+25153G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852871 | |||||||
chr5:138852871 | G | GCACGCGC others(21): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0137 |
2 | HG00642.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1062+25156_1062+25 others(34): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852871 | ||||||
chr5:138852871 | G | GCGCGCGC others(21): Show |
1 | a0001c0001t0001g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1062+25154_1062+25 others(34): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138852871 | ||||||
chr5:138852873 | A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1062+25155A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852873 | |||||||
chr5:138852981 | C | T | 1 | a0001c0004t0004g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1062+25263C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138852981 | |||||||
chr5:138853022 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+25304G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853022 | |||||||
chr5:138853107 | A | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25389A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853107 | |||||||
chr5:138853166 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+25448C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853166 | |||||||
chr5:138853264 | T | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02074.hp2 NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1062+25546T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853264 | |||||||
chr5:138853495 | T | TA | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+25790dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138853495 | ||||||
chr5:138853582 | T | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25864T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853582 | |||||||
chr5:138853585 | G | A | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+25867G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853585 | |||||||
chr5:138853663 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1062+25945G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853663 | |||||||
chr5:138853846 | T | C | 1 | a0001c0002t0003g0048 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1062+26128T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853846 | |||||||
chr5:138853891 | G | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1062+26173G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138853891 | |||||||
chr5:138854009 | A | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1062+26291A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854009 | |||||||
chr5:138854311 | CAG | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+26594_1062+26 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854311 | |||||||
chr5:138854508 | A | G | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+26790A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854508 | |||||||
chr5:138854588 | G | A | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1062+26870G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854588 | |||||||
chr5:138854712 | A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1062+26994A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138854712 | |||||||
chr5:138855097 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1062+27379A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855097 | |||||||
chr5:138855327 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1062+27609G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855327 | |||||||
chr5:138855685 | G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+27967G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855685 | |||||||
chr5:138855704 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1062+27986A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855704 | |||||||
chr5:138855750 | T | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+28032T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855750 | |||||||
chr5:138855992 | A | T | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+28274A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138855992 | |||||||
chr5:138856092 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1062+28374T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856092 | |||||||
chr5:138856349 | T | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1062+28631T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856349 | |||||||
chr5:138856379 | GT | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+28663delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138856379 | ||||||
chr5:138856470 | T | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062+28752T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856470 | |||||||
chr5:138856542 | G | A | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1062+28824G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856542 | |||||||
chr5:138856727 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1062+29009G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856727 | |||||||
chr5:138856817 | C | G | 3 | a0001c0004t0004g0005 a0001c0004t0004g0180 a0001c0009t0004g0006 |
3 | HG02486.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1062+29099C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856817 | |||||||
chr5:138856975 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1063-29237A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138856975 | |||||||
chr5:138857243 | T | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-28969T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857243 | |||||||
chr5:138857308 | A | G | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1063-28904A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857308 | |||||||
chr5:138857487 | A | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1063-28725A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857487 | |||||||
chr5:138857488 | A | AT | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-28717dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138857488 | ||||||
chr5:138857488 | A | T | 21 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0001t0001g0094 others(18): Show |
21 | HG01099.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1063-28724A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857488 | |||||||
chr5:138857592 | C | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-28620C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857592 | |||||||
chr5:138857687 | G | A | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-28525G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857687 | |||||||
chr5:138857784 | C | T | 1 | a0001c0001t0006g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1063-28428C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857784 | |||||||
chr5:138857826 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1063-28386A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857826 | |||||||
chr5:138857973 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-28239G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138857973 | |||||||
chr5:138858076 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1063-28136C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858076 | |||||||
chr5:138858095 | T | C | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1063-28117T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858095 | |||||||
chr5:138858120 | TA | T | 5 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-28084delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858120 | ||||||
chr5:138858128 | AT | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1063-28068delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858128 | ||||||
chr5:138858576 | T | TTTTTTC | 17 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(14): Show |
17 | HG00423.hp2 HG02486.hp2 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063-27618_1063-27 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858576 | ||||||
chr5:138858576 | T | TTTTTTCT others(5): Show |
2 | a0001c0001t0001g0097 a0001c0004t0004g0007 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1063-27624_1063-27 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858576 | ||||||
chr5:138858594 | CT | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0166 a0001c0002t0002g0081 others(3): Show |
6 | HG00438.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063-27599delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858594 | ||||||
chr5:138858595 | T | TTTTTC | 92 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858595 | ||||||
chr5:138858595 | T | TTTTTCTT others(4): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(1): Show |
4 | HG02074.hp2 HG02129.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858595 | ||||||
chr5:138858595 | T | TTTTTCTT others(16): Show |
9 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(6): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(29): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858595 | ||||||
chr5:138858596 | T | TTTTCTTT others(3): Show |
10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1063-27613_1063-27 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858596 | ||||||
chr5:138858596 | T | TTTTCTTT others(9): Show |
1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-27613_1063-27 others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858596 | ||||||
chr5:138858597 | T | TTTCTTTT others(8): Show |
1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-27613_1063-27 others(21): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138858597 | ||||||
chr5:138858676 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1063-27536A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858676 | |||||||
chr5:138858700 | A | G | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(10): Show |
13 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1063-27512A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138858700 | |||||||
chr5:138859188 | G | C | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1063-27024G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859188 | |||||||
chr5:138859299 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1063-26913C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859299 | |||||||
chr5:138859513 | A | G | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1063-26699A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859513 | |||||||
chr5:138859528 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1063-26684T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859528 | |||||||
chr5:138859624 | G | A | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(8): Show |
11 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-26588G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859624 | |||||||
chr5:138859662 | G | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-26550G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138859662 | |||||||
chr5:138860104 | A | G | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1063-26108A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860104 | |||||||
chr5:138860128 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-26084A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860128 | |||||||
chr5:138860181 | A | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-26031A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860181 | |||||||
chr5:138860463 | C | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-25749C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860463 | |||||||
chr5:138860493 | TTTG | T | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1063-25716_1063-25 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138860493 | ||||||
chr5:138860496 | G | GTTTGT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-25696_1063-25 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138860496 | ||||||
chr5:138860500 | GT | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1063-25708delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138860500 | ||||||
chr5:138860584 | C | T | 81 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1063-25628C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860584 | |||||||
chr5:138860759 | A | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1063-25453A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138860759 | |||||||
chr5:138861042 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-25170C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861042 | |||||||
chr5:138861071 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1063-25141G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861071 | |||||||
chr5:138861285 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1063-24927T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861285 | |||||||
chr5:138861470 | A | T | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-24742A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861470 | |||||||
chr5:138861517 | C | G | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1063-24695C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138861517 | |||||||
chr5:138862373 | T | C | 2 | a0001c0003t0002g0062 a0001c0003t0002g0064 |
2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1063-23839T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862373 | |||||||
chr5:138862644 | A | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-23568A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862644 | |||||||
chr5:138862655 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1063-23557T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862655 | |||||||
chr5:138862687 | G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1063-23525G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862687 | |||||||
chr5:138862900 | G | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-23312G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138862900 | |||||||
chr5:138863015 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1063-23197A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863015 | |||||||
chr5:138863182 | T | G | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-23030T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863182 | |||||||
chr5:138863226 | T | A | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-22986T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863226 | |||||||
chr5:138863360 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0017 |
2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1063-22852C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863360 | |||||||
chr5:138863435 | A | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-22777A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863435 | |||||||
chr5:138863490 | C | T | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(10): Show |
13 | HG00423.hp2 HG01243.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1063-22722C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863490 | |||||||
chr5:138863501 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-22711C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863501 | |||||||
chr5:138863671 | G | A | 10 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0136 others(7): Show |
10 | HG01071.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1063-22541G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863671 | |||||||
chr5:138863875 | A | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-22337A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138863875 | |||||||
