Item | Value |
---|---|
geneid | 26005 |
ensemblid | ENSG00000168014.18 |
hgncid | 24564 |
symbol | C2CD3 |
name | C2 domain containing 3 centriole elongation regulator |
refseq_nuc | NM_001286577.2 |
refseq_prot | NP_001273506.1 |
ensembl_nuc | ENST00000334126.12 |
ensembl_prot | ENSP00000334379.7 |
mane_status | MANE Select |
chr | chr11 |
start | 74012718 |
end | 74171002 |
strand | - |
ver | v1.2 |
region | chr11:74012718-74171002 |
region5000 | chr11:74007718-74176002 |
regionname0 | C2CD3_chr11_74012718_74171002 |
regionname5000 | C2CD3_chr11_74007718_74176002 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2353 | 78 | 5 | 15 | 41 | 4 | 11 | 27 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0002 | 0/0 | 2353 | 69 | 16 | 18 | 23 | 6 | 6 | 19 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0003 | 0/0 | 2353 | 60 | 4 | 5 | 41 | 3 | 7 | 28 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0004 | 0/0 | 2353 | 20 | 19 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0005 | 0/0 | 2353 | 13 | 7 | 3 | 0 | 0 | 3 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0006 | 0/0 | 2353 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0007 | 0/0 | 2353 | 10 | 9 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0008 | 0/0 | 2353 | 8 | 0 | 1 | 5 | 0 | 2 | 5 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0009 | 0/0 | 2353 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0010 | 0/0 | 2353 | 6 | 1 | 0 | 4 | 0 | 1 | 4 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0011 | 0/0 | 2353 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0012 | 0/0 | 2353 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0013 | 0/0 | 2353 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0014 | 0/0 | 2353 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0015 | 0/0 | 1123 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(1118): Show |
chr11 | 74007718 | 74176002 |
a0016 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0017 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0018 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0019 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0020 | 0/0 | 2353 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0021 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0022 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0023 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0024 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0025 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0026 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0027 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0028 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0029 | 0/0 | 2353 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0030 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0031 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0032 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0033 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0034 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0035 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
a0036 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | MKQRK others(2348): Show |
chr11 | 74007718 | 74176002 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 7059 | 77 | 5 | 14 | 41 | 4 | 11 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0001c0030 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0002c0003 | 0/0 | 7059 | 49 | 15 | 16 | 6 | 6 | 6 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0002c0005 | 0/0 | 7059 | 19 | 0 | 2 | 17 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0002c0028 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0003c0002 | 0/0 | 7059 | 56 | 1 | 5 | 40 | 3 | 7 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0003c0016 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0003c0034 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0003c0041 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0004c0004 | 0/0 | 7059 | 20 | 19 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0005c0006 | 0/0 | 7059 | 12 | 7 | 3 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0005c0027 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0006c0008 | 0/0 | 7059 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0006c0012 | 0/0 | 7059 | 5 | 5 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0007c0009 | 0/0 | 7059 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0007c0017 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0007c0026 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0008c0007 | 0/0 | 7059 | 8 | 0 | 1 | 5 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0009c0011 | 0/0 | 7059 | 6 | 0 | 0 | 6 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0010c0010 | 0/0 | 7059 | 6 | 1 | 0 | 4 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0011c0015 | 0/0 | 7059 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0011c0018 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0012c0014 | 0/0 | 7059 | 3 | 0 | 1 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0013c0013 | 0/0 | 7059 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0014c0020 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0015c0019 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0016c0023 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0017c0044 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0018c0029 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0019c0043 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0020c0033 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0021c0037 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0022c0032 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0023c0021 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0024c0024 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0025c0040 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0026c0047 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0027c0036 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0028c0045 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0029c0038 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0030c0042 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0031c0025 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0032c0046 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0033c0035 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0034c0031 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0035c0039 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 | ||
a0036c0022 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | ATGAA others(7054): Show |
chr11 | 74007718 | 74176002 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7939 | 77 | 5 | 14 | 41 | 4 | 11 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0001c0030t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0002c0003t0001 | 0/0 | 7939 | 48 | 15 | 16 | 5 | 6 | 6 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0002c0003t0005 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0002c0005t0001 | 0/0 | 7939 | 19 | 0 | 2 | 17 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0002c0028t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0003c0002t0001 | 0/0 | 7939 | 53 | 1 | 4 | 40 | 1 | 7 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0003c0002t0003 | 0/0 | 7939 | 3 | 0 | 1 | 0 | 2 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0003c0016t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0003c0034t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0003c0041t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0004c0004t0001 | 0/0 | 7939 | 20 | 19 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0005c0006t0001 | 0/0 | 7939 | 12 | 7 | 3 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0005c0027t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0006c0008t0001 | 0/0 | 7939 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0006c0012t0001 | 0/0 | 7939 | 5 | 5 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0007c0009t0002 | 0/0 | 7939 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0007c0017t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0007c0026t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0008c0007t0001 | 0/0 | 7939 | 8 | 0 | 1 | 5 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0009c0011t0001 | 0/0 | 7939 | 6 | 0 | 0 | 6 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0010c0010t0001 | 0/0 | 7939 | 6 | 1 | 0 | 4 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0011c0015t0001 | 0/0 | 7939 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0011c0018t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0012c0014t0001 | 0/0 | 7939 | 3 | 0 | 1 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0013c0013t0001 | 0/0 | 7939 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0014c0020t0004 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0015c0019t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0016c0023t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0017c0044t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0018c0029t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0019c0043t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0020c0033t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0021c0037t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0022c0032t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0023c0021t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0024c0024t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0025c0040t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0026c0047t0002 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0027c0036t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0028c0045t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0029c0038t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0030c0042t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0031c0025t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0032c0046t0002 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0033c0035t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0034c0031t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0035c0039t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
a0036c0022t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | GTAGT others(7934): Show |
chr11 | 74007718 | 74176002 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0001c0030t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0003t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0002c0028t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0002t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0016t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0016t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0034t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0003c0041t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0004c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0005c0027t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0012t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0012t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0012t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0006c0012t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0009t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0017t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0017t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0007c0026t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0008c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0009c0011t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0009c0011t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0009c0011t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0009c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0009c0011t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0009c0011t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0010c0010t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0010c0010t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0010c0010t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0010c0010t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0010c0010t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0010c0010t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0011c0015t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0011c0015t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0011c0018t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0011c0018t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0012c0014t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0012c0014t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0012c0014t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0013c0013t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0013c0013t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0013c0013t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0014c0020t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0014c0020t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0015c0019t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0015c0019t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0016c0023t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0017c0044t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0018c0029t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0019c0043t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0020c0033t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0021c0037t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0022c0032t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0023c0021t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0024c0024t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0025c0040t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0026c0047t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0027c0036t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0028c0045t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0029c0038t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0030c0042t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0031c0025t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0032c0046t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0033c0035t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0034c0031t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0035c0039t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
a0036c0022t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0209 | EUR | GBR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00280 | hp1 | a0003 | c0002 | t0001 | g0264 | EUR | FIN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0206 | EUR | FIN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00408 | hp1 | a0003 | c0002 | t0001 | g0251 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00423 | hp1 | a0003 | c0002 | t0001 | g0252 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00438 | hp2 | a0003 | c0002 | t0001 | g0283 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00544 | hp2 | a0003 | c0002 | t0001 | g0278 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00558 | hp2 | a0003 | c0002 | t0001 | g0285 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00597 | hp2 | a0003 | c0002 | t0001 | g0253 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00609 | hp1 | a0003 | c0002 | t0001 | g0291 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00639 | hp1 | a0016 | c0023 | t0001 | g0130 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0208 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00642 | hp1 | a0005 | c0006 | t0001 | g0013 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00642 | hp2 | a0003 | c0002 | t0003 | g0004 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00673 | hp1 | a0003 | c0002 | t0001 | g0259 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00733 | hp1 | a0003 | c0002 | t0001 | g0265 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00733 | hp2 | a0002 | c0005 | t0001 | g0008 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00738 | hp1 | a0002 | c0005 | t0001 | g0049 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00738 | hp2 | a0003 | c0002 | t0001 | g0298 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG00741 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01074 | hp1 | a0008 | c0007 | t0001 | g0177 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01074 | hp2 | a0004 | c0004 | t0001 | g0036 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0196 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01081 | hp2 | a0003 | c0002 | t0001 | g0247 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01099 | hp1 | a0005 | c0006 | t0001 | g0015 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01099 | hp2 | a0017 | c0044 | t0001 | g0089 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01106 | hp2 | a0005 | c0006 | t0001 | g0024 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01109 | hp1 | a0002 | c0003 | t0001 | g0187 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01169 | hp2 | a0018 | c0029 | t0001 | g0198 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0167 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0059 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01258 | hp2 | a0002 | c0003 | t0001 | g0060 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01261 | hp2 | a0019 | c0043 | t0001 | g0084 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0171 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01361 | hp1 | a0012 | c0014 | t0001 | g0135 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0201 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0075 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01433 | hp2 | a0001 | c0030 | t0001 | g0190 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01515 | hp1 | a0020 | c0033 | t0001 | g0178 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01516 | hp1 | a0003 | c0002 | t0003 | g0002 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0210 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01517 | hp1 | a0003 | c0002 | t0003 | g0003 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01884 | hp1 | a0006 | c0008 | t0001 | g0239 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01884 | hp2 | a0011 | c0015 | t0001 | g0001 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01928 | hp2 | a0002 | c0003 | t0001 | g0170 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0169 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0172 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0166 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02015 | hp1 | a0002 | c0005 | t0001 | g0069 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02015 | hp2 | a0021 | c0037 | t0001 | g0273 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02040 | hp2 | a0003 | c0002 | t0001 | g0241 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02055 | hp1 | a0013 | c0013 | t0001 | g0227 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0197 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02056 | hp1 | a0003 | c0002 | t0001 | g0290 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02074 | hp1 | a0003 | c0002 | t0001 | g0292 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02083 | hp2 | a0009 | c0011 | t0001 | g0079 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02129 | hp1 | a0002 | c0003 | t0005 | g0080 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0071 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02145 | hp1 | a0005 | c0006 | t0001 | g0022 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02145 | hp2 | a0007 | c0009 | t0002 | g0313 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02257 | hp2 | a0006 | c0008 | t0001 | g0237 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02258 | hp1 | a0004 | c0004 | t0001 | g0037 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02258 | hp2 | a0006 | c0008 | t0001 | g0236 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02280 | hp1 | a0007 | c0017 | t0001 | g0194 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02280 | hp2 | a0010 | c0010 | t0001 | g0303 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0050 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02451 | hp2 | a0007 | c0017 | t0001 | g0195 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02523 | hp1 | a0003 | c0002 | t0001 | g0288 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02523 | hp2 | a0023 | c0021 | t0001 | g0220 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02572 | hp1 | a0006 | c0008 | t0001 | g0230 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02572 | hp2 | a0002 | c0028 | t0001 | g0011 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0030 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02615 | hp1 | a0006 | c0012 | t0001 | g0235 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02615 | hp2 | a0024 | c0024 | t0001 | g0203 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02622 | hp1 | a0025 | c0040 | t0001 | g0301 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02622 | hp2 | a0004 | c0004 | t0001 | g0048 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02630 | hp2 | a0004 | c0004 | t0001 | g0183 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02647 | hp1 | a0002 | c0003 | t0001 | g0090 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02647 | hp2 | a0004 | c0004 | t0001 | g0032 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02717 | hp1 | a0026 | c0047 | t0002 | g0310 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02717 | hp2 | a0006 | c0012 | t0001 | g0233 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02723 | hp1 | a0006 | c0012 | t0001 | g0232 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02723 | hp2 | a0014 | c0020 | t0004 | g0219 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02735 | hp1 | a0005 | c0027 | t0001 | g0012 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02738 | hp1 | a0012 | c0014 | t0001 | g0134 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0215 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02809 | hp1 | a0002 | c0003 | t0001 | g0056 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02809 | hp2 | a0004 | c0004 | t0001 | g0033 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02818 | hp1 | a0003 | c0002 | t0001 | g0271 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02818 | hp2 | a0004 | c0004 | t0001 | g0046 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02886 | hp1 | a0005 | c0006 | t0001 | g0020 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02886 | hp2 | a0003 | c0016 | t0001 | g0242 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02895 | hp1 | a0004 | c0004 | t0001 | g0043 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0014 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02896 | hp2 | a0015 | c0019 | t0001 | g0028 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02897 | hp1 | a0015 | c0019 | t0001 | g0025 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02897 | hp2 | a0004 | c0004 | t0001 | g0042 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02922 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02922 | hp2 | a0004 | c0004 | t0001 | g0045 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02965 | hp1 | a0011 | c0018 | t0001 | g0132 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02965 | hp2 | a0004 | c0004 | t0001 | g0038 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02970 | hp1 | a0006 | c0008 | t0001 | g0240 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02970 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02976 | hp1 | a0004 | c0004 | t0001 | g0044 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02976 | hp2 | a0006 | c0008 | t0001 | g0229 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03041 | hp1 | a0014 | c0020 | t0004 | g0218 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03041 | hp2 | a0007 | c0009 | t0002 | g0314 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03098 | hp1 | a0003 | c0034 | t0001 | g0185 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0054 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03130 | hp1 | a0011 | c0015 | t0001 | g0223 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03130 | hp2 | a0005 | c0006 | t0001 | g0023 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03139 | hp1 | a0011 | c0018 | t0001 | g0131 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03139 | hp2 | a0027 | c0036 | t0001 | g0287 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03195 | hp1 | a0007 | c0009 | t0002 | g0316 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03195 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0040 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03209 | hp2 | a0028 | c0045 | t0001 | g0224 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03239 | hp1 | a0003 | c0002 | t0001 | g0269 