Item | Value |
---|---|
geneid | 57545 |
ensemblid | ENSG00000048342.18 |
hgncid | 29253 |
symbol | CC2D2A |
name | coiled-coil and C2 domain containing 2A |
refseq_nuc | NM_001378615.1 |
refseq_prot | NP_001365544.1 |
ensembl_nuc | ENST00000424120.6 |
ensembl_prot | ENSP00000403465.1 |
mane_status | MANE Select |
chr | chr4 |
start | 15469882 |
end | 15601552 |
strand | + |
ver | v1.2 |
region | chr4:15469882-15601552 |
region5000 | chr4:15464882-15606552 |
regionname0 | CC2D2A_chr4_15469882_15601552 |
regionname5000 | CC2D2A_chr4_15464882_15606552 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1620 | 262 | 73 | 42 | 99 | 12 | 34 | 77 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0002 | 0/0 | 1620 | 45 | 3 | 9 | 29 | 0 | 4 | 21 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0003 | 0/0 | 1619 | 11 | 1 | 5 | 0 | 2 | 3 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1614): Show |
chr4 | 15464882 | 15606552 |
a0004 | 0/0 | 1620 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0005 | 0/0 | 1620 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0006 | 0/0 | 1620 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0007 | 0/0 | 1620 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0008 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0009 | 0/0 | 1620 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0010 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0011 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0012 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0013 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0014 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0015 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0016 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0017 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0018 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0019 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0020 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0021 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
a0022 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | MNPRE others(1615): Show |
chr4 | 15464882 | 15606552 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4860 | 177 | 58 | 34 | 44 | 10 | 29 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0002 | 0/0 | 4860 | 43 | 2 | 1 | 40 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0004 | 0/0 | 4860 | 22 | 4 | 6 | 6 | 2 | 4 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0006 | 0/0 | 4860 | 11 | 4 | 1 | 5 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0008 | 0/0 | 4860 | 6 | 3 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0015 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0024 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0001c0026 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0002c0003 | 0/0 | 4860 | 34 | 2 | 8 | 22 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0002c0005 | 0/0 | 4860 | 11 | 1 | 1 | 7 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0003c0007 | 0/0 | 4857 | 9 | 1 | 4 | 0 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4852): Show |
chr4 | 15464882 | 15606552 | ||
a0003c0010 | 0/0 | 4857 | 2 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4852): Show |
chr4 | 15464882 | 15606552 | ||
a0004c0013 | 0/0 | 4860 | 2 | 1 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0004c0022 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0005c0011 | 0/0 | 4860 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0005c0032 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0006c0009 | 0/0 | 4860 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0007c0012 | 0/0 | 4860 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0008c0029 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0009c0033 | 0/0 | 4860 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0010c0019 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0011c0030 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0012c0027 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0013c0031 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0014c0025 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0015c0018 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0016c0016 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0017c0023 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0018c0017 | 0/0 | 4860 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0019c0021 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0020c0020 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0021c0014 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 | ||
a0022c0028 | 0/0 | 4860 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | ATGAA others(4855): Show |
chr4 | 15464882 | 15606552 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5184 | 138 | 34 | 28 | 41 | 8 | 27 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0001t0002 | 1/1 | 5184 | 39 | 24 | 6 | 3 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0002t0001 | 0/0 | 5184 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0002t0002 | 0/0 | 5184 | 40 | 2 | 1 | 37 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0004t0002 | 0/0 | 5184 | 22 | 4 | 6 | 6 | 2 | 4 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0006t0001 | 0/0 | 5184 | 8 | 2 | 0 | 5 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0006t0002 | 0/0 | 5184 | 3 | 2 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0008t0002 | 0/0 | 5184 | 6 | 3 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0015t0001 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0024t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0001c0026t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0002c0003t0001 | 0/0 | 5184 | 22 | 2 | 4 | 14 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0002c0003t0002 | 0/0 | 5184 | 12 | 0 | 4 | 8 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0002c0005t0001 | 0/0 | 5184 | 9 | 1 | 1 | 6 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0002c0005t0002 | 0/0 | 5184 | 2 | 0 | 0 | 1 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0003c0007t0002 | 0/0 | 5181 | 9 | 1 | 4 | 0 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5176): Show |
chr4 | 15464882 | 15606552 |
a0003c0010t0002 | 0/0 | 5181 | 2 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5176): Show |
chr4 | 15464882 | 15606552 |
a0004c0013t0003 | 0/0 | 5184 | 2 | 1 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0004c0022t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0005c0011t0001 | 0/0 | 5184 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0005c0032t0001 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0006c0009t0002 | 0/0 | 5184 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0007c0012t0002 | 0/0 | 5184 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0008c0029t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0009c0033t0001 | 0/0 | 5184 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0010c0019t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0011c0030t0002 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0012c0027t0002 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0013c0031t0001 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0014c0025t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0015c0018t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0016c0016t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0017c0023t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0018c0017t0002 | 0/0 | 5184 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0019c0021t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0020c0020t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0021c0014t0002 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
a0022c0028t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | AAGCT others(5179): Show |
chr4 | 15464882 | 15606552 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0001t0002g0323 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0004t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0006t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0008t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0008t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0008t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0008t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0008t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0015t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0024t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0001c0026t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0002c0005t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0007t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0010t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0003c0010t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0004c0013t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0004c0013t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0004c0022t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0005c0011t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0005c0032t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0006c0009t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0006c0009t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0006c0009t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0007c0012t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0007c0012t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0008c0029t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0009c0033t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0010c0019t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0011c0030t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0012c0027t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0013c0031t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0014c0025t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0015c0018t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0016c0016t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0017c0023t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0018c0017t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0019c0021t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0020c0020t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0021c0014t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
a0022c0028t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00140 | hp1 | a0003 | c0007 | t0002 | g0077 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00280 | hp2 | a0001 | c0004 | t0002 | g0059 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00323 | hp1 | a0001 | c0004 | t0002 | g0073 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00408 | hp1 | a0001 | c0006 | t0001 | g0270 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00438 | hp1 | a0002 | c0003 | t0002 | g0302 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00438 | hp2 | a0001 | c0004 | t0002 | g0090 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00558 | hp2 | a0002 | c0003 | t0001 | g0298 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0290 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00609 | hp2 | a0008 | c0029 | t0001 | g0005 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00735 | hp1 | a0001 | c0004 | t0002 | g0060 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01070 | hp2 | a0003 | c0007 | t0002 | g0085 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01081 | hp1 | a0001 | c0006 | t0002 | g0267 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01109 | hp1 | a0004 | c0013 | t0003 | g0140 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01109 | hp2 | a0003 | c0010 | t0002 | g0087 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01167 | hp2 | a0002 | c0003 | t0001 | g0297 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0332 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01243 | hp2 | a0001 | c0004 | t0002 | g0097 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01255 | hp1 | a0002 | c0003 | t0002 | g0277 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01255 | hp2 | a0001 | c0004 | t0002 | g0075 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01257 | hp1 | a0002 | c0003 | t0001 | g0279 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01346 | hp2 | a0001 | c0004 | t0002 | g0098 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01358 | hp1 | a0001 | c0004 | t0002 | g0095 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01358 | hp2 | a0002 | c0003 | t0002 | g0276 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01433 | hp1 | a0002 | c0003 | t0002 | g0275 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01433 | hp2 | a0002 | c0005 | t0001 | g0038 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01515 | hp1 | a0003 | c0007 | t0002 | g0080 | EUR | IBS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0197 | EUR | IBS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01934 | hp1 | a0002 | c0003 | t0002 | g0278 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0274 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01978 | hp1 | a0003 | c0007 | t0002 | g0088 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01978 | hp2 | a0009 | c0033 | t0001 | g0304 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01993 | hp2 | a0003 | c0007 | t0002 | g0084 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02015 | hp1 | a0002 | c0003 | t0001 | g0299 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02015 | hp2 | a0010 | c0019 | t0001 | g0188 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02027 | hp2 | a0001 | c0004 | t0002 | g0093 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0294 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02040 | hp2 | a0001 | c0006 | t0001 | g0273 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02055 | hp2 | a0001 | c0015 | t0001 | g0222 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02056 | hp1 | a0002 | c0003 | t0001 | g0292 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02071 | hp1 | a0001 | c0006 | t0001 | g0272 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02071 | hp2 | a0011 | c0030 | t0002 | g0147 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02132 | hp1 | a0002 | c0005 | t0001 | g0241 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02132 | hp2 | a0012 | c0027 | t0002 | g0151 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02148 | hp1 | a0003 | c0007 | t0002 | g0086 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0295 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02257 | hp2 | a0007 | c0012 | t0002 | g0020 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02280 | hp1 | a0001 | c0004 | t0002 | g0334 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02602 | hp2 | a0003 | c0007 | t0002 | g0081 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02622 | hp1 | a0005 | c0032 | t0001 | g0284 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02647 | hp1 | a0001 | c0024 | t0002 | g0204 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02683 | hp1 | a0001 | c0004 | t0002 | g0099 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02698 | hp2 | a0002 | c0005 | t0002 | g0076 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02723 | hp1 | a0005 | c0011 | t0001 | g0001 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02809 | hp1 | a0001 | c0004 | t0002 | g0029 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02809 | hp2 | a0004 | c0022 | t0002 | g0018 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0266 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02886 | hp2 | a0007 | c0012 | t0002 | g0021 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02895 | hp2 | a0001 | c0008 | t0002 | g0007 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02896 | hp1 | a0001 | c0008 | t0002 | g0007 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02897 | hp1 | a0001 | c0008 | t0002 | g0283 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02965 | hp2 | a0014 | c0025 | t0002 | g0032 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0027 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02976 | hp2 | a0015 | c0018 | t0002 | g0046 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03017 | hp1 | a0001 | c0004 | t0002 | g0096 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03098 | hp1 | a0016 | c0016 | t0002 | g0320 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03130 | hp1 | a0001 | c0006 | t0002 | g0310 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03209 | hp2 | a0017 | c0023 | t0002 | g0012 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03239 | hp1 | a0003 | c0010 | t0002 | g0082 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03453 | hp1 | a0001 | c0006 | t0001 | g0286 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03516 | hp1 | a0001 | c0006 | t0002 | g0308 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03579 | hp1 | a0005 | c0011 | t0001 | g0001 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03654 | hp2 | a0018 | c0017 | t0002 | g0061 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03669 | hp1 | a0001 | c0004 | t0002 | g0063 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03710 | hp1 | a0001 | c0004 | t0002 | g0071 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03710 | hp2 | a0002 | c0005 | t0001 | g0336 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03831 | hp1 | a0001 | c0006 | t0001 | g0271 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0296 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0303 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04228 | hp1 | a0003 | c0007 | t0002 | g0083 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18522 | hp2 | a0019 | c0021 | t0002 | g0035 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18942 | hp1 | a0020 | c0020 | t0001 | g0317 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18943 | hp1 | a0021 | c0014 | t0002 | g0138 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18951 | hp1 | a0002 | c0003 | t0002 | g0291 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0281 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18974 | hp1 | a0002 | c0003 | t0002 | g0306 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18975 | hp2 | a0001 | c0008 | t0002 | g0293 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18977 | hp1 | a0001 | c0004 | t0002 | g0057 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18981 | hp2 | a0002 | c0003 | t0001 | g0315 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18983 | hp1 | a0002 | c0003 | t0002 | g0301 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18985 | hp1 | a0002 | c0003 | t0002 | g0287 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18990 | hp1 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18994 | hp2 | a0001 | c0004 | t0002 | g0094 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19005 | hp2 | a0002 | c0005 | t0001 | g0319 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19006 | hp1 | a0002 | c0005 | t0002 | g0240 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19006 | hp2 | a0002 | c0003 | t0001 | g0269 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19009 | hp2 | a0002 | c0003 | t0001 | g0314 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0028 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0311 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19056 | hp2 | a0002 | c0005 | t0001 | g0242 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19057 | hp1 | a0006 | c0009 | t0002 | g0232 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19057 | hp2 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19058 | hp1 | a0002 | c0003 | t0002 | g0282 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19066 | hp1 | a0001 | c0004 | t0002 | g0091 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19066 | hp2 | a0002 | c0003 | t0002 | g0289 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19067 | hp1 | a0002 | c0003 | t0002 | g0307 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19067 | hp2 | a0006 | c0009 | t0002 | g0231 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19068 | hp1 | a0006 | c0009 | t0002 | g0328 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19078 | hp1 | a0002 | c0005 | t0001 | g0203 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19078 | hp2 | a0001 | c0004 | t0002 | g0092 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19080 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19082 | hp2 | a0001 | c0008 | t0002 | g0305 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19088 | hp2 | a0002 | c0005 | t0001 | g0239 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19090 | hp2 | a0001 | c0026 | t0001 | g0237 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA19091 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20129 | hp1 | a0004 | c0013 | t0003 | g0139 | AFR | ASW | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20129 | hp2 | a0001 | c0006 | t0001 | g0309 | AFR | ASW | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | GIH | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | GIH | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG01123 | hp2 | a0001 | c0004 | t0002 | g0074 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02109 | hp1 | a0001 | c0004 | t0002 | g0254 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02486 | hp2 | a0003 | c0007 | t0002 | g0078 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02559 | hp1 | a0013 | c0031 | t0001 | g0285 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18955 | hp1 | a0001 | c0008 | t0002 | g0288 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA18955 | hp2 | a0022 | c0028 | t0001 | g0255 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0049 | REF | REF | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0323 | REF | REF | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15480737 | G | A | 1 | a0021 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.157G>A | p.Glu53Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/37 | 351/5184 | 157/4863 | 53/1620 | chr4 | 15480737 | |||
chr4:15502513 | C | T | 1 | a0011 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.332C>T | p.Ala111Val | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/37 | 526/5184 | 332/4863 | 111/1620 | chr4 | 15502513 | |||
chr4:15510159 | G | T | 1 | a0008 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.459G>T | p.Arg153Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/37 | 653/5184 | 459/4863 | 153/1620 | chr4 | 15510159 | |||
chr4:15511269 | C | T | 1 | a0022 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.563C>T | p.Ala188Val | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/37 | 757/5184 | 563/4863 | 188/1620 | chr4 | 15511269 | |||
chr4:15511381 | GGAA | G | 1 | a0003 | 11 | HG00140.hp1 HG01070.hp2 HG01109.hp2 others(8): Show |
conservative_inframe_deletion | MODERATE | c.685_687delGAA | p.Glu229del | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/37 | 879/5184 | 685/4863 | 229/1620 | INFO_REALIGN_3_PRIME | chr4 | 15511381 | ||
chr4:15514710 | G | A | 1 | a0016 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.721G>A | p.Glu241Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/37 | 915/5184 | 721/4863 | 241/1620 | chr4 | 15514710 | |||
chr4:15515909 | T | C | 1 | a0018 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.922T>C | p.Phe308Leu | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/37 | 1116/5184 | 922/4863 | 308/1620 | chr4 | 15515909 | |||
chr4:15516734 | A | C | 3 | a0002 a0008 a0009 |
47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
missense_variant | MODERATE | c.1127A>C | p.Glu376Ala | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/37 | 1321/5184 | 1127/4863 | 376/1620 | chr4 | 15516734 | |||
chr4:15538112 | G | A | 1 | a0015 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1978G>A | p.Val660Ile | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/37 | 2172/5184 | 1978/4863 | 660/1620 | chr4 | 15538112 | |||
chr4:15540848 | C | T | 1 | a0009 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2015C>T | p.Ser672Leu | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/37 | 2209/5184 | 2015/4863 | 672/1620 | chr4 | 15540848 | |||
chr4:15540883 | T | A | 1 | a0015 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2050T>A | p.Leu684Ile | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/37 | 2244/5184 | 2050/4863 | 684/1620 | chr4 | 15540883 | |||
chr4:15550839 | G | A | 2 | a0010 a0013 |
2 | HG02015.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.2197G>A | p.Gly733Arg | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/37 | 2391/5184 | 2197/4863 | 733/1620 | chr4 | 15550839 | |||
chr4:15550925 | A | C | 1 | a0014 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2283A>C | p.Glu761Asp | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/37 | 2477/5184 | 2283/4863 | 761/1620 | chr4 | 15550925 | |||
chr4:15553256 | G | A | 1 | a0012 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.2437G>A | p.Gly813Arg | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/37 | 2631/5184 | 2437/4863 | 813/1620 | chr4 | 15553256 | |||
chr4:15559217 | T | C | 1 | a0020 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2882T>C | p.Ile961Thr | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/37 | 3076/5184 | 2882/4863 | 961/1620 | chr4 | 15559217 | |||
chr4:15559247 | A | G | 1 | a0017 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2912A>G | p.Tyr971Cys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/37 | 3106/5184 | 2912/4863 | 971/1620 | chr4 | 15559247 | |||
chr4:15563386 | G | A | 1 | a0005 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.3046G>A | p.Glu1016Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/37 | 3240/5184 | 3046/4863 | 1016/1620 | chr4 | 15563386 | |||
chr4:15570411 | G | A | 2 | a0004 a0019 |
4 | HG01109.hp1 HG02809.hp2 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.3509G>A | p.Arg1170Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/37 | 3703/5184 | 3509/4863 | 1170/1620 | chr4 | 15570411 | |||
chr4:15580121 | C | A | 1 | a0019 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3925C>A | p.Pro1309Thr | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/37 | 4119/5184 | 3925/4863 | 1309/1620 | chr4 | 15580121 | |||
chr4:15589567 | C | G | 1 | a0006 | 3 | NA19057.hp1 NA19067.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.4202C>G | p.Thr1401Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/37 | 4396/5184 | 4202/4863 | 1401/1620 | chr4 | 15589567 | |||
chr4:15597428 | C | T | 1 | a0007 | 2 | HG02257.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.4459C>T | p.Arg1487Cys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/37 | 4653/5184 | 4459/4863 | 1487/1620 | chr4 | 15597428 | |||
chr4:15601264 | T | A | 1 | a0013 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4702T>A | p.Tyr1568Asn | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 37/37 | 4896/5184 | 4702/4863 | 1568/1620 | chr4 | 15601264 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15480736 | C | T | 6 | a0001c0006 a0001c0008 a0002c0003 others(3): Show |
54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
synonymous_variant | LOW | c.156C>T | p.Ser52Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/37 | 350/5184 | 156/4863 | 52/1620 | chr4 | 15480736 | |||
chr4:15502840 | T | C | 1 | a0001c0015 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.355T>C | p.Leu119Leu | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/37 | 549/5184 | 355/4863 | 119/1620 | chr4 | 15502840 | |||
chr4:15514766 | C | T | 6 | a0001c0002 a0001c0008 a0004c0013 others(3): Show |
54 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.777C>T | p.His259His | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/37 | 971/5184 | 777/4863 | 259/1620 | chr4 | 15514766 | |||
chr4:15514775 | C | T | 1 | a0001c0026 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.786C>T | p.Asp262Asp | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/37 | 980/5184 | 786/4863 | 262/1620 | chr4 | 15514775 | |||
chr4:15553294 | C | T | 1 | a0001c0024 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2475C>T | p.Ile825Ile | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/37 | 2669/5184 | 2475/4863 | 825/1620 | chr4 | 15553294 | |||
chr4:15567395 | G | A | 8 | a0001c0004 a0003c0007 a0004c0013 others(5): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
synonymous_variant | LOW | c.3201G>A | p.Ser1067Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 25/37 | 3395/5184 | 3201/4863 | 1067/1620 | chr4 | 15567395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15469989 | G | A | 1 | a0004c0013t0003 | 2 | HG01109.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-87G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/37 | 5944 | chr4 | 15469989 | ||||||
chr4:15601446 | G | C | 15 | a0001c0001t0001 a0001c0002t0001 a0001c0006t0001 others(12): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 37/37 | 21 | chr4 | 15601446 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:15470094 | G | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
40 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.-19+37G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470094 | |||||||
chr4:15470306 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-19+249C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470306 | |||||||
chr4:15470457 | A | G | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+400A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470457 | |||||||
chr4:15470602 | C | G | 1 | a0001c0001t0001g0337 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19+545C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470602 | |||||||
chr4:15470649 | A | ATC | 10 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG01106.hp1 HG01192.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+632_-19+633dup others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | ||||||
chr4:15470649 | A | ATCTC | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0333 others(2): Show |
5 | HG01123.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+630_-19+633dup others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | ||||||
chr4:15470649 | A | ATCTCTC | 5 | a0001c0001t0001g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG01433.hp2 HG03195.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+628_-19+633dup others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | ||||||
chr4:15470649 | A | ATCTCTCT others(3): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-19+624_-19+633dup others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | ||||||
chr4:15470649 | A | ATCTCTCT others(5): Show |
1 | a0001c0001t0001g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19+622_-19+633dup others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | ||||||
chr4:15470649 | A | ATCTCTCT others(7): Show |
1 | a0001c0001t0001g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+620_-19+633dup others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | ||||||
chr4:15470671 | CTCTCTCT others(35): Show |
C | 1 | a0001c0001t0001g0048 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-19+616_-19+657del others(42): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470671 | ||||||
chr4:15470673 | CTCTCTCT others(29): Show |
C | 1 | a0001c0001t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19+618_-19+653del others(36): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470673 | ||||||
chr4:15470675 | CTCTCTCT others(27): Show |
C | 3 | a0001c0001t0001g0263 a0001c0001t0002g0200 a0001c0001t0002g0212 |
3 | HG01952.hp1 HG02293.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-19+620_-19+653del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470675 | ||||||
chr4:15470677 | CTCTCTCT others(11): Show |
C | 1 | a0001c0002t0002g0115 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-19+622_-19+639del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470677 | ||||||
chr4:15470677 | CTCTCTCT others(25): Show |
C | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0221 others(5): Show |
8 | NA18945.hp2 NA18959.hp1 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+622_-19+653del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470677 | ||||||
chr4:15470677 | CTCTCTCT others(27): Show |
C | 8 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0235 others(5): Show |
8 | HG00733.hp1 HG01099.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+622_-19+655del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470677 | ||||||
chr4:15470679 | CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-19+624_-19+637del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | ||||||
chr4:15470679 | CTCTCTCT others(13): Show |