chr5:138864212 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1063-22000A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864212 | |||||||
chr5:138864250 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-21962C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864250 | |||||||
chr5:138864285 | G | A | 1 | a0001c0002t0005g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1063-21927G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864285 | |||||||
chr5:138864340 | A | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1063-21872A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864340 | |||||||
chr5:138864481 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1063-21731C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864481 | |||||||
chr5:138864546 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1063-21666A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864546 | |||||||
chr5:138864638 | A | G | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-21574A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864638 | |||||||
chr5:138864768 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1063-21444G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864768 | |||||||
chr5:138864796 | TTTTTTG | T | 30 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(27): Show |
30 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1063-21385_1063-21 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138864796 | ||||||
chr5:138864797 | TTTTTG | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1063-21410_1063-21 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138864797 | ||||||
chr5:138864797 | TTTTTGTT others(4): Show |
T | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1063-21410_1063-21 others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138864797 | ||||||
chr5:138864876 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0162 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1063-21336G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864876 | |||||||
chr5:138864877 | C | T | 95 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.1063-21335C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138864877 | |||||||
chr5:138865091 | C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-21121C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865091 | |||||||
chr5:138865101 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-21111C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865101 | |||||||
chr5:138865244 | C | T | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-20968C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865244 | |||||||
chr5:138865253 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1063-20959C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865253 | |||||||
chr5:138865308 | C | T | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-20904C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865308 | |||||||
chr5:138865602 | G | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-20610G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865602 | |||||||
chr5:138865746 | A | T | 1 | a0001c0014t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1063-20466A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138865746 | |||||||
chr5:138866241 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1063-19971A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866241 | |||||||
chr5:138866273 | C | CATTT | 52 | a0001c0001t0001g0038 a0001c0001t0001g0086 a0001c0001t0001g0087 others(49): Show |
52 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1063-19886_1063-19 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | C | CATTTATT others(1): Show |
15 | a0001c0001t0001g0096 a0001c0001t0001g0108 a0001c0001t0001g0116 others(12): Show |
15 | HG00099.hp1 HG00323.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-19890_1063-19 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | C | CATTTATT others(5): Show |
2 | a0001c0001t0001g0102 a0001c0005t0001g0168 |
2 | HG03654.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1063-19894_1063-19 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | CATTT | C | 25 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(22): Show |
25 | HG00438.hp1 HG00438.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1063-19886_1063-19 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | CATTTATT others(1): Show |
C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0097 a0001c0001t0001g0103 others(8): Show |
11 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1063-19890_1063-19 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | CATTTATT others(5): Show |
C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0120 a0001c0004t0004g0007 |
3 | HG01993.hp2 HG03492.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1063-19894_1063-19 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | CATTTATT others(9): Show |
C | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1063-19898_1063-19 others(22): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866273 | CATTTATT others(13): Show |
C | 11 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-19902_1063-19 others(26): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866273 | ||||||
chr5:138866289 | T | TATTA | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1063-19920_1063-19 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866289 | ||||||
chr5:138866310 | A | AT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(5): Show |
8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1063-19899dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866310 | ||||||
chr5:138866310 | A | ATTTAT | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-19899_1063-19 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138866310 | ||||||
chr5:138866372 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-19840A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866372 | |||||||
chr5:138866483 | A | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-19729A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866483 | |||||||
chr5:138866554 | G | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-19658G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866554 | |||||||
chr5:138866680 | C | T | 2 | a0001c0001t0001g0109 a0001c0002t0002g0073 |
2 | HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1063-19532C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866680 | |||||||
chr5:138866796 | A | G | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(8): Show |
11 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-19416A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138866796 | |||||||
chr5:138867027 | A | T | 8 | a0001c0002t0002g0056 a0001c0002t0002g0057 a0001c0002t0002g0058 others(5): Show |
8 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1063-19185A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867027 | |||||||
chr5:138867109 | T | C | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-19103T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867109 | |||||||
chr5:138867344 | C | T | 3 | a0001c0002t0002g0061 a0001c0002t0002g0073 a0001c0002t0002g0085 |
3 | HG01361.hp2 HG02735.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1063-18868C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867344 | |||||||
chr5:138867345 | T | G | 64 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(61): Show |
64 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1063-18867T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867345 | |||||||
chr5:138867360 | A | G | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(8): Show |
11 | HG00423.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-18852A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867360 | |||||||
chr5:138867575 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-18637T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867575 | |||||||
chr5:138867743 | C | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-18469C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867743 | |||||||
chr5:138867743 | CTTTCTTT others(7): Show |
C | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1063-18455_1063-18 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138867743 | ||||||
chr5:138867747 | C | CT | 17 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(14): Show |
17 | HG00423.hp2 HG01243.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063-18452dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138867747 | ||||||
chr5:138867747 | CT | C | 62 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0045 others(59): Show |
62 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1063-18452delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138867747 | ||||||
chr5:138867760 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01074.hp2 HG01081.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1063-18452T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138867760 | |||||||
chr5:138868294 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-17918C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868294 | |||||||
chr5:138868322 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1063-17890T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868322 | |||||||
chr5:138868418 | G | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0164 |
2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1063-17794G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868418 | |||||||
chr5:138868567 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-17645C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868567 | |||||||
chr5:138868730 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-17482T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868730 | |||||||
chr5:138868792 | A | G | 29 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0110 others(26): Show |
29 | HG00099.hp2 HG00323.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1063-17420A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138868792 | |||||||
chr5:138869173 | T | TA | 23 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0104 others(20): Show |
23 | HG00423.hp1 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1063-17022dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869173 | ||||||
chr5:138869173 | T | TAA | 34 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(31): Show |
34 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1063-17023_1063-17 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869173 | ||||||
chr5:138869173 | TA | T | 15 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(12): Show |
15 | HG00423.hp2 HG00642.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-17022delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869173 | ||||||
chr5:138869205 | A | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-17007A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869205 | |||||||
chr5:138869272 | A | T | 1 | a0001c0002t0003g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1063-16940A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869272 | |||||||
chr5:138869374 | C | CT | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(8): Show |
11 | HG00423.hp2 HG03516.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-16823dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869374 | ||||||
chr5:138869374 | CT | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-16823delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138869374 | ||||||
chr5:138869459 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1063-16753G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869459 | |||||||
chr5:138869744 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-16468G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138869744 | |||||||
chr5:138870187 | C | T | 5 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-16025C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870187 | |||||||
chr5:138870511 | G | T | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1063-15701G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870511 | |||||||
chr5:138870612 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1063-15600C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870612 | |||||||
chr5:138870786 | A | C | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1063-15426A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138870786 | |||||||
chr5:138871403 | C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-14809C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871403 | |||||||
chr5:138871550 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1063-14662C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871550 | |||||||
chr5:138871791 | A | T | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1063-14421A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871791 | |||||||
chr5:138871844 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1063-14368G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138871844 | |||||||
chr5:138872022 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1063-14190G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872022 | |||||||
chr5:138872027 | A | AGT | 16 | a0001c0001t0001g0038 a0001c0001t0001g0096 a0001c0001t0001g0119 others(13): Show |
16 | HG00099.hp1 HG00438.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1063-14145_1063-14 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | ||||||
chr5:138872027 | A | AGTGT | 17 | a0001c0001t0001g0088 a0001c0001t0001g0102 a0001c0001t0001g0110 others(14): Show |
17 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1063-14147_1063-14 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | ||||||
chr5:138872027 | AGT | A | 35 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(32): Show |
35 | HG00423.hp2 HG00741.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1063-14145_1063-14 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | ||||||
chr5:138872027 | AGTGT | A | 7 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0101 others(4): Show |
7 | HG00423.hp1 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1063-14147_1063-14 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | ||||||
chr5:138872027 | AGTGTGTG others(5): Show |
A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(8): Show |
11 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1063-14155_1063-14 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872027 | ||||||
chr5:138872057 | TGTGTGTG others(5): Show |
T | 27 | a0001c0001t0001g0012 a0001c0002t0002g0035 a0001c0002t0002g0052 others(24): Show |
27 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1063-14153_1063-14 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872057 | ||||||
chr5:138872059 | TGTGTGTG others(3): Show |
T | 26 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG00438.hp2 HG00741.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1063-14151_1063-14 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872059 | ||||||
chr5:138872061 | TGTGTGTG others(1): Show |
T | 5 | a0001c0001t0001g0045 a0001c0002t0003g0021 a0001c0002t0003g0023 others(2): Show |
5 | HG01109.hp2 HG01993.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063-14149_1063-14 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872061 | ||||||
chr5:138872063 | TGTGTGC | T | 2 | a0001c0002t0003g0025 a0001c0012t0003g0019 |
2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1063-14147_1063-14 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872063 | ||||||