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0062 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03453 | hp1 | a0002 | c0003 | t0001 | g0213 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03453 | hp2 | a0004 | c0004 | t0001 | g0034 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0205 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03486 | hp2 | a0006 | c0008 | t0001 | g0238 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03490 | hp2 | a0003 | c0002 | t0001 | g0258 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03491 | hp1 | a0029 | c0038 | t0001 | g0293 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03491 | hp2 | a0005 | c0006 | t0001 | g0007 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03492 | hp1 | a0005 | c0006 | t0001 | g0006 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03492 | hp2 | a0003 | c0002 | t0001 | g0263 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03516 | hp1 | a0006 | c0012 | t0001 | g0231 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03516 | hp2 | a0013 | c0013 | t0001 | g0226 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03540 | hp1 | a0007 | c0009 | t0002 | g0315 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03540 | hp2 | a0005 | c0006 | t0001 | g0021 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03579 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03654 | hp1 | a0003 | c0002 | t0001 | g0268 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03669 | hp2 | a0008 | c0007 | t0001 | g0076 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03704 | hp1 | a0003 | c0002 | t0001 | g0299 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0031 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03831 | hp2 | a0007 | c0026 | t0001 | g0005 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0214 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03927 | hp1 | a0003 | c0002 | t0001 | g0275 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03942 | hp2 | a0008 | c0007 | t0001 | g0217 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG04184 | hp2 | a0003 | c0002 | t0001 | g0270 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG04228 | hp2 | a0010 | c0010 | t0001 | g0302 | SAS | STU | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18522 | hp1 | a0031 | c0025 | t0001 | g0222 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18522 | hp2 | a0032 | c0046 | t0002 | g0309 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18747 | hp2 | a0003 | c0002 | t0001 | g0289 | EAS | CHB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18906 | hp1 | a0013 | c0013 | t0001 | g0225 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18906 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18941 | hp1 | a0003 | c0002 | t0001 | g0255 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18941 | hp2 | a0002 | c0005 | t0001 | g0074 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18942 | hp2 | a0002 | c0005 | t0001 | g0092 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18943 | hp2 | a0010 | c0010 | t0001 | g0305 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18945 | hp1 | a0002 | c0005 | t0001 | g0066 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18946 | hp2 | a0002 | c0005 | t0001 | g0058 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18948 | hp1 | a0002 | c0005 | t0001 | g0189 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18948 | hp2 | a0003 | c0002 | t0001 | g0277 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18949 | hp2 | a0003 | c0002 | t0001 | g0279 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18950 | hp1 | a0003 | c0002 | t0001 | g0262 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18950 | hp2 | a0008 | c0007 | t0001 | g0221 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18956 | hp1 | a0008 | c0007 | t0001 | g0216 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18957 | hp1 | a0003 | c0041 | t0001 | g0297 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18960 | hp2 | a0003 | c0002 | t0001 | g0282 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18962 | hp1 | a0003 | c0002 | t0001 | g0266 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18962 | hp2 | a0002 | c0005 | t0001 | g0067 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18963 | hp1 | a0008 | c0007 | t0001 | g0211 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18963 | hp2 | a0003 | c0002 | t0001 | g0246 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18966 | hp1 | a0002 | c0005 | t0001 | g0086 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18967 | hp1 | a0002 | c0005 | t0001 | g0188 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18970 | hp2 | a0003 | c0002 | t0001 | g0272 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18972 | hp1 | a0003 | c0002 | t0001 | g0284 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18979 | hp1 | a0002 | c0005 | t0001 | g0088 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18979 | hp2 | a0009 | c0011 | t0001 | g0077 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18980 | hp1 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18980 | hp2 | a0003 | c0002 | t0001 | g0286 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18982 | hp1 | a0002 | c0005 | t0001 | g0085 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18982 | hp2 | a0003 | c0002 | t0001 | g0248 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18984 | hp2 | a0010 | c0010 | t0001 | g0308 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18988 | hp1 | a0003 | c0002 | t0001 | g0260 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18989 | hp2 | a0003 | c0002 | t0001 | g0296 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18991 | hp2 | a0003 | c0002 | t0001 | g0294 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18993 | hp2 | a0008 | c0007 | t0001 | g0082 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18995 | hp1 | a0003 | c0002 | t0001 | g0257 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18998 | hp1 | a0003 | c0002 | t0001 | g0261 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18998 | hp2 | a0009 | c0011 | t0001 | g0064 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA18999 | hp2 | a0010 | c0010 | t0001 | g0306 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19003 | hp1 | a0002 | c0005 | t0001 | g0073 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19003 | hp2 | a0010 | c0010 | t0001 | g0307 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19005 | hp1 | a0003 | c0002 | t0001 | g0280 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19009 | hp2 | a0002 | c0005 | t0001 | g0068 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19010 | hp2 | a0003 | c0002 | t0001 | g0256 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19011 | hp2 | a0003 | c0002 | t0001 | g0244 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19030 | hp1 | a0004 | c0004 | t0001 | g0181 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19030 | hp2 | a0007 | c0009 | t0002 | g0312 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19043 | hp1 | a0033 | c0035 | t0001 | g0228 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19043 | hp2 | a0005 | c0006 | t0001 | g0026 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19058 | hp1 | a0003 | c0002 | t0001 | g0254 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19060 | hp1 | a0003 | c0002 | t0001 | g0250 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19062 | hp1 | a0009 | c0011 | t0001 | g0063 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19064 | hp2 | a0002 | c0005 | t0001 | g0168 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19068 | hp1 | a0034 | c0031 | t0001 | g0184 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19068 | hp2 | a0003 | c0002 | t0001 | g0276 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19070 | hp1 | a0008 | c0007 | t0001 | g0212 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19070 | hp2 | a0003 | c0002 | t0001 | g0267 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19074 | hp1 | a0003 | c0002 | t0001 | g0243 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19074 | hp2 | a0009 | c0011 | t0001 | g0065 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19078 | hp1 | a0002 | c0005 | t0001 | g0087 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19078 | hp2 | a0035 | c0039 | t0001 | g0113 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19080 | hp1 | a0002 | c0005 | t0001 | g0072 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19080 | hp2 | a0003 | c0002 | t0001 | g0281 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19081 | hp1 | a0002 | c0005 | t0001 | g0093 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19081 | hp2 | a0003 | c0002 | t0001 | g0274 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19083 | hp1 | a0003 | c0002 | t0001 | g0245 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19085 | hp1 | a0009 | c0011 | t0001 | g0053 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19240 | hp1 | a0004 | c0004 | t0001 | g0041 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA19240 | hp2 | a0007 | c0009 | t0002 | g0317 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20129 | hp2 | a0007 | c0009 | t0002 | g0311 | AFR | ASW | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0200 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0204 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0051 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0207 | SAS | GIH | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20905 | hp2 | a0012 | c0014 | t0001 | g0127 | SAS | GIH | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0202 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG01123 | hp2 | a0003 | c0002 | t0001 | g0300 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02109 | hp1 | a0022 | c0032 | t0001 | g0176 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02486 | hp1 | a0004 | c0004 | t0001 | g0186 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02486 | hp2 | a0011 | c0015 | t0001 | g0001 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03471 | hp1 | a0005 | c0006 | t0001 | g0027 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG03471 | hp2 | a0004 | c0004 | t0001 | g0047 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG06807 | hp1 | a0030 | c0042 | t0001 | g0304 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
HG06807 | hp2 | a0002 | c0003 | t0001 | g0057 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20300 | hp1 | a0006 | c0012 | t0001 | g0234 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA20300 | hp2 | a0036 | c0022 | t0001 | g0295 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA21309 | hp1 | a0003 | c0016 | t0001 | g0249 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
NA21309 | hp2 | a0002 | c0003 | t0001 | g0052 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0098 | REF | REF | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0107 | REF | REF | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74013467 | T | C | 1 | a0032 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.6980A>G | p.Asn2327Ser | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 7190/7939 | 6980/7062 | 2327/2353 | chr11 | 74013467 | |||
chr11:74013495 | A | C | 1 | a0034 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.6952T>G | p.Ser2318Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 7162/7939 | 6952/7062 | 2318/2353 | chr11 | 74013495 | |||
chr11:74033588 | C | G | 1 | a0009 | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
missense_variant | MODERATE | c.6572G>C | p.Gly2191Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6782/7939 | 6572/7062 | 2191/2353 | chr11 | 74033588 | |||
chr11:74033924 | G | A | 1 | a0012 | 3 | HG01361.hp1 HG02738.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.6236C>T | p.Thr2079Met | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6446/7939 | 6236/7062 | 2079/2353 | chr11 | 74033924 | |||
chr11:74033969 | T | C | 1 | a0026 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.6191A>G | p.Tyr2064Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6401/7939 | 6191/7062 | 2064/2353 | chr11 | 74033969 | |||
chr11:74034102 | A | G | 15 | a0004 a0006 a0007 others(12): Show |
66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
missense_variant | MODERATE | c.6058T>C | p.Ser2020Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6268/7939 | 6058/7062 | 2020/2353 | chr11 | 74034102 | |||
chr11:74048206 | T | C | 3 | a0004 a0014 a0022 |
23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
missense_variant&splice_region_variant | MODERATE | c.5494A>G | p.Arg1832Gly | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/33 | 5704/7939 | 5494/7062 | 1832/2353 | chr11 | 74048206 | |||
chr11:74048209 | C | A | 3 | a0004 a0014 a0022 |
23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
missense_variant | MODERATE | c.5491G>T | p.Gly1831Trp | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/33 | 5701/7939 | 5491/7062 | 1831/2353 | chr11 | 74048209 | |||
chr11:74049368 | G | T | 3 | a0010 a0030 a0031 |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
missense_variant | MODERATE | c.5330C>A | p.Ala1777Glu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/33 | 5540/7939 | 5330/7062 | 1777/2353 | chr11 | 74049368 | |||
chr11:74057443 | T | C | 1 | a0025 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.5053A>G | p.Thr1685Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/33 | 5263/7939 | 5053/7062 | 1685/2353 | chr11 | 74057443 | |||
chr11:74057508 | C | T | 2 | a0005 a0015 |
15 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(12): Show |
missense_variant | MODERATE | c.4988G>A | p.Ser1663Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/33 | 5198/7939 | 4988/7062 | 1663/2353 | chr11 | 74057508 | |||
chr11:74074519 | G | C | 1 | a0021 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.4685C>G | p.Ser1562Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/33 | 4895/7939 | 4685/7062 | 1562/2353 | chr11 | 74074519 | |||
chr11:74078681 | T | G | 1 | a0033 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4037A>C | p.Asp1346Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/33 | 4247/7939 | 4037/7062 | 1346/2353 | chr11 | 74078681 | |||
chr11:74085638 | T | C | 2 | a0004 a0014 |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
missense_variant | MODERATE | c.3890A>G | p.Tyr1297Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 4100/7939 | 3890/7062 | 1297/2353 | chr11 | 74085638 | |||
chr11:74085782 | C | T | 1 | a0031 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3746G>A | p.Arg1249Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3956/7939 | 3746/7062 | 1249/2353 | chr11 | 74085782 | |||
chr11:74085833 | T | C | 1 | a0029 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.3695A>G | p.Asn1232Ser | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3905/7939 | 3695/7062 | 1232/2353 | chr11 | 74085833 | |||
chr11:74085857 | T | C | 1 | a0018 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.3671A>G | p.Gln1224Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3881/7939 | 3671/7062 | 1224/2353 | chr11 | 74085857 | |||
chr11:74085872 | C | T | 17 | a0002 a0004 a0005 others(14): Show |
144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
missense_variant | MODERATE | c.3656G>A | p.Arg1219Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3866/7939 | 3656/7062 | 1219/2353 | chr11 | 74085872 | |||
chr11:74092422 | A | T | 1 | a0024 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3511T>A | p.Ser1171Thr | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/33 | 3721/7939 | 3511/7062 | 1171/2353 | chr11 | 74092422 | |||
chr11:74092563 | G | A | 1 | a0015 | 2 | HG02896.hp2 HG02897.hp1 |
stop_gained | HIGH | c.3370C>T | p.Gln1124* | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/33 | 3580/7939 | 3370/7062 | 1124/2353 | chr11 | 74092563 | |||
chr11:74095240 | A | G | 1 | a0027 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.3148T>C | p.Phe1050Leu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/33 | 3358/7939 | 3148/7062 | 1050/2353 | chr11 | 74095240 | |||
chr11:74095398 | C | T | 9 | a0003 a0006 a0013 others(6): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
missense_variant | MODERATE | c.2990G>A | p.Arg997Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/33 | 3200/7939 | 2990/7062 | 997/2353 | chr11 | 74095398 | |||
chr11:74098055 | C | T | 1 | a0020 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2933G>A | p.Arg978Lys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/33 | 3143/7939 | 2933/7062 | 978/2353 | chr11 | 74098055 | |||
chr11:74100598 | C | T | 1 | a0016 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2659G>A | p.Val887Met | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/33 | 2869/7939 | 2659/7062 | 887/2353 | chr11 | 74100598 | |||
chr11:74103210 | C | T | 1 | a0036 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2501G>A | p.Cys834Tyr | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2711/7939 | 2501/7062 | 834/2353 | chr11 | 74103210 | |||
chr11:74103367 | C | T | 1 | a0025 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2344G>A | p.Val782Ile | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2554/7939 | 2344/7062 | 782/2353 | chr11 | 74103367 | |||
chr11:74103393 | G | C | 3 | a0008 a0009 a0020 |
15 | HG01074.hp1 HG01515.hp1 HG02083.hp2 others(12): Show |
missense_variant | MODERATE | c.2318C>G | p.Pro773Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2528/7939 | 2318/7062 | 773/2353 | chr11 | 74103393 | |||
chr11:74114579 | T | C | 1 | a0035 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1535A>G | p.Gln512Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/33 | 1745/7939 | 1535/7062 | 512/2353 | chr11 | 74114579 | |||
chr11:74118334 | C | T | 1 | a0028 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1414G>A | p.Val472Ile | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/33 | 1624/7939 | 1414/7062 | 472/2353 | chr11 | 74118334 | |||
chr11:74132892 | C | T | 1 | a0013 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1169G>A | p.Arg390Lys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/33 | 1379/7939 | 1169/7062 | 390/2353 | chr11 | 74132892 | |||
chr11:74133555 | G | C | 1 | a0030 | 1 | HG06807.hp1 | missense_variant&splice_region_variant | MODERATE | c.958C>G | p.Leu320Val | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/33 | 1168/7939 | 958/7062 | 320/2353 | chr11 | 74133555 | |||
chr11:74138957 | G | C | 2 | a0017 a0019 |
2 | HG01099.hp2 HG01261.hp2 |
missense_variant | MODERATE | c.718C>G | p.His240Asp | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/33 | 928/7939 | 718/7062 | 240/2353 | chr11 | 74138957 | |||
chr11:74161421 | G | C | 1 | a0014 | 2 | HG02723.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.461C>G | p.Ser154Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/33 | 671/7939 | 461/7062 | 154/2353 | chr11 | 74161421 | |||
chr11:74168380 | G | A | 1 | a0014 | 2 | HG02723.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.289C>T | p.Arg97Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/33 | 499/7939 | 289/7062 | 97/2353 | chr11 | 74168380 | |||
chr11:74168538 | G | T | 1 | a0023 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.131C>A | p.Thr44Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/33 | 341/7939 | 131/7062 | 44/2353 | chr11 | 74168538 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74013403 | C | T | 3 | a0007c0009 a0011c0018 a0026c0047 |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
synonymous_variant | LOW | c.7044G>A | p.Gln2348Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 7254/7939 | 7044/7062 | 2348/2353 | chr11 | 74013403 | |||
chr11:74028389 | G | A | 1 | a0005c0027 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.6819C>T | p.Pro2273Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/33 | 7029/7939 | 6819/7062 | 2273/2353 | chr11 | 74028389 | |||
chr11:74048297 | C | T | 1 | a0002c0028 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.5403G>A | p.Thr1801Thr | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/33 | 5613/7939 | 5403/7062 | 1801/2353 | chr11 | 74048297 | |||
chr11:74074281 | T | C | 22 | a0002c0003 a0002c0005 a0002c0028 others(19): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
synonymous_variant | LOW | c.4923A>G | p.Val1641Val | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/33 | 5133/7939 | 4923/7062 | 1641/2353 | chr11 | 74074281 | |||
chr11:74078287 | C | T | 3 | a0010c0010 a0030c0042 a0031c0025 |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
synonymous_variant | LOW | c.4431G>A | p.Arg1477Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/33 | 4641/7939 | 4431/7062 | 1477/2353 | chr11 | 74078287 | |||
chr11:74085664 | C | T | 1 | a0001c0030 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.3864G>A | p.Glu1288Glu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 4074/7939 | 3864/7062 | 1288/2353 | chr11 | 74085664 | |||
chr11:74085715 | C | T | 2 | a0003c0016 a0036c0022 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.3813G>A | p.Leu1271Leu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 4023/7939 | 3813/7062 | 1271/2353 | chr11 | 74085715 | |||
chr11:74093908 | T | C | 2 | a0011c0015 a0028c0045 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.3252A>G | p.Pro1084Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/33 | 3462/7939 | 3252/7062 | 1084/2353 | chr11 | 74093908 | |||
chr11:74098233 | G | A | 1 | a0002c0005 | 19 | HG00733.hp2 HG00738.hp1 HG02015.hp1 others(16): Show |
synonymous_variant | LOW | c.2755C>T | p.Leu919Leu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/33 | 2965/7939 | 2755/7062 | 919/2353 | chr11 | 74098233 | |||
chr11:74103431 | T | G | 5 | a0003c0034 a0006c0008 a0006c0012 others(2): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
synonymous_variant | LOW | c.2280A>C | p.Ala760Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2490/7939 | 2280/7062 | 760/2353 | chr11 | 74103431 | |||
chr11:74103560 | G | A | 1 | a0006c0008 | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.2151C>T | p.Asn717Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2361/7939 | 2151/7062 | 717/2353 | chr11 | 74103560 | |||
chr11:74114458 | T | C | 5 | a0003c0002 a0003c0041 a0021c0037 others(2): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
synonymous_variant | LOW | c.1656A>G | p.Pro552Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/33 | 1866/7939 | 1656/7062 | 552/2353 | chr11 | 74114458 | |||
chr11:74123102 | C | A | 1 | a0025c0040 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1251G>T | p.Gly417Gly | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/33 | 1461/7939 | 1251/7062 | 417/2353 | chr11 | 74123102 | |||
chr11:74123120 | T | C | 1 | a0003c0041 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1233A>G | p.Gln411Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/33 | 1443/7939 | 1233/7062 | 411/2353 | chr11 | 74123120 | |||
chr11:74139628 | G | A | 2 | a0011c0015 a0028c0045 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.684C>T | p.Asn228Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/33 | 894/7939 | 684/7062 | 228/2353 | chr11 | 74139628 | |||
chr11:74168543 | T | C | 3 | a0007c0009 a0026c0047 a0032c0046 |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
synonymous_variant | LOW | c.126A>G | p.Lys42Lys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/33 | 336/7939 | 126/7062 | 42/2353 | chr11 | 74168543 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74012801 | T | C | 1 | a0002c0003t0005 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 584 | chr11 | 74012801 | ||||||
chr11:74013301 | G | A | 1 | a0014c0020t0004 | 2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*84C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 84 | chr11 | 74013301 | ||||||
chr11:74170803 | A | G | 1 | a0003c0002t0003 | 3 | HG00642.hp2 HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-11T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/33 | 11 | chr11 | 74170803 | ||||||
chr11:74170832 | C | A | 3 | a0007c0009t0002 a0026c0047t0002 a0032c0046t0002 |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/33 | 40 | chr11 | 74170832 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74013657 | G | A | 4 | a0002c0003t0001g0052 a0013c0013t0001g0225 a0013c0013t0001g0226 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6922-132C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74013657 | |||||||
chr11:74013790 | C | T | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-265G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74013790 | |||||||
chr11:74013818 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6922-293C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74013818 | |||||||
