Item | Value |
---|---|
geneid | 257062 |
ensemblid | ENSG00000174898.16 |
hgncid | 28598 |
symbol | CATSPERD |
name | cation channel sperm associated auxiliary subunit delta |
refseq_nuc | NM_152784.4 |
refseq_prot | NP_689997.3 |
ensembl_nuc | ENST00000381624.4 |
ensembl_prot | ENSP00000371037.3 |
mane_status | MANE Select |
chr | chr19 |
start | 5720637 |
end | 5778734 |
strand | + |
ver | v1.2 |
region | chr19:5720637-5778734 |
region5000 | chr19:5715637-5783734 |
regionname0 | CATSPERD_chr19_5720637_5778734 |
regionname5000 | CATSPERD_chr19_5715637_5783734 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 798 | 98 | 38 | 32 | 6 | 8 | 13 | 5 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0002 | 0/1 | 798 | 80 | 1 | 26 | 37 | 2 | 13 | 28 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0003 | 0/0 | 798 | 55 | 15 | 6 | 24 | 2 | 8 | 11 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0004 | 0/0 | 798 | 47 | 1 | 3 | 40 | 0 | 3 | 31 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0005 | 0/0 | 798 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0006 | 0/0 | 798 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0007 | 0/0 | 798 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0008 | 0/0 | 798 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0009 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0010 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0011 | 0/0 | 798 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0012 | 0/0 | 798 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0013 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0014 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0015 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0016 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0017 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0018 | 0/0 | 798 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0019 | 0/0 | 798 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0020 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0021 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0022 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0023 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0024 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0025 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0026 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0027 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0028 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0029 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0030 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0031 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0032 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0033 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
a0034 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | MLMLM others(793): Show |
chr19 | 5715637 | 5783734 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2394 | 93 | 37 | 30 | 5 | 8 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0001c0016 | 0/0 | 2394 | 2 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0001c0034 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0001c0040 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0001c0045 | 0/0 | 2394 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0002c0002 | 0/1 | 2394 | 77 | 1 | 25 | 36 | 2 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0002c0019 | 0/0 | 2394 | 2 | 0 | 1 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0002c0027 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0003c0004 | 0/0 | 2394 | 42 | 14 | 6 | 14 | 1 | 7 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0003c0005 | 0/0 | 2394 | 10 | 0 | 0 | 9 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0003c0037 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0003c0041 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0003c0043 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0004c0003 | 0/0 | 2394 | 45 | 1 | 3 | 38 | 0 | 3 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0004c0042 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0004c0044 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0005c0006 | 0/0 | 2394 | 7 | 6 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0006c0007 | 0/0 | 2394 | 5 | 5 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0007c0012 | 0/0 | 2394 | 3 | 0 | 0 | 0 | 2 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0008c0010 | 0/0 | 2394 | 3 | 0 | 2 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0009c0009 | 0/0 | 2394 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0010c0008 | 0/0 | 2394 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0011c0011 | 0/0 | 2394 | 3 | 2 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0012c0030 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0012c0031 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0013c0013 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0014c0017 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0015c0014 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0016c0015 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0017c0018 | 0/0 | 2394 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0018c0025 | 0/0 | 2394 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0019c0046 | 0/0 | 2394 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0020c0038 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0021c0036 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0022c0047 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0023c0023 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0024c0033 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0025c0022 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0026c0032 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0027c0020 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0028c0026 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0029c0039 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0030c0035 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0031c0021 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0032c0029 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0033c0024 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 | ||
a0034c0028 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATGCT others(2389): Show |
chr19 | 5715637 | 5783734 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2556 | 82 | 28 | 28 | 5 | 8 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0001t0002 | 0/0 | 2556 | 8 | 8 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0001t0004 | 0/0 | 2556 | 2 | 1 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0001t0005 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0016t0001 | 0/0 | 2556 | 2 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0034t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0040t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0001c0045t0001 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0002c0002t0001 | 0/1 | 2556 | 73 | 1 | 21 | 36 | 2 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0002c0002t0003 | 0/0 | 2556 | 4 | 0 | 4 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0002c0019t0001 | 0/0 | 2556 | 2 | 0 | 1 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0002c0027t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0003c0004t0001 | 0/0 | 2556 | 41 | 14 | 5 | 14 | 1 | 7 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0003c0004t0003 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0003c0005t0001 | 0/0 | 2556 | 10 | 0 | 0 | 9 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0003c0037t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0003c0041t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0003c0043t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0004c0003t0001 | 0/0 | 2556 | 40 | 1 | 2 | 34 | 0 | 3 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0004c0003t0003 | 0/0 | 2556 | 5 | 0 | 1 | 4 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0004c0042t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0004c0044t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0005c0006t0001 | 0/0 | 2556 | 7 | 6 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0006c0007t0001 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0006c0007t0002 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0007c0012t0001 | 0/0 | 2556 | 3 | 0 | 0 | 0 | 2 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0008c0010t0001 | 0/0 | 2556 | 3 | 0 | 2 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0009c0009t0001 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0010c0008t0001 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0011c0011t0001 | 0/0 | 2556 | 3 | 2 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0012c0030t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0012c0031t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0013c0013t0001 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0014c0017t0002 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0015c0014t0002 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0016c0015t0001 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0017c0018t0001 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0018c0025t0001 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0019c0046t0001 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0020c0038t0002 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0021c0036t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0022c0047t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0023c0023t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0024c0033t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0025c0022t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0026c0032t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0027c0020t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0028c0026t0002 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0029c0039t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0030c0035t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0031c0021t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0032c0029t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0033c0024t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
a0034c0028t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | ATTGA others(2551): Show |
chr19 | 5715637 | 5783734 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0016t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0016t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0034t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0040t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0045t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0019t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0019t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0027t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0037t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0041t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0043t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0042t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0044t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0007c0012t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0007c0012t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0007c0012t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0008c0010t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0008c0010t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0008c0010t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0009c0009t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0009c0009t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0009c0009t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0010c0008t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0010c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0010c0008t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0011c0011t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0011c0011t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0011c0011t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0012c0030t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0012c0031t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0013c0013t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0013c0013t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0014c0017t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0014c0017t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0015c0014t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0015c0014t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0016c0015t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0016c0015t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0017c0018t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0017c0018t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0018c0025t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0019c0046t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0020c0038t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0021c0036t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0022c0047t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0023c0023t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0024c0033t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0025c0022t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0026c0032t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0027c0020t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0028c0026t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0029c0039t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0030c0035t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0031c0021t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0032c0029t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0033c0024t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0034c0028t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0004 | t0001 | g0292 | EUR | GBR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00280 | hp2 | a0003 | c0037 | t0001 | g0220 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0106 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0250 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00438 | hp1 | a0003 | c0004 | t0001 | g0060 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00438 | hp2 | a0004 | c0003 | t0001 | g0306 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00544 | hp1 | a0003 | c0004 | t0001 | g0278 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00544 | hp2 | a0004 | c0003 | t0001 | g0071 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00609 | hp1 | a0003 | c0004 | t0001 | g0322 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00609 | hp2 | a0003 | c0005 | t0001 | g0274 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00621 | hp1 | a0004 | c0003 | t0003 | g0046 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00621 | hp2 | a0012 | c0030 | t0001 | g0288 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00642 | hp1 | a0018 | c0025 | t0001 | g0086 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00741 | hp2 | a0019 | c0046 | t0001 | g0005 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01074 | hp2 | a0003 | c0004 | t0001 | g0140 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01081 | hp2 | a0003 | c0004 | t0001 | g0262 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0328 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01168 | hp1 | a0003 | c0004 | t0001 | g0144 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01169 | hp2 | a0003 | c0004 | t0001 | g0142 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01243 | hp2 | a0001 | c0045 | t0001 | g0151 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0110 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01258 | hp1 | a0003 | c0004 | t0001 | g0246 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0108 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01346 | hp1 | a0002 | c0019 | t0001 | g0332 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0080 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01496 | hp2 | a0003 | c0004 | t0003 | g0125 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01515 | hp1 | a0007 | c0012 | t0001 | g0156 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01517 | hp2 | a0007 | c0012 | t0001 | g0159 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01884 | hp2 | a0005 | c0006 | t0001 | g0227 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01928 | hp1 | a0004 | c0003 | t0001 | g0282 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0122 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01934 | hp1 | a0005 | c0006 | t0001 | g0229 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01934 | hp2 | a0001 | c0016 | t0001 | g0083 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01952 | hp1 | a0002 | c0002 | t0003 | g0145 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01952 | hp2 | a0008 | c0010 | t0001 | g0032 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01975 | hp1 | a0004 | c0003 | t0003 | g0111 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01993 | hp2 | a0008 | c0010 | t0001 | g0031 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02015 | hp1 | a0003 | c0004 | t0001 | g0265 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02027 | hp1 | a0003 | c0041 | t0001 | g0330 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02027 | hp2 | a0004 | c0003 | t0001 | g0240 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02040 | hp1 | a0004 | c0003 | t0001 | g0313 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02040 | hp2 | a0003 | c0005 | t0001 | g0236 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0098 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02056 | hp1 | a0004 | c0003 | t0001 | g0150 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02071 | hp2 | a0003 | c0004 | t0001 | g0244 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02074 | hp1 | a0003 | c0004 | t0001 | g0323 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02074 | hp2 | a0012 | c0031 | t0001 | g0036 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02083 | hp1 | a0003 | c0004 | t0001 | g0325 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02083 | hp2 | a0003 | c0004 | t0001 | g0251 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02129 | hp2 | a0004 | c0003 | t0001 | g0280 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02135 | hp2 | a0004 | c0003 | t0001 | g0119 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0066 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02148 | hp2 | a0004 | c0003 | t0001 | g0247 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02155 | hp1 | a0003 | c0005 | t0001 | g0324 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02155 | hp2 | a0004 | c0003 | t0001 | g0040 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02165 | hp1 | a0003 | c0005 | t0001 | g0307 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02258 | hp1 | a0005 | c0006 | t0001 | g0228 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02451 | hp1 | a0020 | c0038 | t0002 | g0317 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02451 | hp2 | a0021 | c0036 | t0001 | g0294 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02572 | hp1 | a0006 | c0007 | t0001 | g0028 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02572 | hp2 | a0003 | c0004 | t0001 | g0196 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02615 | hp1 | a0009 | c0009 | t0001 | g0016 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02615 | hp2 | a0003 | c0043 | t0001 | g0204 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02622 | hp1 | a0005 | c0006 | t0001 | g0223 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02630 | hp1 | a0022 | c0047 | t0001 | g0004 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02698 | hp1 | a0007 | c0012 | t0001 | g0160 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0217 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02717 | hp1 | a0005 | c0006 | t0001 | g0213 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02717 | hp2 | a0003 | c0004 | t0001 | g0189 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02735 | hp1 | a0023 | c0023 | t0001 | g0118 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02735 | hp2 | a0024 | c0033 | t0001 | g0303 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02809 | hp1 | a0010 | c0008 | t0001 | g0011 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02809 | hp2 | a0013 | c0013 | t0001 | g0012 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02818 | hp1 | a0025 | c0022 | t0001 | g0033 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0333 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0078 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02895 | hp1 | a0009 | c0009 | t0001 | g0019 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02895 | hp2 | a0003 | c0004 | t0001 | g0023 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02896 | hp2 | a0014 | c0017 | t0002 | g0193 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02897 | hp1 | a0014 | c0017 | t0002 | g0194 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02897 | hp2 | a0003 | c0004 | t0001 | g0314 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02922 | hp1 | a0015 | c0014 | t0002 | g0010 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02965 | hp1 | a0026 | c0032 | t0001 | g0334 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02965 | hp2 | a0006 | c0007 | t0002 | g0020 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02970 | hp1 | a0011 | c0011 | t0001 | g0003 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02970 | hp2 | a0010 | c0008 | t0001 | g0014 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02976 | hp1 | a0003 | c0004 | t0001 | g0094 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03041 | hp2 | a0010 | c0008 | t0001 | g0008 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03098 | hp1 | a0009 | c0009 | t0001 | g0015 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0115 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03130 | hp2 | a0016 | c0015 | t0001 | g0081 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03139 | hp1 | a0015 | c0014 | t0002 | g0013 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0075 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03195 | hp2 | a0006 | c0007 | t0001 | g0027 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03209 | hp1 | a0017 | c0018 | t0001 | g0308 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03209 | hp2 | a0003 | c0004 | t0001 | g0097 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03225 | hp2 | a0017 | c0018 | t0001 | g0309 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03239 | hp1 | a0003 | c0004 | t0001 | g0211 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03239 | hp2 | a0004 | c0003 | t0001 | g0129 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03486 | hp2 | a0027 | c0020 | t0001 | g0030 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0283 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03491 | hp2 | a0003 | c0004 | t0001 | g0059 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03516 | hp2 | a0028 | c0026 | t0002 | g0335 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03579 | hp1 | a0013 | c0013 | t0001 | g0009 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03579 | hp2 | a0003 | c0004 | t0001 | g0336 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03654 | hp1 | a0029 | c0039 | t0001 | g0058 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03654 | hp2 | a0030 | c0035 | t0001 | g0152 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03669 | hp1 | a0031 | c0021 | t0001 | g0017 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03669 | hp2 | a0003 | c0004 | t0001 | g0214 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0143 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03710 | hp2 | a0003 | c0004 | t0001 | g0158 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03831 | hp1 | a0002 | c0027 | t0001 | g0291 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03831 | hp2 | a0003 | c0004 | t0001 | g0048 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03834 | hp1 | a0004 | c0003 | t0001 | g0242 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03834 | hp2 | a0001 | c0016 | t0001 | g0167 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03927 | hp1 | a0003 | c0004 | t0001 | g0304 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04184 | hp1 | a0004 | c0003 | t0001 | g0319 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04199 | hp1 | a0011 | c0011 | t0001 | g0315 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04228 | hp2 | a0003 | c0005 | t0001 | g0218 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18522 | hp1 | a0016 | c0015 | t0001 | g0077 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18522 | hp2 | a0005 | c0006 | t0001 | g0215 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18942 | hp2 | a0004 | c0003 | t0001 | g0180 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18943 | hp1 | a0003 | c0005 | t0001 | g0261 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18943 | hp2 | a0002 | c0019 | t0001 | g0331 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18944 | hp2 | a0003 | c0004 | t0001 | g0200 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18946 | hp1 | a0004 | c0042 | t0001 | g0316 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18946 | hp2 | a0004 | c0003 | t0001 | g0326 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18952 | hp2 | a0004 | c0003 | t0001 | g0248 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18954 | hp2 | a0004 | c0003 | t0001 | g0302 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18960 | hp1 | a0004 | c0003 | t0001 | g0121 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18963 | hp1 | a0004 | c0003 | t0001 | g0295 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18966 | hp1 | a0003 | c0005 | t0001 | g0254 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18967 | hp1 | a0003 | c0005 | t0001 | g0239 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18967 | hp2 | a0008 | c0010 | t0001 | g0034 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18969 | hp1 | a0032 | c0029 | t0001 | g0269 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18969 | hp2 | a0004 | c0003 | t0001 | g0169 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18971 | hp2 | a0003 | c0004 | t0001 | g0141 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18972 | hp1 | a0004 | c0003 | t0001 | g0224 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18972 | hp2 | a0003 | c0004 | t0001 | g0235 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18974 | hp1 | a0004 | c0003 | t0003 | g0085 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18983 | hp1 | a0004 | c0003 | t0001 | g0062 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18986 | hp1 | a0004 | c0003 | t0001 | g0054 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18986 | hp2 | a0004 | c0003 | t0001 | g0284 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18990 | hp2 | a0004 | c0003 | t0001 | g0245 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18998 | hp1 | a0004 | c0003 | t0001 | g0267 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18999 | hp1 | a0004 | c0044 | t0001 | g0190 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18999 | hp2 | a0001 | c0040 | t0001 | g0329 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19002 | hp2 | a0004 | c0003 | t0001 | g0272 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19007 | hp1 | a0033 | c0024 | t0001 | g0225 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19007 | hp2 | a0003 | c0005 | t0001 | g0249 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19011 | hp1 | a0003 | c0004 | t0001 | g0207 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19011 | hp2 | a0003 | c0004 | t0001 | g0327 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19012 | hp1 | a0004 | c0003 | t0001 | g0183 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19012 | hp2 | a0004 | c0003 | t0001 | g0171 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19043 | hp2 | a0004 | c0003 | t0001 | g0219 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19060 | hp2 | a0003 | c0004 | t0001 | g0222 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19065 | hp1 | a0004 | c0003 | t0001 | g0253 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19065 | hp2 | a0004 | c0003 | t0003 | g0109 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19066 | hp1 | a0004 | c0003 | t0001 | g0120 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19074 | hp1 | a0004 | c0003 | t0001 | g0173 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19074 | hp2 | a0004 | c0003 | t0003 | g0114 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19077 | hp2 | a0004 | c0003 | t0001 | g0168 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19078 | hp1 | a0004 | c0003 | t0001 | g0035 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19078 | hp2 | a0004 | c0003 | t0001 | g0320 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19079 | hp1 | a0004 | c0003 | t0001 | g0061 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19089 | hp2 | a0004 | c0003 | t0001 | g0237 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19090 | hp1 | a0004 | c0003 | t0001 | g0039 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19090 | hp2 | a0004 | c0003 | t0001 | g0238 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19091 | hp1 | a0003 | c0005 | t0001 | g0185 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19240 | hp1 | a0006 | c0007 | t0002 | g0018 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20905 | hp1 | a0003 | c0004 | t0001 | g0179 | SAS | GIH | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02109 | hp1 | a0001 | c0034 | t0001 | g0025 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0064 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02486 | hp2 | a0006 | c0007 | t0001 | g0029 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02559 | hp2 | a0005 | c0006 | t0001 | g0209 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG06807 | hp1 | a0011 | c0011 | t0001 | g0002 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0299 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA21309 | hp2 | a0034 | c0028 | t0001 | g0102 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0051 | REF | REF | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0163 | REF | REF | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720763 | C | G | 2 | a0019 a0022 |
2 | HG00741.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.26C>G | p.Ala9Gly | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | 127/2556 | 26/2397 | 9/798 | chr19 | 5720763 | |||
chr19:5727298 | C | T | 1 | a0005 | 7 | HG01884.hp2 HG01934.hp1 HG02258.hp1 others(4): Show |
missense_variant | MODERATE | c.157C>T | p.Arg53Cys | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/22 | 258/2556 | 157/2397 | 53/798 | chr19 | 5727298 | |||
chr19:5733859 | G | A | 3 | a0010 a0013 a0015 |
7 | HG02809.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
missense_variant | MODERATE | c.280G>A | p.Gly94Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 381/2556 | 280/2397 | 94/798 | chr19 | 5733859 | |||
chr19:5733863 | T | C | 8 | a0006 a0008 a0009 others(5): Show |
16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
missense_variant | MODERATE | c.284T>C | p.Val95Ala | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 385/2556 | 284/2397 | 95/798 | chr19 | 5733863 | |||
chr19:5733893 | G | C | 1 | a0023 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.314G>C | p.Gly105Ala | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 415/2556 | 314/2397 | 105/798 | chr19 | 5733893 | |||
chr19:5744488 | T | C | 9 | a0006 a0009 a0011 others(6): Show |
17 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
missense_variant | MODERATE | c.635T>C | p.Met212Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/22 | 736/2556 | 635/2397 | 212/798 | chr19 | 5744488 | |||
chr19:5746013 | G | C | 1 | a0018 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.758G>C | p.Gly253Ala | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/22 | 859/2556 | 758/2397 | 253/798 | chr19 | 5746013 | |||
chr19:5748177 | G | A | 1 | a0028 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.826G>A | p.Val276Ile | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/22 | 927/2556 | 826/2397 | 276/798 | chr19 | 5748177 | |||
chr19:5749115 | G | A | 1 | a0034 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.919G>A | p.Ala307Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/22 | 1020/2556 | 919/2397 | 307/798 | chr19 | 5749115 | |||
chr19:5749160 | A | G | 10 | a0006 a0009 a0011 others(7): Show |
18 | HG00741.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
missense_variant | MODERATE | c.964A>G | p.Ile322Val | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/22 | 1065/2556 | 964/2397 | 322/798 | chr19 | 5749160 | |||
chr19:5751791 | A | G | 1 | a0017 | 2 | HG03209.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1132A>G | p.Met378Val | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/22 | 1233/2556 | 1132/2397 | 378/798 | chr19 | 5751791 | |||