chr5:138872065 | TGTGC | T | 6 | a0001c0002t0003g0022 a0001c0002t0003g0029 a0001c0002t0008g0028 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-14145_1063-14 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138872065 | ||||||
chr5:138872067 | T | C | 1 | a0003c0006t0001g0095 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1063-14145T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872067 | |||||||
chr5:138872069 | C | T | 2 | a0001c0002t0003g0020 a0001c0013t0003g0031 |
2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1063-14143C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872069 | |||||||
chr5:138872420 | G | A | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1063-13792G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872420 | |||||||
chr5:138872713 | C | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-13499C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872713 | |||||||
chr5:138872751 | C | T | 3 | a0001c0003t0002g0055 a0001c0003t0002g0076 a0001c0003t0002g0077 |
3 | HG00642.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1063-13461C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872751 | |||||||
chr5:138872752 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-13460A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872752 | |||||||
chr5:138872778 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1063-13434T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872778 | |||||||
chr5:138872820 | A | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0140 others(1): Show |
4 | HG02258.hp2 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-13392A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138872820 | |||||||
chr5:138873064 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1063-13148A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138873064 | |||||||
chr5:138873090 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1063-13122G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138873090 | |||||||
chr5:138873439 | A | G | 2 | a0003c0006t0001g0090 a0003c0006t0001g0095 |
2 | NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1063-12773A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138873439 | |||||||
chr5:138874363 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1063-11849C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874363 | |||||||
chr5:138874798 | A | C | 1 | a0001c0002t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1063-11414A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874798 | |||||||
chr5:138874814 | T | C | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-11398T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874814 | |||||||
chr5:138874883 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-11329A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138874883 | |||||||
chr5:138875206 | C | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-11006C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875206 | |||||||
chr5:138875259 | G | T | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-10953G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875259 | |||||||
chr5:138875283 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1063-10929G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875283 | |||||||
chr5:138875430 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1063-10782G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875430 | |||||||
chr5:138875495 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1063-10717C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875495 | |||||||
chr5:138875702 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1063-10510A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138875702 | |||||||
chr5:138876240 | G | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-9972G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876240 | |||||||
chr5:138876589 | A | G | 5 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063-9623A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876589 | |||||||
chr5:138876605 | C | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-9607C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876605 | |||||||
chr5:138876728 | A | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-9484A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876728 | |||||||
chr5:138876945 | G | A | 1 | a0001c0002t0002g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1063-9267G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138876945 | |||||||
chr5:138877038 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1063-9174G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877038 | |||||||
chr5:138877118 | A | G | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1063-9094A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877118 | |||||||
chr5:138877143 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-9069T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877143 | |||||||
chr5:138877441 | C | CT | 38 | a0001c0001t0001g0046 a0001c0001t0001g0139 a0001c0001t0001g0176 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-8754dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138877441 | ||||||
chr5:138877479 | C | T | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-8733C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877479 | |||||||
chr5:138877512 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1063-8700A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877512 | |||||||
chr5:138877541 | G | A | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1063-8671G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877541 | |||||||
chr5:138877549 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-8663G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877549 | |||||||
chr5:138877603 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1063-8609A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877603 | |||||||
chr5:138877606 | C | T | 11 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0117 others(8): Show |
11 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-8606C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877606 | |||||||
chr5:138877608 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1063-8604C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877608 | |||||||
chr5:138877742 | C | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1063-8470C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877742 | |||||||
chr5:138877917 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1063-8295A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877917 | |||||||
chr5:138877975 | G | A | 1 | a0001c0004t0004g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1063-8237G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138877975 | |||||||
chr5:138878177 | T | A | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-8035T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138878177 | |||||||
chr5:138878405 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1063-7807T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138878405 | |||||||
chr5:138878439 | C | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1063-7773C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138878439 | |||||||
chr5:138879048 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1063-7164G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879048 | |||||||
chr5:138879171 | T | TA | 36 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0091 others(33): Show |
36 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1063-7016dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | ||||||
chr5:138879171 | T | TAA | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
32 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1063-7017_1063-701 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | ||||||
chr5:138879171 | T | TAAA | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(15): Show |
18 | HG01099.hp2 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1063-7018_1063-701 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | ||||||
chr5:138879171 | T | TAAAA | 26 | a0001c0002t0002g0003 a0001c0002t0002g0035 a0001c0002t0002g0051 others(23): Show |
26 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1063-7019_1063-701 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | ||||||
chr5:138879171 | T | TAAAAA | 8 | a0001c0002t0002g0002 a0001c0002t0002g0056 a0001c0002t0002g0058 others(5): Show |
8 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1063-7020_1063-701 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879171 | ||||||
chr5:138879172 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1063-7040A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879172 | |||||||
chr5:138879473 | G | GT | 6 | a0001c0001t0001g0088 a0001c0001t0001g0101 a0001c0001t0001g0176 others(3): Show |
6 | HG01099.hp2 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-6730dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138879473 | ||||||
chr5:138879482 | T | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-6730T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879482 | |||||||
chr5:138879631 | T | A | 1 | a0001c0005t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1063-6581T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879631 | |||||||
chr5:138879639 | G | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1063-6573G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879639 | |||||||
chr5:138879720 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1063-6492A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879720 | |||||||
chr5:138879794 | G | A | 6 | a0001c0002t0003g0004 a0001c0002t0003g0043 a0001c0002t0003g0044 others(3): Show |
6 | HG01167.hp2 HG01243.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063-6418G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138879794 | |||||||
chr5:138880112 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-6100T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880112 | |||||||
chr5:138880221 | T | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063-5991T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880221 | |||||||
chr5:138880314 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1063-5898T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880314 | |||||||
chr5:138880377 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1063-5835T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880377 | |||||||
chr5:138880594 | A | G | 64 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(61): Show |
64 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1063-5618A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880594 | |||||||
chr5:138880723 | A | G | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1063-5489A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880723 | |||||||
chr5:138880763 | A | G | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1063-5449A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880763 | |||||||
chr5:138880936 | G | GA | 39 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(36): Show |
39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1063-5265dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138880936 | ||||||
chr5:138880946 | A | AC | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1063-5266_1063-526 others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880946 | |||||||
chr5:138880971 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1063-5241A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138880971 | |||||||
chr5:138881438 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-4774T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138881438 | |||||||
chr5:138881468 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-4744T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138881468 | |||||||
chr5:138881616 | T | C | 35 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(32): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1063-4596T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138881616 | |||||||
chr5:138881761 | T | TTTG | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1063-4438_1063-443 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138881761 | ||||||
chr5:138882022 | T | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-4190T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882022 | |||||||
chr5:138882061 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-4151T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882061 | |||||||
chr5:138882077 | C | G | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-4135C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882077 | |||||||
chr5:138882115 | A | G | 2 | a0001c0001t0001g0101 a0001c0002t0003g0023 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1063-4097A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882115 | |||||||
chr5:138882134 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1063-4078T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882134 | |||||||
chr5:138882345 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1063-3867A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882345 | |||||||
chr5:138882489 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1063-3723A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882489 | |||||||
chr5:138882956 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-3256G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138882956 | |||||||
chr5:138883158 | C | T | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063-3054C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138883158 | |||||||
chr5:138883373 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-2839C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138883373 | |||||||
chr5:138884190 | G | A | 2 | a0001c0002t0003g0025 a0001c0012t0003g0019 |
2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1063-2022G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138884190 | |||||||
chr5:138884630 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1063-1582A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138884630 | |||||||
chr5:138884668 | T | C | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1063-1544T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138884668 | |||||||
chr5:138885086 | A | G | 13 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(10): Show |
13 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1063-1126A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885086 | |||||||
chr5:138885471 | G | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1063-741G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885471 | |||||||
chr5:138885530 | T | TA | 2 | a0001c0002t0002g0056 a0001c0002t0002g0060 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1063-681dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 138885530 | ||||||
chr5:138885569 | G | A | 1 | a0001c0002t0002g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1063-643G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885569 | |||||||
chr5:138885678 | C | G | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1063-534C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885678 | |||||||
chr5:138885917 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1063-295T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 7/17 | chr5 | 138885917 | |||||||
chr5:138886300 | G | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