chr11:74014012 | G | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.6922-487C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014012 | |||||||
chr11:74014206 | A | G | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-681T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014206 | |||||||
chr11:74014207 | G | A | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-682C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014207 | |||||||
chr11:74014347 | T | G | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6922-822A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014347 | |||||||
chr11:74014399 | A | G | 1 | a0028c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6922-874T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014399 | |||||||
chr11:74014519 | G | GGCCCAGC others(9): Show |
1 | a0001c0001t0001g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6922-1010_6922-995 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014519 | |||||||
chr11:74014519 | GGCCCAGC others(9): Show |
G | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-1010_6922-995 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014519 | |||||||
chr11:74014632 | T | C | 2 | a0010c0010t0001g0303 a0030c0042t0001g0304 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6922-1107A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014632 | |||||||
chr11:74015079 | C | T | 14 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-1554G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015079 | |||||||
chr11:74015100 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6922-1575T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015100 | |||||||
chr11:74015255 | G | C | 4 | a0002c0003t0001g0206 a0002c0003t0001g0208 a0002c0003t0001g0209 others(1): Show |
4 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.6922-1730C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015255 | |||||||
chr11:74015278 | T | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-1753A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015278 | |||||||
chr11:74015498 | C | T | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-1973G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015498 | |||||||
chr11:74015532 | C | T | 1 | a0002c0005t0001g0066 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6922-2007G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015532 | |||||||
chr11:74015887 | G | A | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-2362C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015887 | |||||||
chr11:74015900 | C | CA | 18 | a0003c0002t0001g0299 a0005c0006t0001g0015 a0006c0008t0001g0229 others(15): Show |
19 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.6922-2376dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015900 | |||||||
chr11:74015916 | G | A | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6922-2391C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015916 | |||||||
chr11:74015917 | GA | G | 20 | a0001c0001t0001g0112 a0002c0003t0001g0196 a0002c0003t0001g0197 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.6922-2393delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015917 | |||||||
chr11:74015918 | A | G | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6922-2393T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015918 | |||||||
chr11:74016046 | C | G | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6922-2521G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016046 | |||||||
chr11:74016105 | T | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-2580A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016105 | |||||||
chr11:74016311 | C | CA | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-2787dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016311 | |||||||
chr11:74016511 | C | T | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6922-2986G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016511 | |||||||
chr11:74016573 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0160 a0003c0002t0001g0290 others(1): Show |
4 | HG01952.hp1 HG02056.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.6922-3048C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016573 | |||||||
chr11:74016678 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.6922-3153G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016678 | |||||||
chr11:74016783 | T | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-3258A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016783 | |||||||
chr11:74016796 | G | A | 1 | a0003c0016t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6922-3271C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016796 | |||||||
chr11:74016851 | T | C | 1 | a0002c0005t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.6922-3326A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016851 | |||||||
chr11:74016921 | G | A | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-3396C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016921 | |||||||
chr11:74016940 | G | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6922-3415C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016940 | |||||||
chr11:74016972 | G | A | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-3447C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016972 | |||||||
chr11:74017110 | G | C | 1 | a0018c0029t0001g0198 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6922-3585C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017110 | |||||||
chr11:74017114 | A | G | 123 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0145 others(120): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.6922-3589T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017114 | |||||||
chr11:74017115 | C | T | 1 | a0003c0002t0001g0277 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6922-3590G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017115 | |||||||
chr11:74017138 | G | A | 14 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-3613C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017138 | |||||||
chr11:74017214 | C | T | 2 | a0013c0013t0001g0226 a0013c0013t0001g0227 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6922-3689G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017214 | |||||||
chr11:74017264 | G | A | 1 | a0002c0003t0001g0172 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6922-3739C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017264 | |||||||
chr11:74017383 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6922-3858C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017383 | |||||||
chr11:74017477 | A | G | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-3952T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017477 | |||||||
chr11:74017552 | A | G | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4027T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017552 | |||||||
chr11:74017627 | C | A | 1 | a0006c0008t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6922-4102G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017627 | |||||||
chr11:74017659 | T | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4134A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017659 | |||||||
chr11:74017777 | A | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4252T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017777 | |||||||
chr11:74017797 | TC | T | 12 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(9): Show |
12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-4273delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017797 | |||||||
chr11:74018011 | C | T | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4486G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018011 | |||||||
chr11:74018097 | G | A | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-4572C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018097 | |||||||
chr11:74018155 | A | G | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4630T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018155 | |||||||
chr11:74018174 | CG | C | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-4650delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018174 | |||||||
chr11:74018175 | G | A | 14 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-4650C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018175 | |||||||
chr11:74018177 | G | A | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-4652C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018177 | |||||||
chr11:74018290 | C | T | 2 | a0010c0010t0001g0303 a0030c0042t0001g0304 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6922-4765G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018290 | |||||||
chr11:74018307 | C | A | 1 | a0003c0002t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6922-4782G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018307 | |||||||
chr11:74018336 | C | T | 43 | a0001c0030t0001g0190 a0002c0003t0001g0030 a0002c0003t0001g0031 others(40): Show |
43 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.6922-4811G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018336 | |||||||
chr11:74018344 | C | T | 33 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(30): Show |
34 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(31): Show |
intron_variant | MODIFIER | c.6922-4819G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018344 | |||||||
chr11:74018603 | C | T | 12 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(9): Show |
12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-5078G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018603 | |||||||
chr11:74018674 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6922-5149T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018674 | |||||||
chr11:74018714 | C | T | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6922-5189G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018714 | |||||||
chr11:74018724 | T | C | 19 | a0002c0005t0001g0049 a0002c0005t0001g0058 a0002c0005t0001g0066 others(16): Show |
19 | HG00733.hp1 HG00738.hp1 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.6922-5199A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018724 | |||||||
chr11:74018846 | A | G | 1 | a0023c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6922-5321T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018846 | |||||||
chr11:74018929 | A | T | 1 | a0030c0042t0001g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6922-5404T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018929 | |||||||
chr11:74018957 | C | T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6922-5432G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018957 | |||||||
chr11:74019124 | G | T | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-5599C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019124 | |||||||
chr11:74019234 | G | A | 1 | a0002c0003t0001g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.6922-5709C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019234 | |||||||
chr11:74019235 | C | T | 12 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(9): Show |
12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-5710G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019235 | |||||||
chr11:74019316 | T | TG | 46 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0032 others(43): Show |
47 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.6922-5792dupC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019316 | |||||||
chr11:74019465 | T | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-5940A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019465 | |||||||
chr11:74019563 | T | G | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-6038A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019563 | |||||||
chr11:74019683 | A | ATTTT | 23 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(20): Show |
23 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.6922-6162_6922-615 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019683 | |||||||
chr11:74019683 | A | ATTTTT | 11 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(8): Show |
12 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.6922-6163_6922-615 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019683 | |||||||
chr11:74019695 | C | T | 46 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0032 others(43): Show |
47 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.6922-6170G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019695 | |||||||
chr11:74019704 | T | G | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-6179A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019704 | |||||||
chr11:74019715 | C | T | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-6190G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019715 | |||||||
chr11:74019787 | A | G | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6922-6262T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019787 | |||||||
chr11:74020203 | A | G | 61 | a0002c0003t0001g0052 a0003c0016t0001g0242 a0003c0016t0001g0249 others(58): Show |
62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.6922-6678T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020203 | |||||||
chr11:74020377 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6922-6852T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020377 | |||||||
chr11:74020401 | C | G | 14 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-6876G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020401 | |||||||
chr11:74020531 | T | G | 46 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0032 others(43): Show |
47 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.6922-7006A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020531 | |||||||
chr11:74020538 | C | A | 2 | a0005c0006t0001g0006 a0029c0038t0001g0293 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.6922-7013G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020538 | |||||||
chr11:74020539 | G | C | 34 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(31): Show |
35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-7014C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020539 | |||||||
chr11:74020553 | C | T | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6922-7028G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020553 | |||||||
chr11:74020619 | C | T | 209 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0112 others(206): Show |
210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.6922-7094G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020619 | |||||||
chr11:74020817 | A | G | 3 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 |
3 | HG02280.hp1 HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.6922-7292T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020817 | |||||||
chr11:74020889 | G | A | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-7364C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020889 | |||||||
chr11:74020919 | G | C | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6921+7368C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020919 | |||||||
chr11:74020946 | C | A | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6921+7341G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020946 | |||||||
chr11:74020998 | G | C | 26 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(23): Show |
27 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.6921+7289C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020998 | |||||||
chr11:74021048 | T | C | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6921+7239A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021048 | |||||||
chr11:74021055 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0152 |
2 | HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.6921+7232C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021055 | |||||||
chr11:74021138 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.6921+7149G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021138 | |||||||
chr11:74021198 | C | G | 2 | a0002c0005t0001g0086 a0002c0005t0001g0092 |
2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.6921+7089G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021198 | |||||||
chr11:74021246 | A | AAAAC | 23 | a0003c0002t0001g0276 a0003c0002t0001g0277 a0004c0004t0001g0032 others(20): Show |
23 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.6921+7037_6921+704 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021246 | |||||||
chr11:74021480 | G | T | 27 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0004c0004t0001g0036 others(24): Show |
28 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.6921+6807C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021480 | |||||||
chr11:74021644 | C | T | 16 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(13): Show |
16 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.6921+6643G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021644 | |||||||
chr11:74021767 | C | T | 1 | a0002c0003t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6921+6520G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021767 | |||||||
chr11:74021811 | G | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6921+6476C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021811 | |||||||
chr11:74021836 | G | T | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.6921+6451C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021836 | |||||||
chr11:74021854 | A | G | 2 | a0008c0007t0001g0177 a0020c0033t0001g0178 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.6921+6433T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021854 | |||||||
chr11:74021861 | T | C | 40 | a0002c0003t0001g0054 a0002c0003t0001g0055 a0002c0003t0001g0056 others(37): Show |
41 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(38): Show |
intron_variant | MODIFIER | c.6921+6426A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021861 | |||||||
chr11:74021896 | C | T | 1 | a0002c0003t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.6921+6391G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021896 | |||||||
chr11:74021998 | C | T | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6921+6289G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021998 | |||||||
chr11:74022062 | G | A | 3 | a0013c0013t0001g0226 a0013c0013t0001g0227 a0033c0035t0001g0228 |
3 | HG02055.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6921+6225C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022062 | |||||||
chr11:74022115 | T | A | 18 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(15): Show |
18 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.6921+6172A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022115 | |||||||
chr11:74022116 | T | C | 157 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0112 others(154): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.6921+6171A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022116 | |||||||
chr11:74022127 | G | GA | 6 | a0001c0001t0001g0193 a0006c0008t0001g0230 a0007c0017t0001g0194 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.6921+6159dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022127 | |||||||
chr11:74022238 | T | C | 1 | a0002c0005t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.6921+6049A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022238 | |||||||
chr11:74022317 | G | A | 1 | a0004c0004t0001g0186 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6921+5970C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022317 | |||||||
chr11:74022418 | C | T | 8 | a0002c0003t0001g0213 a0005c0006t0001g0022 a0006c0008t0001g0238 others(5): Show |
8 | HG01884.hp1 HG02145.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.6921+5869G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022418 | |||||||
chr11:74022449 | G | A | 5 | a0002c0003t0001g0196 a0002c0003t0001g0204 a0002c0003t0001g0205 others(2): Show |
5 | HG01081.hp1 HG02738.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.6921+5838C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022449 | |||||||
chr11:74022461 | G | A | 1 | a0003c0002t0001g0288 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.6921+5826C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022461 | |||||||
chr11:74022468 | G | A | 12 | a0003c0034t0001g0185 a0006c0008t0001g0238 a0006c0008t0001g0239 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.6921+5819C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022468 | |||||||
chr11:74022516 | T | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0164 a0012c0014t0001g0127 others(2): Show |
5 | HG01361.hp1 HG02109.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.6921+5771A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022516 | |||||||
chr11:74022575 | G | A | 2 | a0010c0010t0001g0303 a0030c0042t0001g0304 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5712C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022575 | |||||||
chr11:74022611 | ACTGCCGT others(25): Show |
A | 1 | a0002c0003t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6921+5644_6921+567 others(36): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022611 | |||||||
chr11:74022626 | G | A | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.6921+5661C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022626 | |||||||
chr11:74022856 | G | A | 2 | a0010c0010t0001g0303 a0030c0042t0001g0304 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5431C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022856 | |||||||
chr11:74023013 | A | G | 39 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(36): Show |
40 | HG01074.hp2 HG01884.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.6921+5274T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023013 | |||||||
chr11:74023044 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6921+5243G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023044 | |||||||
chr11:74023161 | T | C | 60 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(57): Show |
61 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(58): Show |
intron_variant | MODIFIER | c.6921+5126A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023161 | |||||||
chr11:74023162 | G | A | 3 | a0007c0026t0001g0005 a0010c0010t0001g0303 a0030c0042t0001g0304 |
3 | HG02280.hp2 HG03831.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5125C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023162 | |||||||
chr11:74023189 | C | T | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+5098G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023189 | |||||||
chr11:74023229 | C | T | 3 | a0007c0026t0001g0005 a0010c0010t0001g0303 a0030c0042t0001g0304 |
3 | HG02280.hp2 HG03831.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5058G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023229 | |||||||
chr11:74023329 | A | C | 80 | a0001c0001t0001g0151 a0001c0001t0001g0179 a0001c0030t0001g0190 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.6921+4958T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023329 | |||||||
chr11:74023355 | T | A | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6921+4932A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023355 | |||||||
chr11:74023468 | T | C | 2 | a0010c0010t0001g0303 a0030c0042t0001g0304 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+4819A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023468 | |||||||
chr11:74023542 | T | G | 2 | a0001c0001t0001g0182 a0003c0002t0001g0274 |
2 | NA18949.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.6921+4745A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023542 | |||||||
chr11:74023639 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6921+4648G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023639 | |||||||
chr11:74023655 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6921+4632G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023655 | |||||||
chr11:74023666 | T | C | 1 | a0007c0009t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6921+4621A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023666 | |||||||
chr11:74023688 | T | TC | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+4598dupG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023688 | |||||||
chr11:74023774 | C | T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6921+4513G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023774 | |||||||
chr11:74023782 | C | T | 1 | a0002c0003t0001g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6921+4505G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023782 | |||||||
chr11:74023860 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0174 |
2 | NA18747.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.6921+4427A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023860 | |||||||