chr19:5751792 | T | C | 1 | a0032 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1133T>C | p.Met378Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/22 | 1234/2556 | 1133/2397 | 378/798 | chr19 | 5751792 | |||
chr19:5754216 | C | T | 3 | a0014 a0015 a0021 |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.1249C>T | p.Pro417Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/22 | 1350/2556 | 1249/2397 | 417/798 | chr19 | 5754216 | |||
chr19:5772812 | G | C | 1 | a0007 | 3 | HG01515.hp1 HG01517.hp2 HG02698.hp1 |
missense_variant | MODERATE | c.1788G>C | p.Glu596Asp | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/22 | 1889/2556 | 1788/2397 | 596/798 | chr19 | 5772812 | |||
chr19:5772886 | C | T | 4 | a0004 a0025 a0030 others(1): Show |
50 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(47): Show |
missense_variant | MODERATE | c.1862C>T | p.Ser621Leu | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/22 | 1963/2556 | 1862/2397 | 621/798 | chr19 | 5772886 | |||
chr19:5772939 | G | A | 6 | a0002 a0008 a0012 others(3): Show |
87 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
missense_variant | MODERATE | c.1915G>A | p.Gly639Arg | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/22 | 2016/2556 | 1915/2397 | 639/798 | chr19 | 5772939 | |||
chr19:5776239 | C | T | 1 | a0024 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.2020C>T | p.Arg674Trp | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2121/2556 | 2020/2397 | 674/798 | chr19 | 5776239 | |||
chr19:5776298 | C | G | 1 | a0030 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2079C>G | p.Ile693Met | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2180/2556 | 2079/2397 | 693/798 | chr19 | 5776298 | |||
chr19:5778506 | A | T | 15 | a0003 a0004 a0009 others(12): Show |
120 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(117): Show |
missense_variant | MODERATE | c.2227A>T | p.Thr743Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2328/2556 | 2227/2397 | 743/798 | chr19 | 5778506 | |||
chr19:5778522 | G | A | 1 | a0016 | 2 | HG03130.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.2243G>A | p.Arg748His | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2344/2556 | 2243/2397 | 748/798 | chr19 | 5778522 | |||
chr19:5778543 | T | C | 1 | a0026 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2264T>C | p.Ile755Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2365/2556 | 2264/2397 | 755/798 | chr19 | 5778543 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720785 | G | T | 1 | a0001c0045 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.48G>T | p.Pro16Pro | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | 149/2556 | 48/2397 | 16/798 | chr19 | 5720785 | |||
chr19:5729899 | C | T | 1 | a0001c0045 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.231C>T | p.Asn77Asn | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/22 | 332/2556 | 231/2397 | 77/798 | chr19 | 5729899 | |||
chr19:5733897 | G | C | 8 | a0006c0007 a0008c0010 a0009c0009 others(5): Show |
16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
synonymous_variant | LOW | c.318G>C | p.Ser106Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 419/2556 | 318/2397 | 106/798 | chr19 | 5733897 | |||
chr19:5745996 | C | T | 1 | a0004c0044 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.741C>T | p.Ile247Ile | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/22 | 842/2556 | 741/2397 | 247/798 | chr19 | 5745996 | |||
chr19:5746002 | C | T | 1 | a0003c0043 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.747C>T | p.Pro249Pro | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/22 | 848/2556 | 747/2397 | 249/798 | chr19 | 5746002 | |||
chr19:5748167 | C | G | 4 | a0001c0040 a0002c0019 a0003c0041 others(1): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
synonymous_variant | LOW | c.816C>G | p.Leu272Leu | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/22 | 917/2556 | 816/2397 | 272/798 | chr19 | 5748167 | |||
chr19:5748182 | G | A | 1 | a0002c0027 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.831G>A | p.Arg277Arg | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/22 | 932/2556 | 831/2397 | 277/798 | chr19 | 5748182 | |||
chr19:5751661 | C | T | 1 | a0003c0037 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1002C>T | p.Tyr334Tyr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/22 | 1103/2556 | 1002/2397 | 334/798 | chr19 | 5751661 | |||
chr19:5776190 | C | T | 1 | a0001c0016 | 2 | HG01934.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.1971C>T | p.Asn657Asn | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2072/2556 | 1971/2397 | 657/798 | chr19 | 5776190 | |||
chr19:5776238 | C | G | 1 | a0001c0034 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2019C>G | p.Gly673Gly | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2120/2556 | 2019/2397 | 673/798 | chr19 | 5776238 | |||
chr19:5778586 | C | G | 2 | a0003c0005 a0012c0031 |
11 | HG00609.hp2 HG02040.hp2 HG02074.hp2 others(8): Show |
synonymous_variant | LOW | c.2307C>G | p.Val769Val | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2408/2556 | 2307/2397 | 769/798 | chr19 | 5778586 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720692 | C | G | 3 | a0002c0002t0003 a0003c0004t0003 a0004c0003t0003 |
10 | HG00621.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | chr19 | 5720692 | |||||||
chr19:5720713 | G | C | 1 | a0001c0001t0004 | 2 | HG01109.hp2 HG02896.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | chr19 | 5720713 | |||||||
chr19:5778680 | C | T | 1 | a0001c0001t0005 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 4 | chr19 | 5778680 | ||||||
chr19:5778681 | G | A | 6 | a0001c0001t0002 a0006c0007t0002 a0014c0017t0002 others(3): Show |
16 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 5 | chr19 | 5778681 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720843 | G | A | 3 | a0001c0001t0001g0001 a0011c0011t0001g0002 a0011c0011t0001g0003 |
3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71+35G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720843 | |||||||
chr19:5720962 | C | T | 1 | a0003c0004t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71+154C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720962 | |||||||
chr19:5720968 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.71+160C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720968 | |||||||
chr19:5720996 | C | T | 4 | a0001c0001t0001g0001 a0011c0011t0001g0002 a0011c0011t0001g0003 others(1): Show |
4 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+188C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720996 | |||||||
chr19:5720999 | C | CT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0318 a0001c0040t0001g0329 others(20): Show |
23 | HG00609.hp1 HG01099.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.71+208dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5720999 | ||||||
chr19:5720999 | CT | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(26): Show |
29 | HG01952.hp2 HG01993.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+208delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5720999 | ||||||
chr19:5721007 | T | A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+199T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721007 | |||||||
chr19:5721037 | C | T | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(26): Show |
29 | HG01952.hp2 HG01993.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+229C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721037 | |||||||
chr19:5721045 | C | T | 1 | a0004c0003t0001g0313 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71+237C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721045 | |||||||
chr19:5721059 | C | T | 7 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0002g0311 others(4): Show |
7 | HG02145.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+251C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721059 | |||||||
chr19:5721222 | C | G | 4 | a0001c0001t0001g0001 a0011c0011t0001g0002 a0011c0011t0001g0003 others(1): Show |
4 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+414C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721222 | |||||||
chr19:5721280 | G | C | 1 | a0004c0003t0001g0035 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.71+472G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721280 | |||||||
chr19:5721281 | C | G | 1 | a0004c0003t0001g0035 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.71+473C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721281 | |||||||
chr19:5721552 | T | A | 1 | a0004c0042t0001g0316 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.71+744T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721552 | |||||||
chr19:5721832 | T | A | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71+1024T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721832 | |||||||
chr19:5721878 | A | G | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+1070A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721878 | |||||||
chr19:5721985 | G | GA | 16 | a0001c0001t0001g0001 a0002c0002t0001g0037 a0004c0003t0001g0035 others(13): Show |
16 | HG02074.hp2 HG02257.hp1 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.71+1192dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5721985 | ||||||
chr19:5721985 | GA | G | 9 | a0001c0001t0001g0301 a0002c0002t0001g0305 a0003c0004t0001g0304 others(6): Show |
9 | HG00438.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+1192delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5721985 | ||||||
chr19:5722164 | C | G | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71+1356C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722164 | |||||||
chr19:5722278 | C | A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+1470C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722278 | |||||||
chr19:5722304 | G | A | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.71+1496G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722304 | |||||||
chr19:5722324 | T | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(120): Show |
123 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.71+1516T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722324 | |||||||
chr19:5722351 | G | A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+1543G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722351 | |||||||
chr19:5722392 | C | A | 40 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(37): Show |
40 | HG00741.hp2 HG01243.hp2 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.71+1584C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722392 | |||||||
chr19:5722396 | C | T | 1 | a0026c0032t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71+1588C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722396 | |||||||
chr19:5722400 | C | T | 7 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0002g0311 others(4): Show |
7 | HG02145.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+1592C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722400 | |||||||
chr19:5722413 | G | A | 1 | a0030c0035t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.71+1605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722413 | |||||||
chr19:5722423 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(317): Show |
320 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.71+1615C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722423 | |||||||
chr19:5722428 | T | A | 7 | a0001c0001t0001g0170 a0002c0002t0001g0172 a0002c0002t0001g0174 others(4): Show |
7 | HG02523.hp2 NA18960.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+1620T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722428 | |||||||
chr19:5722458 | A | C | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(31): Show |
34 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.71+1650A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722458 | |||||||
chr19:5722518 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.71+1710G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722518 | |||||||
chr19:5722648 | A | G | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71+1840A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722648 | |||||||
chr19:5722730 | AC | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(230): Show |
233 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.71+1933delC | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5722730 | ||||||
chr19:5722733 | C | A | 1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.71+1925C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722733 | |||||||
chr19:5722734 | C | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0016t0001g0167 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.71+1926C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722734 | |||||||
chr19:5722736 | C | G | 1 | a0001c0001t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.71+1928C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722736 | |||||||
chr19:5722738 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.71+1930C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722738 | |||||||
chr19:5722905 | T | A | 1 | a0026c0032t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72-1903T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722905 | |||||||
chr19:5722919 | GGGCTCAC others(1504): Show |
G | 2 | a0002c0002t0001g0049 a0002c0002t0001g0050 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.72-1868_72-358del | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5722919 | ||||||
chr19:5723018 | C | T | 1 | a0026c0032t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72-1790C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723018 | |||||||
chr19:5723117 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.72-1691G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723117 | |||||||
chr19:5723186 | C | CA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0038 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.72-1608dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723186 | ||||||
chr19:5723226 | T | C | 39 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(36): Show |
39 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.72-1582T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723226 | |||||||
chr19:5723288 | C | A | 35 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(32): Show |
35 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.72-1520C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723288 | |||||||
chr19:5723370 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(303): Show |
306 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.72-1438T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723370 | |||||||
chr19:5723387 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.72-1421C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723387 | |||||||
chr19:5723403 | G | A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.72-1405G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723403 | |||||||
chr19:5723458 | A | AT | 64 | a0001c0001t0001g0082 a0001c0001t0001g0092 a0001c0001t0001g0124 others(61): Show |
64 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.72-1326dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | ||||||
chr19:5723458 | A | ATT | 13 | a0001c0001t0001g0177 a0001c0001t0001g0188 a0001c0001t0001g0230 others(10): Show |
13 | HG01261.hp1 HG01358.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-1327_72-1326dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | ||||||
chr19:5723458 | AT | A | 85 | a0001c0001t0001g0170 a0001c0001t0001g0195 a0001c0001t0001g0256 others(82): Show |
85 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.72-1326delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | ||||||
chr19:5723458 | ATT | A | 25 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(22): Show |
25 | HG01346.hp1 HG01496.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.72-1327_72-1326del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | ||||||
chr19:5723458 | ATTT | A | 6 | a0002c0019t0001g0331 a0003c0041t0001g0330 a0004c0042t0001g0316 others(3): Show |
6 | HG02027.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-1328_72-1326del others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | ||||||
chr19:5723496 | G | A | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.72-1312G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723496 | |||||||
chr19:5723572 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-1236C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723572 | |||||||
chr19:5723576 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.72-1232T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723576 | |||||||
chr19:5723782 | G | GT | 27 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0026 others(24): Show |
27 | HG01261.hp2 HG01346.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.72-1015dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723782 | ||||||
chr19:5723782 | G | GTT | 8 | a0001c0001t0001g0024 a0006c0007t0001g0028 a0006c0007t0001g0029 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-1016_72-1015dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723782 | ||||||
chr19:5723788 | T | G | 5 | a0002c0027t0001g0291 a0003c0004t0001g0322 a0003c0004t0001g0323 others(2): Show |
5 | HG00609.hp1 HG02074.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-1020T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723788 | |||||||
chr19:5723819 | C | T | 1 | a0001c0016t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.72-989C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723819 | |||||||
chr19:5723926 | G | A | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.72-882G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723926 | |||||||
chr19:5724029 | G | A | 4 | a0006c0007t0001g0028 a0006c0007t0002g0018 a0006c0007t0002g0020 others(1): Show |
4 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-779G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724029 | |||||||
chr19:5724248 | A | G | 2 | a0003c0004t0001g0322 a0003c0005t0001g0324 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.72-560A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724248 | |||||||
chr19:5724251 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(77): Show |
80 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.72-557T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724251 | |||||||
chr19:5724308 | C | A | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.72-500C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724308 | |||||||
chr19:5724529 | C | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(31): Show |
34 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.72-279C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724529 | |||||||
chr19:5724596 | G | A | 3 | a0006c0007t0002g0018 a0006c0007t0002g0020 a0009c0009t0001g0019 |
3 | HG02895.hp1 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.72-212G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724596 | |||||||
chr19:5725127 | G | T | 2 | a0001c0001t0001g0300 a0002c0002t0001g0328 |
2 | HG01099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.126+265G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725127 | |||||||
chr19:5725146 | C | G | 2 | a0002c0002t0001g0298 a0002c0002t0001g0299 |
2 | HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+284C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725146 | |||||||
chr19:5725482 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(11): Show |
14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+620G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725482 | |||||||
chr19:5725582 | T | C | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+720T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725582 | |||||||
chr19:5725704 | C | T | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+842C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725704 | |||||||
chr19:5725705 | A | C | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+843A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725705 | |||||||
chr19:5725712 | C | T | 1 | a0004c0042t0001g0316 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.126+850C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725712 | |||||||
chr19:5725880 | G | A | 1 | a0006c0007t0001g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.126+1018G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725880 | |||||||
chr19:5725890 | A | G | 1 | a0002c0002t0001g0297 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.126+1028A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725890 | |||||||
chr19:5725981 | A | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
40 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.126+1119A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725981 | |||||||
chr19:5726008 | C | G | 4 | a0002c0002t0001g0296 a0003c0004t0001g0327 a0004c0003t0001g0295 others(1): Show |
4 | HG02135.hp1 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1146C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726008 | |||||||
chr19:5726036 | G | A | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+1174G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726036 | |||||||
chr19:5726060 | A | AT | 6 | a0001c0001t0001g0164 a0002c0019t0001g0331 a0004c0003t0001g0150 others(3): Show |
6 | HG00741.hp2 HG01175.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1192dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr19 | 5726060 | ||||||
chr19:5726099 | T | A | 1 | a0002c0002t0001g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.127-1169T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726099 | |||||||
chr19:5726637 | C | G | 2 | a0001c0001t0001g0149 a0003c0004t0001g0048 |
2 | HG01346.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.127-631C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726637 | |||||||
chr19:5726662 | G | A | 1 | a0002c0002t0001g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.127-606G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726662 | |||||||
chr19:5726816 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(256): Show |
259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.127-452G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726816 | |||||||
chr19:5726932 | G | A | 87 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0241 others(84): Show |
87 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.127-336G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726932 | |||||||
chr19:5727064 | G | A | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-204G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5727064 | |||||||
chr19:5727067 | C | T | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.127-201C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5727067 | |||||||
chr19:5727068 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-200G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5727068 | |||||||
chr19:5727370 | A | C | 1 | a0003c0004t0001g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.203+26A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727370 | |||||||
chr19:5727403 | C | CT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(117): Show |
120 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.203+59_203+60insT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727403 | |||||||
chr19:5727757 | G | A | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(25): Show |
28 | HG01952.hp2 HG01993.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.203+413G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727757 | |||||||
chr19:5727806 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.203+462C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727806 | |||||||
chr19:5728038 | C | CAAA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(63): Show |
66 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.203+709_203+711dup others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | ||||||
chr19:5728038 | C | CAAAA | 9 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0002c0002t0001g0089 others(6): Show |
9 | HG00642.hp1 HG01175.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+708_203+711dup others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | ||||||
chr19:5728038 | CA | C | 197 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0063 others(194): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.203+711delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | ||||||
chr19:5728038 | CAA | C | 29 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(26): Show |
29 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.203+710_203+711del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | ||||||
chr19:5728085 | C | T | 5 | a0008c0010t0001g0031 a0008c0010t0001g0032 a0008c0010t0001g0034 others(2): Show |
5 | HG01952.hp2 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+741C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728085 | |||||||
chr19:5728125 | C | T | 7 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0002g0311 others(4): Show |
7 | HG02145.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+781C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728125 | |||||||
chr19:5728218 | C | T | 1 | a0003c0005t0001g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.203+874C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728218 | |||||||
chr19:5728238 | G | GTCCCAGC others(3): Show |
1 | a0004c0003t0003g0085 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203+897_203+906dup others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728238 | ||||||
chr19:5728290 | G | A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.203+946G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728290 | |||||||
chr19:5728313 | G | A | 1 | a0003c0005t0001g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.203+969G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728313 | |||||||
chr19:5728344 | G | A | 2 | a0002c0002t0001g0052 a0028c0026t0002g0335 |
2 | HG02056.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.203+1000G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728344 | |||||||
chr19:5728356 | C | CA | 16 | a0001c0001t0001g0164 a0001c0040t0001g0329 a0002c0002t0001g0191 others(13): Show |
16 | HG01175.hp2 HG01346.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.203+1030dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728356 | ||||||
chr19:5728356 | CA | C | 87 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(84): Show |
87 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.203+1030delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728356 | ||||||
chr19:5728364 | A | G | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.203+1020A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728364 | |||||||
chr19:5728369 | AAAAAAGA others(5): Show |
A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.203+1030_203+1041d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728369 | ||||||
chr19:5728371 | A | G | 4 | a0002c0002t0001g0296 a0003c0004t0001g0327 a0004c0003t0001g0295 others(1): Show |
4 | HG02135.hp1 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+1027A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728371 | |||||||
chr19:5728653 | G | A | 4 | a0001c0001t0001g0241 a0002c0002t0001g0234 a0002c0002t0001g0243 others(1): Show |
4 | HG00642.hp2 HG01070.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.204-1219G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728653 | |||||||
chr19:5728705 | C | CT | 71 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(68): Show |
71 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.204-1156dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728705 | ||||||
chr19:5728705 | C | CTT | 10 | a0001c0001t0001g0087 a0001c0001t0001g0139 a0002c0002t0001g0090 others(7): Show |
10 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.204-1157_204-1156d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728705 | ||||||
chr19:5729004 | A | ATC | 8 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0001c0001t0001g0197 others(5): Show |
8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.204-852_204-851dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5729004 | ||||||
chr19:5729101 | C | CT | 6 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0016t0001g0083 others(3): Show |
6 | HG00741.hp1 HG01358.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-760dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5729101 | ||||||
chr19:5729147 | G | A | 2 | a0002c0002t0001g0104 a0003c0004t0001g0244 |
2 | HG02071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.204-725G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729147 | |||||||
chr19:5729231 | G | A | 1 | a0004c0003t0001g0245 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.204-641G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729231 | |||||||
chr19:5729402 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.204-470T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729402 | |||||||
chr19:5729482 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.204-390A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729482 | |||||||
chr19:5730327 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(115): Show |
118 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.276+383A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730327 | |||||||
chr19:5730341 | G | A | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276+397G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730341 | |||||||
chr19:5730399 | C | T | 1 | a0016c0015t0001g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.276+455C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730399 | |||||||
chr19:5730498 | G | A | 1 | a0002c0002t0001g0053 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.276+554G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730498 | |||||||
chr19:5730561 | A | AAAATAAA others(6): Show |
1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276+624_276+625ins others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | ||||||
chr19:5730561 | A | AAAATAAA others(1): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
37 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.276+628_276+635dup others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | ||||||
chr19:5730561 | A | AAAATAAA others(5): Show |
210 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0047 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.276+624_276+635dup others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | ||||||
chr19:5730561 | A | AAAATAAA others(9): Show |
3 | a0001c0001t0001g0201 a0002c0002t0001g0202 a0003c0004t0001g0246 |
3 | HG00738.hp2 HG01258.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.276+620_276+635dup others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | ||||||
chr19:5730561 | A | AAAATAAA others(13): Show |
2 | a0002c0002t0001g0199 a0003c0004t0001g0200 |
2 | NA18944.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.276+635_276+636ins others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | ||||||
chr19:5730715 | T | C | 1 | a0003c0004t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.276+771T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730715 | |||||||
chr19:5730878 | G | A | 1 | a0004c0003t0001g0054 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.276+934G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730878 | |||||||
chr19:5730953 | A | G | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.276+1009A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730953 | |||||||
chr19:5730984 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.276+1040C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730984 | |||||||
chr19:5731058 | C | T | 16 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(13): Show |
16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.276+1114C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731058 | |||||||
chr19:5731079 | G | A | 91 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0241 others(88): Show |
91 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.276+1135G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731079 | |||||||
chr19:5731091 | C | CA | 11 | a0001c0001t0001g0092 a0001c0001t0001g0153 a0001c0001t0001g0164 others(8): Show |
11 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+1164dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731091 | ||||||
chr19:5731091 | CA | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0076 others(9): Show |
12 | HG00280.hp1 HG01070.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.276+1164delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731091 | ||||||
chr19:5731117 | C | T | 1 | a0011c0011t0001g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.276+1173C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731117 | |||||||
chr19:5731217 | C | A | 2 | a0001c0001t0004g0055 a0001c0001t0004g0056 |
2 | HG01109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.276+1273C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731217 | |||||||
chr19:5731330 | AGTGTGGT others(1): Show |
A | 78 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.276+1406_276+1413d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731330 | ||||||