C | 1 | a0001c0002t0001g0112 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-19+624_-19+643del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | ||||||
chr4:15470679 | CTCTCTCT others(15): Show |
C | 1 | a0001c0002t0002g0130 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-19+624_-19+645del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | ||||||
chr4:15470679 | CTCTCTCT others(17): Show |
C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0072 |
2 | HG01099.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-19+624_-19+647del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | ||||||
chr4:15470679 | CTCTCTCT others(25): Show |
C | 5 | a0001c0001t0001g0220 a0001c0001t0001g0258 a0001c0001t0001g0261 others(2): Show |
5 | HG00735.hp2 HG02055.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+624_-19+655del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | ||||||
chr4:15470679 | CTCTCTCT others(27): Show |
C | 15 | a0001c0001t0001g0106 a0001c0001t0001g0198 a0001c0001t0001g0201 others(12): Show |
15 | HG00099.hp2 HG00408.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+624_-19+657del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | ||||||
chr4:15470681 | CTCTCTCT others(7): Show |
C | 2 | a0001c0002t0002g0135 a0001c0002t0002g0136 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-19+626_-19+639del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(11): Show |
C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0120 a0001c0001t0001g0126 others(2): Show |
5 | HG03017.hp2 NA18906.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+626_-19+643del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19+626_-19+645del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(15): Show |
C | 2 | a0001c0004t0002g0090 a0001c0024t0002g0204 |
2 | HG00438.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-19+626_-19+647del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(17): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0067 |
3 | HG01167.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-19+626_-19+649del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(21): Show |
C | 1 | a0001c0006t0002g0310 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19+626_-19+653del others(28): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(25): Show |
C | 8 | a0001c0001t0001g0180 a0001c0001t0001g0196 a0001c0001t0001g0217 others(5): Show |
8 | HG01515.hp2 NA18948.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+626_-19+657del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(27): Show |
C | 13 | a0001c0001t0001g0104 a0001c0001t0001g0199 a0001c0001t0001g0215 others(10): Show |
13 | HG03239.hp2 HG03942.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+626_-19+659del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470681 | CTCTCTCT others(29): Show |
C | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-19+626_-19+661del others(36): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | ||||||
chr4:15470683 | CTCTCTCT others(5): Show |
C | 2 | a0001c0001t0001g0017 a0001c0002t0002g0114 |
2 | HG00558.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-19+628_-19+639del others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(7): Show |
C | 1 | a0021c0014t0002g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-19+628_-19+641del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(11): Show |
C | 3 | a0001c0001t0001g0051 a0001c0002t0002g0122 a0001c0002t0002g0159 |
3 | HG02165.hp2 HG03486.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-19+628_-19+645del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(13): Show |
C | 4 | a0001c0001t0002g0161 a0001c0001t0002g0322 a0001c0002t0002g0100 others(1): Show |
4 | HG02145.hp1 NA18954.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+628_-19+647del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(15): Show |
C | 4 | a0001c0001t0001g0058 a0001c0004t0002g0093 a0004c0013t0003g0139 others(1): Show |
4 | HG00639.hp1 HG01109.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+628_-19+649del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(19): Show |
C | 1 | a0001c0004t0002g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-19+628_-19+653del others(26): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(27): Show |
C | 10 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0250 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+628_-19+661del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470683 | CTCTCTCT others(31): Show |
C | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+628_-19+665del others(38): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | ||||||
chr4:15470685 | CTCTCTAT others(5): Show |
C | 1 | a0002c0003t0001g0300 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-19+630_-19+641del others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(9): Show |
C | 2 | a0001c0002t0001g0137 a0001c0002t0002g0133 |
2 | NA19004.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-19+630_-19+645del others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(11): Show |
C | 7 | a0001c0001t0002g0054 a0001c0002t0002g0118 a0001c0002t0002g0125 others(4): Show |
7 | HG00597.hp2 HG01106.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+630_-19+647del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(13): Show |
C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0089 a0001c0001t0002g0102 others(11): Show |
14 | HG00140.hp1 HG00609.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+630_-19+649del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(15): Show |
C | 4 | a0001c0004t0002g0057 a0001c0004t0002g0071 a0001c0004t0002g0091 others(1): Show |
4 | HG03710.hp1 NA18977.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+630_-19+651del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(17): Show |
C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0002t0002g0148 |
3 | HG00099.hp1 HG02109.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-19+630_-19+653del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(19): Show |
C | 1 | a0001c0004t0002g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+630_-19+655del others(26): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(25): Show |
C | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0253 others(1): Show |
4 | HG01081.hp2 HG01361.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+630_-19+661del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470685 | CTCTCTAT others(27): Show |
C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0213 |
3 | HG02683.hp2 HG03834.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-19+630_-19+663del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | ||||||
chr4:15470687 | CTCTA | C | 4 | a0001c0001t0001g0174 a0001c0001t0001g0183 a0001c0001t0002g0172 others(1): Show |
4 | HG02015.hp2 HG02165.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+632_-19+635del others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | ||||||
chr4:15470687 | CTCTATAT others(7): Show |
C | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-19+632_-19+645del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | ||||||
chr4:15470687 | CTCTATAT others(11): Show |
C | 11 | a0001c0001t0001g0079 a0001c0001t0001g0127 a0001c0001t0001g0128 others(8): Show |
11 | HG01515.hp1 HG02698.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+632_-19+649del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | ||||||
chr4:15470687 | CTCTATAT others(13): Show |
C | 2 | a0001c0001t0001g0062 a0001c0004t0002g0075 |
2 | HG01255.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-19+632_-19+651del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | ||||||
chr4:15470687 | CTCTATAT others(15): Show |
C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0068 others(3): Show |
6 | HG00323.hp1 HG00741.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+632_-19+653del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | ||||||
chr4:15470687 | CTCTATAT others(27): Show |
C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0244 a0001c0001t0001g0246 others(1): Show |
4 | NA18951.hp2 NA18953.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+632_-19+665del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | ||||||
chr4:15470689 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+632C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470689 | |||||||
chr4:15470689 | CTA | C | 8 | a0001c0001t0001g0173 a0001c0001t0001g0337 a0001c0001t0002g0008 others(5): Show |
8 | HG00642.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+676_-19+677del others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATA | C | 21 | a0001c0001t0001g0111 a0001c0001t0001g0178 a0001c0001t0001g0326 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19+674_-19+677del others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATA | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0108 others(19): Show |
23 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-19+672_-19+677del others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(1): Show |
C | 22 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0103 others(19): Show |
22 | HG00408.hp1 HG01257.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+670_-19+677del others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(3): Show |
C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0193 others(6): Show |
9 | HG01255.hp1 HG02040.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+668_-19+677del others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(5): Show |
C | 6 | a0001c0001t0001g0166 a0001c0001t0001g0179 a0001c0006t0001g0286 others(3): Show |
6 | HG01358.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+666_-19+677del others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(7): Show |
C | 4 | a0001c0001t0002g0164 a0002c0005t0002g0076 a0011c0030t0002g0147 others(1): Show |
4 | HG02071.hp2 HG02486.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+664_-19+677del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(9): Show |
C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0149 others(3): Show |
6 | HG00621.hp1 HG02622.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+662_-19+677del others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(11): Show |
C | 14 | a0001c0001t0001g0055 a0001c0001t0001g0119 a0001c0001t0001g0121 others(11): Show |
16 | HG00733.hp2 HG02080.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+660_-19+677del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(13): Show |
C | 3 | a0001c0001t0001g0070 a0001c0004t0002g0059 a0003c0007t0002g0086 |
3 | HG00280.hp2 HG02055.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-19+658_-19+677del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(15): Show |
C | 6 | a0001c0001t0001g0069 a0001c0004t0002g0096 a0001c0004t0002g0097 others(3): Show |
6 | HG01243.hp2 HG01346.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+656_-19+677del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(17): Show |
C | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19+654_-19+677del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470689 | CTATATAT others(27): Show |
C | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-19+644_-19+677del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | ||||||
chr4:15470691 | A | C | 31 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(28): Show |
31 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+634A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470691 | |||||||
chr4:15470693 | A | C | 32 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
32 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-19+636A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470693 | |||||||
chr4:15470695 | A | C | 46 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(43): Show |
46 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-19+638A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470695 | |||||||
chr4:15470697 | A | C | 56 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0034 others(53): Show |
58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-19+640A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470697 | |||||||
chr4:15470699 | A | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0034 others(65): Show |
71 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19+642A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470699 | |||||||
chr4:15470701 | A | C | 59 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0034 others(56): Show |
62 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-19+644A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470701 | |||||||
chr4:15470703 | A | C | 47 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0034 others(44): Show |
50 | HG00408.hp1 HG00438.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.-19+646A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470703 | |||||||
chr4:15470705 | A | C | 28 | a0001c0001t0001g0047 a0001c0001t0001g0103 a0001c0001t0001g0166 others(25): Show |
30 | HG00408.hp1 HG00438.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.-19+648A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470705 | |||||||
chr4:15470707 | A | C | 23 | a0001c0001t0001g0047 a0001c0001t0001g0103 a0001c0001t0001g0166 others(20): Show |
24 | HG00408.hp1 HG01255.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+650A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470707 | |||||||
chr4:15470709 | A | C | 13 | a0001c0001t0001g0121 a0001c0001t0001g0166 a0001c0001t0002g0189 others(10): Show |
15 | HG01255.hp1 HG01358.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19+652A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470709 | |||||||
chr4:15470711 | A | C | 7 | a0001c0001t0001g0121 a0001c0001t0002g0190 a0001c0002t0001g0123 others(4): Show |
8 | HG00280.hp2 HG02080.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+654A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470711 | |||||||
chr4:15470713 | A | C | 3 | a0001c0002t0002g0003 a0001c0002t0002g0134 a0001c0004t0002g0097 |
3 | HG01243.hp2 NA18942.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-19+656A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470713 | |||||||
chr4:15470729 | A | C | 1 | a0006c0009t0002g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+672A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470729 | |||||||
chr4:15470732 | T | A | 1 | a0006c0009t0002g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+675T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470732 | |||||||
chr4:15470733 | A | C | 1 | a0006c0009t0002g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+676A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470733 | |||||||
chr4:15470743 | T | A | 1 | a0006c0009t0002g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+686T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470743 | |||||||
chr4:15470804 | T | C | 331 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(328): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-19+747T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470804 | |||||||
chr4:15471235 | G | A | 2 | a0001c0001t0001g0050 a0005c0011t0001g0001 |
3 | HG02723.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19+1178G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471235 | |||||||
chr4:15471242 | A | G | 1 | a0001c0001t0002g0322 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-19+1185A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471242 | |||||||
chr4:15471391 | TG | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-19+1337delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15471391 | ||||||
chr4:15471551 | A | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
40 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.-19+1494A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471551 | |||||||
chr4:15471559 | C | A | 2 | a0001c0001t0001g0050 a0005c0011t0001g0001 |
3 | HG02723.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19+1502C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471559 | |||||||
chr4:15471628 | C | CA | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG02257.hp1 HG02965.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+1585dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15471628 | ||||||
chr4:15471628 | CA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.-19+1585delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15471628 | ||||||
chr4:15471782 | T | C | 1 | a0001c0002t0002g0107 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-19+1725T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471782 | |||||||
chr4:15471799 | A | T | 1 | a0002c0005t0001g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+1742A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471799 | |||||||
chr4:15471839 | C | T | 3 | a0001c0004t0002g0097 a0001c0004t0002g0098 a0001c0004t0002g0099 |
3 | HG01243.hp2 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-19+1782C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471839 | |||||||
chr4:15471845 | A | G | 1 | a0016c0016t0002g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-19+1788A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471845 | |||||||
chr4:15472147 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-19+2090A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472147 | |||||||
chr4:15472332 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-19+2275G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472332 | |||||||
chr4:15472531 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+2474T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472531 | |||||||
chr4:15472647 | GT | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(287): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-19+2604delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15472647 | ||||||
chr4:15472842 | T | C | 3 | a0001c0001t0001g0196 a0001c0001t0002g0195 a0001c0001t0002g0197 |
3 | HG00735.hp2 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-19+2785T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472842 | |||||||
chr4:15473090 | A | T | 1 | a0001c0001t0001g0318 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-18-2825A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473090 | |||||||
chr4:15473158 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18-2757T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473158 | |||||||
chr4:15473372 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0058 others(42): Show |
46 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-18-2543C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473372 | |||||||
chr4:15473470 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-2445G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473470 | |||||||
chr4:15473476 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(287): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-18-2439A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473476 | |||||||
chr4:15473506 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-18-2409G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473506 | |||||||
chr4:15473539 | A | G | 1 | a0002c0005t0001g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-2376A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473539 | |||||||
chr4:15473581 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18-2334G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473581 | |||||||
chr4:15473830 | GA | G | 3 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-2082delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15473830 | ||||||
chr4:15474164 | C | T | 1 | a0001c0004t0002g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18-1751C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474164 | |||||||
chr4:15474304 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18-1611G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474304 | |||||||
chr4:15474507 | A | G | 1 | a0002c0005t0001g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-18-1408A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474507 | |||||||
chr4:15474620 | A | C | 49 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
50 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-1295A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474620 | |||||||
chr4:15474704 | A | G | 49 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
50 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-1211A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474704 | |||||||
chr4:15474875 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18-1040C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474875 | |||||||
chr4:15474980 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-935A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474980 | |||||||
chr4:15475051 | G | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-864G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475051 | |||||||
chr4:15475100 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-815C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475100 | |||||||
chr4:15475135 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18-780G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475135 | |||||||
chr4:15475187 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18-728T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475187 | |||||||
chr4:15475222 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-693C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475222 | |||||||
chr4:15475246 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0008 others(5): Show |
8 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18-669C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475246 | |||||||
chr4:15475295 | A | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
96 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-18-620A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475295 | |||||||
chr4:15475298 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-617G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475298 | |||||||
chr4:15475327 | C | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
37 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.-18-588C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475327 | |||||||
chr4:15475458 | C | A | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-457C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475458 | |||||||
chr4:15475564 | C | T | 1 | a0020c0020t0001g0317 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-18-351C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475564 | |||||||
chr4:15475778 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-18-137G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475778 | |||||||
chr4:15476031 | C | T | 1 | a0001c0004t0002g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.39+60C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476031 | |||||||
chr4:15476188 | C | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0050 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+217C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476188 | |||||||
chr4:15476406 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.39+435C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476406 | |||||||
chr4:15476477 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0050 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+506G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476477 | |||||||
chr4:15476593 | G | A | 39 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
39 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.39+622G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476593 | |||||||
chr4:15476925 | G | T | 3 | a0002c0003t0001g0313 a0002c0003t0001g0314 a0002c0003t0001g0315 |
3 | NA18981.hp2 NA19009.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.39+954G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476925 | |||||||
chr4:15477000 | C | A | 2 | a0001c0001t0002g0164 a0001c0001t0002g0165 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.39+1029C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477000 | |||||||
chr4:15477068 | C | T | 52 | a0001c0006t0001g0006 a0001c0006t0001g0270 a0001c0006t0001g0271 others(49): Show |
54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.39+1097C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477068 | |||||||
chr4:15477230 | T | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(191): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.39+1259T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477230 | |||||||
chr4:15477242 | C | T | 1 | a0001c0006t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.39+1271C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477242 | |||||||
chr4:15477290 | A | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
40 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.39+1319A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477290 | |||||||
chr4:15477301 | C | CA | 10 | a0001c0001t0001g0105 a0001c0001t0001g0166 a0001c0001t0001g0201 others(7): Show |
10 | HG02293.hp1 HG02293.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+1347dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr4 | 15477301 | ||||||
chr4:15477356 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.40-1367T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477356 | |||||||
chr4:15477775 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | NA18612.hp2 NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.40-948C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477775 | |||||||
chr4:15477920 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-803C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477920 | |||||||
chr4:15478017 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.40-706A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478017 | |||||||
chr4:15478159 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.40-564C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478159 | |||||||
chr4:15478412 | C | A | 1 | a0001c0006t0001g0270 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.40-311C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478412 | |||||||
chr4:15478449 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(287): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.40-274T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478449 | |||||||
chr4:15478544 | A | C | 3 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.40-179A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478544 | |||||||
chr4:15478601 | A | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(287): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.40-122A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478601 | |||||||
chr4:15478858 | G | A | 53 | a0001c0001t0001g0103 a0001c0006t0001g0006 a0001c0006t0001g0270 others(50): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.123+52G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15478858 | |||||||
chr4:15478938 | G | T | 5 | a0001c0001t0001g0023 a0001c0001t0002g0008 a0001c0001t0002g0024 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+132G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15478938 | |||||||
chr4:15479019 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123+213C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479019 | |||||||
chr4:15479024 | G | T | 1 | a0002c0003t0001g0312 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.123+218G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479024 | |||||||
chr4:15479041 | T | G | 52 | a0001c0006t0001g0006 a0001c0006t0001g0270 a0001c0006t0001g0271 others(49): Show |
54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.123+235T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479041 | |||||||
chr4:15479049 | T | C | 49 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
50 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.123+243T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479049 | |||||||
chr4:15479161 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.123+355T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479161 | |||||||
chr4:15479460 | C | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0002g0008 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+654C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479460 | |||||||
chr4:15479485 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0002g0015 a0001c0001t0002g0041 |
3 | HG02622.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123+679G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479485 | |||||||
chr4:15479601 | T | A | 2 | a0001c0006t0001g0271 a0001c0006t0001g0272 |
2 | HG02071.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.123+795T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479601 | |||||||
chr4:15479613 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.123+807G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479613 | |||||||
chr4:15480036 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.124-668C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480036 | |||||||
chr4:15480214 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.124-490G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480214 | |||||||
chr4:15480352 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.124-352A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480352 | |||||||
chr4:15480452 | C | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(22): Show |
25 | HG01243.hp1 HG01433.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-252C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480452 | |||||||
chr4:15480589 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-115C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480589 | |||||||
chr4:15480698 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(84): Show |
89 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
splice_region_variant&intron_variant | LOW | c.124-6C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480698 | |||||||
chr4:15480853 | A | G | 291 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(288): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.247+26A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15480853 | |||||||
chr4:15480874 | G | A | 1 | a0001c0006t0001g0273 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.247+47G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15480874 | |||||||
chr4:15481044 | A | C | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
90 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.247+217A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481044 | |||||||
chr4:15481086 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247+259A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481086 | |||||||
chr4:15481113 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG02109.hp2 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.247+286T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481113 | |||||||
chr4:15481185 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.247+358G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481185 | |||||||
chr4:15481279 | C | T | 4 | a0001c0001t0001g0022 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG01243.hp2 HG01346.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+452C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481279 | |||||||
chr4:15481280 | G | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(25): Show |
28 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.247+453G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481280 | |||||||
chr4:15481372 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.247+545G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481372 | |||||||
chr4:15481380 | G | A | 34 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(31): Show |
34 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.247+553G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481380 | |||||||
chr4:15481466 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0047 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.247+639G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481466 | |||||||
chr4:15481470 | C | A | 2 | a0002c0005t0001g0027 a0002c0005t0001g0038 |
2 | HG01433.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.247+643C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481470 | |||||||
chr4:15481664 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.247+837T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481664 | |||||||
chr4:15481873 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+1046G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481873 | |||||||