splice_region_variant&intron_variant | LOW | c.1143+8G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138886300 | |||||||
chr5:138886641 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1143+349G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138886641 | |||||||
chr5:138886905 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1144-585A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138886905 | |||||||
chr5:138887051 | C | G | 1 | a0001c0014t0001g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1144-439C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887051 | |||||||
chr5:138887139 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1144-351A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887139 | |||||||
chr5:138887191 | G | A | 3 | a0001c0005t0001g0156 a0001c0005t0001g0167 a0001c0005t0001g0168 |
3 | HG00099.hp1 HG00741.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1144-299G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887191 | |||||||
chr5:138887305 | C | G | 53 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(50): Show |
53 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1144-185C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887305 | |||||||
chr5:138887467 | A | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1144-23A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 8/17 | chr5 | 138887467 | |||||||
chr5:138887888 | C | T | 2 | a0001c0002t0005g0050 a0001c0002t0005g0068 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1296+246C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138887888 | |||||||
chr5:138887944 | A | G | 63 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(60): Show |
63 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1296+302A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138887944 | |||||||
chr5:138887983 | C | T | 1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1296+341C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138887983 | |||||||
chr5:138888103 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1296+461A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888103 | |||||||
chr5:138888359 | A | G | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1296+717A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888359 | |||||||
chr5:138888586 | A | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
82 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1296+944A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888586 | |||||||
chr5:138888594 | C | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1296+952C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888594 | |||||||
chr5:138888609 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
82 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1296+967A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888609 | |||||||
chr5:138888746 | C | T | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+1104C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888746 | |||||||
chr5:138888885 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+1243G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138888885 | |||||||
chr5:138889169 | A | G | 1 | a0001c0003t0002g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1296+1527A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138889169 | |||||||
chr5:138889532 | G | A | 1 | a0001c0001t0006g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1296+1890G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138889532 | |||||||
chr5:138889905 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1296+2263C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138889905 | |||||||
chr5:138890264 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+2622T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890264 | |||||||
chr5:138890326 | T | G | 10 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(7): Show |
10 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+2684T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890326 | |||||||
chr5:138890349 | AT | A | 67 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(64): Show |
67 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1296+2710delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138890349 | ||||||
chr5:138890529 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1296+2887G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890529 | |||||||
chr5:138890576 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(5): Show |
8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296+2934A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138890576 | |||||||
chr5:138891039 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+3397A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891039 | |||||||
chr5:138891078 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1296+3436T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891078 | |||||||
chr5:138891376 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
82 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1296+3734A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891376 | |||||||
chr5:138891396 | C | CT | 39 | a0001c0001t0001g0176 a0001c0002t0002g0002 a0001c0002t0002g0003 others(36): Show |
39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1296+3764dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138891396 | ||||||
chr5:138891578 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0002c0007t0001g0099 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+3936G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891578 | |||||||
chr5:138891710 | G | C | 26 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1296+4068G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891710 | |||||||
chr5:138891947 | G | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1296+4305G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138891947 | |||||||
chr5:138892004 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1296+4362G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892004 | |||||||
chr5:138892037 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1296+4395C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892037 | |||||||
chr5:138892090 | T | G | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1296+4448T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892090 | |||||||
chr5:138892328 | G | GT | 28 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0096 others(25): Show |
28 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1296+4715dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | G | GTT | 16 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0128 others(13): Show |
16 | HG00423.hp2 HG00438.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1296+4714_1296+471 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | G | GTTTT | 8 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0092 others(5): Show |
8 | HG02895.hp2 HG03486.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+4712_1296+471 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | G | GTTTTT | 5 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0118 others(2): Show |
5 | HG00741.hp1 HG02486.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+4711_1296+471 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | GT | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0135 a0001c0001t0001g0171 others(10): Show |
13 | HG01071.hp2 HG01361.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.1296+4715delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | GTT | G | 6 | a0001c0002t0003g0020 a0001c0002t0003g0029 a0001c0002t0005g0026 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1296+4714_1296+471 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | GTTTTTTT | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG02451.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1296+4709_1296+471 others(11): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | GTTTTTTT others(3): Show |
G | 33 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(30): Show |
33 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1296+4706_1296+471 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892328 | GTTTTTTT others(4): Show |
G | 1 | a0001c0002t0002g0060 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1296+4705_1296+471 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138892328 | ||||||
chr5:138892939 | C | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5297C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892939 | |||||||
chr5:138892973 | G | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1296+5331G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138892973 | |||||||
chr5:138893159 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5517G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893159 | |||||||
chr5:138893282 | C | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5640C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893282 | |||||||
chr5:138893357 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+5715G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893357 | |||||||
chr5:138893515 | A | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1296+5873A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893515 | |||||||
chr5:138893595 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1296+5953T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893595 | |||||||
chr5:138893632 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1296+5990G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893632 | |||||||
chr5:138893793 | T | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+6151T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893793 | |||||||
chr5:138893843 | C | T | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+6201C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893843 | |||||||
chr5:138893865 | T | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+6223T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138893865 | |||||||
chr5:138894275 | C | CTTTCTT | 36 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(33): Show |
36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1296+6638_1296+663 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894275 | ||||||
chr5:138894279 | C | CTTTT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(33): Show |
36 | HG00438.hp2 HG00741.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1296+6638_1296+663 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894279 | ||||||
chr5:138894280 | T | TTTTTC | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+6638_1296+663 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894280 | |||||||
chr5:138894281 | C | T | 47 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 others(44): Show |
47 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1296+6639C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894281 | |||||||
chr5:138894281 | CT | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0115 a0001c0001t0001g0158 others(2): Show |
5 | HG01070.hp1 HG01099.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1296+6657delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894281 | ||||||
chr5:138894284 | T | TCTTTC | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1296+6642_1296+664 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894284 | |||||||
chr5:138894442 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+6800A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894442 | |||||||
chr5:138894574 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1296+6932A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894574 | |||||||
chr5:138894595 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1296+6953C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894595 | |||||||
chr5:138894641 | C | CTGATTA | 7 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0002t0002g0054 others(4): Show |
7 | HG00423.hp2 HG01433.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1296+7035_1296+704 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894641 | ||||||
chr5:138894641 | CTGATTA | C | 11 | a0001c0001t0001g0036 a0001c0001t0001g0103 a0001c0001t0001g0151 others(8): Show |
11 | HG00639.hp2 HG01099.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1296+7035_1296+704 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894641 | ||||||
chr5:138894641 | CTGATTAT others(5): Show |
C | 12 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(9): Show |
12 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1296+7029_1296+704 others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138894641 | ||||||
chr5:138894753 | T | G | 1 | a0001c0002t0003g0024 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1296+7111T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894753 | |||||||
chr5:138894939 | C | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1296+7297C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894939 | |||||||
chr5:138894962 | T | C | 3 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0072 |
3 | HG01433.hp2 HG01515.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1296+7320T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138894962 | |||||||
chr5:138895269 | A | G | 1 | a0001c0002t0002g0074 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1296+7627A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895269 | |||||||
chr5:138895416 | G | A | 2 | a0001c0002t0005g0050 a0001c0002t0005g0068 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1296+7774G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895416 | |||||||
chr5:138895503 | TG | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1296+7871delG | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138895503 | ||||||
chr5:138895714 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
96 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1296+8072C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895714 | |||||||
chr5:138895956 | C | T | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1296+8314C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138895956 | |||||||
chr5:138896266 | T | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1297-8083T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896266 | |||||||
chr5:138896389 | T | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0165 |
3 | HG02970.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1297-7960T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896389 | |||||||
chr5:138896398 | T | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1297-7951T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896398 | |||||||
chr5:138896545 | T | C | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-7804T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896545 | |||||||
chr5:138896736 | A | G | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1297-7613A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896736 | |||||||
chr5:138896838 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1297-7511G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138896838 | |||||||
chr5:138897050 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-7299A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897050 | |||||||
chr5:138897084 | G | GC | 106 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
106 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1297-7265_1297-726 others(5): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897084 | |||||||