chr19:5731460 | T | A | 2 | a0003c0005t0001g0249 a0004c0003t0001g0248 |
2 | NA18952.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.276+1516T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731460 | |||||||
chr19:5731519 | A | G | 1 | a0002c0002t0001g0290 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.276+1575A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731519 | |||||||
chr19:5731549 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.276+1605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731549 | |||||||
chr19:5731560 | G | GT | 102 | a0001c0001t0001g0043 a0001c0001t0001g0065 a0001c0001t0001g0067 others(99): Show |
102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.276+1642dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTT | 55 | a0001c0001t0001g0203 a0001c0001t0001g0230 a0001c0001t0001g0232 others(52): Show |
55 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.276+1641_276+1642d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTT | 11 | a0001c0040t0001g0329 a0002c0002t0001g0243 a0002c0002t0001g0321 others(8): Show |
11 | HG01070.hp1 HG01346.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+1640_276+1642d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTT | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(12): Show |
15 | HG01993.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.276+1639_276+1642d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTT | 7 | a0001c0001t0001g0001 a0006c0007t0001g0028 a0008c0010t0001g0032 others(4): Show |
7 | HG01952.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+1638_276+1642d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTT | 8 | a0010c0008t0001g0011 a0013c0013t0001g0009 a0013c0013t0001g0012 others(5): Show |
8 | HG02809.hp1 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.276+1637_276+1642d others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT | 22 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0113 others(19): Show |
22 | HG00323.hp1 HG00642.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.276+1636_276+1642d others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT others(1): Show |
31 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(28): Show |
31 | HG00621.hp1 HG01071.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.276+1635_276+1642d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT others(2): Show |
6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0301 others(3): Show |
6 | HG01106.hp1 HG01168.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1634_276+1642d others(11): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT others(3): Show |
7 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0134 others(4): Show |
7 | HG01070.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+1633_276+1642d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT others(4): Show |
7 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0100 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+1632_276+1642d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT others(5): Show |
5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1631_276+1642d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | G | GTTTTTTT others(6): Show |
1 | a0004c0003t0001g0319 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.276+1630_276+1642d others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731560 | GTTTTTTT others(4): Show |
G | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.276+1632_276+1642d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | ||||||
chr19:5731611 | C | G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.276+1667C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731611 | |||||||
chr19:5731616 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276+1672C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731616 | |||||||
chr19:5731636 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(20): Show |
23 | HG01346.hp1 HG02027.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.276+1692C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731636 | |||||||
chr19:5731644 | C | T | 2 | a0003c0004t0001g0064 a0003c0004t0001g0075 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.276+1700C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731644 | |||||||
chr19:5731657 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.276+1713G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731657 | |||||||
chr19:5731720 | C | T | 1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.276+1776C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731720 | |||||||
chr19:5731731 | G | A | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.276+1787G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731731 | |||||||
chr19:5731750 | T | C | 1 | a0004c0003t0001g0295 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.276+1806T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731750 | |||||||
chr19:5732274 | G | T | 1 | a0023c0023t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.277-1582G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732274 | |||||||
chr19:5732381 | A | T | 1 | a0004c0044t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.277-1475A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732381 | |||||||
chr19:5732455 | C | T | 1 | a0001c0016t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.277-1401C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732455 | |||||||
chr19:5732464 | ACT | A | 78 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.277-1389_277-1388d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5732464 | ||||||
chr19:5732493 | C | T | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-1363C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732493 | |||||||
chr19:5732494 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.277-1362G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732494 | |||||||
chr19:5732552 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277-1304C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732552 | |||||||
chr19:5732686 | T | G | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.277-1170T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732686 | |||||||
chr19:5732968 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(261): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.277-888T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732968 | |||||||
chr19:5732972 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(21): Show |
24 | HG01243.hp2 HG01346.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.277-884C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732972 | |||||||
chr19:5732983 | G | GT | 8 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0001c0001t0001g0197 others(5): Show |
8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-865dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5732983 | ||||||
chr19:5733070 | C | G | 16 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(13): Show |
16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-786C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733070 | |||||||
chr19:5733305 | C | CTCTTTCT others(17): Show |
1 | a0001c0001t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.277-550_277-549ins others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733305 | ||||||
chr19:5733305 | C | CTCTTTCT others(25): Show |
1 | a0001c0001t0001g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.277-550_277-549ins others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733305 | ||||||
chr19:5733305 | C | CTCTTTCT others(29): Show |
2 | a0003c0004t0001g0023 a0003c0004t0001g0314 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.277-550_277-549ins others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733305 | ||||||
chr19:5733307 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0003c0004t0001g0023 others(1): Show |
4 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-549T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733307 | |||||||
chr19:5733307 | T | TCTTTCTT others(34): Show |
1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277-549_277-548ins others(41): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733307 | |||||||
chr19:5733307 | T | TTTCTTTC others(44): Show |
1 | a0001c0001t0002g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.277-547_277-546ins others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(13): Show |
3 | a0001c0001t0001g0001 a0011c0011t0001g0002 a0011c0011t0001g0003 |
3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.277-540_277-521dup others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(17): Show |
2 | a0010c0008t0001g0008 a0010c0008t0001g0014 |
2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.277-544_277-521dup others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(21): Show |
1 | a0013c0013t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.277-548_277-521dup others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(25): Show |
3 | a0010c0008t0001g0011 a0013c0013t0001g0012 a0015c0014t0002g0010 |
3 | HG02809.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.277-521_277-520ins others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(29): Show |
1 | a0015c0014t0002g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-521_277-520ins others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(37): Show |
1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.277-521_277-520ins others(44): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733307 | T | TTTTCTTT others(41): Show |
1 | a0001c0034t0001g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277-521_277-520ins others(48): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | ||||||
chr19:5733326 | T | C | 6 | a0006c0007t0001g0028 a0006c0007t0001g0029 a0006c0007t0002g0018 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-530T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733326 | |||||||
chr19:5733332 | T | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(77): Show |
80 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.277-524T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733332 | |||||||
chr19:5733335 | C | CTTTCCTT others(1): Show |
3 | a0001c0045t0001g0151 a0021c0036t0001g0294 a0027c0020t0001g0030 |
3 | HG01243.hp2 HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.277-521_277-520ins others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733335 | |||||||
chr19:5733335 | C | CTTTCTTT others(5): Show |
1 | a0002c0002t0001g0290 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.277-521_277-520ins others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733335 | |||||||
chr19:5733335 | C | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(77): Show |
80 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.277-521C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733335 | |||||||
chr19:5733347 | T | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(85): Show |
88 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.277-509T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733347 | |||||||
chr19:5733347 | T | TCTTC | 156 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0047 others(153): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.277-499_277-496dup others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733347 | ||||||
chr19:5733347 | TCTTCCTT others(9): Show |
T | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-491_277-476del others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733347 | ||||||
chr19:5733349 | TTCCTTCC others(5): Show |
T | 1 | a0003c0005t0001g0274 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.277-495_277-484del others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733349 | ||||||
chr19:5733387 | G | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(263): Show |
266 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.277-469G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733387 | |||||||
chr19:5733407 | CTCCT | C | 39 | a0001c0001t0001g0177 a0001c0001t0001g0188 a0001c0001t0001g0201 others(36): Show |
39 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.277-428_277-425del others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733407 | ||||||
chr19:5733432 | CCTTT | C | 17 | a0002c0002t0001g0250 a0006c0007t0001g0027 a0006c0007t0001g0028 others(14): Show |
17 | HG00323.hp2 HG00741.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.277-409_277-406del others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733432 | ||||||
chr19:5734057 | T | C | 1 | a0012c0031t0001g0036 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.391+87T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734057 | |||||||
chr19:5734228 | T | C | 78 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.391+258T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734228 | |||||||
chr19:5734579 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.391+609G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734579 | |||||||
chr19:5734638 | C | CA | 51 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(48): Show |
51 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.391+681dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5734638 | ||||||
chr19:5734692 | C | T | 1 | a0003c0037t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.391+722C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734692 | |||||||
chr19:5734718 | C | T | 20 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(17): Show |
20 | HG01346.hp1 HG02027.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.391+748C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734718 | |||||||
chr19:5734744 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.391+774G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734744 | |||||||
chr19:5734800 | T | TA | 10 | a0001c0001t0001g0096 a0001c0001t0001g0149 a0001c0001t0001g0186 others(7): Show |
10 | HG01346.hp2 HG01433.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.391+845dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5734800 | ||||||
chr19:5734800 | TA | T | 6 | a0001c0001t0001g0128 a0004c0003t0003g0114 a0006c0007t0001g0028 others(3): Show |
6 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+845delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5734800 | ||||||
chr19:5734805 | A | T | 5 | a0001c0001t0001g0273 a0002c0002t0001g0289 a0003c0004t0001g0251 others(2): Show |
5 | HG02071.hp1 HG02083.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+835A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734805 | |||||||
chr19:5734815 | A | G | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.391+845A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734815 | |||||||
chr19:5734944 | C | T | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391+974C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734944 | |||||||
chr19:5735287 | G | A | 1 | a0013c0013t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.391+1317G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735287 | |||||||
chr19:5735352 | C | T | 2 | a0002c0002t0001g0182 a0002c0002t0001g0271 |
2 | NA18995.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.391+1382C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735352 | |||||||
chr19:5735373 | C | T | 4 | a0002c0002t0001g0041 a0002c0002t0001g0072 a0002c0002t0001g0073 others(1): Show |
4 | HG01074.hp1 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+1403C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735373 | |||||||
chr19:5735421 | C | A | 1 | a0002c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391+1451C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735421 | |||||||
chr19:5735477 | A | AT | 11 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0153 others(8): Show |
11 | HG01070.hp2 HG01192.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+1523dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735477 | ||||||
chr19:5735477 | AT | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(91): Show |
94 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+1523delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735477 | ||||||
chr19:5735505 | G | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(47): Show |
50 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.391+1535G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735505 | |||||||
chr19:5735550 | G | A | 39 | a0001c0001t0001g0177 a0001c0001t0001g0188 a0001c0001t0001g0201 others(36): Show |
39 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.391+1580G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735550 | |||||||
chr19:5735606 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(115): Show |
118 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.392-1532A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735606 | |||||||
chr19:5735607 | G | GGACTACA others(9): Show |
1 | a0004c0003t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.392-1530_392-1515d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735607 | ||||||
chr19:5735720 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(261): Show |
264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.392-1418A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735720 | |||||||
chr19:5735768 | C | T | 1 | a0004c0003t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.392-1370C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735768 | |||||||
chr19:5735774 | A | AT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0133 others(9): Show |
12 | HG00735.hp2 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.392-1344dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735774 | ||||||
chr19:5735774 | AT | A | 192 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0044 others(189): Show |
192 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.392-1344delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735774 | ||||||
chr19:5735774 | ATT | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0139 a0001c0001t0001g0148 others(5): Show |
8 | HG01069.hp1 HG01168.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-1345_392-1344d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735774 | ||||||
chr19:5735844 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(11): Show |
14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.392-1294G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735844 | |||||||
chr19:5735873 | T | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
39 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.392-1265T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735873 | |||||||
chr19:5735874 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0034t0001g0025 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-1264G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735874 | |||||||
chr19:5735940 | C | T | 2 | a0011c0011t0001g0002 a0011c0011t0001g0003 |
2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.392-1198C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735940 | |||||||
chr19:5736029 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(78): Show |
81 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.392-1109A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736029 | |||||||
chr19:5736052 | C | T | 2 | a0002c0002t0001g0049 a0002c0002t0001g0050 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.392-1086C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736052 | |||||||
chr19:5736063 | C | T | 1 | a0003c0005t0001g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.392-1075C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736063 | |||||||
chr19:5736139 | C | T | 5 | a0008c0010t0001g0031 a0008c0010t0001g0032 a0008c0010t0001g0034 others(2): Show |
5 | HG01952.hp2 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-999C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736139 | |||||||
chr19:5736318 | A | T | 1 | a0002c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.392-820A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736318 | |||||||
chr19:5736361 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(75): Show |
78 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.392-777C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736361 | |||||||
chr19:5736362 | G | A | 2 | a0003c0005t0001g0236 a0003c0005t0001g0254 |
2 | HG02040.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.392-776G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736362 | |||||||
chr19:5736444 | C | T | 1 | a0010c0008t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.392-694C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736444 | |||||||
chr19:5736533 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.392-605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736533 | |||||||
chr19:5736538 | G | A | 1 | a0002c0019t0001g0332 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.392-600G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736538 | |||||||
chr19:5736697 | A | G | 2 | a0002c0002t0001g0286 a0032c0029t0001g0269 |
2 | NA18969.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.392-441A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736697 | |||||||
chr19:5736720 | G | A | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-418G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736720 | |||||||
chr19:5736828 | T | G | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.392-310T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736828 | |||||||
chr19:5736857 | A | T | 1 | a0002c0002t0001g0268 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.392-281A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736857 | |||||||
chr19:5736908 | T | C | 16 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(13): Show |
16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-230T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736908 | |||||||
chr19:5736933 | T | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-205T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736933 | |||||||
chr19:5736980 | C | A | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.392-158C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736980 | |||||||
chr19:5737124 | T | C | 1 | a0010c0008t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.392-14T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5737124 | |||||||
chr19:5737492 | A | G | 1 | a0004c0003t0001g0035 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.459+287A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737492 | |||||||
chr19:5737524 | T | C | 9 | a0002c0002t0001g0107 a0002c0002t0001g0127 a0004c0003t0001g0119 others(6): Show |
9 | HG01952.hp2 HG01993.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+319T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737524 | |||||||
chr19:5737536 | AAGACTCT others(3): Show |
A | 1 | a0002c0002t0003g0145 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.459+333_459+342del others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737536 | ||||||
chr19:5737540 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.459+335C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737540 | |||||||
chr19:5737546 | CA | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(225): Show |
228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.459+362delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737546 | ||||||
chr19:5737557 | A | G | 1 | a0003c0004t0001g0023 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.459+352A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737557 | |||||||
chr19:5737836 | G | A | 13 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(10): Show |
13 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+631G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737836 | |||||||
chr19:5737850 | C | CA | 22 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(19): Show |
22 | HG00140.hp1 HG00741.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+659dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737850 | ||||||
chr19:5737850 | CA | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0126 a0001c0001t0001g0128 others(6): Show |
9 | HG01070.hp2 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+659delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737850 | ||||||
chr19:5737871 | A | C | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.459+666A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737871 | |||||||
chr19:5737982 | C | T | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(12): Show |
15 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.459+777C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737982 | |||||||
chr19:5738070 | C | A | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.459+865C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738070 | |||||||
chr19:5738071 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.459+866C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738071 | |||||||
chr19:5738110 | C | T | 2 | a0002c0002t0001g0266 a0004c0003t0001g0267 |
2 | HG00408.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.459+905C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738110 | |||||||
chr19:5738266 | G | C | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-1060G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738266 | |||||||
chr19:5738267 | C | G | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-1059C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738267 | |||||||
chr19:5738352 | C | CA | 6 | a0001c0001t0001g0067 a0002c0002t0001g0234 a0002c0002t0001g0243 others(3): Show |
6 | HG00642.hp2 HG01070.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-956dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5738352 | ||||||
chr19:5738352 | CA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(82): Show |
85 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.460-956delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5738352 | ||||||
chr19:5738352 | CAA | C | 30 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(27): Show |
30 | HG00741.hp2 HG01243.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-957_460-956del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5738352 | ||||||
chr19:5738367 | A | G | 1 | a0002c0002t0001g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.460-959A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738367 | |||||||
chr19:5738462 | G | A | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.460-864G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738462 | |||||||
chr19:5738474 | G | C | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.460-852G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738474 | |||||||
chr19:5738497 | A | C | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-829A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738497 | |||||||
chr19:5738590 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.460-736C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738590 | |||||||
chr19:5738623 | A | C | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-703A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738623 | |||||||
chr19:5738624 | C | A | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-702C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738624 | |||||||
chr19:5738669 | C | T | 1 | a0005c0006t0001g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.460-657C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738669 | |||||||
chr19:5738740 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.460-586C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738740 | |||||||
chr19:5738767 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(100): Show |
103 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.460-559G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738767 | |||||||
chr19:5738775 | C | T | 3 | a0001c0001t0001g0001 a0011c0011t0001g0002 a0011c0011t0001g0003 |
3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.460-551C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738775 | |||||||
chr19:5738777 | T | A | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-549T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738777 | |||||||
chr19:5738783 | C | A | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-543C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738783 | |||||||
chr19:5738970 | C | G | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-356C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738970 | |||||||
chr19:5738971 | G | C | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-355G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738971 | |||||||
chr19:5738991 | G | T | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.460-335G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738991 | |||||||
chr19:5739101 | G | A | 92 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0241 others(89): Show |
92 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.460-225G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5739101 | |||||||
chr19:5739106 | C | CTGCCTGC others(13): Show |
1 | a0001c0001t0001g0113 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.460-219_460-200dup others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5739106 | ||||||
chr19:5739157 | A | G | 1 | a0003c0004t0001g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.460-169A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5739157 | |||||||
chr19:5739306 | T | C | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-20T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5739306 | |||||||
chr19:5739309 | C | CT | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(12): Show |
15 | HG00621.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.460-5dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5739309 | ||||||
chr19:5739630 | G | C | 3 | a0003c0005t0001g0185 a0003c0005t0001g0249 a0004c0003t0001g0248 |
3 | NA18952.hp2 NA19007.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.573+191G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739630 | |||||||
chr19:5739683 | AT | A | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+245delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739683 | |||||||
chr19:5739842 | A | AAAAAAAA others(7): Show |
6 | a0001c0001t0001g0301 a0001c0045t0001g0151 a0004c0003t0001g0302 others(3): Show |
6 | HG00741.hp2 HG01192.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+414_573+415ins others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5739842 | ||||||
chr19:5739842 | A | AAAAAAAA others(6): Show |
109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(106): Show |
109 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.573+414_573+415ins others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5739842 | ||||||
chr19:5739842 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0001g0128 a0001c0001t0001g0133 a0002c0002t0001g0049 others(1): Show |
4 | HG01433.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+404_573+415dup others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5739842 | ||||||
chr19:5739918 | TTAGAGAC others(3): Show |
T | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.573+480_573+489del others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739918 | |||||||
chr19:5739930 | AG | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0034t0001g0025 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+492delG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739930 | |||||||
chr19:5739955 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.573+516C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739955 | |||||||
chr19:5740019 | C | T | 1 | a0002c0002t0001g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.573+580C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740019 | |||||||
chr19:5740027 | A | T | 2 | a0001c0001t0002g0293 a0021c0036t0001g0294 |
2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.573+588A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740027 | |||||||
chr19:5740098 | A | G | 1 | a0003c0004t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.573+659A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740098 | |||||||
chr19:5740482 | G | A | 2 | a0019c0046t0001g0005 a0022c0047t0001g0004 |
2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.573+1043G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740482 | |||||||
chr19:5740575 | G | A | 1 | a0027c0020t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573+1136G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740575 | |||||||
chr19:5740582 | C | T | 1 | a0027c0020t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573+1143C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740582 | |||||||
chr19:5740617 | A | C | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+1178A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740617 | |||||||
chr19:5740680 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.573+1241C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740680 | |||||||
chr19:5740762 | C | CA | 35 | a0001c0001t0001g0063 a0001c0001t0001g0123 a0001c0001t0001g0130 others(32): Show |
35 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.573+1347dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5740762 | ||||||