chr4:15482186 | G | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(25): Show |
28 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.247+1359G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482186 | |||||||
chr4:15482228 | G | C | 1 | a0020c0020t0001g0317 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.247+1401G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482228 | |||||||
chr4:15482262 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.247+1435T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482262 | |||||||
chr4:15482527 | C | T | 287 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(284): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.247+1700C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482527 | |||||||
chr4:15482562 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247+1735A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482562 | |||||||
chr4:15482699 | C | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0002g0008 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+1872C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482699 | |||||||
chr4:15482872 | T | C | 1 | a0002c0005t0001g0203 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.247+2045T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482872 | |||||||
chr4:15482875 | AT | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(49): Show |
54 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.247+2050delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15482875 | ||||||
chr4:15482879 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.247+2052G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482879 | |||||||
chr4:15482899 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247+2072C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482899 | |||||||
chr4:15482900 | G | A | 1 | a0002c0005t0001g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247+2073G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482900 | |||||||
chr4:15483127 | A | T | 1 | a0001c0001t0002g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.247+2300A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483127 | |||||||
chr4:15483391 | T | G | 1 | a0001c0024t0002g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247+2564T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483391 | |||||||
chr4:15483560 | T | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG00323.hp2 HG01074.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+2733T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483560 | |||||||
chr4:15483614 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(49): Show |
54 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.247+2787C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483614 | |||||||
chr4:15483761 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.247+2934G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483761 | |||||||
chr4:15483880 | T | C | 3 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.247+3053T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483880 | |||||||
chr4:15483986 | G | C | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.247+3159G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483986 | |||||||
chr4:15484061 | A | AGTTTATA others(10): Show |
1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247+3235_247+3236i others(19): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15484061 | ||||||
chr4:15484111 | T | C | 6 | a0002c0003t0001g0274 a0002c0003t0001g0279 a0002c0003t0002g0275 others(3): Show |
6 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+3284T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484111 | |||||||
chr4:15484383 | T | C | 4 | a0001c0002t0002g0114 a0001c0002t0002g0115 a0001c0002t0002g0116 others(1): Show |
4 | HG00558.hp1 NA18747.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+3556T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484383 | |||||||
chr4:15484455 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.247+3628G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484455 | |||||||
chr4:15484460 | C | T | 6 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+3633C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484460 | |||||||
chr4:15484545 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.247+3718G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484545 | |||||||
chr4:15484670 | A | G | 1 | a0001c0004t0002g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.247+3843A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484670 | |||||||
chr4:15484694 | T | G | 1 | a0001c0004t0002g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.247+3867T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484694 | |||||||
chr4:15485149 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247+4322G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485149 | |||||||
chr4:15485174 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+4347A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485174 | |||||||
chr4:15485192 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.247+4365A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485192 | |||||||
chr4:15485211 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(138): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.247+4384A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485211 | |||||||
chr4:15485228 | C | G | 12 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+4401C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485228 | |||||||
chr4:15485705 | T | C | 52 | a0001c0006t0001g0006 a0001c0006t0001g0270 a0001c0006t0001g0271 others(49): Show |
54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.247+4878T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485705 | |||||||
chr4:15485739 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.247+4912C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485739 | |||||||
chr4:15485808 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+4981A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485808 | |||||||
chr4:15486030 | G | A | 12 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+5203G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15486030 | |||||||
chr4:15486372 | GT | G | 12 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+5548delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15486372 | ||||||
chr4:15486525 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0002g0008 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+5698G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15486525 | |||||||
chr4:15486588 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.247+5761T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15486588 | |||||||
chr4:15487137 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+6310T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487137 | |||||||
chr4:15487331 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0002g0015 a0001c0001t0002g0041 |
3 | HG02622.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.247+6504G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487331 | |||||||
chr4:15487370 | T | C | 3 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.247+6543T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487370 | |||||||
chr4:15487448 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(289): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.247+6621C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487448 | |||||||
chr4:15487505 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.247+6678C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487505 | |||||||
chr4:15487506 | C | T | 1 | a0016c0016t0002g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.247+6679C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487506 | |||||||
chr4:15487536 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+6709C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487536 | |||||||
chr4:15487572 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0002g0008 a0001c0001t0002g0024 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+6745G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487572 | |||||||
chr4:15487652 | G | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0164 a0001c0001t0002g0165 others(4): Show |
8 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+6825G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487652 | |||||||
chr4:15487665 | G | A | 4 | a0001c0006t0001g0006 a0002c0003t0001g0280 a0002c0003t0001g0281 others(1): Show |
5 | NA18960.hp1 NA18990.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+6838G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487665 | |||||||
chr4:15487780 | T | A | 3 | a0001c0001t0001g0033 a0001c0001t0002g0016 a0014c0025t0002g0032 |
3 | HG02965.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.247+6953T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487780 | |||||||
chr4:15487785 | T | TA | 5 | a0001c0001t0002g0200 a0001c0001t0002g0210 a0001c0001t0002g0211 others(2): Show |
5 | HG01099.hp2 HG01192.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+6965dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15487785 | ||||||
chr4:15487789 | A | AT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+6962_247+6963i others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487789 | |||||||
chr4:15487789 | A | ATT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.247+6962_247+6963i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487789 | |||||||
chr4:15487789 | A | ATTT | 51 | a0001c0006t0001g0006 a0001c0006t0001g0270 a0001c0006t0001g0271 others(48): Show |
53 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.247+6962_247+6963i others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487789 | |||||||
chr4:15487790 | A | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+6963A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487790 | |||||||
chr4:15487791 | A | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+6964A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487791 | |||||||
chr4:15487792 | A | AT | 141 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0055 others(138): Show |
142 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.247+6976dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15487792 | ||||||
chr4:15487792 | A | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(138): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.247+6965A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487792 | |||||||
chr4:15487831 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+7004A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487831 | |||||||
chr4:15487957 | T | TC | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+7136dupC | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15487957 | ||||||
chr4:15488019 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.247+7192G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488019 | |||||||
chr4:15488098 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(102): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.247+7271G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488098 | |||||||
chr4:15488168 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.247+7341G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488168 | |||||||
chr4:15488491 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247+7664T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488491 | |||||||
chr4:15488512 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.247+7685G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488512 | |||||||
chr4:15488614 | C | T | 7 | a0001c0001t0001g0089 a0001c0004t0002g0057 a0001c0004t0002g0090 others(4): Show |
7 | HG00438.hp2 HG02027.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.247+7787C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488614 | |||||||
chr4:15488645 | C | G | 1 | a0010c0019t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.247+7818C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488645 | |||||||
chr4:15488728 | G | A | 2 | a0001c0008t0002g0007 a0001c0008t0002g0283 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.247+7901G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488728 | |||||||
chr4:15488809 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.247+7982G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488809 | |||||||
chr4:15488934 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+8107C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488934 | |||||||
chr4:15489015 | C | A | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+8188C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489015 | |||||||
chr4:15489128 | A | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+8301A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489128 | |||||||
chr4:15489218 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.247+8391T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489218 | |||||||
chr4:15489226 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+8399A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489226 | |||||||
chr4:15489329 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247+8502C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489329 | |||||||
chr4:15489585 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247+8758C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489585 | |||||||
chr4:15489586 | G | A | 1 | a0005c0011t0001g0001 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.247+8759G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489586 | |||||||
chr4:15489706 | T | C | 11 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0120 others(8): Show |
11 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.247+8879T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489706 | |||||||
chr4:15490227 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.247+9400C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490227 | |||||||
chr4:15490389 | A | G | 1 | a0001c0002t0002g0160 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.247+9562A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490389 | |||||||
chr4:15490414 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.247+9587C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490414 | |||||||
chr4:15490448 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.247+9621G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490448 | |||||||
chr4:15490554 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(265): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.247+9727C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490554 | |||||||
chr4:15490644 | A | G | 13 | a0001c0001t0001g0079 a0002c0005t0002g0076 a0003c0007t0002g0077 others(10): Show |
13 | HG00140.hp1 HG01070.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.247+9817A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490644 | |||||||
chr4:15490779 | T | C | 51 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(48): Show |
52 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.247+9952T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490779 | |||||||
chr4:15490820 | G | C | 21 | a0001c0001t0001g0048 a0001c0001t0001g0196 a0001c0001t0001g0227 others(18): Show |
21 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.247+9993G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490820 | |||||||
chr4:15490853 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.247+10026G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490853 | |||||||
chr4:15490867 | CCTGTT | C | 42 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0052 others(39): Show |
43 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.247+10053_247+1005 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15490867 | ||||||
chr4:15490918 | C | G | 1 | a0001c0006t0001g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.247+10091C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490918 | |||||||
chr4:15490921 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.247+10094T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490921 | |||||||
chr4:15490934 | G | A | 24 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0055 others(21): Show |
25 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.247+10107G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490934 | |||||||
chr4:15491003 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0039 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+10176G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491003 | |||||||
chr4:15491037 | G | A | 1 | a0002c0003t0002g0287 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.247+10210G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491037 | |||||||
chr4:15491048 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.247+10221C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491048 | |||||||
chr4:15491098 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.247+10271C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491098 | |||||||
chr4:15491099 | G | A | 1 | a0001c0004t0002g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.247+10272G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491099 | |||||||
chr4:15491126 | G | C | 53 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.247+10299G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491126 | |||||||
chr4:15491147 | C | T | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0051 others(42): Show |
46 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.247+10320C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491147 | |||||||
chr4:15491252 | T | C | 48 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(45): Show |
49 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.247+10425T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491252 | |||||||
chr4:15491366 | T | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG02615.hp2 HG03017.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+10539T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491366 | |||||||
chr4:15491397 | C | G | 1 | a0001c0002t0002g0117 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.247+10570C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491397 | |||||||
chr4:15491415 | C | T | 27 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(24): Show |
28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.247+10588C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491415 | |||||||
chr4:15491849 | T | A | 1 | a0001c0001t0002g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.248-10580T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491849 | |||||||
chr4:15491947 | T | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(24): Show |
28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.248-10482T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491947 | |||||||
chr4:15492030 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.248-10399A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492030 | |||||||
chr4:15492058 | A | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(24): Show |
28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.248-10371A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492058 | |||||||
chr4:15492131 | C | T | 69 | a0001c0001t0001g0048 a0001c0001t0001g0196 a0001c0001t0001g0227 others(66): Show |
69 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.248-10298C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492131 | |||||||
chr4:15492164 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.248-10265A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492164 | |||||||
chr4:15492198 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248-10231C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492198 | |||||||
chr4:15492491 | CTT | C | 25 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0055 others(22): Show |
26 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.248-9931_248-9930d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15492491 | ||||||
chr4:15492500 | G | T | 55 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(52): Show |
56 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.248-9929G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492500 | |||||||
chr4:15492513 | GT | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0047 others(24): Show |
28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.248-9905delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15492513 | ||||||
chr4:15492544 | G | A | 2 | a0003c0007t0002g0077 a0003c0007t0002g0078 |
2 | HG00140.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.248-9885G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492544 | |||||||
chr4:15492571 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.248-9858T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492571 | |||||||
chr4:15492696 | C | G | 3 | a0001c0004t0002g0073 a0001c0004t0002g0074 a0001c0004t0002g0075 |
3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.248-9733C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492696 | |||||||
chr4:15492704 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.248-9725G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492704 | |||||||
chr4:15492788 | C | A | 1 | a0001c0004t0002g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.248-9641C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492788 | |||||||
chr4:15493059 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.248-9370A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493059 | |||||||
chr4:15493130 | T | C | 53 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-9299T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493130 | |||||||
chr4:15493142 | T | G | 53 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-9287T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493142 | |||||||
chr4:15493188 | C | T | 3 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.248-9241C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493188 | |||||||
chr4:15493191 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.248-9238C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493191 | |||||||
chr4:15493245 | A | ATTAT | 53 | a0001c0001t0001g0050 a0001c0001t0001g0198 a0001c0001t0001g0235 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-9160_248-9157d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493245 | ||||||
chr4:15493245 | A | ATTATTTA others(1): Show |
6 | a0001c0001t0001g0196 a0001c0001t0001g0227 a0001c0001t0001g0229 others(3): Show |
6 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-9164_248-9157d others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493245 | ||||||
chr4:15493245 | A | ATTATTTA others(5): Show |
15 | a0001c0001t0001g0048 a0001c0001t0001g0230 a0001c0001t0001g0233 others(12): Show |
15 | HG01099.hp2 HG01192.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.248-9168_248-9157d others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493245 | ||||||
chr4:15493265 | T | TTTAC | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(26): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.248-9161_248-9160i others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493265 | ||||||
chr4:15493269 | T | C | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(26): Show |
30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.248-9160T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493269 | |||||||
chr4:15493269 | T | TTTAC | 44 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(41): Show |
45 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.248-9146_248-9143d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493269 | ||||||
chr4:15493576 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.248-8853T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493576 | |||||||
chr4:15493686 | A | G | 146 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
148 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.248-8743A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493686 | |||||||
chr4:15493688 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.248-8741T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493688 | |||||||
chr4:15493724 | T | C | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.248-8705T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493724 | |||||||
chr4:15494021 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.248-8408C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494021 | |||||||
chr4:15494088 | G | A | 1 | a0014c0025t0002g0032 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.248-8341G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494088 | |||||||
chr4:15494089 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.248-8340T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494089 | |||||||
chr4:15494202 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248-8227G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494202 | |||||||
chr4:15494270 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.248-8159A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494270 | |||||||
chr4:15494379 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.248-8050G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494379 | |||||||
chr4:15494396 | G | C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
27 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.248-8033G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494396 | |||||||
chr4:15494646 | G | A | 53 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-7783G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494646 | |||||||
chr4:15494686 | T | C | 119 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(116): Show |
120 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.248-7743T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494686 | |||||||
chr4:15494963 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.248-7466A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494963 | |||||||
chr4:15495005 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.248-7424G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495005 | |||||||
chr4:15495006 | A | T | 1 | a0001c0001t0002g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.248-7423A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495006 | |||||||
chr4:15495093 | C | G | 41 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(38): Show |
42 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.248-7336C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495093 | |||||||
chr4:15495161 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.248-7268T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495161 | |||||||
chr4:15495297 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.248-7132C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495297 | |||||||
chr4:15495355 | C | G | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-7074C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495355 | |||||||
chr4:15495356 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-7073A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495356 | |||||||
chr4:15495357 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-7072C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495357 | |||||||
chr4:15495750 | G | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.248-6679G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495750 | |||||||
chr4:15495873 | C | A | 2 | a0001c0001t0002g0163 a0001c0001t0002g0184 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.248-6556C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495873 | |||||||
chr4:15496137 | T | G | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-6292T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496137 | |||||||
chr4:15496166 | T | C | 4 | a0001c0001t0001g0017 a0002c0003t0001g0311 a0002c0005t0001g0027 others(1): Show |
4 | HG01433.hp2 HG02976.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-6263T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496166 | |||||||
chr4:15496312 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-6117A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496312 | |||||||
chr4:15496485 | C | T | 48 | a0001c0006t0002g0267 a0001c0008t0002g0288 a0001c0008t0002g0293 others(45): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-5944C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496485 | |||||||
chr4:15496586 | C | T | 1 | a0001c0002t0002g0159 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.248-5843C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496586 | |||||||
chr4:15496980 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.248-5449C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496980 | |||||||
chr4:15496991 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.248-5438A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496991 | |||||||
chr4:15497093 | C | A | 43 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(40): Show |
44 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.248-5336C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497093 | |||||||
chr4:15497177 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-5252G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497177 | |||||||
chr4:15497612 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.248-4817A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497612 | |||||||
chr4:15497627 | T | C | 181 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
184 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.248-4802T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497627 | |||||||
chr4:15497719 | T | C | 60 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0089 others(57): Show |
61 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.248-4710T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497719 | |||||||
chr4:15497848 | C | A | 1 | a0001c0004t0002g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.248-4581C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497848 | |||||||
chr4:15497857 | A | AT | 60 | a0001c0001t0001g0048 a0001c0001t0001g0079 a0001c0001t0001g0089 others(57): Show |
61 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.248-4571dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15497857 | ||||||
chr4:15498097 | G | T | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-4332G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498097 | |||||||
chr4:15498147 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.248-4282A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498147 | |||||||
chr4:15498462 | G | A | 1 | a0002c0003t0002g0289 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.248-3967G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498462 | |||||||
chr4:15498501 | C | A | 1 | a0018c0017t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.248-3928C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498501 | |||||||
chr4:15498654 | ACT | A | 6 | a0002c0003t0001g0279 a0002c0003t0002g0275 a0002c0003t0002g0276 others(3): Show |
6 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-3774_248-3773d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498654 | |||||||
chr4:15498798 | T | C | 3 | a0002c0003t0001g0280 a0002c0003t0001g0281 a0002c0003t0001g0312 |
3 | NA18960.hp1 NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.248-3631T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498798 | |||||||
chr4:15498897 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0002g0161 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.248-3532C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498897 | |||||||
chr4:15498939 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0002g0161 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.248-3490A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498939 | |||||||
chr4:15499211 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.248-3218A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499211 | |||||||
chr4:15499267 | G | A | 2 | a0006c0009t0002g0231 a0006c0009t0002g0232 |
2 | NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.248-3162G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499267 | |||||||
chr4:15499276 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248-3153G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499276 | |||||||
chr4:15499397 | T | A | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-3032T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499397 | |||||||
chr4:15499621 | T | C | 6 | a0001c0001t0002g0004 a0001c0001t0002g0054 a0001c0001t0002g0169 others(3): Show |
7 | HG01891.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-2808T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499621 | |||||||