chr11:74024009 | G | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6921+4278C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024009 | |||||||
chr11:74024043 | G | A | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6921+4244C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024043 | |||||||
chr11:74024044 | T | G | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6921+4243A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024044 | |||||||
chr11:74024114 | C | T | 1 | a0003c0002t0001g0245 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6921+4173G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024114 | |||||||
chr11:74024179 | C | T | 60 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(57): Show |
61 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(58): Show |
intron_variant | MODIFIER | c.6921+4108G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024179 | |||||||
chr11:74024282 | A | G | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+4005T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024282 | |||||||
chr11:74024330 | A | G | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6921+3957T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024330 | |||||||
chr11:74024767 | G | A | 4 | a0002c0003t0001g0054 a0002c0003t0001g0055 a0002c0003t0001g0056 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6921+3520C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024767 | |||||||
chr11:74024780 | G | A | 41 | a0001c0001t0001g0151 a0001c0001t0001g0179 a0002c0003t0001g0052 others(38): Show |
41 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.6921+3507C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024780 | |||||||
chr11:74024839 | T | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6921+3448A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024839 | |||||||
chr11:74025114 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0160 |
2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.6921+3173A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025114 | |||||||
chr11:74025176 | A | G | 7 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6921+3111T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025176 | |||||||
chr11:74025336 | G | A | 1 | a0002c0003t0001g0200 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.6921+2951C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025336 | |||||||
chr11:74025373 | G | A | 7 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6921+2914C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025373 | |||||||
chr11:74025457 | G | A | 2 | a0006c0008t0001g0239 a0006c0008t0001g0240 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6921+2830C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025457 | |||||||
chr11:74025468 | A | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+2819T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025468 | |||||||
chr11:74025547 | C | G | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.6921+2740G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025547 | |||||||
chr11:74025620 | G | A | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6921+2667C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025620 | |||||||
chr11:74025643 | G | A | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+2644C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025643 | |||||||
chr11:74025696 | G | A | 2 | a0006c0008t0001g0239 a0006c0008t0001g0240 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6921+2591C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025696 | |||||||
chr11:74025702 | G | C | 2 | a0005c0006t0001g0026 a0005c0006t0001g0027 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6921+2585C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025702 | |||||||
chr11:74025725 | G | T | 7 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(4): Show |
7 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6921+2562C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025725 | |||||||
chr11:74025756 | C | A | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.6921+2531G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025756 | |||||||
chr11:74025830 | T | C | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.6921+2457A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025830 | |||||||
chr11:74025897 | G | A | 2 | a0006c0008t0001g0239 a0006c0008t0001g0240 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6921+2390C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025897 | |||||||
chr11:74026012 | C | T | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6921+2275G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026012 | |||||||
chr11:74026043 | A | T | 1 | a0008c0007t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6921+2244T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026043 | |||||||
chr11:74026200 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6921+2087G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026200 | |||||||
chr11:74026231 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.6921+2056G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026231 | |||||||
chr11:74026268 | C | T | 1 | a0002c0003t0001g0210 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.6921+2019G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026268 | |||||||
chr11:74026310 | GA | G | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+1976delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026310 | |||||||
chr11:74026321 | A | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6921+1966T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026321 | |||||||
chr11:74026443 | G | A | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.6921+1844C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026443 | |||||||
chr11:74026692 | G | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6921+1595C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026692 | |||||||
chr11:74026735 | T | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6921+1552A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026735 | |||||||
chr11:74026791 | A | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6921+1496T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026791 | |||||||
chr11:74026822 | G | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0103 |
2 | HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.6921+1465C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026822 | |||||||
chr11:74026870 | C | G | 4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6921+1417G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026870 | |||||||
chr11:74026962 | C | CA | 178 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0156 others(175): Show |
179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.6921+1324dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026962 | |||||||
chr11:74026962 | C | CAA | 14 | a0003c0002t0001g0282 a0003c0002t0001g0286 a0003c0002t0003g0002 others(11): Show |
14 | HG01516.hp1 HG01517.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.6921+1323_6921+132 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026962 | |||||||
chr11:74027074 | A | T | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6921+1213T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027074 | |||||||
chr11:74027112 | T | C | 6 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.6921+1175A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027112 | |||||||
chr11:74027210 | G | A | 1 | a0007c0009t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6921+1077C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027210 | |||||||
chr11:74027239 | A | T | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+1048T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027239 | |||||||
chr11:74027244 | C | T | 229 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0151 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.6921+1043G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027244 | |||||||
chr11:74027254 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.6921+1033C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027254 | |||||||
chr11:74027296 | T | C | 1 | a0002c0003t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6921+991A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027296 | |||||||
chr11:74027431 | A | G | 1 | a0006c0012t0001g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6921+856T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027431 | |||||||
chr11:74027451 | A | C | 1 | a0005c0027t0001g0012 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6921+836T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027451 | |||||||
chr11:74027507 | A | G | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.6921+780T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027507 | |||||||
chr11:74027671 | C | T | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.6921+616G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027671 | |||||||
chr11:74027755 | AT | A | 3 | a0003c0002t0001g0298 a0003c0002t0001g0299 a0003c0002t0001g0300 |
3 | HG00738.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.6921+531delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027755 | |||||||
chr11:74027840 | C | T | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+447G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027840 | |||||||
chr11:74027896 | C | T | 2 | a0002c0003t0001g0050 a0002c0003t0001g0051 |
2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.6921+391G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027896 | |||||||
chr11:74027897 | G | A | 1 | a0003c0002t0001g0270 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6921+390C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027897 | |||||||
chr11:74027941 | G | A | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+346C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027941 | |||||||
chr11:74027999 | T | C | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6921+288A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027999 | |||||||
chr11:74028014 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6921+273A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028014 | |||||||
chr11:74028045 | T | C | 31 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(28): Show |
31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+242A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028045 | |||||||
chr11:74028245 | T | G | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6921+42A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028245 | |||||||
chr11:74028256 | T | C | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+31A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028256 | |||||||
chr11:74028608 | C | G | 36 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(33): Show |
36 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.6810-210G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028608 | |||||||
chr11:74028636 | T | C | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6810-238A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028636 | |||||||
chr11:74028712 | T | A | 1 | a0003c0002t0001g0282 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6810-314A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028712 | |||||||
chr11:74028864 | G | A | 36 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(33): Show |
36 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.6810-466C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028864 | |||||||
chr11:74029119 | G | A | 65 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(62): Show |
66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.6810-721C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029119 | |||||||
chr11:74029208 | C | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-810G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029208 | |||||||
chr11:74029210 | C | A | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6810-812G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029210 | |||||||
chr11:74029217 | G | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-819C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029217 | |||||||
chr11:74029355 | G | A | 1 | a0002c0003t0001g0070 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.6810-957C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029355 | |||||||
chr11:74029530 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6810-1132G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029530 | |||||||
chr11:74029606 | CCAGA | C | 5 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG00544.hp1 HG02129.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.6810-1212_6810-120 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029606 | |||||||
chr11:74029630 | G | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6810-1232C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029630 | |||||||
chr11:74029722 | C | G | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6810-1324G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029722 | |||||||
chr11:74029953 | G | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6810-1555C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029953 | |||||||
chr11:74030050 | C | A | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6810-1652G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030050 | |||||||
chr11:74030220 | C | T | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-1822G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030220 | |||||||
chr11:74030253 | T | C | 36 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(33): Show |
36 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.6810-1855A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030253 | |||||||
chr11:74030282 | T | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-1884A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030282 | |||||||
chr11:74030351 | T | C | 1 | a0002c0003t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6810-1953A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030351 | |||||||
chr11:74030354 | T | C | 55 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(52): Show |
56 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(53): Show |
intron_variant | MODIFIER | c.6810-1956A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030354 | |||||||
chr11:74030377 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0103 |
2 | HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.6810-1979A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030377 | |||||||
chr11:74030472 | C | T | 1 | a0002c0003t0001g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6810-2074G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030472 | |||||||
chr11:74030550 | C | T | 6 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.6810-2152G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030550 | |||||||
chr11:74030703 | A | G | 23 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(20): Show |
23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.6810-2305T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030703 | |||||||
chr11:74030794 | G | A | 3 | a0002c0003t0001g0200 a0002c0003t0001g0201 a0002c0003t0001g0202 |
3 | HG01123.hp1 HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.6810-2396C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030794 | |||||||
chr11:74030954 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0152 |
2 | HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.6809+2397G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030954 | |||||||
chr11:74031219 | T | G | 26 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(23): Show |
26 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.6809+2132A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031219 | |||||||
chr11:74031365 | C | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6809+1986G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031365 | |||||||
chr11:74031392 | C | T | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6809+1959G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031392 | |||||||
chr11:74031919 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6809+1432C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031919 | |||||||
chr11:74032284 | T | C | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.6809+1067A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032284 | |||||||
chr11:74032368 | G | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6809+983C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032368 | |||||||
chr11:74032487 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6809+864G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032487 | |||||||
chr11:74032490 | CCT | C | 39 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(36): Show |
40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.6809+859_6809+860d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032490 | |||||||
chr11:74032590 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6809+761C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032590 | |||||||
chr11:74032596 | C | T | 1 | a0003c0002t0001g0276 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6809+755G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032596 | |||||||
chr11:74032640 | G | A | 1 | a0002c0003t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6809+711C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032640 | |||||||
chr11:74032732 | C | G | 41 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(38): Show |
42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.6809+619G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032732 | |||||||
chr11:74032735 | C | T | 8 | a0001c0001t0001g0182 a0003c0002t0001g0257 a0003c0002t0001g0266 others(5): Show |
8 | HG00438.hp2 HG03654.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.6809+616G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032735 | |||||||
chr11:74032817 | G | A | 41 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(38): Show |
42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.6809+534C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032817 | |||||||
chr11:74032839 | T | C | 2 | a0003c0002t0001g0280 a0003c0002t0001g0281 |
2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6809+512A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032839 | |||||||
chr11:74032863 | T | TA | 8 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.6809+487dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032863 | |||||||
chr11:74033056 | T | G | 3 | a0006c0008t0001g0238 a0006c0008t0001g0239 a0006c0008t0001g0240 |
3 | HG01884.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6809+295A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74033056 | |||||||
chr11:74033118 | G | T | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6809+233C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74033118 | |||||||
chr11:74034350 | T | C | 41 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(38): Show |
42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.5882-72A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034350 | |||||||
chr11:74034482 | A | C | 1 | a0004c0004t0001g0036 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5882-204T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034482 | |||||||
chr11:74034499 | G | A | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5882-221C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034499 | |||||||
chr11:74034579 | G | A | 1 | a0003c0002t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5882-301C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034579 | |||||||
chr11:74034633 | T | C | 1 | a0003c0002t0001g0288 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5882-355A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034633 | |||||||
chr11:74034765 | T | G | 1 | a0036c0022t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5882-487A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034765 | |||||||
chr11:74034794 | G | A | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5882-516C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034794 | |||||||
chr11:74034843 | T | C | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5882-565A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034843 | |||||||
chr11:74034890 | A | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5882-612T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034890 | |||||||
chr11:74034942 | T | G | 1 | a0013c0013t0001g0225 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5882-664A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034942 | |||||||
chr11:74035022 | G | A | 2 | a0004c0004t0001g0042 a0004c0004t0001g0043 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5882-744C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035022 | |||||||
chr11:74035119 | G | T | 1 | a0012c0014t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5882-841C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035119 | |||||||
chr11:74035143 | A | G | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5882-865T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035143 | |||||||
chr11:74035236 | C | T | 3 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0026c0047t0002g0310 |
3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5882-958G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035236 | |||||||
chr11:74035244 | A | G | 65 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(62): Show |
66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.5882-966T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035244 | |||||||
chr11:74035402 | G | A | 63 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(60): Show |
64 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.5882-1124C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035402 | |||||||
chr11:74035421 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5882-1143C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035421 | |||||||
chr11:74035635 | T | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5882-1357A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035635 | |||||||
chr11:74035709 | G | GT | 12 | a0001c0001t0001g0094 a0007c0009t0002g0311 a0007c0009t0002g0312 others(9): Show |
12 | HG01255.hp2 HG02145.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5882-1432dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035709 | |||||||
chr11:74035748 | T | C | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5882-1470A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035748 | |||||||
chr11:74035816 | T | C | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5882-1538A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035816 | |||||||
chr11:74035859 | C | CT | 17 | a0003c0002t0001g0257 a0005c0027t0001g0012 a0006c0008t0001g0229 others(14): Show |
18 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.5882-1582dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035859 | |||||||
chr11:74035859 | C | G | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5882-1581G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035859 | |||||||
chr11:74035908 | C | T | 8 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(5): Show |
9 | HG01884.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.5881+1570G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035908 | |||||||
chr11:74035970 | G | C | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5881+1508C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035970 | |||||||
chr11:74036110 | C | G | 1 | a0019c0043t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5881+1368G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036110 | |||||||
chr11:74036175 | C | T | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5881+1303G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036175 | |||||||
chr11:74036216 | G | C | 6 | a0009c0011t0001g0053 a0009c0011t0001g0063 a0009c0011t0001g0064 others(3): Show |
6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.5881+1262C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036216 | |||||||
chr11:74036349 | A | G | 5 | a0003c0002t0001g0252 a0003c0002t0001g0253 a0003c0002t0001g0254 others(2): Show |
5 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.5881+1129T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036349 | |||||||
chr11:74036452 | A | G | 1 | a0003c0002t0001g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5881+1026T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036452 | |||||||
chr11:74036582 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5881+896C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036582 | |||||||