chr19:5740762 | CA | C | 24 | a0001c0001t0001g0116 a0001c0001t0001g0192 a0001c0040t0001g0329 others(21): Show |
24 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.573+1347delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5740762 | ||||||
chr19:5740793 | G | A | 1 | a0029c0039t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.573+1354G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740793 | |||||||
chr19:5740902 | C | A | 1 | a0006c0007t0001g0029 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+1463C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740902 | |||||||
chr19:5740942 | G | A | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+1503G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740942 | |||||||
chr19:5741042 | GCCATTGC others(27): Show |
G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(102): Show |
105 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.573+1606_573+1639d others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741042 | ||||||
chr19:5741118 | C | A | 1 | a0004c0003t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.573+1679C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741118 | |||||||
chr19:5741153 | C | CA | 15 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0002g0018 others(12): Show |
15 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+1715dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741153 | ||||||
chr19:5741273 | A | G | 4 | a0002c0002t0001g0266 a0004c0003t0001g0035 a0004c0003t0001g0267 others(1): Show |
4 | HG00408.hp2 NA18986.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+1834A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741273 | |||||||
chr19:5741630 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.573+2191A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741630 | |||||||
chr19:5741740 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+2301C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741740 | |||||||
chr19:5741741 | G | C | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+2302G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741741 | |||||||
chr19:5741785 | C | CCGGGGGG others(5): Show |
1 | a0001c0001t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.573+2346_573+2347i others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741785 | |||||||
chr19:5741785 | C | CG | 69 | a0001c0001t0001g0065 a0001c0001t0001g0157 a0001c0001t0001g0164 others(66): Show |
69 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.573+2359dupG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGG | 42 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0076 others(39): Show |
42 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.573+2358_573+2359d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGG | 39 | a0001c0001t0001g0038 a0001c0001t0001g0082 a0001c0001t0001g0148 others(36): Show |
39 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.573+2357_573+2359d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(4): Show |
5 | a0001c0001t0001g0087 a0001c0001t0001g0133 a0002c0002t0001g0050 others(2): Show |
5 | HG01433.hp2 HG02293.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+2349_573+2359d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(5): Show |
9 | a0001c0001t0001g0100 a0001c0001t0001g0135 a0002c0002t0001g0106 others(6): Show |
9 | HG00323.hp1 HG00621.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+2348_573+2359d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(6): Show |
14 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0001g0138 others(11): Show |
14 | HG00741.hp2 HG01928.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.573+2347_573+2359d others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(7): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0117 a0001c0001t0001g0131 others(3): Show |
6 | HG00642.hp1 HG01071.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(8): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0113 others(8): Show |
11 | HG01069.hp2 HG01258.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(9): Show |
3 | a0001c0001t0001g0045 a0003c0004t0001g0098 a0004c0003t0003g0114 |
3 | HG02055.hp1 NA19074.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.573+2359_573+2360i others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(10): Show |
6 | a0001c0001t0002g0095 a0002c0002t0001g0127 a0002c0002t0001g0143 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(11): Show |
8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0128 others(5): Show |
8 | HG01071.hp1 HG01346.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(12): Show |
1 | a0001c0001t0001g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(13): Show |
3 | a0001c0001t0001g0126 a0002c0002t0001g0090 a0012c0031t0001g0036 |
3 | HG02074.hp2 HG03492.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.573+2359_573+2360i others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(93): Show |
1 | a0001c0001t0001g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.573+2359_573+2360i others(102): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | CGGGGGGG others(8): Show |
1 | a0022c0047t0001g0004 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | ||||||
chr19:5741785 | C | T | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.573+2346C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741785 | |||||||
chr19:5741786 | G | A | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+2347G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741786 | |||||||
chr19:5741788 | G | A | 2 | a0002c0002t0001g0276 a0002c0002t0001g0287 |
2 | HG01261.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.573+2349G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741788 | |||||||
chr19:5741789 | GGGGGGGG others(3): Show |
G | 2 | a0002c0002t0001g0112 a0002c0002t0001g0184 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.573+2353_573+2362d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741789 | ||||||
chr19:5741792 | G | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+2353G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741792 | |||||||
chr19:5741793 | G | GGGGGGGG others(15): Show |
1 | a0025c0022t0001g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741793 | ||||||
chr19:5741793 | G | GGGGGGGG others(14): Show |
1 | a0031c0021t0001g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741793 | ||||||
chr19:5741794 | G | GC | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0026 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+2355_573+2356i others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741794 | |||||||
chr19:5741794 | G | GGGGTGGG others(14): Show |
2 | a0006c0007t0002g0018 a0006c0007t0002g0020 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.573+2358_573+2359i others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741794 | ||||||
chr19:5741794 | G | GGGTGGGG others(13): Show |
1 | a0009c0009t0001g0019 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.573+2357_573+2358i others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741794 | ||||||
chr19:5741796 | GGGT | G | 61 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0045 others(58): Show |
61 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+2362_573+2364d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741796 | ||||||
chr19:5741799 | T | A | 1 | a0002c0002t0003g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.573+2360T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741799 | |||||||
chr19:5741799 | T | C | 160 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(157): Show |
160 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.573+2360T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741799 | |||||||
chr19:5741799 | T | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0047 others(30): Show |
33 | HG00280.hp1 HG00735.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.573+2360T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741799 | |||||||
chr19:5741799 | T | TGGGGGGG others(17): Show |
1 | a0006c0007t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573+2362_573+2363i others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741799 | ||||||
chr19:5741800 | G | GGGGGGGG others(5): Show |
2 | a0001c0001t0005g0080 a0016c0015t0001g0081 |
2 | HG01433.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.573+2362_573+2363i others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741800 | ||||||
chr19:5741800 | G | GGGGGGGG others(4): Show |
2 | a0001c0001t0001g0043 a0016c0015t0001g0077 |
2 | HG00280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.573+2362_573+2363i others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741800 | ||||||
chr19:5741800 | G | GGGGGGGG others(3): Show |
2 | a0001c0001t0001g0047 a0003c0004t0001g0078 |
2 | HG02886.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.573+2362_573+2363i others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741800 | ||||||
chr19:5741800 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.573+2361G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741800 | |||||||
chr19:5741801 | G | GGGGGGGG others(4): Show |
1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.573+2362_573+2363i others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741801 | |||||||
chr19:5741802 | T | G | 14 | a0004c0042t0001g0316 a0006c0007t0001g0027 a0006c0007t0001g0028 others(11): Show |
14 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.573+2363T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741802 | |||||||
chr19:5741802 | T | TGGGGGGT others(8): Show |
1 | a0027c0020t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573+2364_573+2365i others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741802 | ||||||
chr19:5741925 | T | G | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+2486T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741925 | |||||||
chr19:5741977 | A | G | 3 | a0001c0001t0001g0001 a0011c0011t0001g0002 a0011c0011t0001g0003 |
3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.574-2450A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741977 | |||||||
chr19:5742010 | T | A | 2 | a0004c0003t0003g0085 a0004c0003t0003g0114 |
2 | NA18974.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.574-2417T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742010 | |||||||
chr19:5742058 | C | CA | 5 | a0001c0001t0001g0136 a0001c0001t0001g0164 a0001c0001t0001g0232 others(2): Show |
5 | HG00735.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-2361dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742058 | ||||||
chr19:5742096 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(109): Show |
112 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.574-2331T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742096 | |||||||
chr19:5742127 | TGCGTGTG others(3): Show |
T | 1 | a0002c0002t0001g0041 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.574-2291_574-2282d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742127 | ||||||
chr19:5742129 | C | T | 1 | a0003c0004t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.574-2298C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742129 | |||||||
chr19:5742150 | GTGTGAAC others(23): Show |
G | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-2262_574-2233d others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742150 | ||||||
chr19:5742157 | CGT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(88): Show |
91 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.574-2262_574-2261d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742157 | ||||||
chr19:5742165 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.574-2262T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742165 | |||||||
chr19:5742167 | CGT | C | 46 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(43): Show |
46 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.574-2253_574-2252d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742167 | ||||||
chr19:5742168 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.574-2259G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742168 | |||||||
chr19:5742169 | T | C | 3 | a0006c0007t0002g0018 a0006c0007t0002g0020 a0009c0009t0001g0019 |
3 | HG02895.hp1 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.574-2258T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742169 | |||||||
chr19:5742208 | GCATGTGT others(3): Show |
G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(103): Show |
106 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.574-2209_574-2200d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742208 | ||||||
chr19:5742218 | A | G | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2209A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742218 | |||||||
chr19:5742220 | A | G | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2207A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742220 | |||||||
chr19:5742228 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2199G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742228 | |||||||
chr19:5742232 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2195G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742232 | |||||||
chr19:5742241 | T | A | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2186T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742241 | |||||||
chr19:5742241 | T | C | 13 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(10): Show |
13 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-2186T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742241 | |||||||
chr19:5742287 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-2140T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742287 | |||||||
chr19:5742289 | C | CGT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.574-2133_574-2132d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742289 | ||||||
chr19:5742289 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-2138C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742289 | |||||||
chr19:5742306 | ATG | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(91): Show |
94 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.574-2112_574-2111d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742306 | ||||||
chr19:5742306 | ATGTG | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(11): Show |
14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-2114_574-2111d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742306 | ||||||
chr19:5742315 | T | G | 91 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0241 others(88): Show |
91 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.574-2112T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742315 | |||||||
chr19:5742323 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.574-2104C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742323 | |||||||
chr19:5742330 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00741.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.574-2097A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742330 | |||||||
chr19:5742339 | CAT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(89): Show |
92 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.574-2087_574-2086d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742339 | |||||||
chr19:5742340 | A | G | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(31): Show |
34 | HG00741.hp2 HG01243.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.574-2087A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742340 | |||||||
chr19:5742395 | G | A | 1 | a0002c0002t0001g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.574-2032G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742395 | |||||||
chr19:5742419 | C | T | 2 | a0001c0001t0002g0293 a0021c0036t0001g0294 |
2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.574-2008C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742419 | |||||||
chr19:5742548 | G | A | 47 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(44): Show |
47 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.574-1879G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742548 | |||||||
chr19:5742568 | G | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0044 others(87): Show |
90 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.574-1859G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742568 | |||||||
chr19:5742587 | G | C | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.574-1840G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742587 | |||||||
chr19:5742588 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.574-1839C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742588 | |||||||
chr19:5742601 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(11): Show |
14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-1826G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742601 | |||||||
chr19:5742636 | G | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0044 others(84): Show |
87 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.574-1791G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742636 | |||||||
chr19:5742743 | C | T | 1 | a0004c0003t0001g0267 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.574-1684C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742743 | |||||||
chr19:5742796 | GA | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0301 a0001c0001t0002g0095 |
3 | HG01192.hp2 HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.574-1626delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742796 | ||||||
chr19:5742797 | A | G | 1 | a0003c0004t0003g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.574-1630A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742797 | |||||||
chr19:5742807 | G | T | 2 | a0007c0012t0001g0156 a0007c0012t0001g0159 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.574-1620G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742807 | |||||||
chr19:5742943 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.574-1484C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742943 | |||||||
chr19:5742998 | G | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0044 others(89): Show |
92 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.574-1429G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742998 | |||||||
chr19:5743000 | G | T | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-1427G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743000 | |||||||
chr19:5743085 | C | T | 1 | a0004c0003t0001g0302 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.574-1342C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743085 | |||||||
chr19:5743183 | A | G | 1 | a0003c0004t0001g0304 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.574-1244A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743183 | |||||||
chr19:5743234 | C | T | 1 | a0004c0003t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.574-1193C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743234 | |||||||
chr19:5743317 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(90): Show |
93 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.574-1110G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743317 | |||||||
chr19:5743435 | T | TA | 4 | a0001c0001t0001g0043 a0001c0001t0002g0095 a0001c0001t0005g0080 others(1): Show |
4 | HG00280.hp1 HG01433.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-985dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743435 | ||||||
chr19:5743445 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(265): Show |
268 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.574-982G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743445 | |||||||
chr19:5743450 | T | C | 17 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(14): Show |
17 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.574-977T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743450 | |||||||
chr19:5743548 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.574-879G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743548 | |||||||
chr19:5743606 | G | A | 2 | a0001c0001t0001g0096 a0004c0003t0001g0129 |
2 | HG02647.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.574-821G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743606 | |||||||
chr19:5743606 | G | GAAAAAA | 20 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0099 others(17): Show |
20 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.574-819_574-814dup others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743606 | ||||||
chr19:5743606 | G | GAAAAAAA | 224 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(221): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.574-820_574-814dup others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743606 | ||||||
chr19:5743606 | G | GAAAAAAA others(1): Show |
19 | a0001c0001t0001g0001 a0004c0003t0003g0109 a0006c0007t0001g0027 others(16): Show |
19 | HG00741.hp2 HG02257.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.574-814_574-813ins others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743606 | ||||||
chr19:5743614 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.574-813G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743614 | |||||||
chr19:5743648 | G | GTC | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(118): Show |
121 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.574-763_574-762dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743648 | ||||||
chr19:5743654 | C | T | 6 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(3): Show |
6 | HG01346.hp1 HG02027.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-773C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743654 | |||||||
chr19:5743658 | C | T | 2 | a0001c0001t0002g0205 a0003c0043t0001g0204 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.574-769C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743658 | |||||||
chr19:5743667 | CCTCTCTC others(19): Show |
C | 2 | a0001c0001t0002g0093 a0018c0025t0001g0086 |
2 | HG00642.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-745_574-720del others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743667 | ||||||
chr19:5743677 | T | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(88): Show |
91 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.574-750T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743677 | |||||||
chr19:5743683 | C | CCTCT | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-723_574-720dup others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743683 | ||||||
chr19:5743683 | CCTCTCTC others(1): Show |
C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(86): Show |
89 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.574-727_574-720del others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743683 | ||||||
chr19:5743694 | CTCTCTCT others(7): Show |
C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0092 a0001c0001t0005g0080 |
3 | HG00280.hp1 HG01433.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.574-727_574-714del others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743694 | ||||||
chr19:5743702 | C | CTCTCTCT others(3): Show |
1 | a0006c0007t0001g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.574-720_574-719ins others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743702 | ||||||
chr19:5743702 | C | CTCTCTG | 11 | a0006c0007t0001g0029 a0009c0009t0001g0015 a0009c0009t0001g0016 others(8): Show |
11 | HG00741.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-700_574-695dup others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743702 | ||||||
chr19:5743740 | TG | T | 141 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(138): Show |
141 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.574-684delG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743740 | ||||||
chr19:5743797 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(93): Show |
96 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.574-630C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743797 | |||||||
chr19:5743813 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(88): Show |
91 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.574-614A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743813 | |||||||
chr19:5743863 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.574-564C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743863 | |||||||
chr19:5744073 | G | A | 1 | a0002c0002t0001g0271 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.574-354G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744073 | |||||||
chr19:5744140 | C | T | 1 | a0002c0002t0001g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.574-287C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744140 | |||||||
chr19:5744171 | G | A | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574-256G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744171 | |||||||
chr19:5744227 | G | A | 1 | a0005c0006t0001g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-200G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744227 | |||||||
chr19:5744347 | TTAGA | T | 3 | a0003c0004t0001g0064 a0003c0004t0001g0066 a0003c0004t0001g0075 |
3 | HG02109.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.574-77_574-74delGA others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5744347 | ||||||
chr19:5744579 | G | A | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.657+69G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744579 | |||||||
chr19:5744748 | G | A | 5 | a0001c0040t0001g0329 a0002c0019t0001g0331 a0002c0019t0001g0332 others(2): Show |
5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+238G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744748 | |||||||
chr19:5744815 | G | A | 1 | a0002c0002t0001g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.657+305G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744815 | |||||||
chr19:5744865 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(155): Show |
158 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.657+355G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744865 | |||||||
chr19:5744889 | C | T | 1 | a0006c0007t0001g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657+379C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744889 | |||||||
chr19:5744903 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(109): Show |
112 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.657+393G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744903 | |||||||
chr19:5745036 | G | A | 2 | a0015c0014t0002g0010 a0015c0014t0002g0013 |
2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.657+526G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745036 | |||||||
chr19:5745056 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.657+546C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745056 | |||||||
chr19:5745201 | G | T | 155 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0038 others(152): Show |
155 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.657+691G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745201 | |||||||
chr19:5745242 | C | T | 1 | a0004c0003t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.658-671C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745242 | |||||||
chr19:5745247 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(92): Show |
95 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.658-666G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745247 | |||||||
chr19:5745255 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.658-658G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745255 | |||||||
chr19:5745308 | C | T | 8 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-605C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745308 | |||||||
chr19:5745337 | G | A | 2 | a0005c0006t0001g0209 a0005c0006t0001g0229 |
2 | HG01934.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.658-576G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745337 | |||||||
chr19:5745493 | C | T | 2 | a0001c0001t0001g0318 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.658-420C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745493 | |||||||
chr19:5745621 | AAAAATAA others(3): Show |
A | 2 | a0001c0001t0001g0024 a0001c0001t0002g0026 |
2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.658-273_658-264del others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr19 | 5745621 | ||||||
chr19:5745653 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(97): Show |
100 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.658-260T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745653 | |||||||
chr19:5745683 | G | A | 17 | a0006c0007t0001g0027 a0006c0007t0001g0028 a0006c0007t0001g0029 others(14): Show |
17 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.658-230G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745683 | |||||||
chr19:5745753 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(97): Show |
100 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.658-160G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745753 | |||||||
chr19:5745774 | AG | A | 10 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0198 others(7): Show |
10 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.658-138delG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745774 | |||||||
chr19:5745814 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-99C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745814 | |||||||
chr19:5745821 | C | T | 1 | a0034c0028t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.658-92C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745821 | |||||||
chr19:5746110 | C | CA | 136 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(133): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.808+48dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746110 | ||||||
chr19:5746120 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG01109.hp2 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.808+57G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746120 | |||||||
chr19:5746436 | C | CT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0024 others(99): Show |
102 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.808+383dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746436 | ||||||
chr19:5746516 | CCTCCCGG others(12): Show |
C | 1 | a0002c0002t0001g0182 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.808+457_808+475del others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746516 | ||||||
chr19:5746551 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.808+488C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746551 | |||||||
chr19:5746589 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.808+526C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746589 | |||||||
chr19:5746779 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.808+716T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746779 | |||||||
chr19:5746810 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.808+747T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746810 | |||||||
chr19:5746811 | C | CT | 263 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(260): Show |
263 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.808+758dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746811 | ||||||
chr19:5746811 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.808+748C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746811 | |||||||
chr19:5746848 | C | T | 136 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(133): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.808+785C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746848 | |||||||
chr19:5746849 | G | A | 1 | a0016c0015t0001g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.808+786G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746849 | |||||||
chr19:5746871 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.808+808T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746871 | |||||||
chr19:5747169 | C | CT | 29 | a0001c0001t0001g0076 a0001c0001t0001g0210 a0001c0001t0001g0300 others(26): Show |
29 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.809-970dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747169 | ||||||
chr19:5747169 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(93): Show |
96 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.809-970delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747169 | ||||||
chr19:5747214 | C | T | 1 | a0002c0002t0001g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.809-946C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747214 | |||||||
chr19:5747321 | G | A | 1 | a0002c0019t0001g0332 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.809-839G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747321 | |||||||
chr19:5747543 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.809-617C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747543 | |||||||
chr19:5747610 | CT | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0165 others(11): Show |
14 | HG00438.hp2 HG00609.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.809-530delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747610 | ||||||
chr19:5747610 | CTT | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(249): Show |