chr5:138897294 | A | AC | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1297-7041dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | ||||||
chr5:138897294 | A | ACC | 28 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(25): Show |
28 | HG01071.hp2 HG01074.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1297-7042_1297-704 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | ||||||
chr5:138897294 | A | ACCC | 14 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0092 others(11): Show |
14 | HG00323.hp1 HG00438.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1297-7043_1297-704 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | ||||||
chr5:138897294 | AC | A | 19 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0102 others(16): Show |
19 | HG01099.hp2 HG01109.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1297-7041delC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | ||||||
chr5:138897294 | ACCCCCCC others(4): Show |
A | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1297-7051_1297-704 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138897294 | ||||||
chr5:138897297 | C | G | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1297-7052C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897297 | |||||||
chr5:138897298 | C | G | 3 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 |
3 | HG01109.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1297-7051C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897298 | |||||||
chr5:138897303 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1297-7046C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897303 | |||||||
chr5:138897309 | G | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-7040G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897309 | |||||||
chr5:138897310 | C | G | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
10 | HG00438.hp2 HG00741.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1297-7039C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897310 | |||||||
chr5:138897497 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-6852A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897497 | |||||||
chr5:138897683 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1297-6666C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897683 | |||||||
chr5:138897892 | C | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-6457C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897892 | |||||||
chr5:138897965 | A | G | 1 | a0001c0002t0002g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1297-6384A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138897965 | |||||||
chr5:138898158 | A | AC | 56 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(53): Show |
56 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1297-6182dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138898158 | ||||||
chr5:138898194 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1297-6155C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898194 | |||||||
chr5:138898308 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-6041A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898308 | |||||||
chr5:138898427 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
100 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1297-5922G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898427 | |||||||
chr5:138898441 | G | T | 64 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(61): Show |
64 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1297-5908G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138898441 | |||||||
chr5:138898601 | T | TA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(58): Show |
61 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1297-5732dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138898601 | ||||||
chr5:138898601 | T | TAA | 7 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0001c0002t0002g0082 others(4): Show |
7 | HG02486.hp2 HG02602.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1297-5733_1297-573 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138898601 | ||||||
chr5:138899160 | G | A | 3 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 |
3 | HG01993.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1297-5189G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899160 | |||||||
chr5:138899184 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1297-5165C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899184 | |||||||
chr5:138899348 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1297-5001C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899348 | |||||||
chr5:138899688 | C | A | 1 | a0001c0003t0002g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1297-4661C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899688 | |||||||
chr5:138899851 | A | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-4498A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138899851 | |||||||
chr5:138900011 | T | G | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1297-4338T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138900011 | |||||||
chr5:138900307 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1297-4042A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138900307 | |||||||
chr5:138900379 | TTATGAGA others(2029): Show |
T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-3968_1297-193 others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 138900379 | ||||||
chr5:138900631 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-3718A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138900631 | |||||||
chr5:138901029 | C | G | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1297-3320C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901029 | |||||||
chr5:138901066 | G | A | 63 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(60): Show |
63 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1297-3283G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901066 | |||||||
chr5:138901140 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1297-3209C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901140 | |||||||
chr5:138901218 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1297-3131C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901218 | |||||||
chr5:138901252 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
105 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1297-3097A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901252 | |||||||
chr5:138901262 | A | G | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1297-3087A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901262 | |||||||
chr5:138901572 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1297-2777G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901572 | |||||||
chr5:138901591 | A | G | 1 | a0001c0002t0005g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1297-2758A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901591 | |||||||
chr5:138901604 | T | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2745T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901604 | |||||||
chr5:138901613 | G | C | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1297-2736G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901613 | |||||||
chr5:138901727 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2622C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901727 | |||||||
chr5:138901868 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1297-2481A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901868 | |||||||
chr5:138901944 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-2405G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138901944 | |||||||
chr5:138902069 | A | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2280A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902069 | |||||||
chr5:138902354 | G | A | 67 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(64): Show |
67 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1297-1995G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902354 | |||||||
chr5:138902419 | G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1930G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902419 | |||||||
chr5:138902426 | G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1923G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902426 | |||||||
chr5:138902432 | G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1917G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902432 | |||||||
chr5:138902482 | T | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1867T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902482 | |||||||
chr5:138902511 | T | C | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1838T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902511 | |||||||
chr5:138902513 | A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1836A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902513 | |||||||
chr5:138902565 | G | A | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(7): Show |
10 | HG00423.hp1 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-1784G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902565 | |||||||
chr5:138902602 | G | C | 1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1297-1747G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902602 | |||||||
chr5:138902630 | A | G | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-1719A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902630 | |||||||
chr5:138902641 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1297-1708G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902641 | |||||||
chr5:138902719 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-1630C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902719 | |||||||
chr5:138902736 | A | G | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1297-1613A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902736 | |||||||
chr5:138902854 | A | G | 6 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0114 others(3): Show |
6 | HG02132.hp2 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-1495A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138902854 | |||||||
chr5:138903049 | T | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-1300T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903049 | |||||||
chr5:138903113 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1297-1236A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903113 | |||||||
chr5:138903116 | T | G | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-1233T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903116 | |||||||
chr5:138903118 | T | C | 5 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01070.hp1 HG01109.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297-1231T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903118 | |||||||
chr5:138903158 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1297-1191C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903158 | |||||||
chr5:138903249 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1297-1100C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903249 | |||||||
chr5:138903663 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1297-686C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903663 | |||||||
chr5:138903989 | C | T | 1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1297-360C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138903989 | |||||||
chr5:138904224 | G | A | 1 | a0001c0002t0002g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1297-125G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138904224 | |||||||
chr5:138904235 | C | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-114C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 9/17 | chr5 | 138904235 | |||||||
chr5:138904704 | C | T | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1389+263C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138904704 | |||||||
chr5:138904833 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1389+392G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138904833 | |||||||
chr5:138905018 | T | C | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1389+577T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905018 | |||||||
chr5:138905028 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1389+587A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905028 | |||||||
chr5:138905049 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+608G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905049 | |||||||
chr5:138905093 | C | CA | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
14 | HG00423.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1389+671dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905093 | ||||||
chr5:138905093 | C | CAA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1389+670_1389+671d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905093 | ||||||
chr5:138905111 | A | AAAATACA others(7): Show |
1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1389+671_1389+672i others(16): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | ||||||
chr5:138905111 | A | AAATACAT others(6): Show |
14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0046 others(11): Show |
14 | HG00438.hp2 HG01167.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1389+671_1389+672i others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | ||||||
chr5:138905111 | A | AAATACAT others(10): Show |
5 | a0001c0002t0008g0028 a0001c0004t0004g0005 a0001c0004t0004g0180 others(2): Show |
5 | HG02486.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+671_1389+672i others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | ||||||
chr5:138905111 | A | AATACATA others(5): Show |
45 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0002t0002g0002 others(42): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1389+678_1389+689d others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | ||||||
chr5:138905111 | A | AATACATA others(9): Show |
2 | a0001c0002t0003g0029 a0001c0002t0005g0050 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1389+674_1389+689d others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138905111 | ||||||
chr5:138905111 | A | ACATACAT others(10): Show |
1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1389+670_1389+671i others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905111 | |||||||
chr5:138905185 | G | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1389+744G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905185 | |||||||
chr5:138905243 | T | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+802T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905243 | |||||||
chr5:138905550 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1389+1109A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905550 | |||||||
chr5:138905586 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+1145C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905586 | |||||||
chr5:138905629 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
83 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1389+1188A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905629 | |||||||
chr5:138905824 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+1383C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138905824 | |||||||
chr5:138906076 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1389+1635G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906076 | |||||||