chr4:15499631 | T | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(11): Show |
15 | HG02109.hp2 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.248-2798T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499631 | |||||||
chr4:15499880 | A | G | 52 | a0001c0001t0001g0149 a0001c0001t0001g0316 a0001c0001t0001g0321 others(49): Show |
54 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.248-2549A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499880 | |||||||
chr4:15499928 | GGGA | G | 119 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(116): Show |
121 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.248-2494_248-2492d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15499928 | ||||||
chr4:15500075 | T | TTG | 7 | a0001c0001t0001g0105 a0001c0001t0001g0249 a0002c0003t0001g0269 others(4): Show |
7 | HG00597.hp1 NA18951.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-2322_248-2321d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500075 | T | TTGTG | 39 | a0001c0002t0001g0137 a0001c0002t0002g0125 a0001c0004t0002g0094 others(36): Show |
39 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-2324_248-2321d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500075 | T | TTGTGTG | 5 | a0001c0008t0002g0305 a0002c0003t0001g0332 a0002c0003t0002g0282 others(2): Show |
5 | HG01192.hp2 NA18974.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2326_248-2321d others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500075 | TTGTG | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(10): Show |
14 | HG01243.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.248-2324_248-2321d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500075 | TTGTGTG | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-2326_248-2321d others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500075 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0011 a0007c0012t0002g0021 a0015c0018t0002g0046 |
3 | HG02109.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.248-2328_248-2321d others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500075 | TTGTGTGT others(3): Show |
T | 1 | a0001c0006t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.248-2330_248-2321d others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | ||||||
chr4:15500089 | G | A | 1 | a0001c0002t0002g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.248-2340G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500089 | |||||||
chr4:15500097 | G | A | 8 | a0001c0001t0001g0192 a0001c0001t0002g0008 a0001c0001t0002g0024 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2332G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500097 | |||||||
chr4:15500099 | G | A | 8 | a0001c0001t0001g0192 a0001c0001t0002g0008 a0001c0001t0002g0024 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2330G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500099 | |||||||
chr4:15500099 | G | GTATACA | 2 | a0001c0001t0002g0004 a0001c0001t0002g0171 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.248-2329_248-2328i others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATACAT others(3): Show |
1 | a0001c0001t0002g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.248-2329_248-2328i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATACAT others(7): Show |
4 | a0001c0001t0002g0054 a0001c0001t0002g0164 a0001c0001t0002g0170 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATACAT others(9): Show |
1 | a0001c0001t0002g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.248-2329_248-2328i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATATA | 5 | a0001c0001t0001g0104 a0001c0001t0001g0174 a0001c0001t0001g0181 others(2): Show |
5 | HG01081.hp2 HG01169.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0180 a0001c0001t0001g0201 a0001c0001t0001g0224 others(1): Show |
4 | HG00735.hp1 HG02293.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATATAT others(3): Show |
7 | a0001c0001t0001g0051 a0001c0001t0001g0178 a0001c0001t0001g0218 others(4): Show |
7 | HG02055.hp2 HG03486.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0119 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
5 | HG00733.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0226 a0001c0001t0002g0015 a0010c0019t0001g0188 |
3 | HG02015.hp2 HG02622.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.248-2329_248-2328i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-2329_248-2328i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500099 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.248-2328_248-2315d others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | ||||||
chr4:15500101 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0051 others(44): Show |
48 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-2328G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500101 | |||||||
chr4:15500101 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.248-2327_248-2326i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | ||||||
chr4:15500101 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0183 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.248-2327_248-2326i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | ||||||
chr4:15500101 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-2327_248-2326i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | ||||||
chr4:15500101 | G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.248-2327_248-2326i others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | ||||||
chr4:15500101 | GTGTGTGT others(11): Show |
G | 2 | a0001c0006t0001g0286 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.248-2326_248-2309d others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | ||||||
chr4:15500103 | G | A | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0051 others(59): Show |
64 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.248-2326G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500103 | |||||||
chr4:15500103 | GTGTGTAT others(1): Show |
G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0034 others(8): Show |
11 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.248-2324_248-2317d others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500103 | ||||||
chr4:15500103 | GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0001g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.248-2324_248-2315d others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500103 | ||||||
chr4:15500105 | G | A | 64 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
66 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.248-2324G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500105 | |||||||
chr4:15500107 | G | A | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
67 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.248-2322G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500107 | |||||||
chr4:15500107 | G | GTGTGTA | 3 | a0001c0001t0001g0022 a0002c0003t0002g0276 a0002c0005t0001g0241 |
3 | HG01358.hp2 HG02132.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.248-2321_248-2320i others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTAT others(3): Show |
1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.248-2321_248-2320i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTAT others(5): Show |
4 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(1): Show |
4 | HG01099.hp2 HG01192.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2321_248-2320i others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTGT others(7): Show |
4 | a0001c0001t0001g0233 a0001c0001t0002g0200 a0006c0009t0002g0232 others(1): Show |
4 | HG02293.hp1 NA18747.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2321_248-2320i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTGT others(9): Show |
1 | a0001c0006t0001g0273 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.248-2321_248-2320i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTGT others(7): Show |
6 | a0001c0001t0001g0048 a0001c0001t0001g0227 a0001c0001t0001g0230 others(3): Show |
6 | HG02080.hp1 NA18612.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-2321_248-2320i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0002g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.248-2321_248-2320i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.248-2321_248-2320i others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | G | GTGTGTGT others(9): Show |
2 | a0001c0001t0001g0196 a0001c0001t0002g0197 |
2 | HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.248-2321_248-2320i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | GTA | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.248-2298_248-2297d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500107 | GTATA | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0079 others(13): Show |
17 | HG00642.hp2 HG01515.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.248-2300_248-2297d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | ||||||
chr4:15500109 | A | G | 33 | a0001c0001t0001g0062 a0001c0001t0001g0105 a0001c0001t0001g0205 others(30): Show |
33 | HG00280.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.248-2320A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500109 | |||||||
chr4:15500111 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(130): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.248-2318A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500111 | |||||||
chr4:15500113 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(135): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.248-2316A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500113 | |||||||
chr4:15500115 | A | G | 60 | a0001c0001t0001g0053 a0001c0001t0001g0149 a0001c0001t0001g0208 others(57): Show |
62 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.248-2314A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500115 | |||||||
chr4:15500117 | A | G | 4 | a0001c0002t0002g0101 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00621.hp1 NA18953.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2312A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500117 | |||||||
chr4:15500129 | A | ATG | 3 | a0001c0001t0002g0026 a0001c0001t0002g0030 a0001c0004t0002g0028 |
3 | HG01891.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.248-2299_248-2298i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500129 | ||||||
chr4:15500129 | A | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(15): Show |
19 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.248-2300A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500129 | |||||||
chr4:15500182 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.248-2247T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500182 | |||||||
chr4:15500343 | T | C | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-2086T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500343 | |||||||
chr4:15500350 | G | A | 1 | a0001c0004t0002g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.248-2079G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500350 | |||||||
chr4:15500492 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.248-1937T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500492 | |||||||
chr4:15500684 | T | C | 24 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0196 others(21): Show |
24 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.248-1745T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500684 | |||||||
chr4:15500951 | C | T | 1 | a0002c0005t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.248-1478C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500951 | |||||||
chr4:15501286 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0053 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-1143T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15501286 | |||||||
chr4:15501745 | T | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.248-684T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15501745 | |||||||
chr4:15501797 | T | C | 1 | a0001c0006t0001g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248-632T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15501797 | |||||||
chr4:15502073 | A | T | 52 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(49): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.248-356A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15502073 | |||||||
chr4:15502091 | A | G | 6 | a0001c0002t0002g0100 a0001c0002t0002g0152 a0001c0002t0002g0153 others(3): Show |
6 | HG00609.hp1 HG02132.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-338A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15502091 | |||||||
chr4:15502371 | T | TTTTTC | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
95 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.248-48_248-44dupCT others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15502371 | ||||||
chr4:15502526 | A | T | 1 | a0001c0002t0002g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.336+9A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/36 | chr4 | 15502526 | |||||||
chr4:15502617 | C | T | 1 | a0013c0031t0001g0285 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.336+100C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/36 | chr4 | 15502617 | |||||||
chr4:15502637 | G | C | 2 | a0004c0013t0003g0139 a0004c0013t0003g0140 |
2 | HG01109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.336+120G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/36 | chr4 | 15502637 | |||||||
chr4:15503184 | T | A | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438+261T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503184 | |||||||
chr4:15503196 | G | A | 48 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(45): Show |
50 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.438+273G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503196 | |||||||
chr4:15503272 | C | A | 2 | a0001c0008t0002g0007 a0001c0008t0002g0283 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.438+349C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503272 | |||||||
chr4:15503397 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.438+474C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503397 | |||||||
chr4:15503634 | A | AG | 254 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.438+713dupG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | INFO_REALIGN_3_PRIME | chr4 | 15503634 | ||||||
chr4:15503634 | A | G | 1 | a0001c0026t0001g0237 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+711A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503634 | |||||||
chr4:15503771 | A | C | 2 | a0004c0022t0002g0018 a0019c0021t0002g0035 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.438+848A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503771 | |||||||
chr4:15503820 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0034 others(6): Show |
9 | HG01243.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+897C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503820 | |||||||
chr4:15503933 | G | C | 313 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(310): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.438+1010G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503933 | |||||||
chr4:15503991 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.438+1068C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503991 | |||||||
chr4:15504419 | G | A | 1 | a0002c0003t0001g0294 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.438+1496G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504419 | |||||||
chr4:15504496 | A | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG00323.hp2 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1573A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504496 | |||||||
chr4:15504947 | G | C | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+2024G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504947 | |||||||
chr4:15504955 | C | G | 1 | a0021c0014t0002g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.438+2032C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504955 | |||||||
chr4:15505085 | G | A | 43 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(40): Show |
44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.438+2162G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505085 | |||||||
chr4:15505173 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.438+2250A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505173 | |||||||
chr4:15505188 | T | A | 43 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(40): Show |
44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.438+2265T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505188 | |||||||
chr4:15505409 | T | C | 207 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(204): Show |
211 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.438+2486T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505409 | |||||||
chr4:15505431 | C | A | 1 | a0001c0006t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.438+2508C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505431 | |||||||
chr4:15505545 | G | C | 80 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(77): Show |
80 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.438+2622G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505545 | |||||||
chr4:15505688 | C | T | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.438+2765C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505688 | |||||||
chr4:15505842 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.438+2919C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505842 | |||||||
chr4:15505873 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.438+2950G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505873 | |||||||
chr4:15506068 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+3145G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506068 | |||||||
chr4:15506082 | A | T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+3159A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506082 | |||||||
chr4:15506150 | T | C | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+3227T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506150 | |||||||
chr4:15506207 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.438+3284C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506207 | |||||||
chr4:15506222 | A | T | 1 | a0001c0004t0002g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.438+3299A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506222 | |||||||
chr4:15506224 | T | C | 3 | a0001c0004t0002g0097 a0001c0004t0002g0098 a0001c0004t0002g0099 |
3 | HG01243.hp2 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.438+3301T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506224 | |||||||
chr4:15506246 | A | T | 1 | a0001c0004t0002g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.438+3323A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506246 | |||||||
chr4:15506727 | A | G | 1 | a0001c0004t0002g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.439-3412A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506727 | |||||||
chr4:15506812 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.439-3327G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506812 | |||||||
chr4:15506848 | C | T | 28 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(25): Show |
28 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.439-3291C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506848 | |||||||
chr4:15506858 | G | C | 75 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(72): Show |
75 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.439-3281G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506858 | |||||||
chr4:15507119 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.439-3020C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507119 | |||||||
chr4:15507152 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.439-2987T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507152 | |||||||
chr4:15507244 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0002g0161 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439-2895T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507244 | |||||||
chr4:15507344 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.439-2795T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507344 | |||||||
chr4:15507374 | T | C | 1 | a0001c0004t0002g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.439-2765T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507374 | |||||||
chr4:15507447 | A | G | 2 | a0007c0012t0002g0020 a0007c0012t0002g0021 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.439-2692A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507447 | |||||||
chr4:15507599 | G | A | 55 | a0001c0001t0001g0316 a0001c0001t0001g0321 a0001c0002t0001g0112 others(52): Show |
57 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.439-2540G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507599 | |||||||
chr4:15507668 | G | A | 74 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(71): Show |
74 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.439-2471G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507668 | |||||||
chr4:15507723 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0192 |
3 | HG03195.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.439-2416T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507723 | |||||||
chr4:15507764 | G | A | 74 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(71): Show |
74 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.439-2375G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507764 | |||||||
chr4:15507771 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.439-2368T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507771 | |||||||
chr4:15507777 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.439-2362C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507777 | |||||||
chr4:15507996 | A | G | 1 | a0001c0002t0001g0112 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.439-2143A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507996 | |||||||
chr4:15508112 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0002g0161 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439-2027T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508112 | |||||||
chr4:15508331 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.439-1808A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508331 | |||||||
chr4:15508344 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.439-1795A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508344 | |||||||
chr4:15508375 | T | C | 63 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0166 others(60): Show |
65 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.439-1764T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508375 | |||||||
chr4:15508399 | G | A | 1 | a0002c0003t0001g0292 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.439-1740G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508399 | |||||||
chr4:15508455 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.439-1684A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508455 | |||||||
chr4:15509031 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.439-1108G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509031 | |||||||
chr4:15509237 | C | G | 1 | a0001c0006t0002g0310 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.439-902C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509237 | |||||||
chr4:15509252 | T | C | 2 | a0002c0003t0002g0276 a0002c0003t0002g0277 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.439-887T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509252 | |||||||
chr4:15509277 | C | CT | 179 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.439-848dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | INFO_REALIGN_3_PRIME | chr4 | 15509277 | ||||||
chr4:15509277 | C | CTT | 9 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0069 others(6): Show |
9 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.439-849_439-848dup others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | INFO_REALIGN_3_PRIME | chr4 | 15509277 | ||||||
chr4:15509421 | C | T | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439-718C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509421 | |||||||
chr4:15509431 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.439-708G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509431 | |||||||
chr4:15509599 | G | A | 52 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(49): Show |
54 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.439-540G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509599 | |||||||
chr4:15509660 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.439-479C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509660 | |||||||
chr4:15509703 | G | T | 74 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(71): Show |
74 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.439-436G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509703 | |||||||
chr4:15509764 | G | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.439-375G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509764 | |||||||
chr4:15509945 | G | A | 3 | a0002c0003t0001g0311 a0002c0005t0001g0027 a0002c0005t0001g0038 |
3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.439-194G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509945 | |||||||
chr4:15510032 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(9): Show |
12 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-107G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15510032 | |||||||
chr4:15510407 | A | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.540+167A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510407 | |||||||
chr4:15510705 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.540+465A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510705 | |||||||
chr4:15510767 | A | AAG | 3 | a0001c0001t0002g0030 a0001c0004t0002g0028 a0001c0004t0002g0029 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.541-478_541-477dup others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | INFO_REALIGN_3_PRIME | chr4 | 15510767 | ||||||
chr4:15510767 | A | G | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(112): Show |
119 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.541-480A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510767 | |||||||
chr4:15510917 | A | G | 208 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
212 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.541-330A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510917 | |||||||
chr4:15511222 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-25G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15511222 | |||||||
chr4:15511446 | T | C | 1 | a0001c0001t0002g0008 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.717+23T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15511446 | |||||||
chr4:15511524 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.717+101C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15511524 | |||||||
chr4:15511742 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.717+319T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15511742 | |||||||
chr4:15512143 | A | G | 1 | a0018c0017t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.717+720A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15512143 | |||||||
chr4:15512493 | A | C | 76 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(73): Show |
76 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.717+1070A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15512493 | |||||||
chr4:15512727 | G | A | 1 | a0001c0002t0002g0160 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.717+1304G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15512727 | |||||||
chr4:15512951 | C | CA | 6 | a0001c0001t0001g0318 a0001c0004t0002g0097 a0001c0004t0002g0098 others(3): Show |
6 | HG01243.hp2 HG01346.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+1542dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr4 | 15512951 | ||||||
chr4:15512951 | CA | C | 192 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(189): Show |
196 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.717+1542delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr4 | 15512951 | ||||||
chr4:15513006 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.717+1583A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513006 | |||||||
chr4:15513224 | C | T | 51 | a0001c0001t0001g0022 a0001c0001t0001g0113 a0001c0001t0001g0120 others(48): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.718-1483C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513224 | |||||||
chr4:15513363 | C | T | 1 | a0002c0005t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.718-1344C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513363 | |||||||
chr4:15513427 | C | T | 198 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
202 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.718-1280C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513427 | |||||||
chr4:15513730 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0002g0008 a0001c0001t0002g0024 others(5): Show |
9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.718-977G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513730 | |||||||
chr4:15513805 | T | C | 1 | a0001c0004t0002g0071 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.718-902T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513805 | |||||||
chr4:15514168 | C | T | 199 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(196): Show |
203 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.718-539C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15514168 | |||||||
chr4:15514536 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.718-171C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15514536 | |||||||
chr4:15515194 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.880+325A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/36 | chr4 | 15515194 | |||||||
chr4:15515370 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.881-498G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/36 | chr4 | 15515370 | |||||||
chr4:15515514 | A | G | 8 | a0001c0001t0001g0047 a0001c0001t0002g0008 a0001c0001t0002g0024 others(5): Show |
9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.881-354A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/36 | chr4 | 15515514 | |||||||
chr4:15516005 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01243.hp1 | splice_donor_variant&intron_variant | HIGH | c.1017+1G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | chr4 | 15516005 | |||||||
chr4:15516133 | AT | A | 74 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(71): Show |
75 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.1017+142delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | INFO_REALIGN_3_PRIME | chr4 | 15516133 | ||||||
chr4:15516248 | C | G | 1 | a0001c0002t0002g0160 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1017+244C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | chr4 | 15516248 | |||||||
chr4:15516313 | C | T | 75 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(72): Show |
75 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1017+309C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | chr4 | 15516313 | |||||||
chr4:15516864 | A | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | NA18975.hp1 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1149+108A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15516864 | |||||||
chr4:15516944 | C | CT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0166 others(5): Show |
8 | HG02071.hp1 HG02738.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149+211dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | ||||||
chr4:15516944 | CT | C | 116 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0052 others(113): Show |
119 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1149+211delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | ||||||
chr4:15516944 | CTT | C | 53 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0070 others(50): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1149+210_1149+211d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | ||||||
chr4:15516944 | CTTT | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1149+209_1149+211d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | ||||||
chr4:15516972 | C | T | 73 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(70): Show |