252 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.809-531_809-530del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747610 | ||||||
chr19:5747651 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.809-509C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747651 | |||||||
chr19:5747814 | G | T | 140 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(137): Show |
140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.809-346G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747814 | |||||||
chr19:5747819 | C | T | 1 | a0004c0003t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.809-341C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747819 | |||||||
chr19:5747820 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.809-340C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747820 | |||||||
chr19:5747901 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.809-259C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747901 | |||||||
chr19:5747960 | C | T | 1 | a0003c0004t0001g0323 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.809-200C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747960 | |||||||
chr19:5748037 | C | T | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.809-123C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5748037 | |||||||
chr19:5748115 | C | G | 10 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0096 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-45C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5748115 | |||||||
chr19:5748373 | G | C | 1 | a0004c0003t0001g0319 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.904+118G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748373 | |||||||
chr19:5748397 | G | A | 6 | a0010c0008t0001g0011 a0010c0008t0001g0014 a0013c0013t0001g0009 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.904+142G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748397 | |||||||
chr19:5748429 | G | A | 136 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(133): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.904+174G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748429 | |||||||
chr19:5748612 | C | G | 1 | a0004c0003t0001g0224 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.904+357C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748612 | |||||||
chr19:5748623 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0038 others(93): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.904+387dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748623 | ||||||
chr19:5748623 | C | CAA | 8 | a0001c0001t0001g0088 a0001c0001t0001g0318 a0001c0040t0001g0329 others(5): Show |
8 | HG01346.hp1 HG02559.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+386_904+387dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748623 | ||||||
chr19:5748623 | CA | C | 12 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0126 others(9): Show |
12 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.904+387delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748623 | ||||||
chr19:5748728 | C | CT | 28 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0022 others(25): Show |
28 | HG00741.hp2 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.905-353dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748728 | ||||||
chr19:5748728 | C | CTT | 211 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0038 others(208): Show |
211 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.905-354_905-353dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748728 | ||||||
chr19:5748728 | C | CTTT | 28 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0001g0132 others(25): Show |
28 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.905-355_905-353dup others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748728 | ||||||
chr19:5749059 | C | T | 136 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0065 others(133): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.905-42C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5749059 | |||||||
chr19:5749062 | C | A | 1 | a0004c0003t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.905-39C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5749062 | |||||||
chr19:5749271 | C | T | 1 | a0016c0015t0001g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.987+88C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749271 | |||||||
chr19:5749286 | G | T | 1 | a0029c0039t0001g0058 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.987+103G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749286 | |||||||
chr19:5749399 | G | T | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.987+216G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749399 | |||||||
chr19:5749497 | G | C | 1 | a0002c0002t0001g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.987+314G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749497 | |||||||
chr19:5749573 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(24): Show |
27 | HG00741.hp2 HG01346.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.987+390G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749573 | |||||||
chr19:5749803 | A | AT | 131 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0063 others(128): Show |
131 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.987+638dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5749803 | ||||||
chr19:5749843 | G | A | 1 | a0003c0005t0001g0239 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.987+660G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749843 | |||||||
chr19:5749975 | T | C | 1 | a0004c0003t0001g0061 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.987+792T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749975 | |||||||
chr19:5749976 | G | A | 1 | a0004c0003t0001g0180 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.987+793G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749976 | |||||||
chr19:5750084 | G | A | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.987+901G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750084 | |||||||
chr19:5750176 | T | C | 3 | a0001c0001t0001g0079 a0004c0003t0001g0240 a0010c0008t0001g0011 |
3 | HG01169.hp1 HG02027.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.987+993T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750176 | |||||||
chr19:5750187 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987+1004G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750187 | |||||||
chr19:5750204 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.987+1021C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750204 | |||||||
chr19:5750210 | T | A | 1 | a0002c0002t0001g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.987+1027T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750210 | |||||||
chr19:5750215 | A | G | 2 | a0002c0002t0001g0052 a0003c0004t0001g0322 |
2 | HG00609.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.987+1032A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750215 | |||||||
chr19:5750219 | T | C | 1 | a0003c0004t0001g0322 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.987+1036T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750219 | |||||||
chr19:5750223 | C | T | 3 | a0001c0001t0001g0201 a0002c0002t0001g0260 a0004c0003t0001g0282 |
3 | HG00738.hp2 HG01928.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.987+1040C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750223 | |||||||
chr19:5750234 | T | G | 1 | a0002c0002t0001g0260 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.987+1051T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750234 | |||||||
chr19:5750246 | T | A | 18 | a0001c0001t0001g0157 a0001c0001t0001g0170 a0001c0001t0001g0256 others(15): Show |
18 | HG00140.hp2 HG00544.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.987+1063T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750246 | |||||||
chr19:5750260 | A | G | 12 | a0001c0001t0001g0138 a0001c0001t0001g0187 a0001c0001t0002g0205 others(9): Show |
12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+1077A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750260 | |||||||
chr19:5750264 | C | T | 1 | a0003c0004t0001g0325 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.987+1081C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750264 | |||||||
chr19:5750265 | G | A | 1 | a0004c0003t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.987+1082G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750265 | |||||||
chr19:5750274 | C | T | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987+1091C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750274 | |||||||
chr19:5750275 | C | G | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987+1092C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750275 | |||||||
chr19:5750276 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0004g0055 a0003c0004t0001g0064 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1093G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750276 | |||||||
chr19:5750312 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.987+1129C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750312 | |||||||
chr19:5750374 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.987+1191C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750374 | |||||||
chr19:5750399 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.987+1216A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750399 | |||||||
chr19:5750420 | T | C | 2 | a0002c0002t0001g0049 a0003c0004t0001g0325 |
2 | HG02083.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.988-1227T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750420 | |||||||
chr19:5750450 | C | CA | 33 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0065 others(30): Show |
33 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.988-1174dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | C | CAA | 175 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0076 others(172): Show |
175 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.988-1175_988-1174d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | C | CAAA | 30 | a0001c0001t0001g0021 a0001c0001t0001g0123 a0001c0001t0001g0154 others(27): Show |
30 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.988-1176_988-1174d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | C | CAAAA | 8 | a0002c0002t0001g0257 a0003c0004t0001g0235 a0004c0003t0001g0071 others(5): Show |
8 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1177_988-1174d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | C | CAAAAAAA others(7): Show |
1 | a0003c0004t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.988-1187_988-1174d others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | C | CAAAAAAA others(9): Show |
1 | a0003c0004t0001g0214 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.988-1189_988-1174d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | C | CAAAAAAA others(25): Show |
1 | a0002c0002t0001g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.988-1174_988-1173i others(34): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750450 | CA | C | 19 | a0001c0001t0001g0116 a0001c0001t0001g0136 a0001c0001t0001g0138 others(16): Show |
19 | HG00735.hp1 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.988-1174delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | ||||||
chr19:5750475 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0192 a0010c0008t0001g0011 others(2): Show |
5 | HG00741.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1172G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750475 | |||||||
chr19:5750689 | C | T | 5 | a0001c0001t0002g0293 a0003c0043t0001g0204 a0006c0007t0001g0028 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-958C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750689 | |||||||
chr19:5750702 | T | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0136 a0001c0001t0001g0175 others(7): Show |
10 | HG00735.hp1 HG02257.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.988-945T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750702 | |||||||
chr19:5750741 | A | G | 1 | a0004c0003t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.988-906A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750741 | |||||||
chr19:5750742 | G | A | 1 | a0004c0003t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.988-905G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750742 | |||||||
chr19:5750829 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0124 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-818C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750829 | |||||||
chr19:5750835 | C | T | 11 | a0001c0001t0001g0136 a0001c0001t0001g0175 a0002c0002t0001g0049 others(8): Show |
11 | HG00735.hp1 HG02027.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-812C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750835 | |||||||
chr19:5750882 | T | C | 16 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0099 others(13): Show |
16 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.988-765T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750882 | |||||||
chr19:5750936 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.988-711C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750936 | |||||||
chr19:5751069 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(242): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.988-578C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751069 | |||||||
chr19:5751141 | T | C | 1 | a0003c0004t0001g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.988-506T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751141 | |||||||
chr19:5751142 | G | T | 1 | a0003c0004t0001g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.988-505G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751142 | |||||||
chr19:5751151 | T | C | 1 | a0002c0002t0001g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.988-496T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751151 | |||||||
chr19:5751192 | C | T | 1 | a0006c0007t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.988-455C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751192 | |||||||
chr19:5751197 | CAAAA | C | 10 | a0001c0001t0001g0100 a0003c0004t0001g0023 a0003c0004t0001g0314 others(7): Show |
10 | HG02486.hp2 HG02572.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.988-408_988-405del others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-412_988-405del others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(5): Show |
C | 2 | a0006c0007t0002g0020 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.988-416_988-405del others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0147 a0009c0009t0001g0016 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.988-420_988-405del others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(10): Show |
C | 8 | a0001c0001t0001g0116 a0001c0001t0001g0138 a0001c0001t0001g0146 others(5): Show |
8 | HG01109.hp2 HG01361.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.988-421_988-405del others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(11): Show |
C | 1 | a0003c0004t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.988-422_988-405del others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(12): Show |
C | 8 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0099 others(5): Show |
8 | HG01884.hp1 HG02165.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-423_988-405del others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(13): Show |
C | 40 | a0001c0001t0001g0132 a0001c0001t0001g0153 a0001c0001t0001g0230 others(37): Show |
40 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.988-424_988-405del others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(14): Show |
C | 143 | a0001c0001t0001g0044 a0001c0001t0001g0076 a0001c0001t0001g0079 others(140): Show |
143 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.988-425_988-405del others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(15): Show |
C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0139 others(14): Show |
17 | HG00735.hp1 HG01169.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.988-426_988-405del others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(16): Show |
C | 2 | a0001c0001t0002g0293 a0003c0043t0001g0204 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.988-427_988-405del others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(18): Show |
C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0312 others(2): Show |
5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-429_988-405del others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(19): Show |
C | 1 | a0001c0001t0004g0056 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.988-430_988-405del others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(20): Show |
C | 4 | a0001c0001t0001g0082 a0003c0004t0001g0064 a0003c0004t0001g0066 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-431_988-405del others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(21): Show |
C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0001g0232 others(1): Show |
4 | HG00741.hp1 HG02559.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-432_988-405del others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751197 | CAAAAAAA others(22): Show |
C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0024 others(49): Show |
52 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.988-433_988-405del others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | ||||||
chr19:5751300 | G | A | 1 | a0004c0003t0001g0219 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.988-347G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751300 | |||||||
chr19:5751321 | G | C | 5 | a0002c0002t0001g0266 a0004c0003t0001g0035 a0004c0003t0001g0062 others(2): Show |
5 | HG00408.hp2 NA18983.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-326G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751321 | |||||||
chr19:5751419 | A | T | 189 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0076 others(186): Show |
189 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.988-228A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751419 | |||||||
chr19:5751451 | G | A | 2 | a0001c0001t0002g0293 a0003c0043t0001g0204 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.988-196G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751451 | |||||||
chr19:5751512 | A | C | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.988-135A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751512 | |||||||
chr19:5751520 | T | C | 1 | a0003c0004t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.988-127T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751520 | |||||||
chr19:5751531 | C | CA | 12 | a0001c0001t0001g0021 a0001c0001t0001g0100 a0001c0001t0001g0161 others(9): Show |
12 | HG02109.hp1 HG02148.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.988-79dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | C | CAAAAAAA others(4): Show |
1 | a0003c0043t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.988-89_988-79dupAA others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0293 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.988-94_988-79dupAA others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CA | C | 11 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0067 others(8): Show |
11 | HG00738.hp1 HG01168.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-79delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAA | C | 6 | a0001c0001t0001g0123 a0001c0001t0001g0153 a0001c0001t0001g0273 others(3): Show |
6 | HG01192.hp1 HG02071.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-81_988-79delAA others(1): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAA | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0076 a0001c0001t0001g0082 others(55): Show |
58 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.988-82_988-79delAA others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAA | C | 117 | a0001c0001t0001g0105 a0001c0001t0001g0113 a0001c0001t0001g0124 others(114): Show |
117 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.988-83_988-79delAA others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAA | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0270 others(5): Show |
8 | HG00408.hp1 HG01255.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.988-84_988-79delAA others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0001g0154 a0001c0001t0002g0026 a0002c0002t0001g0049 others(1): Show |
4 | HG01255.hp1 HG02027.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-89_988-79delAA others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAAA others(5): Show |
C | 18 | a0001c0001t0001g0116 a0001c0001t0001g0136 a0001c0001t0001g0138 others(15): Show |
18 | HG00735.hp1 HG01109.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.988-90_988-79delAA others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAAA others(6): Show |
C | 15 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0099 others(12): Show |
15 | HG01106.hp2 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.988-91_988-79delAA others(11): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAAA others(7): Show |
C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0024 others(44): Show |
47 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.988-92_988-79delAA others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0130 a0001c0001t0002g0205 a0005c0006t0001g0229 |
3 | HG01934.hp1 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.988-93_988-79delAA others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751531 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-94_988-79delAA others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | ||||||
chr19:5751900 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0099 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+77C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5751900 | |||||||
chr19:5751980 | T | C | 2 | a0001c0001t0002g0293 a0003c0043t0001g0204 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1164+157T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5751980 | |||||||
chr19:5751997 | C | CA | 7 | a0001c0001t0001g0130 a0001c0001t0001g0195 a0001c0001t0001g0197 others(4): Show |
7 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+183dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5751997 | ||||||
chr19:5752006 | A | T | 3 | a0001c0001t0001g0318 a0006c0007t0002g0020 a0020c0038t0002g0317 |
3 | HG02451.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1164+183A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752006 | |||||||
chr19:5752007 | T | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0241 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1164+184T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752007 | |||||||
chr19:5752202 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0195 a0001c0001t0001g0197 others(4): Show |
7 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+379C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752202 | |||||||
chr19:5752203 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0004g0056 |
2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1164+380G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752203 | |||||||
chr19:5752239 | G | T | 2 | a0001c0001t0002g0293 a0003c0043t0001g0204 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1164+416G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752239 | |||||||
chr19:5752303 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1164+480C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752303 | |||||||
chr19:5752420 | G | C | 3 | a0001c0001t0001g0318 a0006c0007t0002g0020 a0020c0038t0002g0317 |
3 | HG02451.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1164+597G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752420 | |||||||
chr19:5752428 | G | A | 2 | a0001c0001t0002g0293 a0003c0043t0001g0204 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1164+605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752428 | |||||||
chr19:5752582 | G | A | 1 | a0006c0007t0002g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1164+759G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752582 | |||||||
chr19:5752624 | A | G | 1 | a0003c0005t0001g0307 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1164+801A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752624 | |||||||
chr19:5752660 | C | T | 5 | a0001c0001t0001g0116 a0001c0001t0001g0138 a0001c0001t0001g0146 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+837C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752660 | |||||||
chr19:5752762 | T | C | 14 | a0001c0001t0001g0136 a0001c0001t0001g0175 a0001c0001t0002g0205 others(11): Show |
14 | HG00735.hp1 HG02027.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1164+939T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752762 | |||||||
chr19:5752794 | G | A | 4 | a0001c0001t0001g0210 a0002c0002t0001g0283 a0002c0002t0001g0296 others(1): Show |
4 | HG02135.hp1 HG03490.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+971G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752794 | |||||||
chr19:5752908 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1164+1085A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752908 | |||||||
chr19:5753007 | G | A | 12 | a0001c0001t0001g0130 a0001c0001t0001g0195 a0001c0001t0001g0197 others(9): Show |
12 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1165-1125G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753007 | |||||||
chr19:5753027 | C | CA | 16 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0001g0155 others(13): Show |
16 | HG00642.hp2 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1165-1088dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753027 | ||||||
chr19:5753027 | CA | C | 33 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0096 others(30): Show |
33 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1165-1088delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753027 | ||||||
chr19:5753105 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(264): Show |
267 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.1165-1027C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753105 | |||||||
chr19:5753280 | G | T | 2 | a0003c0005t0001g0185 a0003c0005t0001g0249 |
2 | NA19007.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1165-852G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753280 | |||||||
chr19:5753281 | G | C | 3 | a0003c0004t0001g0064 a0003c0004t0001g0066 a0003c0004t0001g0075 |
3 | HG02109.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1165-851G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753281 | |||||||
chr19:5753291 | T | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0100 a0001c0001t0001g0230 others(25): Show |
28 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1165-841T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753291 | |||||||
chr19:5753298 | C | T | 1 | a0003c0004t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165-834C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753298 | |||||||
chr19:5753300 | C | G | 1 | a0003c0004t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165-832C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753300 | |||||||
chr19:5753314 | G | A | 1 | a0003c0005t0001g0239 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1165-818G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753314 | |||||||
chr19:5753335 | T | C | 117 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0076 others(114): Show |
117 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1165-797T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753335 | |||||||
chr19:5753363 | T | A | 83 | a0001c0001t0001g0021 a0001c0001t0001g0076 a0001c0001t0001g0082 others(80): Show |
83 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1165-769T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753363 | |||||||
chr19:5753364 | T | G | 75 | a0001c0001t0001g0021 a0001c0001t0001g0076 a0001c0001t0001g0082 others(72): Show |
75 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1165-768T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753364 | |||||||
chr19:5753371 | T | TAA | 3 | a0002c0002t0001g0206 a0002c0002t0001g0212 a0002c0002t0001g0221 |
3 | NA18963.hp2 NA18971.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1165-760_1165-759d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753371 | ||||||
chr19:5753394 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1165-738C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753394 | |||||||
chr19:5753423 | G | A | 4 | a0001c0001t0001g0312 a0001c0001t0001g0318 a0001c0001t0002g0057 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-709G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753423 | |||||||
chr19:5753434 | C | T | 1 | a0002c0002t0003g0122 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1165-698C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753434 | |||||||
chr19:5753518 | C | T | 1 | a0004c0044t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1165-614C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753518 | |||||||
chr19:5753529 | C | T | 1 | a0003c0004t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165-603C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753529 | |||||||
chr19:5753567 | A | G | 5 | a0001c0001t0001g0099 a0003c0004t0001g0064 a0003c0004t0001g0066 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-565A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753567 | |||||||
chr19:5753594 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1165-538C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753594 | |||||||
chr19:5753595 | G | A | 3 | a0004c0003t0001g0320 a0004c0003t0003g0085 a0004c0003t0003g0114 |
3 | NA18974.hp1 NA19074.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1165-537G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753595 | |||||||
chr19:5753626 | T | G | 5 | a0002c0002t0001g0226 a0002c0002t0001g0233 a0003c0004t0001g0200 others(2): Show |
5 | HG01081.hp2 HG01496.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-506T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753626 | |||||||
chr19:5753683 | A | T | 2 | a0002c0002t0001g0234 a0002c0002t0001g0243 |
2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1165-449A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753683 | |||||||
chr19:5753698 | G | T | 3 | a0001c0001t0001g0021 a0001c0034t0001g0025 a0009c0009t0001g0019 |
3 | HG02109.hp1 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1165-434G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753698 | |||||||
chr19:5753706 | T | TA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0002c0002t0001g0277 others(3): Show |
6 | HG01496.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-414dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753706 | ||||||
chr19:5753730 | G | A | 1 | a0002c0002t0001g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1165-402G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753730 | |||||||
chr19:5753859 | C | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0312 a0001c0001t0001g0318 others(2): Show |
5 | HG02109.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-273C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753859 | |||||||
chr19:5753872 | C | CA | 12 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0195 others(9): Show |
12 | HG01884.hp1 HG02074.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1165-250dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753872 | ||||||
chr19:5753910 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1165-222C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753910 | |||||||
chr19:5753911 | G | A | 1 | a0002c0002t0001g0275 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1165-221G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753911 | |||||||
chr19:5753947 | G | A | 1 | a0002c0002t0001g0290 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1165-185G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753947 | |||||||
chr19:5754090 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1165-42A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5754090 | |||||||
chr19:5754267 | T | C | 1 | a0003c0004t0001g0200 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1278+22T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754267 | |||||||
chr19:5754375 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0105 |
3 | HG01255.hp2 HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1278+130T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754375 | |||||||
chr19:5754393 | C | CT | 20 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0123 others(17): Show |
20 | HG00438.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1278+171dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | ||||||
chr19:5754393 | C | CTT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0044 others(128): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1278+170_1278+171d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | ||||||
chr19:5754393 | C | CTTT | 34 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0128 others(31): Show |