chr5:138906131 | C | G | 64 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(61): Show |
64 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1389+1690C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906131 | |||||||
chr5:138906309 | A | G | 1 | a0004c0010t0001g0169 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1389+1868A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906309 | |||||||
chr5:138906840 | T | C | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1389+2399T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138906840 | |||||||
chr5:138907211 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+2770G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907211 | |||||||
chr5:138907409 | G | A | 68 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(65): Show |
68 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1389+2968G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907409 | |||||||
chr5:138907468 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+3027C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907468 | |||||||
chr5:138907470 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1389+3029G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907470 | |||||||
chr5:138907481 | G | C | 1 | a0001c0002t0005g0068 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1389+3040G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907481 | |||||||
chr5:138907523 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1389+3082C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907523 | |||||||
chr5:138907577 | G | A | 7 | a0001c0001t0001g0094 a0001c0001t0001g0108 a0001c0001t0001g0109 others(4): Show |
7 | HG00423.hp2 HG02132.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+3136G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907577 | |||||||
chr5:138907739 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+3298T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907739 | |||||||
chr5:138907924 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+3483G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907924 | |||||||
chr5:138907965 | C | T | 2 | a0001c0003t0002g0062 a0001c0003t0002g0064 |
2 | HG01346.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1389+3524C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138907965 | |||||||
chr5:138907969 | C | CTT | 19 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(16): Show |
19 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1389+3537_1389+353 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138907969 | ||||||
chr5:138908130 | A | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1389+3689A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908130 | |||||||
chr5:138908342 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+3901C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908342 | |||||||
chr5:138908579 | C | CGCTTGAG others(12): Show |
4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+4153_1389+415 others(23): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138908579 | ||||||
chr5:138908579 | C | T | 84 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1389+4138C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908579 | |||||||
chr5:138908587 | C | T | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1389+4146C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908587 | |||||||
chr5:138908703 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1389+4262A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138908703 | |||||||
chr5:138908773 | AAG | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1389+4335_1389+433 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138908773 | ||||||
chr5:138909033 | C | A | 1 | a0001c0002t0002g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1389+4592C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909033 | |||||||
chr5:138909234 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1389+4793A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909234 | |||||||
chr5:138909359 | C | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0043 a0001c0002t0003g0044 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+4918C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909359 | |||||||
chr5:138909462 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1389+5021A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909462 | |||||||
chr5:138909531 | A | T | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1389+5090A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909531 | |||||||
chr5:138909720 | G | T | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1389+5279G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909720 | |||||||
chr5:138909740 | T | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+5299T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138909740 | |||||||
chr5:138910226 | C | CT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0134 a0001c0001t0001g0147 others(3): Show |
6 | HG00438.hp1 HG01099.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+5812dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910226 | CT | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
56 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1389+5812delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910226 | CTT | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(37): Show |
40 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1389+5811_1389+581 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910226 | CTTT | C | 7 | a0001c0001t0001g0124 a0001c0002t0002g0003 a0001c0002t0002g0052 others(4): Show |
7 | HG01433.hp1 HG01515.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+5810_1389+581 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910226 | CTTTT | C | 10 | a0001c0002t0003g0004 a0001c0002t0003g0020 a0001c0002t0003g0025 others(7): Show |
10 | HG00741.hp1 HG01243.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1389+5809_1389+581 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910226 | CTTTTT | C | 6 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(3): Show |
6 | HG01109.hp2 HG01167.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1389+5808_1389+581 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910226 | CTTTTTTT others(4): Show |
C | 2 | a0001c0004t0004g0005 a0001c0012t0003g0019 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1389+5802_1389+581 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138910226 | ||||||
chr5:138910252 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1389+5811T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910252 | |||||||
chr5:138910412 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1389+5971G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910412 | |||||||
chr5:138910472 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389+6031G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910472 | |||||||
chr5:138910542 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+6101C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910542 | |||||||
chr5:138910639 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
78 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1389+6198G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910639 | |||||||
chr5:138910787 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1389+6346A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138910787 | |||||||
chr5:138911089 | T | C | 59 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(56): Show |
59 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1389+6648T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911089 | |||||||
chr5:138911376 | C | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-6366C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911376 | |||||||
chr5:138911458 | A | AC | 17 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0003g0004 others(14): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1390-6275dupC | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138911458 | ||||||
chr5:138911459 | C | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1390-6283C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911459 | |||||||
chr5:138911515 | G | T | 1 | a0001c0002t0002g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1390-6227G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911515 | |||||||
chr5:138911891 | A | G | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-5851A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911891 | |||||||
chr5:138911948 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1390-5794C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138911948 | |||||||
chr5:138912226 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-5516G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912226 | |||||||
chr5:138912338 | G | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-5404G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912338 | |||||||
chr5:138912376 | TAGA | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-5359_1390-535 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138912376 | ||||||
chr5:138912699 | C | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-5043C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912699 | |||||||
chr5:138912758 | TTA | T | 63 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(60): Show |
63 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1390-4979_1390-497 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138912758 | ||||||
chr5:138912885 | T | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1390-4857T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912885 | |||||||
chr5:138912885 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0018 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1390-4857T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912885 | |||||||
chr5:138912965 | C | T | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1390-4777C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138912965 | |||||||
chr5:138913054 | G | A | 1 | a0001c0011t0001g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1390-4688G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913054 | |||||||
chr5:138913058 | CT | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1390-4672delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138913058 | ||||||
chr5:138913058 | CTT | C | 59 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(56): Show |
59 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1390-4673_1390-467 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138913058 | ||||||
chr5:138913076 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1390-4666T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913076 | |||||||
chr5:138913316 | G | T | 9 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(6): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1390-4426G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913316 | |||||||
chr5:138913569 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | HG00099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1390-4173G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913569 | |||||||
chr5:138913583 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1390-4143delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138913583 | ||||||
chr5:138913670 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1390-4072G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913670 | |||||||
chr5:138913860 | A | G | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(7): Show |
10 | HG00423.hp1 NA18946.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390-3882A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913860 | |||||||
chr5:138913887 | G | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0114 others(5): Show |
8 | HG02132.hp2 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1390-3855G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913887 | |||||||
chr5:138913892 | T | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0161 |
3 | HG01070.hp1 HG01109.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1390-3850T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913892 | |||||||
chr5:138913895 | G | T | 9 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0001g0140 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1390-3847G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913895 | |||||||
chr5:138913996 | G | T | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1390-3746G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138913996 | |||||||
chr5:138914251 | C | A | 63 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(60): Show |
63 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1390-3491C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914251 | |||||||
chr5:138914417 | G | A | 63 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(60): Show |
63 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1390-3325G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914417 | |||||||
chr5:138914630 | G | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1390-3112G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914630 | |||||||
chr5:138914932 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-2810G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138914932 | |||||||
chr5:138915104 | G | A | 7 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(4): Show |
7 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1390-2638G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915104 | |||||||
chr5:138915235 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1390-2507C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915235 | |||||||
chr5:138915407 | T | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0166 a0001c0001t0001g0170 |
3 | HG00323.hp2 HG02129.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1390-2335T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915407 | |||||||
chr5:138915516 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-2226G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915516 | |||||||
chr5:138915587 | A | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-2155A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915587 | |||||||
chr5:138915634 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1390-2108T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138915634 | |||||||
chr5:138916000 | G | A | 59 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(56): Show |
59 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1390-1742G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916000 | |||||||
chr5:138916003 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1390-1739C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916003 | |||||||
chr5:138916067 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1390-1675A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916067 | |||||||
chr5:138916177 | C | CAAA | 5 | a0001c0001t0001g0101 a0001c0002t0003g0021 a0001c0002t0003g0022 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-1553_1390-155 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(2): Show |
29 | a0001c0002t0002g0003 a0001c0002t0002g0035 a0001c0002t0002g0052 others(26): Show |
29 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1390-1559_1390-155 others(13): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(3): Show |
17 | a0001c0002t0002g0002 a0001c0002t0002g0051 a0001c0002t0002g0054 others(14): Show |