73 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1149+216C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15516972 | |||||||
chr4:15517009 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+253G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517009 | |||||||
chr4:15517011 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0194 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+255G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517011 | |||||||
chr4:15517040 | C | T | 1 | a0001c0002t0002g0146 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1149+284C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517040 | |||||||
chr4:15517097 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1149+341G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517097 | |||||||
chr4:15517104 | C | A | 8 | a0001c0001t0001g0047 a0001c0001t0002g0008 a0001c0001t0002g0024 others(5): Show |
9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+348C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517104 | |||||||
chr4:15517109 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0250 others(2): Show |
5 | HG00741.hp2 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+353G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517109 | |||||||
chr4:15517324 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0002g0008 a0001c0001t0002g0024 others(5): Show |
9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+568G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517324 | |||||||
chr4:15517915 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0194 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+1159G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517915 | |||||||
chr4:15517951 | C | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+1195C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517951 | |||||||
chr4:15517970 | G | T | 1 | a0001c0002t0002g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1149+1214G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517970 | |||||||
chr4:15518008 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0072 |
2 | HG01099.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1149+1252G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518008 | |||||||
chr4:15518036 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0034 others(6): Show |
9 | HG01243.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+1280G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518036 | |||||||
chr4:15518457 | C | T | 2 | a0007c0012t0002g0020 a0007c0012t0002g0021 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1149+1701C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518457 | |||||||
chr4:15518791 | C | T | 1 | a0002c0003t0001g0294 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1149+2035C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518791 | |||||||
chr4:15518824 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(48): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1149+2068G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518824 | |||||||
chr4:15518848 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1149+2092C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518848 | |||||||
chr4:15518980 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1149+2224A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518980 | |||||||
chr4:15519776 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1149+3020C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519776 | |||||||
chr4:15519779 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1149+3023C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519779 | |||||||
chr4:15519780 | G | A | 73 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(70): Show |
73 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1149+3024G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519780 | |||||||
chr4:15519977 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1149+3221G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519977 | |||||||
chr4:15520121 | G | T | 1 | a0001c0002t0002g0145 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1149+3365G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520121 | |||||||
chr4:15520352 | C | T | 73 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(70): Show |
73 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1149+3596C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520352 | |||||||
chr4:15520379 | C | A | 1 | a0002c0005t0001g0203 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1149+3623C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520379 | |||||||
chr4:15520586 | T | C | 80 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(77): Show |
80 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1149+3830T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520586 | |||||||
chr4:15520659 | C | T | 43 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(40): Show |
44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1149+3903C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520659 | |||||||
chr4:15520745 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1149+3989C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520745 | |||||||
chr4:15520749 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1149+3993T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520749 | |||||||
chr4:15520797 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0002g0190 a0001c0001t0002g0194 |
3 | HG02451.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+4041G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520797 | |||||||
chr4:15521170 | A | C | 1 | a0002c0005t0001g0319 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1149+4414A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521170 | |||||||
chr4:15521191 | A | G | 1 | a0009c0033t0001g0304 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1149+4435A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521191 | |||||||
chr4:15521192 | C | T | 44 | a0002c0003t0001g0266 a0002c0003t0001g0269 a0002c0003t0001g0274 others(41): Show |
44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1149+4436C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521192 | |||||||
chr4:15521324 | T | C | 46 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(43): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1149+4568T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521324 | |||||||
chr4:15521445 | C | G | 1 | a0001c0006t0002g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1149+4689C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521445 | |||||||
chr4:15521513 | T | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0002g0015 others(2): Show |
5 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149+4757T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521513 | |||||||
chr4:15521585 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1149+4829G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521585 | |||||||
chr4:15522106 | C | T | 1 | a0001c0008t0002g0293 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1150-5341C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522106 | |||||||
chr4:15522155 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1150-5292C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522155 | |||||||
chr4:15522167 | C | T | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1150-5280C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522167 | |||||||
chr4:15522176 | G | A | 7 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(4): Show |
8 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-5271G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522176 | |||||||
chr4:15522230 | C | T | 7 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(4): Show |
8 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-5217C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522230 | |||||||
chr4:15522292 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0002g0190 a0001c0001t0002g0194 |
3 | HG02451.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-5155G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522292 | |||||||
chr4:15522343 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1150-5104C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522343 | |||||||
chr4:15522415 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1150-5032A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522415 | |||||||
chr4:15522508 | G | GT | 6 | a0001c0001t0001g0331 a0001c0001t0002g0008 a0001c0001t0002g0024 others(3): Show |
6 | HG01106.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-4927dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15522508 | ||||||
chr4:15522508 | GT | G | 55 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0050 others(52): Show |
55 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1150-4927delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15522508 | ||||||
chr4:15522540 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1150-4907G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522540 | |||||||
chr4:15522632 | T | A | 1 | a0001c0002t0002g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1150-4815T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522632 | |||||||
chr4:15522901 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1150-4546C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522901 | |||||||
chr4:15522947 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1150-4500G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522947 | |||||||
chr4:15522985 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0048 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1150-4462A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522985 | |||||||
chr4:15523031 | T | G | 1 | a0002c0003t0002g0289 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1150-4416T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15523031 | |||||||
chr4:15523114 | CA | C | 45 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(42): Show |
46 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1150-4318delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15523114 | ||||||
chr4:15523180 | G | GTCCT | 52 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(49): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1150-4245_1150-424 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15523180 | ||||||
chr4:15523180 | GTCCT | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0036 others(1): Show |
4 | HG02630.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-4245_1150-424 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15523180 | ||||||
chr4:15523248 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1150-4199G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15523248 | |||||||
chr4:15523487 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0121 |
2 | HG02615.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1150-3960C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15523487 | |||||||
chr4:15524171 | T | G | 1 | a0022c0028t0001g0255 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1150-3276T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524171 | |||||||
chr4:15524229 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1150-3218G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524229 | |||||||
chr4:15524281 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1150-3166C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524281 | |||||||
chr4:15524295 | G | A | 2 | a0007c0012t0002g0020 a0007c0012t0002g0021 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1150-3152G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524295 | |||||||
chr4:15524428 | G | GCCTTCTG others(334): Show |
1 | a0001c0001t0001g0259 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1150-3002_1150-300 others(345): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524428 | ||||||
chr4:15524447 | A | AT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0327 a0001c0001t0002g0161 others(5): Show |
8 | HG01978.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-2979dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | ||||||
chr4:15524447 | A | ATTTTTTT | 46 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0235 others(43): Show |
46 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1150-2985_1150-297 others(11): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | ||||||
chr4:15524447 | A | ATTTTTTT others(1): Show |
10 | a0001c0001t0001g0113 a0001c0001t0001g0198 a0001c0001t0001g0236 others(7): Show |
10 | HG00621.hp2 HG01952.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-2986_1150-297 others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | ||||||
chr4:15524447 | AT | A | 51 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(48): Show |
52 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1150-2979delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | ||||||
chr4:15524447 | ATTTT | A | 23 | a0001c0001t0001g0048 a0001c0001t0001g0196 a0001c0001t0001g0227 others(20): Show |
23 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150-2982_1150-297 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | ||||||
chr4:15524512 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1150-2935G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524512 | |||||||
chr4:15524543 | C | T | 60 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0166 others(57): Show |
62 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1150-2904C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524543 | |||||||
chr4:15524595 | T | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-2852T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524595 | |||||||
chr4:15524610 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1150-2837T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524610 | |||||||
chr4:15524652 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0134 |
3 | NA18942.hp2 NA18945.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1150-2795C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524652 | |||||||
chr4:15524653 | G | A | 87 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1150-2794G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524653 | |||||||
chr4:15524663 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1150-2784G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524663 | |||||||
chr4:15524672 | C | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-2775C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524672 | |||||||
chr4:15524673 | G | A | 50 | a0001c0001t0001g0017 a0001c0001t0002g0030 a0001c0004t0002g0028 others(47): Show |
50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1150-2774G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524673 | |||||||
chr4:15524702 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1150-2745T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524702 | |||||||
chr4:15524740 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0072 |
2 | HG01099.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1150-2707C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524740 | |||||||
chr4:15524743 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150-2704A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524743 | |||||||
chr4:15525420 | A | T | 52 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(49): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1150-2027A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525420 | |||||||
chr4:15525423 | C | G | 1 | a0001c0004t0002g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1150-2024C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525423 | |||||||
chr4:15525453 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1150-1994G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525453 | |||||||
chr4:15525474 | A | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0048 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1150-1973A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525474 | |||||||
chr4:15525475 | A | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0048 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1150-1972A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525475 | |||||||
chr4:15525476 | T | G | 22 | a0001c0001t0001g0048 a0001c0001t0001g0196 a0001c0001t0001g0227 others(19): Show |
22 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1150-1971T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525476 | |||||||
chr4:15525555 | T | G | 1 | a0002c0003t0001g0280 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1150-1892T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525555 | |||||||
chr4:15525726 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1150-1721C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525726 | |||||||
chr4:15525865 | T | C | 2 | a0001c0004t0002g0254 a0001c0004t0002g0334 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1150-1582T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525865 | |||||||
chr4:15526185 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1150-1262A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526185 | |||||||
chr4:15526274 | AC | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1150-1172delC | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526274 | |||||||
chr4:15526440 | C | A | 1 | a0001c0002t0002g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1150-1007C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526440 | |||||||
chr4:15526656 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1150-791A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526656 | |||||||
chr4:15526741 | C | T | 46 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(43): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1150-706C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526741 | |||||||
chr4:15526764 | C | A | 43 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(40): Show |
44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1150-683C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526764 | |||||||
chr4:15526833 | C | A | 43 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0104 others(40): Show |
44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1150-614C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526833 | |||||||
chr4:15527106 | T | G | 1 | a0002c0003t0001g0295 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1150-341T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15527106 | |||||||
chr4:15527171 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1150-276G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15527171 | |||||||
chr4:15527289 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0002g0190 a0001c0001t0002g0194 |
3 | HG02451.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-158C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15527289 | |||||||
chr4:15527682 | T | A | 1 | a0001c0006t0002g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1359+26T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15527682 | |||||||
chr4:15527760 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1359+104C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15527760 | |||||||
chr4:15528468 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1360-152A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528468 | |||||||
chr4:15528501 | C | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1360-119C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528501 | |||||||
chr4:15528505 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1360-115C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528505 | |||||||
chr4:15528528 | A | G | 1 | a0002c0003t0001g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1360-92A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528528 | |||||||
chr4:15528957 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0042 |
3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1466+231C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15528957 | |||||||
chr4:15529163 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1466+437T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529163 | |||||||
chr4:15529262 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1466+536G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529262 | |||||||
chr4:15529378 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1466+652A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529378 | |||||||
chr4:15529381 | C | CA | 8 | a0001c0001t0001g0056 a0001c0001t0001g0260 a0001c0001t0002g0008 others(5): Show |
9 | HG00741.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466+668dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529381 | ||||||
chr4:15529483 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1466+757A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529483 | |||||||
chr4:15529650 | T | C | 2 | a0006c0009t0002g0231 a0006c0009t0002g0232 |
2 | NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1466+924T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529650 | |||||||
chr4:15529673 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1466+947G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529673 | |||||||
chr4:15529685 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1466+959T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529685 | |||||||
chr4:15529816 | C | CT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0149 others(3): Show |
6 | HG00280.hp2 HG01978.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1466+1102dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529816 | ||||||
chr4:15529843 | CATTT | C | 61 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0166 others(58): Show |
63 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1466+1127_1466+113 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529843 | ||||||
chr4:15529878 | ATTTTTTA others(8): Show |
A | 1 | a0001c0001t0002g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1466+1159_1466+117 others(19): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529878 | ||||||
chr4:15529892 | AT | A | 75 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0113 others(72): Show |
75 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1466+1174delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529892 | ||||||
chr4:15529900 | T | A | 3 | a0001c0006t0001g0270 a0001c0006t0001g0286 a0001c0024t0002g0204 |
3 | HG00408.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1466+1174T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529900 | |||||||
chr4:15529904 | TTTATTA | T | 48 | a0001c0001t0001g0256 a0002c0003t0001g0266 a0002c0003t0001g0269 others(45): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1466+1185_1466+119 others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529904 | ||||||
chr4:15530003 | ACT | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1466+1280_1466+128 others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15530003 | ||||||
chr4:15530038 | T | C | 2 | a0001c0002t0002g0129 a0001c0002t0002g0130 |
2 | HG01106.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1466+1312T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530038 | |||||||
chr4:15530041 | G | C | 1 | a0001c0002t0002g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1466+1315G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530041 | |||||||
chr4:15530083 | C | T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466+1357C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530083 | |||||||
chr4:15530086 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1466+1360C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530086 | |||||||
chr4:15530113 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1466+1387A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530113 | |||||||
chr4:15530164 | C | G | 2 | a0007c0012t0002g0020 a0007c0012t0002g0021 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1466+1438C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530164 | |||||||
chr4:15530183 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0002g0161 |
3 | HG02145.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1466+1457A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530183 | |||||||
chr4:15530207 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0329 |
2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1466+1481G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530207 | |||||||
chr4:15530933 | C | A | 1 | a0002c0003t0001g0295 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1466+2207C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530933 | |||||||
chr4:15531241 | G | A | 40 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0002c0003t0001g0266 others(37): Show |
40 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1467-1952G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531241 | |||||||
chr4:15531342 | C | G | 26 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0196 others(23): Show |
26 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1467-1851C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531342 | |||||||
chr4:15531414 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1467-1779C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531414 | |||||||
chr4:15531446 | C | T | 40 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0002c0003t0001g0266 others(37): Show |
40 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1467-1747C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531446 | |||||||
chr4:15531646 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1467-1547C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531646 | |||||||
chr4:15531713 | C | T | 5 | a0002c0003t0001g0279 a0002c0003t0002g0275 a0002c0003t0002g0276 others(2): Show |
5 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1467-1480C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531713 | |||||||
chr4:15531900 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | NA18612.hp1 NA18953.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467-1293G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531900 | |||||||
chr4:15532218 | G | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1467-975G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532218 | |||||||
chr4:15532348 | C | T | 63 | a0001c0001t0001g0321 a0001c0002t0001g0112 a0001c0002t0001g0123 others(60): Show |
65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1467-845C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532348 | |||||||
chr4:15532489 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1467-704T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532489 | |||||||
chr4:15532492 | A | T | 1 | a0002c0003t0001g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1467-701A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532492 | |||||||
chr4:15532668 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1467-525G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532668 | |||||||
chr4:15533023 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1467-170C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15533023 | |||||||
chr4:15533029 | GACATCCT others(9): Show |
G | 6 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1467-159_1467-144d others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15533029 | ||||||
chr4:15533090 | G | A | 40 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0002c0003t0001g0266 others(37): Show |
40 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1467-103G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15533090 | |||||||
chr4:15533373 | T | C | 1 | a0003c0007t0002g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1607+40T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15533373 | |||||||
chr4:15533472 | A | G | 309 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1607+139A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15533472 | |||||||
chr4:15533598 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1607+265A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15533598 | |||||||
chr4:15534114 | G | A | 1 | a0001c0004t0002g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1607+781G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534114 | |||||||
chr4:15534216 | T | C | 2 | a0001c0004t0002g0254 a0001c0004t0002g0334 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1607+883T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534216 | |||||||
chr4:15534589 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1607+1256G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534589 | |||||||
chr4:15534628 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG00639.hp2 HG01070.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1607+1295T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534628 | |||||||
chr4:15534883 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1607+1550A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534883 | |||||||
chr4:15535005 | G | GA | 10 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0192 others(7): Show |
11 | HG02027.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1607+1682dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | INFO_REALIGN_3_PRIME | chr4 | 15535005 | ||||||
chr4:15535155 | T | C | 1 | a0001c0001t0001g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1608-1765T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15535155 | |||||||
chr4:15535218 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1608-1702C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15535218 | |||||||
chr4:15535401 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1608-1519C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15535401 | |||||||
chr4:15536084 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1608-836C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536084 | |||||||
chr4:15536089 | G | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1608-831G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536089 | |||||||
chr4:15536144 | C | A | 2 | a0004c0022t0002g0018 a0019c0021t0002g0035 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1608-776C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536144 | |||||||
chr4:15536307 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1608-613G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536307 | |||||||
chr4:15536341 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1608-579G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536341 | |||||||
chr4:15536349 | C | T | 1 | a0001c0002t0002g0144 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1608-571C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536349 | |||||||
chr4:15536354 | T | C | 43 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(40): Show |
43 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1608-566T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536354 | |||||||
chr4:15536563 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1608-357T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536563 | |||||||
chr4:15536761 | A | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0192 others(6): Show |
10 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608-159A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536761 | |||||||
chr4:15536768 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1608-152T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536768 | |||||||
chr4:15536800 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1608-120T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536800 | |||||||
chr4:15537121 | T | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1764+45T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537121 | |||||||
chr4:15537299 | G | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0050 others(140): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1764+223G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537299 | |||||||
chr4:15537576 | G | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1765-323G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537576 | |||||||
chr4:15537579 | T | C | 43 | a0001c0001t0001g0198 a0001c0001t0001g0235 a0001c0001t0001g0236 others(40): Show |
43 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1765-320T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537579 | |||||||
chr4:15537830 | A | G | 45 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0198 others(42): Show |
45 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1765-69A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537830 | |||||||
chr4:15537875 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0050 others(142): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1765-24A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537875 | |||||||