34 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1278+169_1278+171d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | ||||||
chr19:5754393 | CT | C | 25 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0117 others(22): Show |
25 | HG01884.hp2 HG01934.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1278+171delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | ||||||
chr19:5754421 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1278+176C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754421 | |||||||
chr19:5754430 | G | A | 2 | a0001c0001t0001g0105 a0003c0004t0001g0333 |
2 | HG01257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1278+185G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754430 | |||||||
chr19:5754459 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1278+214C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754459 | |||||||
chr19:5754460 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1278+215G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754460 | |||||||
chr19:5754562 | C | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1278+317C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754562 | |||||||
chr19:5754629 | C | G | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+384C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754629 | |||||||
chr19:5754650 | G | A | 3 | a0001c0001t0001g0079 a0003c0004t0001g0322 a0003c0041t0001g0330 |
3 | HG00609.hp1 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1278+405G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754650 | |||||||
chr19:5754716 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+471C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754716 | |||||||
chr19:5754725 | G | T | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1278+480G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754725 | |||||||
chr19:5754759 | T | A | 1 | a0003c0004t0001g0189 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1278+514T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754759 | |||||||
chr19:5754788 | G | A | 1 | a0003c0037t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1278+543G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754788 | |||||||
chr19:5754828 | C | G | 3 | a0001c0001t0001g0100 a0001c0001t0002g0026 a0006c0007t0002g0018 |
3 | HG02976.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1278+583C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754828 | |||||||
chr19:5754847 | C | CT | 85 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0084 others(82): Show |
85 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1278+617dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754847 | ||||||
chr19:5755144 | C | T | 1 | a0004c0003t0001g0237 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1278+899C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755144 | |||||||
chr19:5755199 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0162 |
3 | HG00738.hp1 HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1278+954C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755199 | |||||||
chr19:5755386 | G | A | 3 | a0001c0001t0002g0093 a0006c0007t0002g0020 a0020c0038t0002g0317 |
3 | HG02257.hp2 HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1278+1141G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755386 | |||||||
chr19:5755458 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(230): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1278+1213A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755458 | |||||||
chr19:5755635 | T | C | 1 | a0003c0004t0001g0189 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1278+1390T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755635 | |||||||
chr19:5755714 | G | A | 1 | a0003c0004t0001g0196 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1278+1469G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755714 | |||||||
chr19:5755773 | C | CAATA | 37 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0076 others(34): Show |
37 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1278+1551_1278+155 others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5755773 | ||||||
chr19:5755869 | A | C | 1 | a0004c0003t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1278+1624A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755869 | |||||||
chr19:5755919 | T | G | 1 | a0002c0002t0001g0268 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1278+1674T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755919 | |||||||
chr19:5756009 | G | A | 1 | a0003c0004t0003g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1278+1764G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756009 | |||||||
chr19:5756132 | T | G | 5 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0003c0004t0001g0094 others(2): Show |
5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-1711T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756132 | |||||||
chr19:5756187 | G | A | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1279-1656G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756187 | |||||||
chr19:5756284 | G | GA | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(168): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1279-1548dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5756284 | ||||||
chr19:5756379 | G | A | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-1464G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756379 | |||||||
chr19:5756440 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(240): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1279-1403C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756440 | |||||||
chr19:5756493 | A | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0192 a0001c0001t0001g0318 others(4): Show |
7 | HG00741.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1279-1350A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756493 | |||||||
chr19:5756555 | C | T | 2 | a0001c0001t0002g0101 a0006c0007t0001g0027 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1279-1288C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756555 | |||||||
chr19:5756559 | T | A | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1279-1284T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756559 | |||||||
chr19:5756634 | G | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0136 a0001c0001t0001g0165 others(3): Show |
6 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1209G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756634 | |||||||
chr19:5756654 | G | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0003c0004t0001g0094 others(2): Show |
5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-1189G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756654 | |||||||
chr19:5756748 | C | T | 1 | a0003c0004t0001g0094 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1279-1095C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756748 | |||||||
chr19:5756865 | C | T | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-978C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756865 | |||||||
chr19:5756950 | A | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0192 a0001c0001t0001g0318 others(4): Show |
7 | HG00741.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1279-893A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756950 | |||||||
chr19:5756978 | G | A | 4 | a0002c0002t0001g0091 a0002c0002t0001g0112 a0002c0002t0001g0143 others(1): Show |
4 | HG00323.hp2 HG01175.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-865G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756978 | |||||||
chr19:5757084 | T | G | 5 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0003c0004t0001g0094 others(2): Show |
5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-759T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757084 | |||||||
chr19:5757097 | A | G | 1 | a0013c0013t0001g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1279-746A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757097 | |||||||
chr19:5757119 | G | A | 2 | a0009c0009t0001g0019 a0028c0026t0002g0335 |
2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1279-724G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757119 | |||||||
chr19:5757259 | G | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(235): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1279-584G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757259 | |||||||
chr19:5757297 | CT | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(284): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1279-529delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757297 | ||||||
chr19:5757297 | CTT | C | 31 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0042 others(28): Show |
31 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.1279-530_1279-529d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757297 | ||||||
chr19:5757525 | G | A | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1279-318G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757525 | |||||||
chr19:5757547 | T | C | 1 | a0013c0013t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279-296T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757547 | |||||||
chr19:5757581 | G | A | 8 | a0001c0001t0001g0099 a0003c0004t0001g0064 a0003c0004t0001g0075 others(5): Show |
8 | HG02109.hp2 HG02622.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279-262G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757581 | |||||||
chr19:5757599 | A | AT | 8 | a0001c0001t0001g0087 a0003c0004t0001g0097 a0003c0004t0001g0098 others(5): Show |
8 | HG02055.hp1 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279-222dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | ||||||
chr19:5757599 | AT | A | 88 | a0001c0001t0001g0043 a0001c0001t0001g0063 a0001c0001t0001g0067 others(85): Show |
88 | HG00280.hp1 HG00438.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.1279-222delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | ||||||
chr19:5757599 | ATT | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(198): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1279-223_1279-222d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | ||||||
chr19:5757599 | ATTT | A | 9 | a0001c0001t0001g0103 a0001c0001t0002g0093 a0002c0002t0001g0089 others(6): Show |
9 | HG01258.hp2 HG01517.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279-224_1279-222d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | ||||||
chr19:5757599 | ATTTTTTT others(3): Show |
A | 1 | a0008c0010t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1279-231_1279-222d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | ||||||
chr19:5757656 | G | A | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-187G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757656 | |||||||
chr19:5757706 | G | C | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-137G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757706 | |||||||
chr19:5757793 | G | A | 2 | a0015c0014t0002g0010 a0015c0014t0002g0013 |
2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1279-50G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757793 | |||||||
chr19:5758171 | G | A | 1 | a0003c0004t0001g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1368+239G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758171 | |||||||
chr19:5758261 | G | A | 8 | a0002c0002t0001g0041 a0002c0002t0001g0106 a0002c0002t0001g0258 others(5): Show |
8 | HG00323.hp1 HG01261.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368+329G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758261 | |||||||
chr19:5758454 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0192 a0001c0001t0001g0318 others(3): Show |
6 | HG00741.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368+522G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758454 | |||||||
chr19:5758545 | T | C | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1369-541T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758545 | |||||||
chr19:5758573 | C | CA | 18 | a0001c0001t0001g0082 a0001c0001t0001g0099 a0001c0001t0002g0057 others(15): Show |
18 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1369-493dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758573 | ||||||
chr19:5758573 | CA | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(250): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1369-493delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758573 | ||||||
chr19:5758573 | CAA | C | 11 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0007 others(8): Show |
11 | HG00642.hp2 HG01081.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369-494_1369-493d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758573 | ||||||
chr19:5758599 | C | T | 1 | a0030c0035t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1369-487C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758599 | |||||||
chr19:5758658 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1369-428G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758658 | |||||||
chr19:5758692 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1369-394G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758692 | |||||||
chr19:5758730 | G | A | 10 | a0001c0001t0001g0087 a0001c0001t0001g0195 a0003c0004t0001g0066 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369-356G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758730 | |||||||
chr19:5758758 | GA | G | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369-320delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758758 | ||||||
chr19:5758923 | C | CA | 32 | a0001c0001t0001g0044 a0001c0001t0001g0088 a0001c0001t0001g0117 others(29): Show |
32 | HG00621.hp2 HG00741.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1369-140dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758923 | ||||||
chr19:5758923 | CA | C | 19 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0139 others(16): Show |
19 | HG00280.hp1 HG01099.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1369-140delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758923 | ||||||
chr19:5759220 | T | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(246): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1427+76T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759220 | |||||||
chr19:5759247 | C | A | 1 | a0004c0003t0001g0319 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1427+103C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759247 | |||||||
chr19:5759259 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0310 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1427+115G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759259 | |||||||
chr19:5759372 | G | T | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1427+228G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759372 | |||||||
chr19:5759380 | G | A | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1427+236G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759380 | |||||||
chr19:5759390 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1427+246C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759390 | |||||||
chr19:5759405 | A | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(211): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1427+261A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759405 | |||||||
chr19:5759407 | A | T | 1 | a0001c0001t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1427+263A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759407 | |||||||
chr19:5759480 | G | T | 15 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(12): Show |
15 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1427+336G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759480 | |||||||
chr19:5759552 | T | A | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+408T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759552 | |||||||
chr19:5759566 | CA | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1427+441delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5759566 | ||||||
chr19:5759572 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1427+428A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759572 | |||||||
chr19:5759611 | G | A | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+467G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759611 | |||||||
chr19:5759737 | G | A | 1 | a0002c0002t0001g0275 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1427+593G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759737 | |||||||
chr19:5759747 | T | C | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+603T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759747 | |||||||
chr19:5759801 | C | T | 3 | a0001c0001t0002g0026 a0006c0007t0002g0018 a0028c0026t0002g0335 |
3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1427+657C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759801 | |||||||
chr19:5759814 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1427+670A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759814 | |||||||
chr19:5759927 | A | T | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+783A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759927 | |||||||
chr19:5759950 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1427+806G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759950 | |||||||
chr19:5760000 | G | A | 2 | a0001c0001t0002g0293 a0011c0011t0001g0003 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1427+856G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760000 | |||||||
chr19:5760073 | C | CA | 188 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0038 others(185): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1427+953dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760073 | ||||||
chr19:5760073 | C | CAA | 49 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(46): Show |
49 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1427+952_1427+953d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760073 | ||||||
chr19:5760102 | G | A | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1427+958G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760102 | |||||||
chr19:5760170 | G | A | 1 | a0030c0035t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1427+1026G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760170 | |||||||
chr19:5760173 | G | A | 51 | a0001c0001t0001g0001 a0002c0002t0001g0042 a0002c0002t0001g0070 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1427+1029G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760173 | |||||||
chr19:5760323 | C | T | 11 | a0001c0001t0002g0095 a0003c0004t0001g0023 a0003c0004t0001g0064 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1427+1179C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760323 | |||||||
chr19:5760398 | C | CA | 115 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0044 others(112): Show |
115 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1427+1268dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760398 | ||||||
chr19:5760398 | C | CAA | 16 | a0002c0002t0001g0050 a0002c0002t0001g0089 a0002c0002t0001g0127 others(13): Show |
16 | HG00438.hp2 HG00544.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1427+1267_1427+126 others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760398 | ||||||
chr19:5760398 | CA | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0147 a0001c0001t0002g0026 others(49): Show |
52 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1427+1268delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760398 | ||||||
chr19:5760415 | A | G | 1 | a0009c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1427+1271A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760415 | |||||||
chr19:5760471 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1427+1327C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760471 | |||||||
chr19:5760472 | T | A | 51 | a0001c0001t0001g0001 a0002c0002t0001g0042 a0002c0002t0001g0070 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1427+1328T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760472 | |||||||
chr19:5760477 | G | A | 1 | a0003c0004t0001g0304 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1427+1333G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760477 | |||||||
chr19:5760486 | C | T | 5 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+1342C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760486 | |||||||
chr19:5760530 | A | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(240): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1427+1386A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760530 | |||||||
chr19:5760619 | GGACCAAG others(4): Show |
G | 1 | a0004c0003t0003g0085 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1427+1476_1427+148 others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760619 | |||||||
chr19:5760767 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1427+1623G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760767 | |||||||
chr19:5760797 | T | G | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1427+1653T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760797 | |||||||
chr19:5760916 | G | A | 1 | a0002c0002t0001g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1427+1772G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760916 | |||||||
chr19:5760939 | CA | C | 12 | a0001c0001t0001g0165 a0003c0004t0001g0023 a0003c0004t0001g0064 others(9): Show |
12 | HG02074.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1427+1809delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760939 | ||||||
chr19:5761006 | C | G | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+1862C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761006 | |||||||
chr19:5761042 | GT | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(205): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1427+1909delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761042 | ||||||
chr19:5761333 | C | T | 5 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428-1882C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761333 | |||||||
chr19:5761345 | G | A | 51 | a0001c0001t0001g0001 a0002c0002t0001g0042 a0002c0002t0001g0070 others(48): Show |
51 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1428-1870G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761345 | |||||||
chr19:5761416 | A | AATGG | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1428-1774_1428-177 others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761416 | ||||||
chr19:5761416 | AATGGATG others(1): Show |
A | 3 | a0004c0003t0001g0119 a0004c0003t0001g0280 a0004c0003t0001g0302 |
3 | HG02129.hp2 HG02135.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1428-1778_1428-177 others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761416 | ||||||
chr19:5761441 | A | ATGGATGG others(5): Show |
5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428-1771_1428-177 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761441 | ||||||
chr19:5761445 | C | A | 30 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0099 others(27): Show |
30 | HG01884.hp1 HG01891.hp2 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.1428-1770C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761445 | |||||||
chr19:5761463 | G | GGCTGGAT others(148): Show |
221 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(218): Show |
221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1428-1750_1428-159 others(159): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761463 | ||||||
chr19:5761463 | G | GGCTGGAT others(303): Show |
2 | a0001c0001t0002g0293 a0011c0011t0001g0003 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1428-1596_1428-159 others(314): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761463 | ||||||
chr19:5761463 | G | GGCTGGCT others(148): Show |
13 | a0002c0002t0001g0042 a0002c0002t0001g0070 a0002c0002t0001g0090 others(10): Show |
13 | HG00408.hp1 HG01099.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1428-1747_1428-174 others(159): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761463 | ||||||
chr19:5761469 | A | C | 1 | a0002c0002t0001g0252 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1428-1746A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761469 | |||||||
chr19:5761703 | C | CT | 33 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0099 others(30): Show |
33 | HG00609.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1428-1498dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761703 | ||||||
chr19:5761783 | A | G | 1 | a0002c0002t0001g0127 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1428-1432A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761783 | |||||||
chr19:5761791 | C | T | 21 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0099 others(18): Show |
21 | HG01884.hp1 HG01934.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1428-1424C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761791 | |||||||
chr19:5761822 | C | T | 1 | a0021c0036t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1428-1393C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761822 | |||||||
chr19:5761913 | T | G | 10 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1428-1302T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761913 | |||||||
chr19:5761937 | C | T | 75 | a0001c0001t0001g0084 a0001c0001t0001g0131 a0001c0001t0001g0132 others(72): Show |
75 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1428-1278C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761937 | |||||||
chr19:5761989 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1428-1226T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761989 | |||||||
chr19:5761990 | G | A | 1 | a0006c0007t0001g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1428-1225G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761990 | |||||||
chr19:5762041 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0043 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1428-1167_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762041 | ||||||
chr19:5762041 | C | CATATATA others(7): Show |
1 | a0001c0001t0005g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1428-1169_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762041 | ||||||
chr19:5762041 | C | CATATATA others(9): Show |
3 | a0004c0003t0001g0062 a0004c0003t0001g0245 a0004c0003t0001g0248 |
3 | NA18952.hp2 NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1428-1171_1428-115 others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762041 | ||||||
chr19:5762048 | ATATATAT others(5): Show |
A | 3 | a0014c0017t0002g0193 a0015c0014t0002g0010 a0015c0014t0002g0013 |
3 | HG02896.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1428-1165_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762048 | ||||||
chr19:5762048 | ATATATAT others(6): Show |
A | 2 | a0014c0017t0002g0194 a0021c0036t0001g0294 |
2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1428-1165_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762048 | ||||||
chr19:5762056 | A | AT | 4 | a0002c0002t0001g0007 a0002c0002t0001g0107 a0003c0004t0001g0115 others(1): Show |
4 | HG02155.hp1 HG02523.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1158dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762056 | ||||||
chr19:5762056 | A | T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0162 others(2): Show |
5 | HG00738.hp1 HG01243.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-1159A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762056 | |||||||
chr19:5762057 | TA | T | 5 | a0002c0002t0001g0255 a0002c0002t0001g0289 a0004c0003t0001g0120 others(2): Show |
5 | HG02129.hp1 NA18960.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-1157delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762057 | |||||||
chr19:5762058 | A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(6): Show |
5 | a0002c0002t0001g0264 a0002c0002t0001g0268 a0003c0004t0001g0189 others(2): Show |
5 | HG00408.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(10): Show |
2 | a0004c0003t0001g0282 a0034c0028t0001g0102 |
2 | HG01928.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(52): Show |
1 | a0001c0001t0001g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(63): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(40): Show |
1 | a0033c0024t0001g0225 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(40): Show |
1 | a0001c0001t0001g0079 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(45): Show |
1 | a0001c0016t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(56): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(46): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(48): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(40): Show |
1 | a0001c0016t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(33): Show |
2 | a0001c0001t0001g0006 a0004c0003t0001g0180 |
2 | NA18942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(44): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(34): Show |
1 | a0003c0004t0001g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(45): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(47): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(38): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(39): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0103 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(45): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(35): Show |
1 | a0003c0037t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(46): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(25): Show |
1 | a0004c0003t0001g0224 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0124 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(42): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(22): Show |
1 | a0003c0004t0001g0325 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(38): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(40): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(30): Show |
2 | a0001c0001t0001g0105 a0003c0004t0001g0179 |
2 | HG01257.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(41): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(24): Show |
1 | a0001c0001t0002g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(35): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(25): Show |
1 | a0003c0004t0001g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(33): Show |
1 | a0002c0002t0001g0290 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(44): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(21): Show |
1 | a0002c0027t0001g0291 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(22): Show |
2 | a0002c0002t0001g0037 a0004c0003t0001g0071 |
2 | HG00544.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0149 a0002c0002t0001g0296 |
2 | HG01346.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(34): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(24): Show |
2 | a0002c0002t0001g0283 a0006c0007t0002g0018 |
2 | HG03490.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(35): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(30): Show |
2 | a0001c0001t0001g0232 a0003c0004t0001g0023 |
2 | HG00741.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(41): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0301 a0002c0002t0001g0233 a0002c0002t0001g0259 |
3 | HG01192.hp2 HG02273.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(20): Show |
1 | a0004c0044t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(21): Show |
2 | a0002c0002t0001g0191 a0005c0006t0001g0215 |
2 | HG03942.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0273 a0012c0031t0001g0036 |
2 | HG02071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(29): Show |
1 | a0003c0004t0001g0314 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(40): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0013c0013t0001g0009 |
3 | HG02818.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0210 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
8 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(18): Show |
7 | a0001c0001t0001g0136 a0001c0001t0001g0230 a0001c0001t0001g0256 others(4): Show |
7 | HG00735.hp1 HG03239.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0177 a0003c0004t0001g0075 a0003c0004t0001g0158 |
3 | HG02683.hp1 HG03195.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(20): Show |
4 | a0002c0002t0001g0226 a0002c0002t0001g0275 a0004c0003t0001g0313 others(1): Show |
4 | HG02040.hp1 NA18954.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(22): Show |
1 | a0002c0002t0001g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0116 a0010c0008t0001g0008 a0017c0018t0001g0309 |
3 | HG03041.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0084 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0132 a0002c0002t0001g0178 |
2 | HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
8 | a0002c0002t0001g0049 a0002c0002t0001g0068 a0002c0002t0001g0112 others(5): Show |
8 | HG00438.hp2 HG01109.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(18): Show |
6 | a0001c0001t0001g0170 a0002c0002t0001g0089 a0002c0002t0001g0143 others(3): Show |
6 | HG00642.hp1 HG02027.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(19): Show |
2 | a0002c0002t0001g0199 a0003c0004t0001g0214 |
2 | HG03669.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(20): Show |