17 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1390-1560_1390-155 others(14): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(4): Show |
2 | a0001c0002t0003g0047 a0001c0002t0005g0050 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1390-1561_1390-155 others(15): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(6): Show |
3 | a0001c0002t0003g0020 a0001c0002t0003g0029 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1390-1563_1390-155 others(17): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(7): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.1390-1564_1390-155 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(19): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(9): Show |
1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(20): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0003g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(23): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(13): Show |
1 | a0001c0012t0003g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(24): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(19): Show |
2 | a0001c0001t0001g0092 a0002c0007t0001g0100 |
2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(30): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(20): Show |
1 | a0002c0007t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(31): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0104 a0003c0006t0001g0095 |
2 | HG00423.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(33): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(25): Show |
1 | a0003c0006t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(36): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(29): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0093 others(1): Show |
4 | HG02723.hp2 HG06807.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(40): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(30): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0179 |
2 | NA18986.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1390-1551_1390-155 others(41): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(42): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(33): Show |
1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(44): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(34): Show |
1 | a0001c0001t0001g0086 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(45): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916177 | C | CAAAAAAA others(42): Show |
1 | a0001c0001t0001g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1390-1551_1390-155 others(53): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916177 | ||||||
chr5:138916312 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-1430C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916312 | |||||||
chr5:138916395 | C | CT | 18 | a0001c0001t0001g0101 a0001c0001t0001g0176 a0001c0001t0006g0174 others(15): Show |
18 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1390-1332dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916395 | ||||||
chr5:138916779 | A | AT | 50 | a0001c0001t0001g0094 a0001c0001t0001g0151 a0001c0001t0001g0162 others(47): Show |
50 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1390-953dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916779 | ||||||
chr5:138916779 | A | ATT | 13 | a0001c0002t0003g0004 a0001c0002t0003g0021 a0001c0002t0003g0022 others(10): Show |
13 | HG00741.hp1 HG01109.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1390-954_1390-953d others(4): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916779 | ||||||
chr5:138916782 | T | TA | 3 | a0001c0002t0003g0020 a0001c0002t0003g0025 a0001c0012t0003g0019 |
3 | HG02280.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1390-960_1390-959i others(3): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916782 | |||||||
chr5:138916783 | T | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0001c0001t0001g0176 others(4): Show |
7 | HG01099.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-959T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916783 | |||||||
chr5:138916797 | C | G | 1 | a0001c0003t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1390-945C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916797 | |||||||
chr5:138916961 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1390-781A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916961 | |||||||
chr5:138916962 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-780C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138916962 | |||||||
chr5:138916982 | C | CA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-759dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138916982 | ||||||
chr5:138917052 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-690C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138917052 | |||||||
chr5:138917454 | A | C | 3 | a0001c0001t0001g0176 a0001c0001t0006g0174 a0001c0001t0006g0175 |
3 | HG01099.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1390-288A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138917454 | |||||||
chr5:138917531 | TTTTA | T | 35 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(32): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1390-207_1390-204d others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 138917531 | ||||||
chr5:138917731 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1390-11A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 10/17 | chr5 | 138917731 | |||||||
chr5:138917982 | A | G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0119 others(6): Show |
9 | HG01099.hp1 HG01168.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+84A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138917982 | |||||||
chr5:138918194 | G | GA | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546+297dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138918194 | ||||||
chr5:138918456 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1546+558A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918456 | |||||||
chr5:138918568 | G | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1546+670G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918568 | |||||||
chr5:138918635 | G | C | 4 | a0001c0002t0003g0021 a0001c0002t0003g0022 a0001c0002t0003g0023 others(1): Show |
4 | HG01109.hp2 HG01993.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+737G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918635 | |||||||
chr5:138918858 | G | A | 8 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(5): Show |
8 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+960G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138918858 | |||||||
chr5:138919243 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1546+1345A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138919243 | |||||||
chr5:138919410 | CA | C | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1546+1513delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138919410 | |||||||
chr5:138919857 | G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1546+1959G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138919857 | |||||||
chr5:138919967 | A | AT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0176 a0001c0002t0002g0059 others(7): Show |
10 | HG01074.hp1 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+2095dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | ||||||
chr5:138919967 | AT | A | 102 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1546+2095delT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | ||||||
chr5:138919967 | ATT | A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0153 others(2): Show |
5 | HG01074.hp2 HG01515.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+2094_1546+209 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | ||||||
chr5:138919967 | ATTT | A | 9 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(6): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+2093_1546+209 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138919967 | ||||||
chr5:138920040 | G | A | 9 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(6): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+2142G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920040 | |||||||
chr5:138920272 | G | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1546+2374G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920272 | |||||||
chr5:138920279 | C | G | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1546+2381C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920279 | |||||||
chr5:138920329 | T | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
77 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1546+2431T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920329 | |||||||
chr5:138920410 | G | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1546+2512G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920410 | |||||||
chr5:138920450 | C | T | 35 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(32): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1546+2552C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920450 | |||||||
chr5:138920497 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1546+2599G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920497 | |||||||
chr5:138920589 | C | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1546+2691C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920589 | |||||||
chr5:138920608 | T | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1546+2710T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920608 | |||||||
chr5:138920616 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2718A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920616 | |||||||
chr5:138920964 | A | T | 1 | a0001c0008t0003g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1546+3066A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138920964 | |||||||
chr5:138921596 | A | AT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | HG00323.hp2 HG01891.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1547-2891dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | ||||||
chr5:138921596 | A | ATT | 7 | a0001c0001t0001g0018 a0001c0002t0002g0003 a0001c0002t0002g0061 others(4): Show |
7 | HG01975.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-2892_1547-289 others(6): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | ||||||
chr5:138921596 | A | ATTT | 39 | a0001c0002t0002g0035 a0001c0002t0002g0051 a0001c0002t0002g0052 others(36): Show |
39 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1547-2893_1547-289 others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | ||||||
chr5:138921596 | A | ATTTT | 5 | a0001c0002t0002g0002 a0001c0002t0002g0058 a0001c0002t0002g0072 others(2): Show |
5 | HG01981.hp1 HG02258.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-2894_1547-289 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | ||||||
chr5:138921596 | A | ATTTTT | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(19): Show |
22 | HG00423.hp1 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1547-2895_1547-289 others(9): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921596 | ||||||
chr5:138921821 | G | A | 1 | a0001c0002t0003g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1547-2689G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138921821 | |||||||
chr5:138921907 | C | G | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1547-2603C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138921907 | |||||||
chr5:138921907 | C | T | 1 | a0001c0002t0002g0073 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1547-2603C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138921907 | |||||||
chr5:138921917 | A | AT | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(9): Show |
12 | HG00423.hp1 HG02258.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-2580dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138921917 | ||||||
chr5:138922163 | C | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG01433.hp1 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-2347C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922163 | |||||||
chr5:138922181 | A | T | 1 | a0001c0002t0002g0079 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1547-2329A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922181 | |||||||
chr5:138922220 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(91): Show |
94 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1547-2290T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922220 | |||||||
chr5:138922488 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
89 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.1547-2022G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922488 | |||||||
chr5:138922664 | C | T | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1547-1846C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922664 | |||||||
chr5:138922672 | C | A | 9 | a0001c0002t0003g0004 a0001c0002t0003g0032 a0001c0002t0003g0033 others(6): Show |
9 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1547-1838C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922672 | |||||||
chr5:138922672 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0149 |
2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1547-1838C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922672 | |||||||
chr5:138922894 | G | A | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1547-1616G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922894 | |||||||
chr5:138922930 | TA | T | 52 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0002t0002g0002 others(49): Show |
52 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1547-1566delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138922930 | ||||||
chr5:138922947 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1547-1563G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138922947 | |||||||
chr5:138923001 | T | TGTTTAA | 75 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(72): Show |
75 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1547-1509_1547-150 others(10): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923001 | |||||||
chr5:138923061 | A | G | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1547-1449A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923061 | |||||||
chr5:138923113 | A | C | 75 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(72): Show |
75 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1547-1397A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923113 | |||||||
chr5:138923636 | C | T | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-874C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923636 | |||||||
chr5:138923754 | C | T | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1547-756C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923754 | |||||||
chr5:138923853 | T | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1547-657T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923853 | |||||||
chr5:138923953 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1547-557G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138923953 | |||||||
chr5:138924149 | T | TA | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1547-360dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138924149 | ||||||
chr5:138924282 | G | GT | 45 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(42): Show |
45 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1547-215dupT | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138924282 | ||||||