chr4:15538156 | C | T | 26 | a0001c0001t0001g0022 a0001c0001t0001g0048 a0001c0001t0001g0196 others(23): Show |
26 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2003+19C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538156 | |||||||
chr4:15538234 | C | T | 3 | a0002c0003t0001g0311 a0002c0005t0001g0027 a0002c0005t0001g0038 |
3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2003+97C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538234 | |||||||
chr4:15538521 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2003+384C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538521 | |||||||
chr4:15538663 | A | T | 310 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(307): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2003+526A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538663 | |||||||
chr4:15538857 | G | A | 7 | a0001c0002t0002g0003 a0001c0002t0002g0101 a0001c0002t0002g0134 others(4): Show |
8 | NA18942.hp2 NA18945.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.2003+720G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538857 | |||||||
chr4:15538867 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2003+730A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538867 | |||||||
chr4:15538915 | C | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.2003+778C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538915 | |||||||
chr4:15539099 | A | G | 1 | a0001c0002t0002g0146 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2003+962A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539099 | |||||||
chr4:15539458 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2003+1321C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539458 | |||||||
chr4:15539522 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2004-1315C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539522 | |||||||
chr4:15539553 | T | G | 2 | a0001c0008t0002g0007 a0001c0008t0002g0283 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2004-1284T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539553 | |||||||
chr4:15539772 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2004-1065T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539772 | |||||||
chr4:15539969 | A | C | 1 | a0021c0014t0002g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2004-868A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539969 | |||||||
chr4:15539986 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.2004-851G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539986 | |||||||
chr4:15540045 | A | C | 1 | a0003c0007t0002g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2004-792A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540045 | |||||||
chr4:15540101 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0039 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004-736T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540101 | |||||||
chr4:15540136 | A | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0002g0161 others(3): Show |
6 | HG01433.hp2 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-701A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540136 | |||||||
chr4:15540159 | A | C | 1 | a0015c0018t0002g0046 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-678A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540159 | |||||||
chr4:15540288 | G | GT | 6 | a0001c0001t0001g0106 a0001c0001t0002g0161 a0002c0003t0001g0300 others(3): Show |
6 | HG01433.hp2 HG02145.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2004-538dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | INFO_REALIGN_3_PRIME | chr4 | 15540288 | ||||||
chr4:15540574 | A | G | 76 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0067 others(73): Show |
78 | HG00733.hp2 HG00741.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.2004-263A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540574 | |||||||
chr4:15540623 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0002g0040 others(1): Show |
4 | HG03195.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004-214A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540623 | |||||||
chr4:15540788 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2004-49T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540788 | |||||||
chr4:15540825 | C | A | 1 | a0002c0003t0001g0294 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2004-12C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540825 | |||||||
chr4:15541159 | A | G | 61 | a0001c0001t0002g0163 a0001c0001t0002g0184 a0001c0002t0001g0123 others(58): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2181+145A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541159 | |||||||
chr4:15541212 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2181+198G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541212 | |||||||
chr4:15541297 | C | T | 1 | a0003c0010t0002g0082 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2181+283C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541297 | |||||||
chr4:15541339 | T | A | 25 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0036 others(22): Show |
26 | HG00639.hp1 HG01891.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.2181+325T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541339 | |||||||
chr4:15541388 | C | G | 113 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2181+374C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541388 | |||||||
chr4:15541601 | G | A | 1 | a0013c0031t0001g0285 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2181+587G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541601 | |||||||
chr4:15541668 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2181+654A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541668 | |||||||
chr4:15541744 | A | G | 2 | a0001c0001t0001g0055 a0013c0031t0001g0285 |
2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2181+730A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541744 | |||||||
chr4:15542045 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2181+1031C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542045 | |||||||
chr4:15542282 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1268G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542282 | |||||||
chr4:15542299 | A | G | 1 | a0002c0005t0001g0203 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2181+1285A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542299 | |||||||
chr4:15542437 | C | A | 1 | a0001c0001t0002g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2181+1423C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542437 | |||||||
chr4:15542540 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1526A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542540 | |||||||
chr4:15542777 | G | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2181+1763G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542777 | |||||||
chr4:15542853 | C | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2181+1839C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542853 | |||||||
chr4:15542917 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1903C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542917 | |||||||
chr4:15543093 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2181+2079C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543093 | |||||||
chr4:15543172 | A | T | 1 | a0002c0003t0001g0312 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2181+2158A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543172 | |||||||
chr4:15543316 | G | A | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+2302G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543316 | |||||||
chr4:15543693 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2181+2679C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543693 | |||||||
chr4:15543787 | G | A | 54 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0031 others(51): Show |
55 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.2181+2773G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543787 | |||||||
chr4:15543908 | C | T | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+2894C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543908 | |||||||
chr4:15544043 | T | C | 5 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0221 others(2): Show |
5 | NA18945.hp2 NA18994.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181+3029T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544043 | |||||||
chr4:15544060 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2181+3046A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544060 | |||||||
chr4:15544073 | GAAGCCTC others(7): Show |
G | 1 | a0001c0001t0001g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2181+3060_2181+307 others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544073 | |||||||
chr4:15544107 | C | T | 1 | a0001c0024t0002g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2181+3093C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544107 | |||||||
chr4:15544118 | G | A | 1 | a0001c0006t0002g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2181+3104G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544118 | |||||||
chr4:15544239 | C | T | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2181+3225C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544239 | |||||||
chr4:15544443 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2181+3429C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544443 | |||||||
chr4:15544471 | A | T | 1 | a0001c0001t0001g0333 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2181+3457A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544471 | |||||||
chr4:15544586 | A | G | 1 | a0001c0004t0002g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2181+3572A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544586 | |||||||
chr4:15544590 | C | A | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+3576C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544590 | |||||||
chr4:15544643 | C | A | 1 | a0001c0001t0002g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2181+3629C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544643 | |||||||
chr4:15544790 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2181+3776A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544790 | |||||||
chr4:15544926 | T | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0056 others(15): Show |
19 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2181+3912T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544926 | |||||||
chr4:15545042 | G | A | 1 | a0001c0002t0002g0115 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2181+4028G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545042 | |||||||
chr4:15545511 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0036 others(1): Show |
4 | HG02630.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+4497G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545511 | |||||||
chr4:15545514 | T | A | 1 | a0001c0004t0002g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2181+4500T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545514 | |||||||
chr4:15545514 | T | C | 1 | a0001c0004t0002g0057 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2181+4500T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545514 | |||||||
chr4:15545691 | C | A | 104 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0163 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2181+4677C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545691 | |||||||
chr4:15545710 | AATGGGAA others(1): Show |
A | 149 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2181+4706_2181+471 others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15545710 | ||||||
chr4:15545715 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2181+4701G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545715 | |||||||
chr4:15545752 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2181+4738A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545752 | |||||||
chr4:15545869 | G | T | 1 | a0002c0003t0001g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2181+4855G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545869 | |||||||
chr4:15545890 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2181+4876C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545890 | |||||||
chr4:15545985 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2182-4839C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545985 | |||||||
chr4:15546086 | G | C | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-4738G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546086 | |||||||
chr4:15546281 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0042 |
3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182-4543C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546281 | |||||||
chr4:15546636 | G | A | 1 | a0001c0015t0001g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2182-4188G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546636 | |||||||
chr4:15546688 | C | T | 35 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0064 others(32): Show |
35 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2182-4136C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546688 | |||||||
chr4:15546792 | C | T | 40 | a0001c0001t0001g0053 a0001c0004t0002g0028 a0001c0004t0002g0029 others(37): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.2182-4032C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546792 | |||||||
chr4:15546793 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2182-4031G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546793 | |||||||
chr4:15546892 | A | C | 3 | a0002c0003t0001g0311 a0002c0005t0001g0027 a0002c0005t0001g0038 |
3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2182-3932A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546892 | |||||||
chr4:15546905 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2182-3919T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546905 | |||||||
chr4:15546927 | T | C | 109 | a0001c0001t0001g0053 a0001c0001t0001g0108 a0001c0001t0001g0109 others(106): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2182-3897T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546927 | |||||||
chr4:15547093 | A | C | 154 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2182-3731A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547093 | |||||||
chr4:15547340 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2182-3484T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547340 | |||||||
chr4:15547362 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0056 others(15): Show |
19 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2182-3462G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547362 | |||||||
chr4:15547611 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2182-3213C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547611 | |||||||
chr4:15547628 | T | C | 154 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2182-3196T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547628 | |||||||
chr4:15547630 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2182-3194G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547630 | |||||||
chr4:15547646 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2182-3178A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547646 | |||||||
chr4:15547672 | A | T | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-3152A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547672 | |||||||
chr4:15547757 | T | C | 5 | a0002c0003t0002g0282 a0002c0003t0002g0291 a0002c0003t0002g0306 others(2): Show |
5 | NA18951.hp1 NA18974.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.2182-3067T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547757 | |||||||
chr4:15547988 | G | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-2836G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547988 | |||||||
chr4:15548070 | G | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2182-2754G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548070 | |||||||
chr4:15548121 | A | AT | 114 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(111): Show |
118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2182-2690dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15548121 | ||||||
chr4:15548145 | G | C | 4 | a0001c0001t0001g0168 a0001c0001t0001g0173 a0001c0001t0001g0183 others(1): Show |
4 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182-2679G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548145 | |||||||
chr4:15548147 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2182-2677T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548147 | |||||||
chr4:15548148 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2182-2676A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548148 | |||||||
chr4:15548155 | G | A | 64 | a0001c0001t0002g0030 a0001c0001t0002g0163 a0001c0001t0002g0167 others(61): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2182-2669G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548155 | |||||||
chr4:15548161 | T | A | 1 | a0001c0006t0001g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2182-2663T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548161 | |||||||
chr4:15548179 | G | A | 1 | a0001c0024t0002g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182-2645G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548179 | |||||||
chr4:15548187 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2182-2637T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548187 | |||||||
chr4:15548281 | C | T | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-2543C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548281 | |||||||
chr4:15548362 | C | T | 104 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0163 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2182-2462C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548362 | |||||||
chr4:15548487 | A | C | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-2337A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548487 | |||||||
chr4:15548570 | C | CA | 73 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
75 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2182-2240dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15548570 | ||||||
chr4:15548570 | CA | C | 7 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0001c0001t0001g0217 others(4): Show |
7 | HG02559.hp1 HG02683.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182-2240delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15548570 | ||||||
chr4:15549041 | T | C | 1 | a0022c0028t0001g0255 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2182-1783T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549041 | |||||||
chr4:15549484 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2182-1340G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549484 | |||||||
chr4:15549506 | A | C | 6 | a0004c0013t0003g0139 a0004c0013t0003g0140 a0004c0022t0002g0018 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182-1318A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549506 | |||||||
chr4:15549664 | G | A | 15 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0016 others(12): Show |
16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2182-1160G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549664 | |||||||
chr4:15549675 | C | T | 63 | a0001c0001t0002g0163 a0001c0001t0002g0184 a0001c0002t0001g0123 others(60): Show |
65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.2182-1149C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549675 | |||||||
chr4:15549693 | C | T | 104 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0163 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2182-1131C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549693 | |||||||
chr4:15549732 | G | A | 2 | a0002c0003t0001g0281 a0002c0003t0001g0312 |
2 | NA18960.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2182-1092G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549732 | |||||||
chr4:15550159 | G | T | 1 | a0001c0024t0002g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182-665G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550159 | |||||||
chr4:15550176 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0014c0025t0002g0032 |
3 | HG02622.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2182-648G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550176 | |||||||
chr4:15550335 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2182-489C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550335 | |||||||
chr4:15550443 | T | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-381T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550443 | |||||||
chr4:15550495 | G | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
39 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2182-329G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550495 | |||||||
chr4:15550575 | T | C | 113 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0103 others(110): Show |
115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2182-249T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550575 | |||||||
chr4:15550672 | A | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
39 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2182-152A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550672 | |||||||
chr4:15550800 | C | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2182-24C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550800 | |||||||
chr4:15551396 | A | G | 40 | a0001c0001t0001g0053 a0001c0004t0002g0028 a0001c0004t0002g0029 others(37): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.2338+416A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551396 | |||||||
chr4:15551403 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0260 |
2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2338+423C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551403 | |||||||
chr4:15551448 | T | C | 5 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0250 others(2): Show |
5 | HG00741.hp2 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338+468T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551448 | |||||||
chr4:15551496 | T | A | 8 | a0003c0007t0002g0077 a0003c0007t0002g0078 a0003c0007t0002g0080 others(5): Show |
8 | HG00140.hp1 HG01070.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2338+516T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551496 | |||||||
chr4:15551505 | T | C | 1 | a0001c0001t0001g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2338+525T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551505 | |||||||
chr4:15551520 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2338+540C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551520 | |||||||
chr4:15551608 | C | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2338+628C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551608 | |||||||
chr4:15551652 | T | C | 2 | a0001c0002t0002g0132 a0001c0002t0002g0214 |
2 | HG00408.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2338+672T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551652 | |||||||
chr4:15551829 | T | C | 1 | a0002c0003t0001g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2338+849T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551829 | |||||||
chr4:15552127 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2339-1031G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552127 | |||||||
chr4:15552148 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2339-1010G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552148 | |||||||
chr4:15552246 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2339-912T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552246 | |||||||
chr4:15552344 | A | C | 1 | a0001c0004t0002g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2339-814A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552344 | |||||||
chr4:15552345 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2339-813G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552345 | |||||||
chr4:15552403 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2339-755A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552403 | |||||||
chr4:15552458 | T | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2339-700T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552458 | |||||||
chr4:15552534 | A | G | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2339-624A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552534 | |||||||
chr4:15552596 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2339-562T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552596 | |||||||
chr4:15553077 | G | C | 1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2339-81G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15553077 | |||||||
chr4:15553445 | GGTAAAAA others(8): Show |
G | 9 | a0001c0001t0001g0126 a0002c0003t0001g0269 a0002c0005t0001g0005 others(6): Show |
9 | HG00609.hp2 HG02132.hp1 NA19005.hp2 others(6): Show |
intron_variant | MODIFIER | c.2486+143_2486+157d others(17): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | INFO_REALIGN_3_PRIME | chr4 | 15553445 | ||||||
chr4:15553474 | C | T | 1 | a0001c0006t0002g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2486+169C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553474 | |||||||
chr4:15553528 | G | A | 1 | a0002c0003t0001g0300 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2486+223G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553528 | |||||||
chr4:15553919 | T | C | 1 | a0021c0014t0002g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2486+614T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553919 | |||||||
chr4:15553934 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2486+629C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553934 | |||||||
chr4:15554034 | G | A | 1 | a0001c0006t0002g0310 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2486+729G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554034 | |||||||
chr4:15554057 | A | G | 14 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2486+752A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554057 | |||||||
chr4:15554063 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2486+758A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554063 | |||||||
chr4:15554360 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2487-712G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554360 | |||||||
chr4:15554361 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2487-711C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554361 | |||||||
chr4:15554422 | G | A | 64 | a0001c0001t0002g0030 a0001c0001t0002g0163 a0001c0001t0002g0167 others(61): Show |
66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2487-650G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554422 | |||||||
chr4:15554573 | G | A | 15 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0016 others(12): Show |
16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2487-499G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554573 | |||||||
chr4:15554607 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2487-465T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554607 | |||||||
chr4:15554630 | C | T | 7 | a0001c0002t0001g0123 a0001c0002t0002g0114 a0001c0002t0002g0115 others(4): Show |
7 | HG00558.hp1 HG02080.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.2487-442C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554630 | |||||||
chr4:15554641 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2487-431G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554641 | |||||||
chr4:15554780 | A | G | 110 | a0001c0001t0001g0053 a0001c0001t0001g0108 a0001c0001t0001g0109 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.2487-292A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554780 | |||||||
chr4:15555061 | C | G | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2487-11C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15555061 | |||||||
chr4:15555413 | C | T | 2 | a0001c0001t0002g0161 a0001c0002t0002g0158 |
2 | HG02145.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2625+203C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555413 | |||||||
chr4:15555414 | G | A | 1 | a0001c0024t0002g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2625+204G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555414 | |||||||
chr4:15555477 | G | C | 7 | a0002c0003t0001g0274 a0002c0003t0001g0290 a0002c0003t0001g0295 others(4): Show |
7 | HG00558.hp2 HG00597.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2625+267G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555477 | |||||||
chr4:15555486 | T | C | 6 | a0001c0004t0002g0057 a0001c0004t0002g0090 a0001c0004t0002g0091 others(3): Show |
6 | HG00438.hp2 HG02027.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2625+276T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555486 | |||||||
chr4:15555721 | G | C | 1 | a0022c0028t0001g0255 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2625+511G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555721 | |||||||
chr4:15555819 | C | A | 40 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2625+609C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555819 | |||||||
chr4:15555868 | A | T | 104 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0163 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2625+658A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555868 | |||||||
chr4:15556015 | T | G | 15 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0016 others(12): Show |
16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2625+805T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556015 | |||||||
chr4:15556290 | C | T | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-1014C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556290 | |||||||
chr4:15556332 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2626-972C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556332 | |||||||
chr4:15556454 | T | C | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | NA18612.hp2 NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2626-850T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556454 | |||||||
chr4:15556497 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0322 |
2 | NA18974.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2626-807T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556497 | |||||||
chr4:15556563 | C | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2626-741C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556563 | |||||||
chr4:15556609 | C | G | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-695C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556609 | |||||||
chr4:15556720 | C | T | 104 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0163 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2626-584C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556720 | |||||||
chr4:15556729 | A | C | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-575A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556729 | |||||||
chr4:15556744 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2626-560G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556744 | |||||||
chr4:15556784 | T | C | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2626-520T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556784 | |||||||
chr4:15556895 | G | T | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2626-409G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556895 | |||||||
chr4:15557044 | G | A | 10 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG02055.hp2 NA18945.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.2626-260G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15557044 | |||||||
chr4:15557045 | T | C | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-259T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15557045 | |||||||
chr4:15557223 | T | A | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-81T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15557223 | |||||||
chr4:15557262 | TCTGA | T | 3 | a0001c0002t0002g0146 a0001c0002t0002g0150 a0001c0002t0002g0160 |
3 | NA19054.hp2 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2626-38_2626-35del others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | INFO_REALIGN_3_PRIME | chr4 | 15557262 | ||||||
chr4:15557552 | A | G | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+45A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557552 | |||||||