1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0024 a0005c0006t0001g0229 |
2 | HG01934.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(10): Show |
2 | a0003c0005t0001g0274 a0004c0003t0001g0320 |
2 | HG00609.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0293 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(13): Show |
1 | a0011c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(14): Show |
2 | a0006c0007t0001g0027 a0022c0047t0001g0004 |
2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(15): Show |
2 | a0005c0006t0001g0223 a0017c0018t0001g0308 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(16): Show |
2 | a0001c0001t0002g0101 a0001c0001t0002g0311 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
12 | a0002c0002t0001g0069 a0002c0002t0001g0073 a0002c0002t0001g0074 others(9): Show |
12 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0134 a0002c0002t0001g0243 a0002c0002t0003g0122 others(1): Show |
4 | HG01070.hp1 HG01070.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0131 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(8): Show |
1 | a0003c0005t0001g0236 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(9): Show |
2 | a0004c0003t0003g0085 a0004c0003t0003g0114 |
2 | NA18974.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(10): Show |
1 | a0007c0012t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0022 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(15): Show |
1 | a0003c0004t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(16): Show |
3 | a0003c0004t0001g0262 a0003c0004t0003g0125 a0011c0011t0001g0315 |
3 | HG01081.hp2 HG01496.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
4 | a0002c0002t0001g0041 a0002c0002t0001g0072 a0002c0002t0001g0104 others(1): Show |
4 | HG00323.hp1 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(18): Show |
4 | a0002c0002t0001g0053 a0002c0002t0001g0276 a0002c0002t0001g0305 others(1): Show |
4 | HG01261.hp2 HG01358.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(5): Show |
3 | a0001c0001t0002g0093 a0003c0004t0001g0336 a0008c0010t0001g0031 |
3 | HG01993.hp2 HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(6): Show |
8 | a0001c0001t0001g0001 a0002c0002t0001g0181 a0002c0002t0001g0252 others(5): Show |
8 | HG01069.hp1 HG01258.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(7): Show |
4 | a0003c0004t0001g0235 a0003c0004t0001g0304 a0003c0004t0001g0333 others(1): Show |
4 | HG02886.hp1 HG03486.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(10): Show |
2 | a0007c0012t0001g0156 a0007c0012t0001g0159 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0312 |
2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(15): Show |
2 | a0005c0006t0001g0209 a0029c0039t0001g0058 |
2 | HG02559.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0123 a0002c0002t0001g0271 |
2 | HG03486.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
1 | a0010c0008t0001g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(3): Show |
2 | a0006c0007t0002g0020 a0020c0038t0002g0317 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(5): Show |
2 | a0003c0004t0001g0144 a0024c0033t0001g0303 |
2 | HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(6): Show |
11 | a0002c0002t0001g0042 a0002c0002t0001g0070 a0002c0002t0001g0090 others(8): Show |
11 | HG01074.hp2 HG01099.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(7): Show |
11 | a0002c0002t0001g0298 a0003c0004t0001g0207 a0003c0004t0001g0222 others(8): Show |
11 | HG00544.hp1 HG00621.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(8): Show |
2 | a0003c0004t0001g0094 a0003c0005t0001g0239 |
2 | HG02976.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(17): Show |
1 | a0002c0002t0001g0277 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0154 a0001c0001t0001g0197 a0003c0004t0001g0292 others(1): Show |
4 | HG00140.hp1 HG01255.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(7): Show |
1 | a0003c0005t0001g0249 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0088 a0003c0004t0001g0322 |
2 | HG00609.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0117 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATTT others(6): Show |
3 | a0001c0001t0001g0318 a0003c0004t0001g0196 a0028c0026t0002g0335 |
3 | HG02572.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATTATA others(21): Show |
1 | a0004c0003t0001g0326 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATTTTT others(6): Show |
2 | a0001c0001t0001g0096 a0001c0001t0001g0310 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | ATATTTTT others(7): Show |
2 | a0001c0001t0001g0192 a0019c0046t0001g0005 |
2 | HG00741.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | ||||||
chr19:5762058 | A | T | 55 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0067 others(52): Show |
55 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1428-1157A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762058 | |||||||
chr19:5762059 | T | TATATATA others(8): Show |
5 | a0001c0001t0001g0047 a0001c0001t0001g0135 a0001c0001t0001g0188 others(2): Show |
5 | HG01106.hp2 HG01261.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762059 | |||||||
chr19:5762059 | T | TATATATA others(10): Show |
1 | a0016c0015t0001g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762059 | |||||||
chr19:5762059 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0231 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762059 | |||||||
chr19:5762060 | T | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0092 a0001c0001t0001g0198 |
3 | HG00280.hp1 HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1428-1155T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762060 | |||||||
chr19:5762061 | T | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0135 a0001c0001t0001g0188 others(5): Show |
8 | HG01106.hp2 HG01261.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428-1154T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762061 | |||||||
chr19:5762063 | T | A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0135 a0001c0001t0001g0188 others(4): Show |
7 | HG01106.hp2 HG01261.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1428-1152T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762063 | |||||||
chr19:5762103 | G | T | 1 | a0002c0002t0001g0286 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1428-1112G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762103 | |||||||
chr19:5762422 | A | G | 1 | a0001c0016t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1428-793A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762422 | |||||||
chr19:5762533 | T | C | 1 | a0002c0002t0001g0184 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1428-682T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762533 | |||||||
chr19:5762617 | G | GTGGA | 5 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0067 others(2): Show |
5 | HG01168.hp2 HG02004.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-572_1428-569d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762617 | ||||||
chr19:5762817 | T | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1428-398T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762817 | |||||||
chr19:5762858 | G | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1428-357G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762858 | |||||||
chr19:5763203 | G | A | 1 | a0003c0043t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1428-12G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5763203 | |||||||
chr19:5763318 | C | T | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1506+25C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5763318 | |||||||
chr19:5763761 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1506+468C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5763761 | |||||||
chr19:5763847 | C | CTTTT | 10 | a0001c0001t0002g0311 a0003c0004t0001g0023 a0003c0004t0001g0064 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+569_1506+572d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTT | 21 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0099 others(18): Show |
21 | HG01884.hp1 HG01891.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.1506+568_1506+572d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(1): Show |
27 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0105 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1506+565_1506+572d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(2): Show |
11 | a0001c0001t0001g0103 a0001c0001t0001g0164 a0001c0001t0001g0170 others(8): Show |
11 | HG00741.hp1 HG01175.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1506+564_1506+572d others(11): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(3): Show |
41 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0132 others(38): Show |
41 | HG00408.hp1 HG00544.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.1506+563_1506+572d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(4): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0088 others(23): Show |
26 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1506+562_1506+572d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(5): Show |
6 | a0003c0004t0001g0196 a0003c0004t0001g0222 a0003c0004t0001g0235 others(3): Show |
6 | HG00140.hp1 HG02027.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+561_1506+572d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(13): Show |
1 | a0002c0002t0001g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(15): Show |
1 | a0002c0002t0001g0226 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1506+572_1506+573i others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(16): Show |
1 | a0002c0002t0001g0233 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1506+572_1506+573i others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0275 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(18): Show |
1 | a0002c0002t0003g0110 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1506+572_1506+573i others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(19): Show |
15 | a0001c0001t0005g0080 a0002c0002t0001g0037 a0002c0002t0001g0049 others(12): Show |
15 | HG00323.hp1 HG00323.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(20): Show |
39 | a0001c0001t0001g0043 a0001c0001t0001g0208 a0001c0001t0001g0210 others(36): Show |
39 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(21): Show |
19 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0135 others(16): Show |
19 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(22): Show |
5 | a0001c0001t0001g0136 a0001c0001t0001g0165 a0002c0002t0001g0234 others(2): Show |
5 | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0166 a0001c0001t0002g0095 |
2 | HG02055.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1506+572_1506+573i others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(24): Show |
5 | a0002c0002t0001g0053 a0002c0002t0001g0068 a0002c0002t0001g0212 others(2): Show |
5 | HG01109.hp1 HG01358.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(35): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763847 | C | CTTTTTTT others(30): Show |
1 | a0034c0028t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(39): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | ||||||
chr19:5763911 | G | C | 6 | a0002c0002t0001g0127 a0004c0003t0001g0054 a0004c0003t0001g0071 others(3): Show |
6 | HG00438.hp2 HG00544.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+618G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5763911 | |||||||
chr19:5764029 | AGAAGAAA others(4): Show |
A | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1506+738_1506+748d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764029 | ||||||
chr19:5764039 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(235): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1506+746G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764039 | |||||||
chr19:5764041 | G | T | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1506+748G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764041 | |||||||
chr19:5764092 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0003c0004t0001g0094 others(1): Show |
4 | HG02559.hp1 HG02976.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+799G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764092 | |||||||
chr19:5764101 | GGCCTCCC others(78): Show |
G | 2 | a0002c0002t0001g0181 a0004c0003t0001g0237 |
2 | NA18942.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1506+829_1506+913d others(87): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764101 | ||||||
chr19:5764228 | C | G | 6 | a0002c0002t0001g0174 a0002c0002t0001g0266 a0002c0002t0001g0289 others(3): Show |
6 | HG00408.hp2 HG02129.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+935C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764228 | |||||||
chr19:5764235 | A | AT | 10 | a0001c0001t0001g0021 a0001c0001t0001g0170 a0001c0001t0001g0192 others(7): Show |
10 | HG00741.hp2 HG02965.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.1506+955dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764235 | ||||||
chr19:5764235 | A | ATT | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1506+954_1506+955d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764235 | ||||||
chr19:5764235 | A | ATTT | 7 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(4): Show |
7 | HG01358.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1506+953_1506+955d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764235 | ||||||
chr19:5764379 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(236): Show |
239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1506+1086G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764379 | |||||||
chr19:5764425 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(233): Show |
236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1506+1132T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764425 | |||||||
chr19:5764460 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1506+1167C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764460 | |||||||
chr19:5764461 | G | A | 76 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0135 others(73): Show |
76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1506+1168G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764461 | |||||||
chr19:5764461 | G | C | 1 | a0004c0003t0001g0320 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1506+1168G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764461 | |||||||
chr19:5764464 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(238): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1506+1171T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764464 | |||||||
chr19:5764547 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0043 others(185): Show |
188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1506+1254G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764547 | |||||||
chr19:5764647 | A | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1506+1354A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764647 | |||||||
chr19:5764657 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1506+1364T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764657 | |||||||
chr19:5764690 | C | T | 10 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+1397C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764690 | |||||||
chr19:5764739 | G | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0076 a0001c0001t0001g0136 others(4): Show |
7 | HG00735.hp1 HG01192.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-1364G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764739 | |||||||
chr19:5764751 | T | A | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1507-1352T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764751 | |||||||
chr19:5764862 | G | A | 1 | a0003c0004t0001g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1507-1241G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764862 | |||||||
chr19:5765071 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(242): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1507-1032T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765071 | |||||||
chr19:5765091 | T | C | 1 | a0002c0002t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1507-1012T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765091 | |||||||
chr19:5765205 | G | A | 1 | a0003c0005t0001g0239 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1507-898G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765205 | |||||||
chr19:5765225 | C | T | 5 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-878C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765225 | |||||||
chr19:5765283 | A | G | 1 | a0003c0005t0001g0261 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1507-820A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765283 | |||||||
chr19:5765353 | GCTCT | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0192 a0001c0001t0001g0197 others(2): Show |
5 | HG00741.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-745_1507-742d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765353 | ||||||
chr19:5765401 | GATTTATT others(9): Show |
G | 3 | a0002c0002t0001g0226 a0002c0002t0001g0233 a0002c0002t0001g0275 |
3 | NA18954.hp1 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1507-698_1507-683d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765401 | ||||||
chr19:5765405 | T | TATTC | 5 | a0001c0001t0001g0148 a0002c0002t0001g0202 a0003c0004t0001g0059 others(2): Show |
5 | HG01168.hp2 HG03209.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-651_1507-648d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | ||||||
chr19:5765405 | TATTC | T | 45 | a0001c0001t0001g0082 a0001c0001t0001g0092 a0001c0001t0001g0175 others(42): Show |
45 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1507-651_1507-648d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | ||||||
chr19:5765405 | TATTCATT others(1): Show |
T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0099 others(13): Show |
16 | HG00438.hp2 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1507-655_1507-648d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | ||||||
chr19:5765405 | TATTCATT others(5): Show |
T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0044 others(50): Show |
53 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1507-659_1507-648d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | ||||||
chr19:5765405 | TATTCATT others(9): Show |
T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(160): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1507-663_1507-648d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | ||||||
chr19:5765405 | TATTCATT others(13): Show |
T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(4): Show |
7 | HG02015.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-667_1507-648d others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | ||||||
chr19:5765417 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1507-686C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765417 | |||||||
chr19:5765421 | C | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0001g0138 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1507-682C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765421 | |||||||
chr19:5765425 | C | T | 21 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0001c0001t0001g0192 others(18): Show |
21 | HG00741.hp2 HG01934.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1507-678C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765425 | |||||||
chr19:5765446 | A | T | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1507-657A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765446 | |||||||
chr19:5765466 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1507-637G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765466 | |||||||
chr19:5765518 | A | G | 2 | a0001c0001t0002g0026 a0006c0007t0002g0018 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1507-585A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765518 | |||||||
chr19:5765641 | G | A | 2 | a0001c0001t0002g0026 a0006c0007t0002g0018 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1507-462G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765641 | |||||||
chr19:5765684 | C | T | 5 | a0002c0002t0001g0174 a0002c0002t0001g0266 a0004c0003t0001g0035 others(2): Show |
5 | HG00408.hp2 NA18960.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-419C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765684 | |||||||
chr19:5765701 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(230): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1507-402A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765701 | |||||||
chr19:5765709 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(230): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1507-394A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765709 | |||||||
chr19:5765760 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(314): Show |
317 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.1507-343T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765760 | |||||||
chr19:5765858 | G | A | 53 | a0001c0001t0001g0175 a0001c0001t0001g0241 a0002c0002t0001g0007 others(50): Show |
53 | HG00408.hp2 HG00621.hp1 HG01952.hp2 others(50): Show |
intron_variant | MODIFIER | c.1507-245G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765858 | |||||||
chr19:5765867 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1507-236C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765867 | |||||||
chr19:5766024 | T | C | 6 | a0002c0002t0001g0127 a0004c0003t0001g0054 a0004c0003t0001g0071 others(3): Show |
6 | HG00438.hp2 HG00544.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1507-79T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5766024 | |||||||
chr19:5766079 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(228): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1507-24T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5766079 | |||||||
chr19:5766288 | T | TA | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1559+133_1559+134i others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766288 | |||||||
chr19:5766289 | G | A | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1559+134G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766289 | |||||||
chr19:5766289 | G | GA | 7 | a0001c0001t0001g0084 a0001c0001t0001g0105 a0001c0001t0001g0132 others(4): Show |
7 | HG01106.hp1 HG01257.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1559+150dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766289 | ||||||
chr19:5766289 | G | GAA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(196): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1559+149_1559+150d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766289 | ||||||
chr19:5766289 | G | GAAA | 23 | a0001c0001t0001g0210 a0001c0001t0001g0232 a0001c0001t0002g0293 others(20): Show |
23 | HG00438.hp2 HG00544.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1559+148_1559+150d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766289 | ||||||
chr19:5766311 | C | T | 1 | a0034c0028t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1559+156C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766311 | |||||||
chr19:5766312 | G | A | 2 | a0001c0001t0002g0293 a0011c0011t0001g0003 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1559+157G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766312 | |||||||
chr19:5766336 | G | A | 2 | a0001c0001t0002g0026 a0006c0007t0002g0018 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1559+181G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766336 | |||||||
chr19:5766349 | G | C | 1 | a0011c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1559+194G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766349 | |||||||
chr19:5766459 | GA | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1559+318delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766459 | ||||||
chr19:5766574 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1559+419C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766574 | |||||||
chr19:5766579 | AT | A | 88 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(85): Show |
88 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1559+427delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766579 | ||||||
chr19:5766697 | AT | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(228): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1559+555delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766697 | ||||||
chr19:5766743 | A | C | 1 | a0002c0027t0001g0291 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1559+588A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766743 | |||||||
chr19:5766931 | G | T | 2 | a0003c0004t0001g0189 a0003c0043t0001g0204 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1559+776G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766931 | |||||||
chr19:5767141 | C | T | 1 | a0031c0021t0001g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1559+986C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767141 | |||||||
chr19:5767174 | G | A | 1 | a0002c0002t0001g0286 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1560-994G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767174 | |||||||
chr19:5767224 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1560-944G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767224 | |||||||
chr19:5767253 | C | T | 3 | a0007c0012t0001g0156 a0007c0012t0001g0159 a0007c0012t0001g0160 |
3 | HG01515.hp1 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1560-915C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767253 | |||||||
chr19:5767289 | C | G | 5 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1560-879C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767289 | |||||||
chr19:5767316 | C | CA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(187): Show |
190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1560-834dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767316 | ||||||
chr19:5767316 | C | CAA | 44 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0024 others(41): Show |
44 | HG00741.hp1 HG01081.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.1560-835_1560-834d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767316 | ||||||
chr19:5767321 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1560-847A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767321 | |||||||
chr19:5767339 | G | T | 1 | a0002c0002t0001g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1560-829G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767339 | |||||||
chr19:5767413 | G | GT | 8 | a0001c0001t0001g0133 a0001c0001t0002g0205 a0002c0002t0001g0042 others(5): Show |
8 | HG00544.hp2 HG01175.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1560-742dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767413 | ||||||
chr19:5767413 | GT | G | 17 | a0001c0001t0002g0095 a0003c0004t0001g0023 a0003c0004t0001g0064 others(14): Show |
17 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1560-742delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767413 | ||||||
chr19:5767449 | T | G | 1 | a0002c0002t0001g0266 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1560-719T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767449 | |||||||
chr19:5767484 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1560-684T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767484 | |||||||
chr19:5767494 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1560-674A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767494 | |||||||
chr19:5767574 | G | A | 35 | a0002c0002t0001g0042 a0002c0002t0001g0070 a0002c0002t0001g0090 others(32): Show |
35 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1560-594G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767574 | |||||||
chr19:5767588 | T | C | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1560-580T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767588 | |||||||
chr19:5767631 | C | T | 11 | a0002c0002t0001g0090 a0003c0004t0001g0023 a0003c0004t0001g0064 others(8): Show |
11 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1560-537C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767631 | |||||||
chr19:5767709 | G | A | 19 | a0002c0002t0001g0037 a0002c0002t0001g0068 a0002c0002t0001g0069 others(16): Show |
19 | HG00438.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1560-459G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767709 | |||||||
chr19:5767763 | C | A | 3 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 |
3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1560-405C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767763 | |||||||
chr19:5767765 | CTTTT | C | 10 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1560-400_1560-397d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767765 | ||||||
chr19:5767781 | ATTATT | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(237): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1560-378_1560-374d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767781 | ||||||
chr19:5767786 | T | A | 2 | a0003c0004t0001g0023 a0003c0004t0001g0314 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1560-382T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767786 | |||||||
chr19:5767857 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(242): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1560-311T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767857 | |||||||
chr19:5767943 | C | G | 9 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0001c0001t0001g0192 others(6): Show |
9 | HG00741.hp2 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1560-225C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767943 | |||||||
chr19:5767987 | G | A | 1 | a0008c0010t0001g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1560-181G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767987 | |||||||
chr19:5768291 | G | T | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1634+49G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768291 | |||||||
chr19:5768320 | T | TTTTA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(211): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1634+101_1634+104d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5768320 | ||||||
chr19:5768320 | T | TTTTATTT others(1): Show |
23 | a0001c0001t0001g0021 a0001c0001t0001g0088 a0001c0001t0001g0096 others(20): Show |
23 | HG00741.hp2 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634+97_1634+104du others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5768320 | ||||||
chr19:5768320 | T | TTTTATTT others(5): Show |
8 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0205 others(5): Show |
8 | HG01934.hp2 HG02015.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1634+93_1634+104du others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5768320 | ||||||
chr19:5768384 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(239): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1634+142T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768384 | |||||||
chr19:5768406 | G | A | 10 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(7): Show |
10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634+164G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768406 | |||||||
chr19:5768438 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634+196A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768438 | |||||||
chr19:5768449 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1634+207G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768449 | |||||||
chr19:5768601 | G | A | 1 | a0006c0007t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1634+359G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768601 | |||||||
chr19:5768697 | G | A | 1 | a0018c0025t0001g0086 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1634+455G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768697 | |||||||
chr19:5768702 | T | C | 1 | a0003c0004t0001g0325 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1634+460T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768702 | |||||||
chr19:5768807 | C | G | 1 | a0002c0002t0001g0290 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1634+565C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768807 | |||||||
chr19:5768807 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1634+565C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768807 | |||||||
chr19:5768883 | T | C | 2 | a0001c0001t0002g0026 a0006c0007t0002g0018 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1634+641T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768883 | |||||||
chr19:5768920 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(235): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1634+678G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768920 | |||||||
chr19:5769000 | G | A | 1 | a0004c0003t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1634+758G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769000 | |||||||
chr19:5769046 | C | T | 2 | a0002c0002t0001g0178 a0002c0002t0001g0217 |
2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1634+804C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769046 | |||||||