chr11:74037100 | T | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5881+378A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037100 | |||||||
chr11:74037115 | C | T | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5881+363G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037115 | |||||||
chr11:74037134 | T | C | 39 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(36): Show |
40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5881+344A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037134 | |||||||
chr11:74037163 | T | C | 1 | a0012c0014t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5881+315A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037163 | |||||||
chr11:74037208 | C | T | 41 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(38): Show |
42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.5881+270G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037208 | |||||||
chr11:74037336 | T | TA | 13 | a0001c0001t0001g0141 a0002c0003t0001g0197 a0005c0006t0001g0015 others(10): Show |
13 | HG00597.hp1 HG01099.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.5881+141dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037336 | |||||||
chr11:74037711 | G | A | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5661-13C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74037711 | |||||||
chr11:74037752 | A | T | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.5661-54T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74037752 | |||||||
chr11:74037841 | C | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0149 others(1): Show |
4 | HG00140.hp1 HG01106.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.5661-143G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74037841 | |||||||
chr11:74038364 | A | G | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5661-666T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038364 | |||||||
chr11:74038507 | C | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5661-809G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038507 | |||||||
chr11:74038670 | A | G | 4 | a0010c0010t0001g0305 a0010c0010t0001g0306 a0010c0010t0001g0307 others(1): Show |
4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.5661-972T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038670 | |||||||
chr11:74038923 | C | T | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5661-1225G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038923 | |||||||
chr11:74039064 | C | T | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5661-1366G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039064 | |||||||
chr11:74039183 | T | C | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5661-1485A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039183 | |||||||
chr11:74039187 | C | T | 41 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(38): Show |
42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.5661-1489G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039187 | |||||||
chr11:74039204 | G | T | 1 | a0004c0004t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5661-1506C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039204 | |||||||
chr11:74039388 | T | C | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5661-1690A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039388 | |||||||
chr11:74039391 | C | T | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5661-1693G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039391 | |||||||
chr11:74039392 | G | A | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5661-1694C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039392 | |||||||
chr11:74039504 | C | G | 6 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5661-1806G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039504 | |||||||
chr11:74039506 | T | C | 1 | a0003c0002t0001g0268 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5661-1808A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039506 | |||||||
chr11:74039556 | G | A | 4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.5661-1858C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039556 | |||||||
chr11:74039657 | T | C | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5661-1959A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039657 | |||||||
chr11:74039759 | C | T | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5661-2061G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039759 | |||||||
chr11:74040122 | G | A | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5660+1932C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040122 | |||||||
chr11:74040369 | C | T | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5660+1685G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040369 | |||||||
chr11:74040436 | G | T | 55 | a0001c0030t0001g0190 a0002c0003t0001g0030 a0002c0003t0001g0031 others(52): Show |
55 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.5660+1618C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040436 | |||||||
chr11:74040457 | G | A | 1 | a0002c0003t0001g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5660+1597C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040457 | |||||||
chr11:74040572 | T | C | 1 | a0019c0043t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5660+1482A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040572 | |||||||
chr11:74040657 | G | C | 1 | a0003c0002t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5660+1397C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040657 | |||||||
chr11:74040884 | C | G | 1 | a0006c0012t0001g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5660+1170G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040884 | |||||||
chr11:74040899 | C | T | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5660+1155G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040899 | |||||||
chr11:74040908 | GCA | G | 39 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(36): Show |
40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5660+1144_5660+114 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040908 | |||||||
chr11:74040925 | C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5660+1129G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040925 | |||||||
chr11:74040964 | A | AT | 78 | a0001c0001t0001g0193 a0001c0030t0001g0190 a0002c0003t0001g0030 others(75): Show |
78 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.5660+1089dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040964 | |||||||
chr11:74040964 | ATT | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5660+1088_5660+108 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040964 | |||||||
chr11:74040964 | ATTT | A | 29 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(26): Show |
30 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.5660+1087_5660+108 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040964 | |||||||
chr11:74041015 | A | T | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5660+1039T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041015 | |||||||
chr11:74041095 | T | C | 39 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(36): Show |
40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5660+959A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041095 | |||||||
chr11:74041158 | C | T | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5660+896G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041158 | |||||||
chr11:74041176 | C | T | 39 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(36): Show |
40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5660+878G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041176 | |||||||
chr11:74041339 | C | T | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5660+715G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041339 | |||||||
chr11:74041746 | A | C | 65 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(62): Show |
66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.5660+308T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041746 | |||||||
chr11:74041866 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0103 |
2 | HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.5660+188A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041866 | |||||||
chr11:74041879 | A | G | 11 | a0006c0008t0001g0230 a0007c0017t0001g0194 a0007c0017t0001g0195 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5660+175T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041879 | |||||||
chr11:74042024 | T | C | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.5660+30A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74042024 | |||||||
chr11:74042223 | C | CA | 23 | a0002c0003t0001g0018 a0004c0004t0001g0047 a0006c0008t0001g0229 others(20): Show |
23 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.5496-6dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042223 | |||||||
chr11:74042223 | CA | C | 9 | a0002c0005t0001g0067 a0002c0005t0001g0069 a0002c0005t0001g0073 others(6): Show |
9 | HG01074.hp2 HG02015.hp1 HG02886.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.5496-6delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042223 | |||||||
chr11:74042243 | G | A | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.5496-25C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042243 | |||||||
chr11:74042360 | C | CT | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5496-143dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042360 | |||||||
chr11:74042490 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5496-272G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042490 | |||||||
chr11:74042564 | T | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5496-346A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042564 | |||||||
chr11:74042574 | G | A | 1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5496-356C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042574 | |||||||
chr11:74042626 | G | A | 41 | a0001c0030t0001g0190 a0002c0003t0001g0030 a0002c0003t0001g0031 others(38): Show |
41 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.5496-408C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042626 | |||||||
chr11:74042677 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5496-459A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042677 | |||||||
chr11:74042752 | TA | T | 65 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0193 others(62): Show |
66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.5496-535delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042752 | |||||||
chr11:74042787 | A | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5496-569T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042787 | |||||||
chr11:74042812 | C | T | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-594G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042812 | |||||||
chr11:74042992 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0192 |
2 | HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5496-774G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042992 | |||||||
chr11:74043025 | A | G | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.5496-807T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043025 | |||||||
chr11:74043034 | T | C | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.5496-816A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043034 | |||||||
chr11:74043405 | G | A | 5 | a0004c0004t0001g0037 a0004c0004t0001g0038 a0004c0004t0001g0039 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.5496-1187C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043405 | |||||||
chr11:74043470 | T | C | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5496-1252A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043470 | |||||||
chr11:74043509 | A | AT | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5496-1292dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043509 | |||||||
chr11:74043585 | T | A | 5 | a0009c0011t0001g0053 a0009c0011t0001g0063 a0009c0011t0001g0064 others(2): Show |
5 | HG02083.hp2 NA18998.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.5496-1367A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043585 | |||||||
chr11:74043591 | C | T | 23 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(20): Show |
23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.5496-1373G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043591 | |||||||
chr11:74043603 | A | T | 1 | a0002c0003t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5496-1385T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043603 | |||||||
chr11:74043619 | T | G | 9 | a0005c0006t0001g0020 a0005c0006t0001g0021 a0005c0006t0001g0022 others(6): Show |
9 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.5496-1401A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043619 | |||||||
chr11:74043663 | C | G | 9 | a0003c0002t0001g0246 a0003c0002t0001g0248 a0003c0002t0001g0256 others(6): Show |
9 | NA18948.hp2 NA18950.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.5496-1445G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043663 | |||||||
chr11:74043689 | T | C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5496-1471A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043689 | |||||||
chr11:74043762 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5496-1544C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043762 | |||||||
chr11:74043999 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5496-1781A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043999 | |||||||
chr11:74044072 | G | A | 3 | a0004c0004t0001g0035 a0004c0004t0001g0044 a0004c0004t0001g0045 |
3 | HG02922.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5496-1854C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044072 | |||||||
chr11:74044091 | C | T | 4 | a0002c0003t0001g0054 a0002c0003t0001g0055 a0002c0003t0001g0056 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5496-1873G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044091 | |||||||
chr11:74044137 | C | T | 1 | a0003c0002t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5496-1919G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044137 | |||||||
chr11:74044205 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5496-1987G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044205 | |||||||
chr11:74044253 | C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5496-2035G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044253 | |||||||
chr11:74044287 | C | G | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-2069G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044287 | |||||||
chr11:74044338 | C | T | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5496-2120G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044338 | |||||||
chr11:74044353 | G | A | 13 | a0002c0003t0001g0196 a0002c0003t0001g0204 a0002c0003t0001g0205 others(10): Show |
13 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.5496-2135C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044353 | |||||||
chr11:74044392 | T | C | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-2174A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044392 | |||||||
chr11:74044444 | A | ACT | 60 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(57): Show |
61 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(58): Show |
intron_variant | MODIFIER | c.5496-2228_5496-222 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044444 | |||||||
chr11:74044451 | C | CA | 11 | a0001c0001t0001g0157 a0003c0002t0001g0275 a0004c0004t0001g0037 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5496-2234dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044451 | |||||||
chr11:74044468 | G | T | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-2250C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044468 | |||||||
chr11:74044494 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5496-2276T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044494 | |||||||
chr11:74044746 | A | C | 38 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(35): Show |
39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.5496-2528T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044746 | |||||||
chr11:74044865 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5496-2647G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044865 | |||||||
chr11:74045144 | C | T | 62 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(59): Show |
63 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(60): Show |
intron_variant | MODIFIER | c.5496-2926G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045144 | |||||||
chr11:74045254 | C | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+2951G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045254 | |||||||
chr11:74045511 | G | C | 38 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(35): Show |
39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.5495+2694C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045511 | |||||||
chr11:74045524 | T | C | 1 | a0003c0002t0001g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5495+2681A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045524 | |||||||
chr11:74045575 | TC | T | 30 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(27): Show |
31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5495+2629delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045575 | |||||||
chr11:74045577 | CT | C | 191 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0149 others(188): Show |
191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.5495+2627delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045577 | |||||||
chr11:74045719 | G | A | 1 | a0010c0010t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5495+2486C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045719 | |||||||
chr11:74046160 | C | CATTA | 30 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(27): Show |
31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5495+2041_5495+204 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046160 | |||||||
chr11:74046194 | C | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+2011G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046194 | |||||||
chr11:74046271 | C | A | 12 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(9): Show |
12 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.5495+1934G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046271 | |||||||
chr11:74046331 | A | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0160 |
2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.5495+1874T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046331 | |||||||
chr11:74046491 | G | A | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.5495+1714C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046491 | |||||||
chr11:74046650 | G | GCT | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+1553_5495+155 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046650 | |||||||
chr11:74046659 | C | T | 1 | a0030c0042t0001g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5495+1546G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046659 | |||||||
chr11:74046678 | A | G | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.5495+1527T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046678 | |||||||
chr11:74046755 | C | T | 9 | a0003c0002t0001g0246 a0003c0002t0001g0248 a0003c0002t0001g0256 others(6): Show |
9 | NA18948.hp2 NA18950.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.5495+1450G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046755 | |||||||
chr11:74046956 | A | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+1249T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046956 | |||||||
chr11:74047065 | G | C | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5495+1140C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047065 | |||||||
chr11:74047302 | C | A | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5495+903G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047302 | |||||||
chr11:74047315 | A | G | 2 | a0003c0002t0001g0254 a0003c0002t0001g0255 |
2 | NA18941.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5495+890T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047315 | |||||||
chr11:74047426 | A | G | 1 | a0002c0003t0001g0202 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5495+779T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047426 | |||||||
chr11:74047647 | C | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5495+558G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047647 | |||||||
chr11:74047699 | C | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+506G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047699 | |||||||
chr11:74047846 | G | A | 10 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(7): Show |
10 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.5495+359C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047846 | |||||||
chr11:74048411 | G | A | 38 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(35): Show |
39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.5362-73C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048411 | |||||||
chr11:74048499 | T | C | 6 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5362-161A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048499 | |||||||
chr11:74048574 | T | C | 43 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(40): Show |
43 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.5362-236A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048574 | |||||||
chr11:74048619 | T | G | 6 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5362-281A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048619 | |||||||
chr11:74048780 | G | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5362-442C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048780 | |||||||
chr11:74048867 | C | T | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5361+470G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048867 | |||||||
chr11:74048889 | A | ATTC | 220 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0101 others(217): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.5361+445_5361+447d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048889 | |||||||
chr11:74048894 | T | TC | 4 | a0002c0003t0001g0215 a0003c0002t0001g0253 a0003c0002t0001g0278 others(1): Show |
4 | HG00544.hp2 HG00597.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.5361+442_5361+443i others(3): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048894 | |||||||
chr11:74048927 | C | T | 1 | a0024c0024t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5361+410G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048927 | |||||||
chr11:74049032 | TAG | T | 5 | a0004c0004t0001g0033 a0004c0004t0001g0034 a0004c0004t0001g0042 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5361+303_5361+304d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049032 | |||||||
chr11:74049058 | C | T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5361+279G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049058 | |||||||
chr11:74049086 | T | C | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5361+251A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049086 | |||||||
chr11:74049209 | A | G | 4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.5361+128T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049209 | |||||||
chr11:74049570 | A | G | 2 | a0008c0007t0001g0082 a0008c0007t0001g0221 |
2 | NA18950.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.5156-28T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049570 | |||||||
chr11:74049641 | A | G | 62 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(59): Show |
63 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(60): Show |
intron_variant | MODIFIER | c.5156-99T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049641 | |||||||
chr11:74049700 | C | A | 1 | a0024c0024t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5156-158G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049700 | |||||||
chr11:74049744 | G | A | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5156-202C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049744 | |||||||
chr11:74049765 | A | G | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5156-223T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049765 | |||||||
chr11:74049771 | TTC | T | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5156-231_5156-230d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049771 | |||||||
chr11:74049891 | C | CCAAGTAG others(19): Show |
18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5156-350_5156-349i others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049891 | |||||||
chr11:74049894 | C | A | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5156-352G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049894 | |||||||