chr4:15557748 | A | C | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+241A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557748 | |||||||
chr4:15557761 | A | G | 2 | a0007c0012t0002g0020 a0007c0012t0002g0021 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2829+254A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557761 | |||||||
chr4:15557831 | G | C | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+324G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557831 | |||||||
chr4:15557840 | T | C | 35 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0064 others(32): Show |
35 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2829+333T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557840 | |||||||
chr4:15557884 | G | T | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+377G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557884 | |||||||
chr4:15557896 | A | G | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+389A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557896 | |||||||
chr4:15557975 | T | G | 162 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2829+468T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557975 | |||||||
chr4:15558009 | C | T | 2 | a0001c0001t0002g0161 a0017c0023t0002g0012 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+502C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558009 | |||||||
chr4:15558075 | T | C | 106 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0161 others(103): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2829+568T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558075 | |||||||
chr4:15558201 | A | G | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2829+694A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558201 | |||||||
chr4:15558374 | G | A | 15 | a0001c0001t0002g0102 a0001c0001t0002g0190 a0001c0001t0002g0195 others(12): Show |
15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2830-791G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558374 | |||||||
chr4:15558475 | C | A | 40 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2830-690C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558475 | |||||||
chr4:15558702 | A | C | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2830-463A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558702 | |||||||
chr4:15558719 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2830-446G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558719 | |||||||
chr4:15558821 | G | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.2830-344G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558821 | |||||||
chr4:15558881 | T | C | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2830-284T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558881 | |||||||
chr4:15558950 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2830-215C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558950 | |||||||
chr4:15559008 | C | G | 153 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2830-157C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15559008 | |||||||
chr4:15559068 | A | G | 1 | a0001c0006t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2830-97A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15559068 | |||||||
chr4:15559127 | G | T | 39 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
39 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2830-38G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15559127 | |||||||
chr4:15559469 | C | A | 14 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2922+212C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559469 | |||||||
chr4:15559473 | A | G | 148 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2922+216A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559473 | |||||||
chr4:15559563 | T | A | 1 | a0002c0005t0001g0242 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2922+306T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559563 | |||||||
chr4:15559630 | A | G | 104 | a0001c0001t0001g0053 a0001c0001t0002g0030 a0001c0001t0002g0163 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2922+373A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559630 | |||||||
chr4:15559660 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2922+403G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559660 | |||||||
chr4:15559667 | C | CTGTTTCC others(9): Show |
2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+411_2922+412i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | INFO_REALIGN_3_PRIME | chr4 | 15559667 | ||||||
chr4:15559669 | T | G | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+412T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559669 | |||||||
chr4:15559669 | T | TTTTCCTT others(9): Show |
58 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): Show |
59 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.2922+423_2922+424i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | INFO_REALIGN_3_PRIME | chr4 | 15559669 | ||||||
chr4:15559720 | A | AC | 60 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(57): Show |
61 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.2922+463_2922+464i others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559720 | |||||||
chr4:15559865 | C | T | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+608C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559865 | |||||||
chr4:15559882 | A | G | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+625A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559882 | |||||||
chr4:15560033 | C | T | 1 | a0001c0002t0002g0160 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2923-498C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15560033 | |||||||
chr4:15560091 | C | CA | 109 | a0001c0001t0001g0053 a0001c0001t0001g0108 a0001c0001t0001g0109 others(106): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2923-437dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | INFO_REALIGN_3_PRIME | chr4 | 15560091 | ||||||
chr4:15560390 | C | T | 13 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2923-141C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15560390 | |||||||
chr4:15560719 | C | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.3014+97C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560719 | |||||||
chr4:15560830 | T | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.3014+208T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560830 | |||||||
chr4:15560844 | C | G | 43 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.3014+222C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560844 | |||||||
chr4:15560903 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0124 others(1): Show |
4 | HG03486.hp1 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3014+281C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560903 | |||||||
chr4:15561061 | T | G | 2 | a0004c0022t0002g0018 a0019c0021t0002g0035 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3014+439T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561061 | |||||||
chr4:15561084 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3014+462G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561084 | |||||||
chr4:15561200 | C | A | 15 | a0001c0001t0002g0102 a0001c0001t0002g0190 a0001c0001t0002g0195 others(12): Show |
15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.3014+578C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561200 | |||||||
chr4:15561203 | A | T | 15 | a0001c0001t0002g0102 a0001c0001t0002g0190 a0001c0001t0002g0195 others(12): Show |
15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.3014+581A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561203 | |||||||
chr4:15561348 | C | A | 1 | a0007c0012t0002g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3014+726C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561348 | |||||||
chr4:15561477 | C | A | 2 | a0001c0001t0001g0321 a0017c0023t0002g0012 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3014+855C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561477 | |||||||
chr4:15561507 | C | T | 1 | a0022c0028t0001g0255 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3014+885C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561507 | |||||||
chr4:15561537 | G | GT | 19 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0056 others(16): Show |
20 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.3014+925dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | INFO_REALIGN_3_PRIME | chr4 | 15561537 | ||||||
chr4:15561690 | T | C | 1 | a0001c0002t0001g0137 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3014+1068T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561690 | |||||||
chr4:15561747 | G | A | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3014+1125G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561747 | |||||||
chr4:15561787 | T | A | 123 | a0001c0001t0001g0053 a0001c0001t0002g0004 a0001c0001t0002g0015 others(120): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.3014+1165T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561787 | |||||||
chr4:15561992 | C | T | 164 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(161): Show |
167 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3015-1363C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561992 | |||||||
chr4:15562258 | A | G | 1 | a0002c0005t0002g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3015-1097A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562258 | |||||||
chr4:15562337 | A | G | 4 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3015-1018A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562337 | |||||||
chr4:15562415 | A | C | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3015-940A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562415 | |||||||
chr4:15562460 | A | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3015-895A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562460 | |||||||
chr4:15562476 | G | A | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3015-879G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562476 | |||||||
chr4:15562560 | T | C | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3015-795T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562560 | |||||||
chr4:15562835 | C | A | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3015-520C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562835 | |||||||
chr4:15563060 | T | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0197 |
2 | HG00735.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.3015-295T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15563060 | |||||||
chr4:15563086 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3015-269G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15563086 | |||||||
chr4:15563192 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3015-163C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15563192 | |||||||
chr4:15563545 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3182+23G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563545 | |||||||
chr4:15563585 | T | C | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3182+63T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563585 | |||||||
chr4:15563657 | A | T | 1 | a0001c0001t0001g0149 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3182+135A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563657 | |||||||
chr4:15563961 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3182+439C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563961 | |||||||
chr4:15564113 | A | T | 81 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(78): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.3182+591A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564113 | |||||||
chr4:15564135 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3182+613C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564135 | |||||||
chr4:15564212 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3182+690A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564212 | |||||||
chr4:15564236 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3182+714C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564236 | |||||||
chr4:15564251 | G | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
68 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.3182+729G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564251 | |||||||
chr4:15564447 | A | T | 1 | a0001c0006t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3182+925A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564447 | |||||||
chr4:15564520 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3182+998A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564520 | |||||||
chr4:15564630 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3182+1108C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564630 | |||||||
chr4:15564668 | C | G | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3182+1146C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564668 | |||||||
chr4:15564812 | G | A | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3182+1290G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564812 | |||||||
chr4:15564836 | C | T | 3 | a0001c0001t0002g0030 a0001c0006t0002g0308 a0001c0006t0002g0310 |
3 | HG01891.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3182+1314C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564836 | |||||||
chr4:15564947 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3182+1425G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564947 | |||||||
chr4:15565024 | G | T | 320 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(317): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.3182+1502G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565024 | |||||||
chr4:15565070 | T | C | 2 | a0001c0002t0002g0145 a0001c0002t0002g0248 |
2 | HG02056.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3182+1548T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565070 | |||||||
chr4:15565282 | T | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3182+1760T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565282 | |||||||
chr4:15565399 | G | GT | 138 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.3182+1892dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | INFO_REALIGN_3_PRIME | chr4 | 15565399 | ||||||
chr4:15565399 | G | GTT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0105 a0001c0001t0001g0149 others(5): Show |
8 | HG01123.hp1 HG01243.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.3182+1891_3182+189 others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | INFO_REALIGN_3_PRIME | chr4 | 15565399 | ||||||
chr4:15565399 | GT | G | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.3182+1892delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | INFO_REALIGN_3_PRIME | chr4 | 15565399 | ||||||
chr4:15565728 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3183-1649C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565728 | |||||||
chr4:15565988 | A | G | 2 | a0001c0002t0001g0123 a0001c0002t0002g0162 |
2 | HG02080.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3183-1389A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565988 | |||||||
chr4:15566260 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3183-1117C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566260 | |||||||
chr4:15566286 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3183-1091G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566286 | |||||||
chr4:15566642 | C | T | 1 | a0001c0004t0002g0075 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3183-735C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566642 | |||||||
chr4:15566701 | G | C | 1 | a0001c0004t0002g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3183-676G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566701 | |||||||
chr4:15566834 | G | C | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3183-543G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566834 | |||||||
chr4:15566968 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3183-409C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566968 | |||||||
chr4:15566979 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3183-398A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566979 | |||||||
chr4:15567084 | A | C | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3183-293A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15567084 | |||||||
chr4:15567262 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3183-115C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15567262 | |||||||
chr4:15567369 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
splice_region_variant&intron_variant | LOW | c.3183-8T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15567369 | |||||||
chr4:15567523 | A | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3288+41A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 25/36 | chr4 | 15567523 | |||||||
chr4:15567617 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3289-60G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 25/36 | chr4 | 15567617 | |||||||
chr4:15567917 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3398+131C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15567917 | |||||||
chr4:15568180 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3398+394T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15568180 | |||||||
chr4:15568566 | C | T | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3399-727C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15568566 | |||||||
chr4:15568648 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3399-645T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15568648 | |||||||
chr4:15569480 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3495+91G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569480 | |||||||
chr4:15569597 | A | G | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3495+208A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569597 | |||||||
chr4:15569600 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3495+211G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569600 | |||||||
chr4:15569811 | C | T | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3495+422C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569811 | |||||||
chr4:15570141 | A | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3496-257A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15570141 | |||||||
chr4:15570582 | C | T | 1 | a0001c0002t0002g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3594+86C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15570582 | |||||||
chr4:15570748 | CGGGAGGC others(25): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0321 |
3 | HG02145.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3594+273_3594+304d others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15570748 | ||||||
chr4:15570883 | A | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(37): Show |
40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.3594+387A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15570883 | |||||||
chr4:15570909 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3594+413A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15570909 | |||||||
chr4:15571021 | C | T | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3594+525C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571021 | |||||||
chr4:15571092 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3594+596T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571092 | |||||||
chr4:15571430 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3594+934G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571430 | |||||||
chr4:15571446 | G | C | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3594+950G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571446 | |||||||
chr4:15571497 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0260 |
2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3594+1001C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571497 | |||||||
chr4:15571606 | C | CA | 180 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.3594+1124dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15571606 | ||||||
chr4:15571606 | C | CAA | 38 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(35): Show |
38 | HG00642.hp1 HG00741.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.3594+1123_3594+112 others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15571606 | ||||||
chr4:15571884 | A | G | 2 | a0002c0003t0001g0295 a0002c0003t0001g0299 |
2 | HG02015.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.3594+1388A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571884 | |||||||
chr4:15571895 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3594+1399C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571895 | |||||||
chr4:15571910 | C | T | 37 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.3594+1414C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571910 | |||||||
chr4:15571987 | C | T | 13 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.3594+1491C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571987 | |||||||
chr4:15572413 | T | C | 1 | a0002c0003t0001g0290 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3595-1737T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572413 | |||||||
chr4:15572433 | C | T | 3 | a0002c0003t0001g0311 a0002c0005t0001g0027 a0002c0005t0001g0038 |
3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3595-1717C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572433 | |||||||
chr4:15572794 | G | A | 10 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG02055.hp2 NA18945.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.3595-1356G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572794 | |||||||
chr4:15572843 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3595-1307T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572843 | |||||||
chr4:15572878 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3595-1272G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572878 | |||||||
chr4:15573042 | T | C | 111 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(108): Show |
113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.3595-1108T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573042 | |||||||
chr4:15573139 | C | CAAGTT | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3595-1011_3595-101 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573139 | |||||||
chr4:15573334 | AGGCTGGA others(18): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3595-811_3595-787d others(27): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15573334 | ||||||
chr4:15573571 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3595-579G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573571 | |||||||
chr4:15573598 | G | A | 1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3595-552G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573598 | |||||||
chr4:15573801 | C | T | 13 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.3595-349C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573801 | |||||||
chr4:15573893 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG00639.hp2 HG01074.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.3595-257G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573893 | |||||||
chr4:15574039 | A | T | 1 | a0006c0009t0002g0231 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3595-111A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15574039 | |||||||
chr4:15574095 | C | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.3595-55C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15574095 | |||||||
chr4:15574128 | C | T | 106 | a0001c0001t0002g0030 a0001c0001t0002g0040 a0001c0001t0002g0163 others(103): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3595-22C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15574128 | |||||||
chr4:15574581 | T | G | 1 | a0021c0014t0002g0138 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3771+255T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574581 | |||||||
chr4:15574641 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3771+315A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574641 | |||||||
chr4:15574737 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3771+411C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574737 | |||||||
chr4:15574762 | T | G | 6 | a0004c0013t0003g0139 a0004c0013t0003g0140 a0004c0022t0002g0018 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3771+436T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574762 | |||||||
chr4:15574791 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3771+465A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574791 | |||||||
chr4:15574808 | T | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3771+482T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574808 | |||||||
chr4:15574903 | T | C | 1 | a0001c0002t0002g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3771+577T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574903 | |||||||
chr4:15574922 | G | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3771+596G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574922 | |||||||
chr4:15575065 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3771+739T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575065 | |||||||
chr4:15575341 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3771+1015C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575341 | |||||||
chr4:15575669 | T | C | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+1343T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575669 | |||||||
chr4:15575702 | A | G | 93 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(90): Show |
94 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3771+1376A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575702 | |||||||
chr4:15575726 | T | A | 1 | a0003c0007t0002g0084 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3771+1400T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575726 | |||||||
chr4:15575791 | T | C | 321 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3771+1465T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575791 | |||||||
chr4:15575804 | A | T | 1 | a0002c0005t0001g0241 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3771+1478A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575804 | |||||||
chr4:15575893 | G | A | 1 | a0001c0006t0001g0273 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3771+1567G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575893 | |||||||
chr4:15575939 | G | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.3771+1613G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575939 | |||||||
chr4:15575964 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3771+1638A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575964 | |||||||
chr4:15576115 | G | A | 106 | a0001c0001t0002g0030 a0001c0001t0002g0040 a0001c0001t0002g0163 others(103): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3771+1789G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576115 | |||||||
chr4:15576445 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3771+2119T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576445 | |||||||
chr4:15576458 | A | T | 1 | a0006c0009t0002g0231 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3771+2132A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576458 | |||||||
chr4:15576622 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0034 others(7): Show |
10 | HG01243.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3771+2296A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576622 | |||||||
chr4:15576623 | A | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0034 others(7): Show |
10 | HG01243.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3771+2297A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576623 | |||||||
chr4:15576781 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3771+2455T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576781 | |||||||
chr4:15576865 | G | A | 1 | a0002c0003t0001g0300 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3771+2539G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576865 | |||||||
chr4:15577122 | TACTG | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+2797_3771+280 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577122 | |||||||
chr4:15577128 | G | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+2802G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577128 | |||||||
chr4:15577129 | A | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+2803A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577129 | |||||||
chr4:15577428 | CTTAAT | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3772-2537_3772-253 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15577428 | ||||||
chr4:15577505 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3772-2463T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577505 | |||||||
chr4:15577577 | A | G | 4 | a0001c0001t0002g0030 a0001c0001t0002g0167 a0001c0006t0002g0308 others(1): Show |
4 | HG01891.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3772-2391A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577577 | |||||||
chr4:15578093 | T | G | 1 | a0001c0006t0001g0272 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3772-1875T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578093 | |||||||
chr4:15578379 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3772-1589G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578379 | |||||||
chr4:15578395 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3772-1573G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578395 | |||||||
chr4:15578787 | GGTTT | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0002c0003t0001g0295 others(1): Show |
4 | HG00323.hp2 HG02015.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.3772-1152_3772-114 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578787 | ||||||
chr4:15578799 | TG | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0321 |
3 | HG02109.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3772-1168delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578799 | |||||||
chr4:15578803 | TGTTTG | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0262 |
3 | HG00642.hp1 HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3772-1164_3772-116 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578803 | |||||||
chr4:15578804 | G | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3772-1164G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578804 | |||||||
chr4:15578807 | TG | T | 87 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0052 others(84): Show |
89 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3772-1160delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578807 | |||||||
chr4:15578808 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3772-1160G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578808 | |||||||
chr4:15578811 | TG | T | 10 | a0001c0001t0001g0119 a0001c0001t0002g0184 a0001c0002t0002g0135 others(7): Show |
10 | HG00438.hp1 HG00597.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.3772-1156delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578811 | |||||||
chr4:15578812 | G | GT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0056 others(7): Show |
11 | HG00099.hp1 HG00733.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.3772-1153dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578812 | ||||||
chr4:15578812 | G | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
97 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.3772-1156G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578812 | |||||||
chr4:15578815 | TG | T | 40 | a0001c0001t0001g0103 a0001c0001t0002g0040 a0001c0004t0002g0028 others(37): Show |
40 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.3772-1152delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578815 | |||||||
chr4:15578816 | G | GT | 18 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(15): Show |
19 | HG00639.hp1 HG02080.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3772-1147dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578816 | ||||||
chr4:15578816 | G | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.3772-1152G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578816 | |||||||
chr4:15578816 | GT | G | 5 | a0001c0001t0001g0055 a0001c0004t0002g0029 a0001c0004t0002g0059 others(2): Show |
5 | HG00280.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3772-1147delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578816 | ||||||