chr19:5769086 | A | G | 3 | a0001c0001t0002g0293 a0001c0001t0002g0311 a0011c0011t0001g0003 |
3 | HG01891.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1634+844A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769086 | |||||||
chr19:5769150 | T | G | 10 | a0001c0001t0002g0095 a0003c0004t0001g0023 a0003c0004t0001g0064 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634+908T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769150 | |||||||
chr19:5769162 | A | AAG | 13 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0105 others(10): Show |
13 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1634+935_1634+936d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5769162 | ||||||
chr19:5769293 | CA | C | 6 | a0002c0002t0001g0289 a0003c0004t0001g0094 a0003c0004t0001g0142 others(3): Show |
6 | HG01169.hp2 HG02129.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+1072delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5769293 | ||||||
chr19:5769314 | A | AT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0096 others(22): Show |
25 | HG00741.hp2 HG01099.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1634+1072_1634+107 others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769314 | |||||||
chr19:5769314 | A | T | 232 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0024 others(229): Show |
232 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.1634+1072A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769314 | |||||||
chr19:5769329 | G | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1634+1087G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769329 | |||||||
chr19:5769376 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1634+1134T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769376 | |||||||
chr19:5769385 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1634+1143A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769385 | |||||||
chr19:5769433 | C | A | 16 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0100 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1634+1191C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769433 | |||||||
chr19:5769435 | G | A | 2 | a0002c0002t0001g0049 a0002c0002t0001g0104 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1634+1193G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769435 | |||||||
chr19:5769572 | C | T | 1 | a0006c0007t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1634+1330C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769572 | |||||||
chr19:5769574 | C | T | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1634+1332C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769574 | |||||||
chr19:5769672 | G | A | 1 | a0004c0003t0001g0295 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1635-1272G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769672 | |||||||
chr19:5769705 | G | A | 9 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(6): Show |
9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-1239G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769705 | |||||||
chr19:5769860 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(295): Show |
298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1635-1084A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769860 | |||||||
chr19:5769914 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(295): Show |
298 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1635-1030T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769914 | |||||||
chr19:5769963 | C | T | 1 | a0001c0016t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1635-981C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769963 | |||||||
chr19:5770076 | G | A | 2 | a0001c0001t0001g0197 a0026c0032t0001g0334 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1635-868G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770076 | |||||||
chr19:5770088 | C | CA | 13 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0300 others(10): Show |
13 | HG01175.hp2 HG01433.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1635-839dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5770088 | ||||||
chr19:5770112 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1635-832A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770112 | |||||||
chr19:5770168 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1635-776C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770168 | |||||||
chr19:5770190 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1635-754G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770190 | |||||||
chr19:5770235 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1635-709C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770235 | |||||||
chr19:5770258 | A | T | 9 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(6): Show |
9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-686A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770258 | |||||||
chr19:5770430 | C | CA | 26 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0162 others(23): Show |
26 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1635-498dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5770430 | ||||||
chr19:5770430 | C | CAA | 7 | a0001c0001t0001g0133 a0001c0016t0001g0083 a0001c0016t0001g0167 others(4): Show |
7 | HG01433.hp2 HG01934.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-499_1635-498d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5770430 | ||||||
chr19:5770459 | G | A | 1 | a0002c0002t0001g0199 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1635-485G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770459 | |||||||
chr19:5770536 | T | A | 3 | a0007c0012t0001g0156 a0007c0012t0001g0159 a0007c0012t0001g0160 |
3 | HG01515.hp1 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1635-408T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770536 | |||||||
chr19:5770598 | C | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0100 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1635-346C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770598 | |||||||
chr19:5770651 | C | T | 3 | a0004c0003t0001g0183 a0004c0003t0001g0238 a0004c0003t0001g0272 |
3 | NA19002.hp2 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1635-293C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770651 | |||||||
chr19:5770652 | G | A | 31 | a0001c0001t0001g0092 a0001c0001t0001g0130 a0001c0001t0001g0147 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.1635-292G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770652 | |||||||
chr19:5770713 | G | A | 1 | a0003c0005t0001g0274 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1635-231G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770713 | |||||||
chr19:5770720 | G | A | 4 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0002c0002t0001g0290 others(1): Show |
4 | HG01934.hp2 HG02015.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-224G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770720 | |||||||
chr19:5770751 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0131 others(3): Show |
6 | HG00280.hp1 HG00642.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635-193A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770751 | |||||||
chr19:5771114 | G | A | 5 | a0001c0001t0002g0311 a0001c0016t0001g0083 a0001c0016t0001g0167 others(2): Show |
5 | HG01934.hp2 HG02015.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1763+42G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771114 | |||||||
chr19:5771165 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0096 others(9): Show |
12 | HG00741.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763+93C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771165 | |||||||
chr19:5771177 | A | G | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1763+105A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771177 | |||||||
chr19:5771206 | G | T | 1 | a0004c0003t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1763+134G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771206 | |||||||
chr19:5771223 | A | G | 1 | a0011c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+151A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771223 | |||||||
chr19:5771229 | C | T | 1 | a0002c0002t0001g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1763+157C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771229 | |||||||
chr19:5771303 | C | T | 2 | a0002c0002t0001g0178 a0002c0002t0001g0217 |
2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1763+231C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771303 | |||||||
chr19:5771440 | G | A | 51 | a0002c0002t0001g0286 a0002c0002t0001g0321 a0004c0003t0001g0035 others(48): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1763+368G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771440 | |||||||
chr19:5771480 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1763+408C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771480 | |||||||
chr19:5771557 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1763+485C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771557 | |||||||
chr19:5771583 | C | CT | 22 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0133 others(19): Show |
22 | HG01175.hp1 HG01433.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1763+527dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5771583 | ||||||
chr19:5771583 | CT | C | 10 | a0001c0001t0001g0164 a0001c0001t0002g0311 a0002c0002t0001g0106 others(7): Show |
10 | HG00323.hp1 HG01175.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1763+527delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5771583 | ||||||
chr19:5771603 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1763+531C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771603 | |||||||
chr19:5771690 | C | T | 1 | a0011c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+618C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771690 | |||||||
chr19:5771717 | C | T | 1 | a0028c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1763+645C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771717 | |||||||
chr19:5771905 | A | C | 1 | a0004c0003t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1763+833A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771905 | |||||||
chr19:5772044 | CCTTTT | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0138 a0001c0001t0001g0146 |
3 | HG02818.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1764-743_1764-739d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772044 | |||||||
chr19:5772052 | C | CT | 11 | a0002c0002t0001g0283 a0003c0004t0001g0023 a0003c0004t0001g0059 others(8): Show |
11 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1764-723dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772052 | ||||||
chr19:5772052 | CT | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0100 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1764-723delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772052 | ||||||
chr19:5772101 | C | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(276): Show |
279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.1764-687C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772101 | |||||||
chr19:5772214 | A | AT | 100 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0047 others(97): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1764-543dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | A | ATT | 45 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0084 others(42): Show |
45 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1764-544_1764-543d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | A | ATTT | 12 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(9): Show |
12 | HG00642.hp1 HG01109.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1764-545_1764-543d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | A | ATTTTTT | 6 | a0001c0001t0002g0101 a0003c0004t0001g0064 a0003c0004t0001g0075 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1764-548_1764-543d others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | AT | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0096 others(17): Show |
20 | HG00140.hp1 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1764-543delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | ATT | A | 24 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0147 others(21): Show |
24 | HG00280.hp2 HG00544.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1764-544_1764-543d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0067 others(3): Show |
6 | HG01168.hp2 HG02004.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1764-552_1764-543d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | ATTTTTTT others(4): Show |
A | 10 | a0001c0001t0001g0146 a0004c0003t0001g0062 a0004c0003t0001g0238 others(7): Show |
10 | HG01928.hp1 HG02027.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1764-553_1764-543d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | ATTTTTTT others(5): Show |
A | 39 | a0004c0003t0001g0035 a0004c0003t0001g0039 a0004c0003t0001g0040 others(36): Show |
39 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1764-554_1764-543d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772214 | ATTTTTTT others(9): Show |
A | 2 | a0003c0004t0001g0060 a0003c0004t0001g0325 |
2 | HG00438.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1764-558_1764-543d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | ||||||
chr19:5772239 | T | G | 1 | a0004c0003t0001g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1764-549T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772239 | |||||||
chr19:5772259 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1764-529G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772259 | |||||||
chr19:5772284 | G | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0044 a0001c0001t0001g0047 others(27): Show |
30 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1764-504G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772284 | |||||||
chr19:5772313 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(278): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1764-475T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772313 | |||||||
chr19:5772314 | G | A | 51 | a0004c0003t0001g0035 a0004c0003t0001g0039 a0004c0003t0001g0040 others(48): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1764-474G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772314 | |||||||
chr19:5772328 | C | T | 51 | a0001c0001t0001g0139 a0004c0003t0001g0035 a0004c0003t0001g0039 others(48): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1764-460C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772328 | |||||||
chr19:5772352 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1764-436C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772352 | |||||||
chr19:5772365 | T | C | 15 | a0004c0003t0001g0054 a0004c0003t0001g0062 a0004c0003t0001g0071 others(12): Show |
15 | HG00438.hp2 HG00544.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1764-423T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772365 | |||||||
chr19:5772375 | C | A | 1 | a0002c0002t0001g0053 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1764-413C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772375 | |||||||
chr19:5772389 | G | T | 3 | a0003c0004t0001g0094 a0003c0004t0001g0333 a0027c0020t0001g0030 |
3 | HG02886.hp1 HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1764-399G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772389 | |||||||
chr19:5772448 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1764-340C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772448 | |||||||
chr19:5772474 | G | A | 1 | a0006c0007t0001g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1764-314G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772474 | |||||||
chr19:5772516 | C | T | 2 | a0001c0001t0002g0101 a0006c0007t0001g0028 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1764-272C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772516 | |||||||
chr19:5772729 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1764-59C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772729 | |||||||
chr19:5773177 | G | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(278): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1941+212G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773177 | |||||||
chr19:5773221 | G | A | 2 | a0002c0002t0001g0221 a0002c0002t0001g0250 |
2 | HG00323.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1941+256G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773221 | |||||||
chr19:5773328 | T | C | 12 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0003c0004t0001g0023 others(9): Show |
12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1941+363T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773328 | |||||||
chr19:5773466 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0192 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1941+501A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773466 | |||||||
chr19:5773582 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1941+617G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773582 | |||||||
chr19:5773678 | A | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(278): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1941+713A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773678 | |||||||
chr19:5773693 | CT | C | 199 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0043 others(196): Show |
199 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1941+745delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773693 | ||||||
chr19:5773693 | CTT | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(25): Show |
28 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1941+744_1941+745d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773693 | ||||||
chr19:5773773 | T | C | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1941+808T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773773 | |||||||
chr19:5773774 | C | T | 1 | a0002c0002t0001g0283 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1941+809C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773774 | |||||||
chr19:5773884 | C | T | 1 | a0004c0003t0001g0040 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1941+919C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773884 | |||||||
chr19:5773968 | C | CT | 200 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0043 others(197): Show |
200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1941+1020dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773968 | ||||||
chr19:5773968 | C | CTT | 12 | a0001c0001t0001g0154 a0001c0001t0001g0164 a0001c0001t0001g0203 others(9): Show |
12 | HG01175.hp2 HG01255.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1941+1019_1941+102 others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773968 | ||||||
chr19:5773968 | CT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(46): Show |
49 | HG00280.hp2 HG00544.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1941+1020delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773968 | ||||||
chr19:5774029 | G | A | 1 | a0004c0003t0003g0109 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1941+1064G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774029 | |||||||
chr19:5774129 | G | C | 1 | a0021c0036t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1941+1164G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774129 | |||||||
chr19:5774209 | G | A | 2 | a0001c0016t0001g0083 a0001c0016t0001g0167 |
2 | HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1941+1244G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774209 | |||||||
chr19:5774366 | T | G | 1 | a0002c0002t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1941+1401T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774366 | |||||||
chr19:5774603 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(23): Show |
26 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1942-1558C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774603 | |||||||
chr19:5774613 | T | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(310): Show |
313 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.1942-1548T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774613 | |||||||
chr19:5774675 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-1486C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774675 | |||||||
chr19:5774715 | AAAAT | A | 11 | a0001c0016t0001g0083 a0001c0016t0001g0167 a0003c0004t0001g0023 others(8): Show |
11 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1942-1434_1942-143 others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5774715 | ||||||
chr19:5774932 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-1229G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774932 | |||||||
chr19:5775303 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0162 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1942-858G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775303 | |||||||
chr19:5775326 | G | C | 58 | a0003c0004t0001g0048 a0003c0004t0001g0059 a0003c0004t0001g0060 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1942-835G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775326 | |||||||
chr19:5775481 | C | CA | 15 | a0001c0001t0001g0092 a0001c0001t0001g0131 a0001c0001t0001g0134 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1942-662dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775481 | ||||||
chr19:5775481 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1942-662delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775481 | ||||||
chr19:5775481 | CAA | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1942-663_1942-662d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775481 | ||||||
chr19:5775523 | C | T | 1 | a0034c0028t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1942-638C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775523 | |||||||
chr19:5775598 | G | A | 148 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0096 others(145): Show |
148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1942-563G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775598 | |||||||
chr19:5775599 | A | C | 111 | a0003c0004t0001g0048 a0003c0004t0001g0059 a0003c0004t0001g0060 others(108): Show |
111 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1942-562A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775599 | |||||||
chr19:5775624 | G | A | 1 | a0003c0004t0001g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1942-537G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775624 | |||||||
chr19:5775648 | C | CA | 99 | a0002c0027t0001g0291 a0003c0004t0001g0048 a0003c0004t0001g0060 others(96): Show |
99 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1942-494dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775648 | ||||||
chr19:5775648 | C | CAA | 41 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0096 others(38): Show |
41 | HG01515.hp1 HG01517.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1942-495_1942-494d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775648 | ||||||
chr19:5775648 | CA | C | 20 | a0001c0001t0002g0101 a0001c0001t0004g0056 a0001c0016t0001g0083 others(17): Show |
20 | HG00323.hp1 HG01884.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.1942-494delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775648 | ||||||
chr19:5775664 | A | G | 2 | a0001c0016t0001g0083 a0001c0016t0001g0167 |
2 | HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1942-497A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775664 | |||||||
chr19:5775699 | G | A | 1 | a0004c0003t0001g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1942-462G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775699 | |||||||
chr19:5775827 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-334C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775827 | |||||||
chr19:5775835 | G | A | 9 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(6): Show |
9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1942-326G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775835 | |||||||
chr19:5775900 | C | G | 6 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0095 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1942-261C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775900 | |||||||
chr19:5775926 | C | T | 2 | a0002c0002t0001g0184 a0002c0002t0001g0216 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1942-235C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775926 | |||||||
chr19:5776038 | G | C | 1 | a0003c0005t0001g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1942-123G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5776038 | |||||||
chr19:5776052 | C | T | 110 | a0003c0004t0001g0048 a0003c0004t0001g0059 a0003c0004t0001g0060 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1942-109C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5776052 | |||||||
chr19:5776089 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1942-72G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5776089 | |||||||
chr19:5776360 | C | T | 4 | a0003c0004t0001g0094 a0003c0004t0001g0333 a0027c0020t0001g0030 others(1): Show |
4 | HG02886.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2096+45C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776360 | |||||||
chr19:5776380 | T | G | 5 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0001g0138 others(2): Show |
5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096+65T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776380 | |||||||
chr19:5776383 | G | A | 1 | a0001c0016t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2096+68G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776383 | |||||||
chr19:5776416 | C | T | 55 | a0003c0004t0001g0094 a0003c0004t0001g0333 a0004c0003t0001g0035 others(52): Show |
55 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2096+101C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776416 | |||||||
chr19:5776423 | C | T | 1 | a0021c0036t0001g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2096+108C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776423 | |||||||
chr19:5776432 | C | G | 3 | a0001c0001t0002g0101 a0001c0016t0001g0083 a0001c0016t0001g0167 |
3 | HG01884.hp1 HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2096+117C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776432 | |||||||
chr19:5776482 | T | A | 1 | a0003c0004t0001g0059 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2096+167T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776482 | |||||||
chr19:5776548 | G | A | 1 | a0011c0011t0001g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2096+233G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776548 | |||||||
chr19:5776788 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2096+473C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776788 | |||||||
chr19:5776837 | C | T | 6 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0095 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096+522C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776837 | |||||||
chr19:5776870 | T | G | 51 | a0004c0003t0001g0035 a0004c0003t0001g0039 a0004c0003t0001g0040 others(48): Show |
51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2096+555T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776870 | |||||||
chr19:5776877 | C | CA | 27 | a0001c0001t0001g0164 a0001c0001t0002g0095 a0001c0001t0002g0101 others(24): Show |
27 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.2096+579dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5776877 | ||||||
chr19:5776877 | CA | C | 18 | a0001c0001t0001g0022 a0001c0001t0001g0186 a0001c0001t0001g0187 others(15): Show |
18 | HG01109.hp2 HG01169.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2096+579delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5776877 | ||||||
chr19:5776935 | C | T | 10 | a0004c0003t0001g0062 a0004c0003t0001g0120 a0004c0003t0001g0237 others(7): Show |
10 | HG01928.hp1 NA18952.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.2096+620C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776935 | |||||||
chr19:5776947 | A | G | 14 | a0003c0004t0001g0060 a0003c0004t0001g0141 a0003c0004t0001g0200 others(11): Show |
14 | HG00438.hp1 HG00609.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.2096+632A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776947 | |||||||
chr19:5776954 | A | G | 6 | a0001c0001t0002g0057 a0001c0001t0002g0093 a0001c0001t0002g0095 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096+639A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776954 | |||||||
chr19:5776958 | T | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0192 others(4): Show |
7 | HG00741.hp2 HG02257.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2096+643T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776958 | |||||||
chr19:5777120 | A | C | 4 | a0014c0017t0002g0193 a0014c0017t0002g0194 a0015c0014t0002g0010 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2096+805A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777120 | |||||||
chr19:5777223 | T | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0001g0138 others(2): Show |
5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096+908T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777223 | |||||||
chr19:5777226 | T | TGCCTTCT others(11): Show |
5 | a0003c0004t0001g0207 a0003c0004t0001g0222 a0003c0004t0001g0235 others(2): Show |
5 | HG00609.hp1 HG02027.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096+912_2096+929d others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5777226 | ||||||
chr19:5777265 | G | A | 2 | a0001c0001t0001g0024 a0005c0006t0001g0229 |
2 | HG01934.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2096+950G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777265 | |||||||
chr19:5777304 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2096+989T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777304 | |||||||
chr19:5777312 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
177 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.2096+997A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777312 | |||||||
chr19:5777404 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(164): Show |
167 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.2097-972T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777404 | |||||||
chr19:5777463 | G | C | 1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2097-913G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777463 | |||||||
chr19:5777559 | G | C | 9 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(6): Show |
9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2097-817G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777559 | |||||||
chr19:5777614 | A | G | 9 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(6): Show |
9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2097-762A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777614 | |||||||
chr19:5777767 | C | T | 1 | a0004c0003t0001g0295 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2097-609C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777767 | |||||||
chr19:5777856 | T | C | 113 | a0001c0001t0002g0101 a0003c0004t0001g0048 a0003c0004t0001g0059 others(110): Show |
113 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2097-520T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777856 | |||||||
chr19:5778058 | T | G | 1 | a0002c0002t0001g0271 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2097-318T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778058 | |||||||
chr19:5778066 | C | T | 8 | a0003c0004t0001g0023 a0003c0004t0001g0064 a0003c0004t0001g0075 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2097-310C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778066 | |||||||
chr19:5778115 | G | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0001g0138 others(2): Show |
5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2097-261G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778115 | |||||||
chr19:5778139 | G | C | 16 | a0001c0001t0002g0026 a0001c0001t0002g0057 a0001c0001t0002g0093 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2097-237G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778139 | |||||||
chr19:5778156 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2097-220G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778156 | |||||||
chr19:5778196 | G | A | 23 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0096 others(20): Show |
23 | HG01515.hp1 HG01517.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2097-180G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778196 | |||||||
chr19:5778207 | C | CA | 105 | a0001c0001t0001g0022 a0001c0001t0001g0088 a0001c0001t0001g0092 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2097-152dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5778207 | ||||||
chr19:5778331 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2097-45C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778331 | |||||||
chr19:5778333 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2097-43A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778333 |