chr11:74049895 | T | C | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5156-353A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049895 | |||||||
chr11:74049944 | C | T | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5156-402G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049944 | |||||||
chr11:74049986 | G | T | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5156-444C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049986 | |||||||
chr11:74049992 | G | A | 3 | a0006c0008t0001g0238 a0006c0008t0001g0239 a0006c0008t0001g0240 |
3 | HG01884.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5156-450C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049992 | |||||||
chr11:74050046 | T | C | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5156-504A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050046 | |||||||
chr11:74050121 | A | T | 1 | a0002c0003t0001g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5156-579T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050121 | |||||||
chr11:74050216 | A | G | 6 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5156-674T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050216 | |||||||
chr11:74050282 | T | C | 30 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(27): Show |
31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5156-740A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050282 | |||||||
chr11:74050383 | T | C | 3 | a0003c0002t0001g0298 a0003c0002t0001g0299 a0003c0002t0001g0300 |
3 | HG00738.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.5156-841A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050383 | |||||||
chr11:74050390 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.5156-848C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050390 | |||||||
chr11:74050428 | A | G | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5156-886T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050428 | |||||||
chr11:74050566 | A | G | 7 | a0002c0003t0001g0197 a0002c0003t0001g0199 a0002c0003t0001g0200 others(4): Show |
7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.5156-1024T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050566 | |||||||
chr11:74050711 | GTTTGGAC others(559): Show |
G | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5156-1735_5156-117 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050711 | |||||||
chr11:74050715 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.5156-1173C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050715 | |||||||
chr11:74050830 | T | C | 1 | a0003c0002t0001g0282 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5156-1288A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050830 | |||||||
chr11:74051013 | C | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5156-1471G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051013 | |||||||
chr11:74051015 | G | T | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5156-1473C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051015 | |||||||
chr11:74051125 | A | AAAAAC | 7 | a0001c0001t0001g0120 a0001c0001t0001g0182 a0003c0002t0001g0257 others(4): Show |
7 | NA18949.hp1 NA18949.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.5156-1588_5156-158 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051125 | |||||||
chr11:74051301 | G | GA | 25 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(22): Show |
26 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.5156-1760dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051301 | |||||||
chr11:74051571 | T | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5156-2029A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051571 | |||||||
chr11:74051590 | C | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5156-2048G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051590 | |||||||
chr11:74052068 | G | A | 2 | a0007c0026t0001g0005 a0032c0046t0002g0309 |
2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5156-2526C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052068 | |||||||
chr11:74052237 | C | T | 1 | a0003c0002t0001g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5155+2370G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052237 | |||||||
chr11:74052443 | T | C | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5155+2164A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052443 | |||||||
chr11:74052562 | T | A | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.5155+2045A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052562 | |||||||
chr11:74052664 | G | A | 5 | a0004c0004t0001g0033 a0004c0004t0001g0034 a0004c0004t0001g0042 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5155+1943C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052664 | |||||||
chr11:74052988 | G | T | 1 | a0002c0003t0001g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5155+1619C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052988 | |||||||
chr11:74052998 | G | A | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+1609C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052998 | |||||||
chr11:74053034 | A | C | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+1573T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053034 | |||||||
chr11:74053049 | A | G | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5155+1558T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053049 | |||||||
chr11:74053124 | G | A | 1 | a0004c0004t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5155+1483C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053124 | |||||||
chr11:74053284 | A | C | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+1323T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053284 | |||||||
chr11:74053468 | A | G | 1 | a0007c0009t0002g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5155+1139T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053468 | |||||||
chr11:74053687 | C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5155+920G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053687 | |||||||
chr11:74053705 | G | A | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5155+902C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053705 | |||||||
chr11:74053789 | A | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+818T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053789 | |||||||
chr11:74053882 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5155+725G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053882 | |||||||
chr11:74053885 | AGGCAGGA others(6): Show |
A | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+709_5155+721d others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053885 | |||||||
chr11:74054039 | G | A | 14 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.5155+568C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054039 | |||||||
chr11:74054043 | C | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5155+564G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054043 | |||||||
chr11:74054069 | G | C | 1 | a0003c0002t0001g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5155+538C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054069 | |||||||
chr11:74054078 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5155+529G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054078 | |||||||
chr11:74054145 | G | A | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5155+462C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054145 | |||||||
chr11:74054190 | T | G | 1 | a0002c0003t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5155+417A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054190 | |||||||
chr11:74054226 | C | G | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5155+381G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054226 | |||||||
chr11:74054271 | C | CA | 8 | a0001c0001t0001g0151 a0001c0001t0001g0158 a0001c0001t0001g0182 others(5): Show |
8 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.5155+335dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | |||||||
chr11:74054271 | C | CAA | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5155+334_5155+335d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | |||||||
chr11:74054271 | CA | C | 37 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0117 others(34): Show |
37 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.5155+335delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | |||||||
chr11:74054271 | CAA | C | 78 | a0001c0001t0001g0115 a0002c0003t0001g0030 a0002c0003t0001g0031 others(75): Show |
78 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.5155+334_5155+335d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | |||||||
chr11:74054271 | CAAA | C | 11 | a0002c0005t0001g0073 a0007c0009t0002g0311 a0007c0009t0002g0312 others(8): Show |
11 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.5155+333_5155+335d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | |||||||
chr11:74054312 | T | C | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+295A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054312 | |||||||
chr11:74054314 | T | C | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+293A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054314 | |||||||
chr11:74054395 | C | CA | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5155+211dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054395 | |||||||
chr11:74054407 | T | A | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+200A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054407 | |||||||
chr11:74054441 | C | T | 2 | a0007c0009t0002g0316 a0007c0009t0002g0317 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5155+166G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054441 | |||||||
chr11:74054449 | T | C | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.5155+158A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054449 | |||||||
chr11:74054507 | G | GA | 25 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0109 others(22): Show |
25 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.5155+99dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | |||||||
chr11:74054507 | GA | G | 27 | a0001c0001t0001g0115 a0002c0005t0001g0058 a0003c0002t0001g0254 others(24): Show |
27 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.5155+99delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | |||||||
chr11:74054507 | GAA | G | 8 | a0004c0004t0001g0186 a0010c0010t0001g0302 a0010c0010t0001g0303 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.5155+98_5155+99del others(2): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | |||||||
chr11:74054507 | GAAA | G | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5155+97_5155+99del others(3): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | |||||||
chr11:74054507 | GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5155+87_5155+99del others(13): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | |||||||
chr11:74054546 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5155+61C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054546 | |||||||
chr11:74054686 | A | C | 15 | a0008c0007t0001g0076 a0008c0007t0001g0082 a0008c0007t0001g0177 others(12): Show |
15 | HG01074.hp1 HG01515.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.5091-15T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054686 | |||||||
chr11:74054710 | G | C | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5091-39C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054710 | |||||||
chr11:74054742 | G | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5091-71C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054742 | |||||||
chr11:74054767 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5091-96A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054767 | |||||||
chr11:74054854 | G | A | 1 | a0014c0020t0004g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5091-183C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054854 | |||||||
chr11:74054943 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5091-272C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054943 | |||||||
chr11:74055047 | G | A | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5091-376C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055047 | |||||||
chr11:74055098 | C | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0103 others(2): Show |
5 | HG01192.hp2 HG01975.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.5091-427G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055098 | |||||||
chr11:74055143 | G | A | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5091-472C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055143 | |||||||
chr11:74055190 | A | G | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5091-519T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055190 | |||||||
chr11:74055251 | C | A | 2 | a0002c0003t0001g0055 a0002c0003t0001g0057 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5091-580G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055251 | |||||||
chr11:74055251 | C | T | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5091-580G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055251 | |||||||
chr11:74055373 | TATATATT others(2): Show |
T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5091-711_5091-703d others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055373 | |||||||
chr11:74055545 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.5091-874G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055545 | |||||||
chr11:74055645 | T | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5091-974A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055645 | |||||||
chr11:74055741 | A | G | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5091-1070T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055741 | |||||||
chr11:74056023 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5091-1352T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056023 | |||||||
chr11:74056107 | T | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5090+1299A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056107 | |||||||
chr11:74056228 | G | A | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5090+1178C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056228 | |||||||
chr11:74056452 | G | A | 123 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(120): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.5090+954C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056452 | |||||||
chr11:74056527 | A | G | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5090+879T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056527 | |||||||
chr11:74056612 | A | G | 4 | a0005c0006t0001g0006 a0005c0006t0001g0007 a0005c0006t0001g0013 others(1): Show |
4 | HG00642.hp1 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.5090+794T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056612 | |||||||
chr11:74056618 | G | C | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5090+788C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056618 | |||||||
chr11:74056630 | G | A | 57 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(54): Show |
57 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.5090+776C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056630 | |||||||
chr11:74056901 | A | AT | 125 | a0001c0001t0001g0104 a0001c0001t0001g0123 a0001c0001t0001g0133 others(122): Show |
125 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.5090+504dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056901 | |||||||
chr11:74056901 | AT | A | 20 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(17): Show |
20 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.5090+504delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056901 | |||||||
chr11:74056901 | ATT | A | 30 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(27): Show |
31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5090+503_5090+504d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056901 | |||||||
chr11:74057009 | AC | A | 16 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(13): Show |
16 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.5090+396delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057009 | |||||||
chr11:74057112 | C | G | 3 | a0003c0002t0001g0298 a0003c0002t0001g0299 a0003c0002t0001g0300 |
3 | HG00738.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.5090+294G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057112 | |||||||
chr11:74057180 | G | A | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5090+226C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057180 | |||||||
chr11:74057185 | A | G | 1 | a0002c0003t0001g0200 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5090+221T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057185 | |||||||
chr11:74057393 | G | A | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5090+13C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057393 | |||||||
chr11:74057954 | G | GTCAA | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-414_4952-411d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74057954 | |||||||
chr11:74058096 | A | C | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4952-552T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058096 | |||||||
chr11:74058392 | C | G | 1 | a0003c0002t0001g0265 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4952-848G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058392 | |||||||
chr11:74058490 | A | G | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-946T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058490 | |||||||
chr11:74058672 | C | T | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-1128G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058672 | |||||||
chr11:74058731 | G | C | 1 | a0002c0003t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4952-1187C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058731 | |||||||
chr11:74058860 | T | C | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4952-1316A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058860 | |||||||
chr11:74058944 | C | T | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-1400G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058944 | |||||||
chr11:74058980 | T | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4952-1436A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058980 | |||||||
chr11:74059027 | C | T | 61 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(58): Show |
62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.4952-1483G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059027 | |||||||
chr11:74059075 | G | A | 23 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(20): Show |
23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.4952-1531C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059075 | |||||||
chr11:74059219 | C | G | 43 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(40): Show |
44 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.4952-1675G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059219 | |||||||
chr11:74059250 | C | A | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.4952-1706G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059250 | |||||||
chr11:74059271 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4952-1727G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059271 | |||||||
chr11:74059298 | C | G | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4952-1754G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059298 | |||||||
chr11:74059319 | G | A | 3 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 |
3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4952-1775C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059319 | |||||||
chr11:74059343 | G | A | 1 | a0013c0013t0001g0225 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4952-1799C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059343 | |||||||
chr11:74059398 | G | A | 1 | a0003c0002t0001g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4952-1854C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059398 | |||||||
chr11:74059410 | C | CA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0106 others(20): Show |
23 | HG01081.hp2 HG01255.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.4952-1867dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059410 | C | CAA | 6 | a0006c0008t0001g0239 a0006c0012t0001g0232 a0006c0012t0001g0234 others(3): Show |
7 | HG01884.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4952-1868_4952-186 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059410 | C | CAAA | 17 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(14): Show |
17 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.4952-1869_4952-186 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059410 | C | CAAAAA | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01074.hp2 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4952-1871_4952-186 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059410 | C | CAAAAAA | 6 | a0004c0004t0001g0042 a0004c0004t0001g0181 a0004c0004t0001g0186 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4952-1872_4952-186 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059410 | C | CAAAAAAA | 7 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(4): Show |
7 | HG02630.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4952-1873_4952-186 others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059410 | CA | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0002c0003t0001g0091 others(5): Show |
8 | HG01516.hp2 HG01975.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.4952-1867delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | |||||||
chr11:74059462 | C | T | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4952-1918G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059462 | |||||||
chr11:74059496 | C | G | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-1952G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059496 | |||||||
chr11:74059672 | G | A | 4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4952-2128C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059672 | |||||||
chr11:74059711 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4952-2167G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059711 | |||||||
chr11:74059729 | C | T | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4952-2185G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059729 | |||||||
chr11:74059809 | C | T | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-2265G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059809 | |||||||
chr11:74059928 | A | C | 10 | a0003c0002t0001g0243 a0003c0002t0001g0244 a0003c0002t0001g0245 others(7): Show |
10 | HG00558.hp2 HG02056.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.4952-2384T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059928 | |||||||
chr11:74059968 | G | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4952-2424C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059968 | |||||||
chr11:74059976 | C | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-2432G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059976 | |||||||
chr11:74060008 | C | G | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-2464G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060008 | |||||||
chr11:74060012 | G | A | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-2468C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060012 | |||||||
chr11:74060078 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-2534G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060078 | |||||||
chr11:74060284 | C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-2740G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060284 | |||||||
chr11:74060493 | C | T | 3 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0026c0047t0002g0310 |
3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4952-2949G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060493 | |||||||
chr11:74060661 | T | C | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4952-3117A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060661 | |||||||
chr11:74060672 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4952-3128G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060672 | |||||||
chr11:74060708 | G | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4952-3164C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060708 | |||||||
chr11:74060714 | C | T | 61 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(58): Show |
62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.4952-3170G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060714 | |||||||