chr4:15579024 | C | CA | 315 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(312): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.3772-936dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15579024 | ||||||
chr4:15579131 | T | G | 93 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(90): Show |
94 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3772-837T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579131 | |||||||
chr4:15579275 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3772-693G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579275 | |||||||
chr4:15579635 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3772-333C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579635 | |||||||
chr4:15579929 | T | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0014c0025t0002g0032 |
3 | HG02622.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3772-39T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579929 | |||||||
chr4:15580256 | G | A | 1 | a0001c0004t0002g0254 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3975+85G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580256 | |||||||
chr4:15580362 | A | G | 214 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.3975+191A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580362 | |||||||
chr4:15580415 | A | T | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3975+244A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580415 | |||||||
chr4:15580593 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.3975+422G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580593 | |||||||
chr4:15580637 | C | CA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(65): Show |
70 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.3975+488dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15580637 | ||||||
chr4:15580637 | CA | C | 12 | a0001c0001t0001g0034 a0001c0001t0001g0070 a0001c0001t0001g0183 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3975+488delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15580637 | ||||||
chr4:15580637 | CAA | C | 135 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(132): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.3975+487_3975+488d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15580637 | ||||||
chr4:15580743 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3975+572A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580743 | |||||||
chr4:15580885 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3975+714A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580885 | |||||||
chr4:15580994 | C | T | 2 | a0001c0004t0002g0028 a0001c0004t0002g0029 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3975+823C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580994 | |||||||
chr4:15581019 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG00639.hp2 HG01070.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.3975+848T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581019 | |||||||
chr4:15581100 | A | G | 4 | a0001c0001t0001g0196 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.3975+929A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581100 | |||||||
chr4:15581159 | A | C | 1 | a0001c0001t0001g0325 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3975+988A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581159 | |||||||
chr4:15581453 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3975+1282C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581453 | |||||||
chr4:15581808 | T | C | 3 | a0001c0002t0002g0129 a0001c0002t0002g0135 a0001c0002t0002g0136 |
3 | HG01106.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3975+1637T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581808 | |||||||
chr4:15582040 | A | G | 1 | a0002c0003t0001g0300 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3975+1869A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582040 | |||||||
chr4:15582224 | TTAAA | T | 31 | a0001c0004t0002g0057 a0001c0004t0002g0059 a0001c0004t0002g0060 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.3975+2057_3975+206 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15582224 | ||||||
chr4:15582292 | G | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
6 | HG00099.hp1 HG01099.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3975+2121G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582292 | |||||||
chr4:15582520 | G | C | 1 | a0001c0002t0002g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3975+2349G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582520 | |||||||
chr4:15582562 | T | C | 40 | a0001c0004t0002g0028 a0001c0004t0002g0029 a0001c0004t0002g0057 others(37): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.3975+2391T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582562 | |||||||
chr4:15582631 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3975+2460C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582631 | |||||||
chr4:15582960 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0124 others(1): Show |
4 | HG03486.hp1 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3975+2789A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582960 | |||||||
chr4:15583185 | T | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3976-2972T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583185 | |||||||
chr4:15583328 | T | C | 1 | a0002c0003t0001g0299 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3976-2829T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583328 | |||||||
chr4:15583456 | AACTGTTA others(4): Show |
A | 1 | a0001c0002t0002g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3976-2700_3976-269 others(15): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583456 | |||||||
chr4:15583509 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3976-2648A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583509 | |||||||
chr4:15583599 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3976-2558T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583599 | |||||||
chr4:15583702 | C | G | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3976-2455C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583702 | |||||||
chr4:15583721 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3976-2436G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583721 | |||||||
chr4:15583724 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3976-2433C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583724 | |||||||
chr4:15583731 | C | T | 82 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(79): Show |
83 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.3976-2426C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583731 | |||||||
chr4:15583776 | C | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3976-2381C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583776 | |||||||
chr4:15583808 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3976-2349G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583808 | |||||||
chr4:15583837 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0034 others(6): Show |
9 | HG01243.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3976-2320G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583837 | |||||||
chr4:15583950 | C | CA | 7 | a0001c0001t0001g0009 a0001c0001t0002g0030 a0001c0001t0002g0161 others(4): Show |
7 | HG01891.hp2 HG02132.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3976-2193dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15583950 | ||||||
chr4:15583960 | AAAAAG | A | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3976-2182_3976-217 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15583960 | ||||||
chr4:15584004 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3976-2153G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584004 | |||||||
chr4:15584032 | T | C | 3 | a0003c0007t0002g0077 a0003c0007t0002g0078 a0003c0007t0002g0081 |
3 | HG00140.hp1 HG02486.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3976-2125T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584032 | |||||||
chr4:15584124 | G | A | 14 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3976-2033G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584124 | |||||||
chr4:15584198 | T | A | 1 | a0022c0028t0001g0255 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3976-1959T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584198 | |||||||
chr4:15584324 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3976-1833T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584324 | |||||||
chr4:15584385 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3976-1772G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584385 | |||||||
chr4:15584602 | G | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.3976-1555G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584602 | |||||||
chr4:15584653 | A | G | 22 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(19): Show |
22 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.3976-1504A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584653 | |||||||
chr4:15584757 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3976-1400G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584757 | |||||||
chr4:15584971 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3976-1186C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584971 | |||||||
chr4:15584986 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3976-1171A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584986 | |||||||
chr4:15585910 | A | G | 1 | a0002c0003t0001g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3976-247A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15585910 | |||||||
chr4:15586274 | A | T | 320 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(317): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.4065+28A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586274 | |||||||
chr4:15586475 | A | C | 2 | a0001c0008t0002g0007 a0001c0008t0002g0283 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4065+229A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586475 | |||||||
chr4:15586632 | T | A | 3 | a0001c0001t0002g0030 a0001c0006t0002g0308 a0001c0006t0002g0310 |
3 | HG01891.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4065+386T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586632 | |||||||
chr4:15586850 | G | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0321 |
3 | HG02145.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4065+604G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586850 | |||||||
chr4:15587267 | C | T | 114 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(111): Show |
116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.4066-549C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587267 | |||||||
chr4:15587341 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4066-475T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587341 | |||||||
chr4:15587567 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4066-249G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587567 | |||||||
chr4:15587648 | T | C | 1 | a0002c0003t0002g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4066-168T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587648 | |||||||
chr4:15587691 | C | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.4066-125C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587691 | |||||||
chr4:15587692 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4066-124G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587692 | |||||||
chr4:15587722 | C | T | 109 | a0001c0001t0002g0030 a0001c0001t0002g0040 a0001c0001t0002g0163 others(106): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.4066-94C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587722 | |||||||
chr4:15588176 | G | A | 2 | a0001c0004t0002g0028 a0001c0004t0002g0029 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4179+247G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588176 | |||||||
chr4:15588621 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4179+692A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588621 | |||||||
chr4:15588637 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4179+708T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588637 | |||||||
chr4:15588744 | C | G | 37 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.4180-801C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588744 | |||||||
chr4:15588843 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4180-702G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588843 | |||||||
chr4:15588979 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4180-566G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588979 | |||||||
chr4:15589234 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4180-311C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589234 | |||||||
chr4:15589288 | T | C | 1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4180-257T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589288 | |||||||
chr4:15589348 | G | C | 1 | a0001c0002t0002g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4180-197G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589348 | |||||||
chr4:15589472 | G | A | 1 | a0001c0002t0002g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4180-73G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589472 | |||||||
chr4:15589508 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4180-37T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589508 | |||||||
chr4:15589784 | A | AAT | 138 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(135): Show |
140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.4314+119_4314+120d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15589784 | ||||||
chr4:15589784 | A | AATAT | 71 | a0001c0001t0001g0198 a0001c0001t0002g0257 a0001c0002t0002g0003 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.4314+117_4314+120d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15589784 | ||||||
chr4:15589800 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.4314+121C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15589800 | |||||||
chr4:15589821 | TA | T | 333 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.4314+146delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15589821 | ||||||
chr4:15589842 | C | T | 112 | a0001c0001t0002g0030 a0001c0001t0002g0040 a0001c0001t0002g0163 others(109): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.4314+163C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15589842 | |||||||
chr4:15589858 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4314+179T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15589858 | |||||||
chr4:15590091 | C | A | 1 | a0006c0009t0002g0328 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4314+412C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590091 | |||||||
chr4:15590259 | A | C | 1 | a0002c0003t0001g0292 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4314+580A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590259 | |||||||
chr4:15590313 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4314+634G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590313 | |||||||
chr4:15590328 | A | T | 1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4314+649A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590328 | |||||||
chr4:15590360 | C | T | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4314+681C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590360 | |||||||
chr4:15590475 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4314+796A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590475 | |||||||
chr4:15590636 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4314+957G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590636 | |||||||
chr4:15590898 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4314+1219G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590898 | |||||||
chr4:15591008 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0036 others(1): Show |
4 | HG02630.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4314+1329G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591008 | |||||||
chr4:15591168 | T | C | 1 | a0001c0004t0002g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4314+1489T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591168 | |||||||
chr4:15591219 | AT | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(297): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.4314+1557delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15591219 | ||||||
chr4:15591241 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.4314+1562C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591241 | |||||||
chr4:15591295 | A | G | 117 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(114): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4314+1616A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591295 | |||||||
chr4:15591313 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4314+1634G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591313 | |||||||
chr4:15591449 | C | A | 2 | a0002c0003t0001g0266 a0002c0003t0001g0332 |
2 | HG01192.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4314+1770C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591449 | |||||||
chr4:15591453 | A | C | 87 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(84): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.4314+1774A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591453 | |||||||
chr4:15591509 | G | A | 1 | a0002c0003t0002g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4314+1830G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591509 | |||||||
chr4:15591546 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4314+1867C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591546 | |||||||
chr4:15591569 | T | C | 1 | a0001c0004t0002g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4314+1890T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591569 | |||||||
chr4:15591708 | A | G | 5 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4314+2029A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591708 | |||||||
chr4:15591758 | A | T | 2 | a0001c0002t0002g0115 a0001c0002t0002g0116 |
2 | NA18948.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.4314+2079A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591758 | |||||||
chr4:15591837 | T | C | 1 | a0002c0003t0002g0302 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4314+2158T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591837 | |||||||
chr4:15592069 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.4314+2390C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592069 | |||||||
chr4:15592292 | A | G | 1 | a0001c0002t0002g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4314+2613A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592292 | |||||||
chr4:15592339 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4314+2660A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592339 | |||||||
chr4:15592676 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0002g0190 |
2 | HG02717.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.4314+2997A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592676 | |||||||
chr4:15592685 | T | G | 15 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(12): Show |
15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.4314+3006T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592685 | |||||||
chr4:15592920 | T | C | 26 | a0001c0001t0001g0215 a0002c0003t0001g0266 a0002c0003t0001g0269 others(23): Show |
26 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4315-3165T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592920 | |||||||
chr4:15592930 | G | A | 1 | a0001c0001t0002g0008 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4315-3155G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592930 | |||||||
chr4:15593153 | G | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.4315-2932G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593153 | |||||||
chr4:15593275 | T | C | 42 | a0001c0001t0001g0017 a0001c0001t0001g0079 a0001c0001t0001g0089 others(39): Show |
43 | HG00323.hp2 HG00621.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.4315-2810T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593275 | |||||||
chr4:15593338 | C | A | 1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4315-2747C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593338 | |||||||
chr4:15593675 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4315-2410T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593675 | |||||||
chr4:15593791 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4315-2294G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593791 | |||||||
chr4:15593967 | G | C | 1 | a0001c0006t0001g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4315-2118G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593967 | |||||||
chr4:15594251 | G | T | 1 | a0002c0003t0002g0289 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4315-1834G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15594251 | |||||||
chr4:15594401 | G | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.4315-1684G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15594401 | |||||||
chr4:15594830 | A | T | 261 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(258): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.4315-1255A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15594830 | |||||||
chr4:15595256 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4315-829T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15595256 | |||||||
chr4:15595607 | G | T | 1 | a0001c0006t0001g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4315-478G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15595607 | |||||||
chr4:15595660 | G | A | 1 | a0017c0023t0002g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4315-425G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15595660 | |||||||
chr4:15596276 | A | G | 2 | a0006c0009t0002g0231 a0006c0009t0002g0232 |
2 | NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.4437+69A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596276 | |||||||
chr4:15596361 | C | T | 315 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(312): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.4437+154C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596361 | |||||||
chr4:15596407 | G | A | 1 | a0001c0002t0002g0155 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4437+200G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596407 | |||||||
chr4:15596428 | T | TAA | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(73): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.4437+223_4437+224d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | INFO_REALIGN_3_PRIME | chr4 | 15596428 | ||||||
chr4:15596493 | C | A | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4437+286C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596493 | |||||||
chr4:15596758 | C | T | 11 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0200 others(8): Show |
11 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.4437+551C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596758 | |||||||
chr4:15596855 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): Show |
61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4438-552C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596855 | |||||||
chr4:15596914 | A | G | 117 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(114): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4438-493A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596914 | |||||||
chr4:15596985 | C | T | 315 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(312): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.4438-422C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596985 | |||||||
chr4:15597017 | ATGT | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): Show |
61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4438-385_4438-383d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | INFO_REALIGN_3_PRIME | chr4 | 15597017 | ||||||
chr4:15597169 | G | C | 2 | a0001c0001t0002g0040 a0001c0024t0002g0204 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4438-238G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15597169 | |||||||
chr4:15597270 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0013c0031t0001g0285 |
3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4438-137T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15597270 | |||||||
chr4:15597398 | C | A | 2 | a0002c0003t0001g0281 a0002c0003t0001g0312 |
2 | NA18960.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.4438-9C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15597398 | |||||||
chr4:15597513 | A | C | 1 | a0001c0002t0002g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4496+48A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597513 | |||||||
chr4:15597531 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4496+66A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597531 | |||||||
chr4:15597607 | G | T | 2 | a0005c0011t0001g0001 a0005c0032t0001g0284 |
3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4496+142G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597607 | |||||||
chr4:15597628 | T | G | 10 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG02055.hp2 NA18945.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.4496+163T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597628 | |||||||
chr4:15597730 | T | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4496+265T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597730 | |||||||
chr4:15597938 | C | T | 1 | a0001c0002t0002g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4496+473C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597938 | |||||||
chr4:15598049 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4496+584T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598049 | |||||||
chr4:15598188 | A | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0174 a0001c0001t0001g0333 |
3 | HG03942.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4496+723A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598188 | |||||||
chr4:15598222 | C | T | 117 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(114): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4496+757C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598222 | |||||||
chr4:15598234 | C | G | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4496+769C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598234 | |||||||
chr4:15598476 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.4496+1011G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598476 | |||||||
chr4:15598494 | G | A | 1 | a0020c0020t0001g0317 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4496+1029G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598494 | |||||||
chr4:15598582 | C | T | 261 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(258): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.4497-947C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598582 | |||||||
chr4:15598707 | C | G | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | NA18612.hp2 NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.4497-822C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598707 | |||||||
chr4:15598738 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4497-791T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598738 | |||||||
chr4:15598740 | A | G | 16 | a0001c0001t0002g0102 a0001c0001t0002g0161 a0001c0001t0002g0190 others(13): Show |
16 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.4497-789A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598740 | |||||||
chr4:15598827 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4497-702T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598827 | |||||||
chr4:15599176 | A | G | 127 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(124): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.4497-353A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15599176 | |||||||
chr4:15599367 | G | A | 1 | a0016c0016t0002g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4497-162G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15599367 | |||||||
chr4:15599430 | T | C | 2 | a0001c0004t0002g0028 a0001c0004t0002g0029 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4497-99T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15599430 | |||||||
chr4:15600138 | T | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0192 others(29): Show |
33 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.4674+432T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600138 | |||||||
chr4:15600184 | C | G | 1 | a0002c0003t0001g0292 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4674+478C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600184 | |||||||
chr4:15600484 | C | T | 1 | a0001c0002t0002g0146 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4675-753C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600484 | |||||||
chr4:15600593 | T | C | 37 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.4675-644T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600593 | |||||||
chr4:15600625 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4675-612G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600625 | |||||||
chr4:15600629 | G | C | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(119): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4675-608G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600629 | |||||||
chr4:15600635 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): Show |
61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4675-602G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600635 | |||||||
chr4:15600793 | C | G | 1 | a0001c0002t0002g0148 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4675-444C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600793 | |||||||
chr4:15600873 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): Show |
61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4675-364G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600873 | |||||||
chr4:15600896 | C | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0036 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4675-341C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600896 | |||||||
chr4:15600903 | C | CA | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0192 others(45): Show |
49 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.4675-316dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600903 | ||||||
chr4:15600903 | C | CAA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(83): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4675-317_4675-316d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600903 | ||||||
chr4:15600903 | C | CAAA | 50 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.4675-318_4675-316d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600903 | ||||||
chr4:15600913 | A | AAG | 85 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0023 others(82): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.4675-323_4675-322i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600913 | ||||||
chr4:15600915 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4675-322A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600915 | |||||||
chr4:15600917 | A | AAG | 37 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(34): Show |
37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.4675-319_4675-318i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600917 | ||||||
chr4:15601068 | A | C | 2 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.4675-169A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601068 | |||||||
chr4:15601148 | C | CT | 14 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.4675-89_4675-88ins others(1): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601148 | |||||||
chr4:15601149 | A | T | 14 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.4675-88A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601149 | |||||||
chr4:15601150 | C | A | 14 | a0001c0001t0002g0102 a0001c0001t0002g0195 a0001c0001t0002g0197 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.4675-87C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601150 | |||||||
chr4:15601150 | C | CTTA | 302 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(299): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.4675-85_4675-83dup others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15601150 |