chr5:138924282 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1547-228G>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138924282 | |||||||
chr5:138924295 | TA | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(15): Show |
18 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1547-210delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 138924295 | ||||||
chr5:138924296 | A | T | 56 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1547-214A>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138924296 | |||||||
chr5:138924301 | C | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1547-209C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 11/17 | chr5 | 138924301 | |||||||
chr5:138924907 | G | A | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1747+197G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 12/17 | chr5 | 138924907 | |||||||
chr5:138924916 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18946.hp2 NA19003.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1747+206C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 12/17 | chr5 | 138924916 | |||||||
chr5:138925114 | A | G | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-142A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 12/17 | chr5 | 138925114 | |||||||
chr5:138925425 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1899+18A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925425 | |||||||
chr5:138925765 | T | C | 1 | a0001c0002t0008g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1899+358T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925765 | |||||||
chr5:138925859 | T | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1899+452T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925859 | |||||||
chr5:138925982 | C | T | 48 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(45): Show |
48 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1899+575C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138925982 | |||||||
chr5:138926060 | T | C | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1899+653T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926060 | |||||||
chr5:138926172 | C | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1899+765C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926172 | |||||||
chr5:138926187 | C | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1899+780C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926187 | |||||||
chr5:138926301 | A | G | 38 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(35): Show |
38 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1899+894A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926301 | |||||||
chr5:138926526 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1899+1119G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926526 | |||||||
chr5:138926546 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0097 |
2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1899+1139G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926546 | |||||||
chr5:138926601 | G | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG02257.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1899+1194G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926601 | |||||||
chr5:138926728 | GA | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(11): Show |
14 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1899+1330delA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138926728 | ||||||
chr5:138926910 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1899+1503A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926910 | |||||||
chr5:138926967 | G | A | 2 | a0001c0002t0002g0002 a0001c0002t0002g0003 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1899+1560G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926967 | |||||||
chr5:138926981 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
56 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1899+1574A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138926981 | |||||||
chr5:138927102 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1899+1695C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927102 | |||||||
chr5:138927126 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1899+1719A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927126 | |||||||
chr5:138927211 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1899+1804C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927211 | |||||||
chr5:138927442 | C | T | 1 | a0001c0002t0003g0029 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1900-1804C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927442 | |||||||
chr5:138927478 | C | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1900-1768C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927478 | |||||||
chr5:138927560 | G | A | 35 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(32): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1900-1686G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927560 | |||||||
chr5:138927710 | T | TAATG | 29 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0045 others(26): Show |
29 | HG00099.hp2 HG00741.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1900-1502_1900-149 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | ||||||
chr5:138927710 | T | TAATGAAT others(1): Show |
7 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0001c0002t0003g0004 others(4): Show |
7 | HG01167.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1900-1506_1900-149 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | ||||||
chr5:138927710 | TAATG | T | 8 | a0001c0001t0001g0171 a0001c0002t0003g0021 a0001c0002t0003g0022 others(5): Show |
8 | HG01109.hp2 HG01361.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1900-1502_1900-149 others(8): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | ||||||
chr5:138927710 | TAATGAAT others(1): Show |
T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0006g0174 others(1): Show |
4 | HG01243.hp2 HG03486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1900-1506_1900-149 others(12): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138927710 | ||||||
chr5:138927710 | TAATGAAT others(7): Show |
T | 35 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(32): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1900-1535_1900-152 others(18): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927710 | |||||||
chr5:138927871 | C | T | 10 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0032 others(7): Show |
10 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1900-1375C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927871 | |||||||
chr5:138927916 | T | G | 2 | a0001c0002t0002g0056 a0001c0002t0002g0060 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1900-1330T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927916 | |||||||
chr5:138927934 | G | A | 20 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0159 others(17): Show |
20 | HG01070.hp1 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1900-1312G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927934 | |||||||
chr5:138927938 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1900-1308A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138927938 | |||||||
chr5:138928369 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
75 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1900-877C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928369 | |||||||
chr5:138928387 | CTCTTT | C | 3 | a0001c0002t0005g0026 a0001c0002t0005g0050 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1900-852_1900-848d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138928387 | ||||||
chr5:138928724 | A | G | 1 | a0001c0002t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1900-522A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928724 | |||||||
chr5:138928735 | A | G | 35 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(32): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1900-511A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928735 | |||||||
chr5:138928762 | C | T | 15 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(12): Show |
15 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1900-484C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928762 | |||||||
chr5:138928790 | C | T | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1900-456C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928790 | |||||||
chr5:138928859 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1900-387C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928859 | |||||||
chr5:138928876 | A | G | 2 | a0001c0001t0006g0174 a0001c0001t0006g0175 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1900-370A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928876 | |||||||
chr5:138928931 | G | A | 1 | a0001c0004t0004g0007 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-315G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928931 | |||||||
chr5:138928940 | G | GA | 65 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(62): Show |
65 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1900-295dupA | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 138928940 | ||||||
chr5:138928973 | T | C | 10 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0032 others(7): Show |
10 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1900-273T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138928973 | |||||||
chr5:138929030 | C | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0138 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1900-216C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138929030 | |||||||
chr5:138929105 | T | C | 2 | a0001c0004t0004g0005 a0001c0009t0004g0006 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1900-141T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138929105 | |||||||
chr5:138929222 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1900-24C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 13/17 | chr5 | 138929222 | |||||||
chr5:138929476 | G | A | 11 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0022 others(8): Show |
11 | HG01109.hp2 HG01993.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010+120G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138929476 | |||||||
chr5:138929867 | T | C | 3 | a0001c0002t0003g0029 a0001c0002t0008g0028 a0001c0013t0003g0031 |
3 | HG02723.hp1 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2010+511T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138929867 | |||||||
chr5:138930208 | G | A | 3 | a0001c0002t0002g0066 a0001c0002t0002g0067 a0001c0002t0002g0083 |
3 | HG00323.hp1 HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2011-265G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138930208 | |||||||
chr5:138930377 | A | G | 10 | a0001c0002t0003g0004 a0001c0002t0003g0027 a0001c0002t0003g0032 others(7): Show |
10 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2011-96A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138930377 | |||||||
chr5:138930399 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2011-74A>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 14/17 | chr5 | 138930399 | |||||||
chr5:138930696 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2192+42T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 15/17 | chr5 | 138930696 | |||||||
chr5:138931188 | C | T | 1 | a0001c0002t0003g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2298+253C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931188 | |||||||
chr5:138931252 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2298+317C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931252 | |||||||
chr5:138931358 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2298+423G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931358 | |||||||
chr5:138931374 | A | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2298+439A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931374 | |||||||
chr5:138931394 | T | C | 72 | a0001c0001t0001g0039 a0001c0001t0001g0086 a0001c0001t0001g0087 others(69): Show |
72 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2298+459T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931394 | |||||||
chr5:138931525 | T | G | 23 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(20): Show |
23 | HG00423.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2298+590T>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931525 | |||||||
chr5:138931688 | G | A | 59 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(56): Show |
59 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2298+753G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138931688 | |||||||
chr5:138932053 | TTACTC | T | 3 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0034 |
3 | HG00741.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2299-524_2299-520d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932053 | |||||||
chr5:138932127 | A | G | 75 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(72): Show |
75 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.2299-451A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932127 | |||||||
chr5:138932289 | G | A | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2299-289G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932289 | |||||||
chr5:138932376 | G | A | 1 | a0001c0002t0003g0020 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2299-202G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932376 | |||||||
chr5:138932503 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2299-75T>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 16/17 | chr5 | 138932503 | |||||||
chr5:138933111 | G | C | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2433+399G>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933111 | |||||||
chr5:138933130 | TCAAAA | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0017 |
2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2433+425_2433+429d others(7): Show |
CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 138933130 | ||||||
chr5:138933141 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0149 a0002c0007t0001g0099 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+429C>T | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933141 | |||||||
chr5:138933293 | T | C | 4 | a0001c0004t0004g0005 a0001c0004t0004g0007 a0001c0004t0004g0180 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2434-509T>C | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933293 | |||||||
chr5:138933316 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2434-486A>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933316 | |||||||
chr5:138933459 | G | A | 36 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0035 others(33): Show |
36 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.2434-343G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933459 | |||||||
chr5:138933609 | G | A | 1 | a0001c0001t0006g0175 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2434-193G>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933609 | |||||||
chr5:138933653 | C | G | 1 | a0001c0009t0004g0006 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2434-149C>G | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933653 | |||||||
chr5:138933774 | C | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG02257.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2434-28C>A | CTNNA1 | ENSG00000044115.21 | transcript | ENST00000302763.12 | protein_coding | 17/17 | chr5 | 138933774 |