chr11:74060740 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4952-3196C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060740 | |||||||
chr11:74060749 | G | A | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4952-3205C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060749 | |||||||
chr11:74060753 | C | T | 5 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0160 others(2): Show |
5 | HG01952.hp1 HG02056.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.4952-3209G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060753 | |||||||
chr11:74060764 | G | A | 1 | a0003c0002t0001g0265 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4952-3220C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060764 | |||||||
chr11:74060780 | G | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4952-3236C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060780 | |||||||
chr11:74060798 | T | C | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-3254A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060798 | |||||||
chr11:74060814 | T | A | 7 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(4): Show |
7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.4952-3270A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060814 | |||||||
chr11:74060891 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4952-3347C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060891 | |||||||
chr11:74061045 | A | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-3501T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061045 | |||||||
chr11:74061155 | G | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4952-3611C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061155 | |||||||
chr11:74061322 | T | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0154 others(1): Show |
4 | HG02083.hp1 HG04184.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.4952-3778A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061322 | |||||||
chr11:74061591 | C | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-4047G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061591 | |||||||
chr11:74061659 | C | T | 1 | a0003c0002t0001g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4952-4115G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061659 | |||||||
chr11:74061728 | T | C | 61 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.4952-4184A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061728 | |||||||
chr11:74061827 | G | A | 7 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(4): Show |
7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.4952-4283C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061827 | |||||||
chr11:74061982 | T | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0175 others(1): Show |
4 | HG02040.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.4952-4438A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061982 | |||||||
chr11:74062130 | C | T | 1 | a0005c0006t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4952-4586G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062130 | |||||||
chr11:74062218 | G | A | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4952-4674C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062218 | |||||||
chr11:74062270 | G | A | 26 | a0002c0003t0001g0171 a0004c0004t0001g0032 a0004c0004t0001g0033 others(23): Show |
26 | HG01074.hp2 HG01358.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.4952-4726C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062270 | |||||||
chr11:74062456 | C | T | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4952-4912G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062456 | |||||||
chr11:74062717 | G | A | 43 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(40): Show |
44 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.4952-5173C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062717 | |||||||
chr11:74062736 | C | T | 4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4952-5192G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062736 | |||||||
chr11:74062738 | T | C | 36 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(33): Show |
37 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.4952-5194A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062738 | |||||||
chr11:74062757 | G | C | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-5213C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062757 | |||||||
chr11:74062784 | T | C | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-5240A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062784 | |||||||
chr11:74062792 | G | A | 27 | a0001c0001t0001g0133 a0001c0001t0001g0152 a0004c0004t0001g0032 others(24): Show |
27 | HG01074.hp2 HG01358.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4952-5248C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062792 | |||||||
chr11:74062814 | C | A | 1 | a0002c0005t0001g0069 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4952-5270G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062814 | |||||||
chr11:74062830 | T | C | 2 | a0008c0007t0001g0177 a0020c0033t0001g0178 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.4952-5286A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062830 | |||||||
chr11:74063061 | C | T | 18 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(15): Show |
18 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.4952-5517G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063061 | |||||||
chr11:74063160 | C | A | 4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4952-5616G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063160 | |||||||
chr11:74063171 | T | C | 123 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(120): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.4952-5627A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063171 | |||||||
chr11:74063373 | T | C | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4952-5829A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063373 | |||||||
chr11:74063374 | C | G | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4952-5830G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063374 | |||||||
chr11:74063409 | A | ATGGATTC others(3): Show |
1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5866_4952-586 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063409 | |||||||
chr11:74063410 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5866G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063410 | |||||||
chr11:74063416 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5872T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063416 | |||||||
chr11:74063418 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5874T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063418 | |||||||
chr11:74063730 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4952-6186A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063730 | |||||||
chr11:74063768 | A | T | 123 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(120): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.4952-6224T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063768 | |||||||
chr11:74064143 | C | T | 1 | a0002c0003t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4952-6599G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064143 | |||||||
chr11:74064145 | G | T | 3 | a0003c0002t0001g0268 a0003c0002t0001g0283 a0003c0041t0001g0297 |
3 | HG00438.hp2 HG03654.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.4952-6601C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064145 | |||||||
chr11:74064166 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4952-6622G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064166 | |||||||
chr11:74064261 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4952-6717G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064261 | |||||||
chr11:74064381 | T | C | 2 | a0003c0002t0001g0251 a0003c0002t0001g0292 |
2 | HG00408.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.4952-6837A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064381 | |||||||
chr11:74064430 | T | A | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4952-6886A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064430 | |||||||
chr11:74064477 | G | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4952-6933C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064477 | |||||||
chr11:74064540 | A | C | 3 | a0005c0006t0001g0006 a0005c0006t0001g0007 a0005c0006t0001g0013 |
3 | HG00642.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4952-6996T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064540 | |||||||
chr11:74064568 | C | T | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4952-7024G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064568 | |||||||
chr11:74064604 | G | A | 1 | a0005c0006t0001g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4952-7060C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064604 | |||||||
chr11:74064620 | C | A | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-7076G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064620 | |||||||
chr11:74064629 | A | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4952-7085T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064629 | |||||||
chr11:74064889 | C | T | 1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4952-7345G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064889 | |||||||
chr11:74064989 | C | T | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4952-7445G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064989 | |||||||
chr11:74065129 | C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-7585G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065129 | |||||||
chr11:74065137 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4952-7593A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065137 | |||||||
chr11:74065145 | A | C | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-7601T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065145 | |||||||
chr11:74065317 | C | T | 1 | a0002c0005t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4952-7773G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065317 | |||||||
chr11:74065428 | G | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4952-7884C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065428 | |||||||
chr11:74065552 | C | A | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4952-8008G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065552 | |||||||
chr11:74065613 | C | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-8069G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065613 | |||||||
chr11:74065734 | TA | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-8191delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065734 | |||||||
chr11:74065831 | G | A | 1 | a0010c0010t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4952-8287C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065831 | |||||||
chr11:74065913 | G | A | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4951+8340C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065913 | |||||||
chr11:74066134 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4951+8119G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066134 | |||||||
chr11:74066135 | G | A | 2 | a0003c0002t0003g0002 a0003c0002t0003g0003 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4951+8118C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066135 | |||||||
chr11:74066153 | T | C | 3 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 |
3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4951+8100A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066153 | |||||||
chr11:74066214 | A | G | 53 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(50): Show |
54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.4951+8039T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066214 | |||||||
chr11:74066264 | A | AGGAGGGG others(42): Show |
294 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(291): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.4951+7988_4951+798 others(53): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066264 | |||||||
chr11:74066264 | A | AGGAGGGG others(43): Show |
16 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0118 others(13): Show |
16 | HG00544.hp1 HG00609.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4951+7988_4951+798 others(54): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066264 | |||||||
chr11:74066264 | A | AGGAGGGG others(44): Show |
1 | a0001c0001t0001g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4951+7988_4951+798 others(55): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066264 | |||||||
chr11:74066267 | A | AGGGGGAA others(43): Show |
2 | a0002c0003t0001g0070 a0024c0024t0001g0203 |
2 | HG02615.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.4951+7985_4951+798 others(54): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066267 | |||||||
chr11:74066267 | A | AGGGGGAA others(45): Show |
1 | a0001c0001t0001g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4951+7985_4951+798 others(56): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066267 | |||||||
chr11:74066267 | A | AGGGGGAA others(44): Show |
1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4951+7985_4951+798 others(55): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066267 | |||||||
chr11:74066292 | TA | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+7960delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066292 | |||||||
chr11:74066342 | CA | C | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4951+7910delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066342 | |||||||
chr11:74066436 | A | AAAAG | 87 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(84): Show |
87 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.4951+7813_4951+781 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066436 | |||||||
chr11:74066447 | A | G | 28 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4951+7806T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066447 | |||||||
chr11:74066502 | T | C | 57 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(54): Show |
57 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.4951+7751A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066502 | |||||||
chr11:74066592 | A | C | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+7661T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066592 | |||||||
chr11:74066601 | A | G | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4951+7652T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066601 | |||||||
chr11:74066654 | C | CT | 207 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(204): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.4951+7598dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066654 | |||||||
chr11:74066725 | C | G | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4951+7528G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066725 | |||||||
chr11:74066937 | A | G | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4951+7316T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066937 | |||||||
chr11:74067054 | T | C | 1 | a0002c0003t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4951+7199A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067054 | |||||||
chr11:74067091 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4951+7162A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067091 | |||||||
chr11:74067311 | G | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4951+6942C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067311 | |||||||
chr11:74067407 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4951+6846A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067407 | |||||||
chr11:74067535 | C | CA | 61 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(58): Show |
62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.4951+6717dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067535 | |||||||
chr11:74067576 | AATGGTAG others(35): Show |
A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6635_4951+667 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067576 | |||||||
chr11:74067578 | T | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+6675A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067578 | |||||||
chr11:74067619 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6634T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067619 | |||||||
chr11:74067627 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6626A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067627 | |||||||
chr11:74067632 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6621G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067632 | |||||||
chr11:74067633 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6620A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067633 | |||||||
chr11:74067634 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6619T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067634 | |||||||
chr11:74067898 | A | G | 211 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(208): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.4951+6355T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067898 | |||||||
chr11:74068118 | C | G | 2 | a0003c0016t0001g0242 a0036c0022t0001g0295 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4951+6135G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068118 | |||||||
chr11:74068519 | C | A | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4951+5734G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068519 | |||||||
chr11:74068523 | A | G | 1 | a0026c0047t0002g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4951+5730T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068523 | |||||||
chr11:74068567 | C | T | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+5686G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068567 | |||||||
chr11:74068595 | G | T | 10 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4951+5658C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068595 | |||||||
chr11:74068752 | A | G | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4951+5501T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068752 | |||||||
chr11:74068875 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4951+5378C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068875 | |||||||
chr11:74068887 | C | T | 1 | a0007c0009t0002g0311 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4951+5366G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068887 | |||||||
chr11:74068934 | T | C | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4951+5319A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068934 | |||||||
chr11:74069078 | A | G | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+5175T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069078 | |||||||
chr11:74069079 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+5174A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069079 | |||||||
chr11:74069122 | G | A | 123 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(120): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.4951+5131C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069122 | |||||||
chr11:74069241 | T | C | 1 | a0003c0002t0001g0268 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4951+5012A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069241 | |||||||
chr11:74069262 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4951+4991C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069262 | |||||||
chr11:74069689 | G | A | 3 | a0006c0008t0001g0238 a0006c0008t0001g0239 a0006c0008t0001g0240 |
3 | HG01884.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4951+4564C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069689 | |||||||
chr11:74069750 | C | T | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4951+4503G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069750 | |||||||
chr11:74069798 | A | G | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4951+4455T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069798 | |||||||
chr11:74069933 | C | G | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+4320G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069933 | |||||||
chr11:74069961 | A | C | 2 | a0002c0003t0001g0196 a0002c0003t0001g0204 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4951+4292T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069961 | |||||||
chr11:74070046 | T | G | 1 | a0002c0005t0001g0087 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4951+4207A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070046 | |||||||
chr11:74070085 | A | G | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4951+4168T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070085 | |||||||
chr11:74070109 | T | C | 1 | a0003c0002t0001g0257 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4951+4144A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070109 | |||||||
chr11:74070169 | A | T | 18 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(15): Show |
19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4951+4084T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070169 | |||||||
chr11:74070190 | A | G | 25 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(22): Show |
25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+4063T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070190 | |||||||
chr11:74070446 | G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+3807C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070446 | |||||||
chr11:74070460 | C | G | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4951+3793G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070460 | |||||||
chr11:74070555 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+3698A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070555 | |||||||
chr11:74070669 | G | A | 176 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(173): Show |
176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.4951+3584C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070669 | |||||||
chr11:74070716 | G | A | 35 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(32): Show |
35 | HG01074.hp2 HG02109.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.4951+3537C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070716 | |||||||
chr11:74070717 | C | G | 35 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(32): Show |
35 | HG01074.hp2 HG02109.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.4951+3536G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070717 | |||||||
chr11:74070718 | A | G | 23 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(20): Show |
23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.4951+3535T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070718 | |||||||
chr11:74070948 | A | G | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4951+3305T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070948 | |||||||
chr11:74070953 | T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4951+3300A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070953 | |||||||
chr11:74071137 | T | C | 1 | a0010c0010t0001g0307 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4951+3116A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071137 | |||||||
chr11:74071264 | A | G | 23 | a0002c0003t0001g0056 a0004c0004t0001g0032 a0004c0004t0001g0033 others(20): Show |
23 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.4951+2989T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071264 | |||||||
chr11:74071502 | G | A | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.4951+2751C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071502 | |||||||
chr11:74071588 | A | G | 12 | a0006c0012t0001g0234 a0007c0009t0002g0311 a0007c0009t0002g0312 others(9): Show |
12 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.4951+2665T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071588 | |||||||
chr11:74071832 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4951+2421C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071832 | |||||||
chr11:74071918 | T | G | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4951+2335A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071918 | |||||||
chr11:74071920 | G | A | 209 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4951+2333C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071920 | |||||||
chr11:74071951 | G | A | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4951+2302C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071951 | |||||||
chr11:74072033 | C | T | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4951+2220G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072033 | |||||||
chr11:74072178 | A | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+2075T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072178 | |||||||
chr11:74072232 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4951+2021G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072232 | |||||||
chr11:74072248 | C | T | 11 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0059 others(8): Show |
11 | HG01192.hp1 HG01255.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4951+2005G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072248 | |||||||
chr11:74072293 | T | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+1960A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072293 | |||||||
chr11:74072392 | T | C | 169 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4951+1861A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072392 | |||||||
chr11:74072433 | A | T | 177 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.4951+1820T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072433 | |||||||
chr11:74072716 | C | CT | 177 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(174): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.4951+1536dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072716 | |||||||
chr11:74072716 | C | CTT | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4951+1535_4951+153 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072716 | |||||||
chr11:74072840 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+1413A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072840 | |||||||
chr11:74072953 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4951+1300A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072953 | |||||||
chr11:74073102 | G | C | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4951+1151C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073102 | |||||||
chr11:74073112 | CTCTGGCA others(8): Show |
C | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4951+1126_4951+114 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073112 | |||||||
chr11:74073325 | G | A | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4951+928C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073325 | |||||||
chr11:74073352 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4951+901A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073352 | |||||||
chr11:74073384 | C | T | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4951+869G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073384 | |||||||
chr11:74073535 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.4951+718G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073535 | |||||||
chr11:74073561 | T | A | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4951+692A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073561 | |||||||
chr11:74073565 | C | T | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4951+688G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073565 | |||||||
chr11:74073571 | A | G | 169 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4951+682T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073571 | |||||||
chr11:74073586 | CA | C | 170 | a0001c0001t0001g0105 a0001c0001t0001g0128 a0001c0001t0001g0151 others(167): Show |
170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.4951+666delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073586 | |||||||
chr11:74073586 | CAA | C | 29 | a0003c0002t0001g0247 a0003c0002t0001g0254 a0003c0002t0001g0298 others(26): Show |
29 | HG00738.hp2 HG01074.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.4951+665_4951+666d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073586 | |||||||
chr11:74073605 | A | G | 9 | a0003c0002t0001g0246 a0003c0002t0001g0248 a0003c0002t0001g0256 others(6): Show |
9 | NA18948.hp2 NA18950.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.4951+648T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073605 | |||||||
chr11:74073709 | C | T | 1 | a0003c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4951+544G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073709 | |||||||
chr11:74073725 | T | C | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4951+528A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073725 | |||||||
chr11:74074074 | A | C | 169 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4951+179T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74074074 | |||||||
chr11:74074694 | C | T | 2 | a0003c0002t0001g0266 a0003c0002t0001g0267 |
2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.4604-94G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074694 | |||||||
chr11:74074841 | C | T | 12 | a0005c0006t0001g0014 a0005c0006t0001g0015 a0005c0006t0001g0020 others(9): Show |
12 | HG01099.hp1 HG01106.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.4604-241G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074841 | |||||||
chr11:74074918 | TACAAAAA others(2): Show |
T | 43 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(40): Show |
43 | HG01074.hp2 HG02055.hp1 HG02145.hp2 others(40): Show |
intron_variant | MODIFIER | c.4604-327_4604-319d others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074918 | |||||||
chr11:74074953 | G | A | 1 | a0008c0007t0001g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4604-353C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074953 | |||||||
chr11:74075040 | C | T | 63 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(60): Show |
63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.4604-440G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075040 | |||||||
chr11:74075135 | A | C | 1 | a0002c0003t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4604-535T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075135 | |||||||
chr11:74075198 | C | T | 11 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0010c0010t0001g0302 others(8): Show |
11 | HG02280.hp2 HG02717.hp1 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.4604-598G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075198 | |||||||
chr11:74075354 | C | T | 1 | a0006c0008t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4604-754G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075354 | |||||||
chr11:74075358 | C | T | 1 | a0010c0010t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4604-758G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075358 | |||||||
chr11:74075366 | TG | T | 303 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(300): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.4604-767delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075366 | |||||||
chr11:74075369 | G | T | 20 | a0001c0001t0001g0125 a0001c0001t0001g0164 a0002c0003t0001g0196 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.4604-769C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075369 | |||||||
chr11:74075377 | G | C | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4604-777C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075377 | |||||||
chr11:74075417 | C | T | 222 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(219): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.4604-817G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075417 | |||||||
chr11:74075466 | G | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4604-866C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075466 | |||||||
chr11:74075480 | T | C | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4604-880A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075480 | |||||||
chr11:74075482 | C | G | 2 | a0003c0002t0001g0280 a0003c0002t0001g0281 |
2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4604-882G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075482 | |||||||
chr11:74075577 | G | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4604-977C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075577 | |||||||
chr11:74075808 | T | G | 6 | a0009c0011t0001g0053 a0009c0011t0001g0063 a0009c0011t0001g0064 others(3): Show |
6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.4604-1208A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075808 | |||||||
chr11:74075956 | C | T | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4604-1356G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075956 | |||||||
chr11:74076031 | C | A | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4604-1431G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076031 | |||||||
chr11:74076154 | T | C | 10 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(7): Show |
10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4604-1554A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076154 | |||||||
chr11:74076279 | C | T | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4604-1679G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076279 | |||||||
chr11:74076336 | G | A | 209 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4604-1736C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076336 | |||||||
chr11:74076337 | A | G | 1 | a0003c0002t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4604-1737T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076337 | |||||||
chr11:74076549 | T | C | 1 | a0003c0002t0001g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4603+1566A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076549 | |||||||
chr11:74076584 | A | G | 1 | a0003c0002t0001g0296 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4603+1531T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076584 | |||||||
chr11:74076728 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4603+1387A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076728 | |||||||
chr11:74077043 | G | A | 1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4603+1072C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077043 | |||||||
chr11:74077112 | A | G | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4603+1003T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077112 | |||||||
chr11:74077210 | G | C | 4 | a0003c0002t0001g0259 a0003c0002t0001g0260 a0003c0002t0001g0261 others(1): Show |
4 | HG00544.hp2 HG00673.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.4603+905C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077210 | |||||||
chr11:74077442 | T | G | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4603+673A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077442 | |||||||
chr11:74077546 | G | A | 1 | a0024c0024t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4603+569C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077546 | |||||||
chr11:74077725 | T | A | 4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4603+390A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077725 | |||||||
chr11:74077771 | GTATA | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0111 |
3 | HG00423.hp2 HG00544.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.4603+340_4603+343d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(1): Show |
G | 7 | a0001c0001t0001g0101 a0001c0001t0001g0115 a0001c0001t0001g0137 others(4): Show |
7 | HG00408.hp2 HG00639.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.4603+336_4603+343d others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(3): Show |
G | 11 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0108 others(8): Show |
11 | HG01261.hp1 HG01952.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.4603+334_4603+343d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(5): Show |
G | 10 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0109 others(7): Show |
10 | HG00438.hp1 HG01975.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.4603+332_4603+343d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(7): Show |
G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0136 a0001c0001t0001g0153 others(4): Show |
7 | HG00558.hp1 HG00741.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.4603+330_4603+343d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(9): Show |
G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0118 a0001c0001t0001g0128 others(2): Show |
5 | HG01433.hp2 HG02602.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.4603+328_4603+343d others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(11): Show |
G | 5 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0143 others(2): Show |
5 | HG01099.hp2 HG02040.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.4603+326_4603+343d others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(13): Show |
G | 1 | a0001c0001t0001g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4603+324_4603+343d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(15): Show |
G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0116 a0001c0001t0001g0142 |
3 | HG01255.hp2 HG02300.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.4603+322_4603+343d others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0139 |
2 | HG01169.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.4603+320_4603+343d others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4603+318_4603+343d others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(23): Show |
G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0182 a0022c0032t0001g0176 |
3 | HG02109.hp1 NA18949.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.4603+314_4603+343d others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(25): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4603+312_4603+343d others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(29): Show |
G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0158 |
2 | HG00609.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.4603+308_4603+343d others(38): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(33): Show |
G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0141 others(3): Show |
6 | HG00597.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4603+304_4603+343d others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(35): Show |
G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0161 |
2 | HG02559.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.4603+302_4603+343d others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(37): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4603+300_4603+343d others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(39): Show |
G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4603+298_4603+343d others(48): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(41): Show |
G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0001g0165 |
3 | HG01106.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.4603+296_4603+343d others(50): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(51): Show |
G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | NA18967.hp2 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.4603+286_4603+343d others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077771 | GTATATAT others(55): Show |
G | 1 | a0035c0039t0001g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.4603+282_4603+343d others(64): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | |||||||
chr11:74077793 | ATATATAT others(47): Show |
A | 7 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(4): Show |
7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.4603+268_4603+321d others(56): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077793 | |||||||
chr11:74077795 | A | G | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.4603+320T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077795 | |||||||
chr11:74077795 | ATATATAT others(45): Show |
A | 7 | a0002c0003t0001g0061 a0002c0003t0001g0070 a0002c0003t0001g0071 others(4): Show |
7 | HG02129.hp1 HG02132.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.4603+268_4603+319d others(54): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077795 | |||||||
chr11:74077797 | A | G | 6 | a0007c0009t0002g0311 a0007c0009t0002g0313 a0007c0009t0002g0314 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4603+318T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077797 | |||||||
chr11:74077797 | ATATATAT others(43): Show |
A | 3 | a0006c0008t0001g0230 a0006c0008t0001g0238 a0006c0008t0001g0239 |
3 | HG01884.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4603+268_4603+317d others(52): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077797 | |||||||
chr11:74077799 | A | G | 8 | a0007c0009t0002g0311 a0007c0009t0002g0313 a0007c0009t0002g0314 others(5): Show |
8 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.4603+316T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077799 | |||||||
chr11:74077799 | ATATATAT others(41): Show |
A | 8 | a0005c0006t0001g0006 a0005c0006t0001g0007 a0005c0006t0001g0013 others(5): Show |
8 | HG00642.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4603+268_4603+315d others(50): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077799 | |||||||
chr11:74077801 | A | G | 4 | a0007c0009t0002g0314 a0007c0009t0002g0317 a0007c0026t0001g0005 others(1): Show |
4 | HG03041.hp2 HG03831.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.4603+314T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077801 | |||||||
chr11:74077803 | ATATATAT others(37): Show |
A | 1 | a0003c0002t0001g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4603+268_4603+311d others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077803 | |||||||
chr11:74077805 | ATATATAT others(35): Show |
A | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4603+268_4603+309d others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077805 | |||||||
chr11:74077807 | ATATATAT others(33): Show |
A | 3 | a0002c0003t0001g0213 a0003c0016t0001g0249 a0005c0006t0001g0014 |
3 | HG02895.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4603+268_4603+307d others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077807 | |||||||
chr11:74077811 | ATATATAT others(29): Show |
A | 3 | a0003c0002t0001g0268 a0003c0002t0001g0294 a0003c0034t0001g0185 |
3 | HG03098.hp1 HG03654.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4603+268_4603+303d others(38): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077811 | |||||||
chr11:74077813 | ATATATAT others(27): Show |
A | 5 | a0003c0002t0001g0270 a0003c0002t0001g0276 a0003c0002t0001g0296 others(2): Show |
5 | HG02015.hp2 HG03139.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.4603+268_4603+301d others(36): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077813 | |||||||
chr11:74077815 | ATATATAT others(25): Show |
A | 26 | a0002c0003t0001g0052 a0002c0003t0001g0081 a0002c0003t0001g0214 others(23): Show |
26 | HG00280.hp1 HG00438.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.4603+268_4603+299d others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077815 | |||||||
chr11:74077817 | ATATATAT others(23): Show |
A | 46 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0056 others(43): Show |
46 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.4603+268_4603+297d others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077817 | |||||||
chr11:74077819 | ATATATAT others(21): Show |
A | 15 | a0002c0003t0001g0018 a0002c0003t0001g0170 a0002c0003t0001g0187 others(12): Show |
15 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.4603+268_4603+295d others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077819 | |||||||
chr11:74077821 | ATATATAT others(19): Show |
A | 17 | a0001c0001t0001g0133 a0002c0003t0001g0051 a0002c0003t0001g0167 others(14): Show |
17 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.4603+268_4603+293d others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077821 | |||||||
chr11:74077823 | ATATATAT others(16): Show |
A | 1 | a0002c0003t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4603+269_4603+291d others(25): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077823 | |||||||
chr11:74077823 | ATATATAT others(17): Show |
A | 25 | a0002c0003t0001g0059 a0002c0003t0001g0201 a0002c0003t0001g0208 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.4603+268_4603+291d others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077823 | |||||||
chr11:74077825 | ATATATAT others(15): Show |
A | 27 | a0002c0003t0001g0019 a0002c0003t0001g0030 a0002c0003t0001g0031 others(24): Show |
28 | HG01074.hp1 HG01123.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.4603+268_4603+289d others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077825 | |||||||
chr11:74077827 | ATATATAT others(13): Show |
A | 12 | a0001c0001t0001g0152 a0001c0001t0001g0179 a0002c0005t0001g0066 others(9): Show |
12 | HG01358.hp2 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.4603+268_4603+287d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077827 | |||||||
chr11:74077829 | ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0180 a0002c0005t0001g0074 a0002c0005t0001g0092 others(3): Show |
6 | NA18941.hp2 NA18942.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.4603+268_4603+285d others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077829 | |||||||
chr11:74077831 | ATATATAT others(9): Show |
A | 4 | a0002c0003t0001g0083 a0002c0005t0001g0189 a0009c0011t0001g0065 others(1): Show |
4 | HG02074.hp2 HG02622.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.4603+268_4603+283d others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077831 | |||||||
chr11:74077833 | ATATATAT others(7): Show |
A | 5 | a0002c0003t0001g0210 a0002c0005t0001g0085 a0002c0005t0001g0086 others(2): Show |
5 | HG01516.hp2 HG02717.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.4603+268_4603+281d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077833 | |||||||
chr11:74077835 | ATATATAT others(5): Show |
A | 2 | a0002c0003t0001g0197 a0002c0005t0001g0058 |
2 | HG02055.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.4603+268_4603+279d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077835 | |||||||
chr11:74077847 | T | A | 2 | a0007c0009t0002g0312 a0007c0026t0001g0005 |
2 | HG03831.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4603+268A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077847 | |||||||
chr11:74077848 | A | G | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.4603+267T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077848 | |||||||
chr11:74077868 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0151 |
2 | NA18956.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.4603+247G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077868 | |||||||
chr11:74077931 | A | G | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4603+184T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077931 | |||||||
chr11:74077983 | A | T | 1 | a0010c0010t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4603+132T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077983 | |||||||
chr11:74078100 | A | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4603+15T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74078100 | |||||||
chr11:74078732 | T | G | 228 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(225): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.4001-15A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078732 | |||||||
chr11:74078832 | C | T | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-115G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078832 | |||||||
chr11:74078920 | G | C | 1 | a0002c0005t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4001-203C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078920 | |||||||
chr11:74078980 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4001-263A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078980 | |||||||
chr11:74079107 | A | AGT | 209 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4001-392_4001-391d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079107 | |||||||
chr11:74079162 | T | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001-445A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079162 | |||||||
chr11:74079198 | C | T | 169 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4001-481G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079198 | |||||||
chr11:74079304 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4001-587A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079304 | |||||||
chr11:74079364 | G | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4001-647C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079364 | |||||||
chr11:74079427 | G | C | 4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001-710C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079427 | |||||||
chr11:74079782 | C | T | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0104 others(6): Show |
9 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.4001-1065G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079782 | |||||||
chr11:74079879 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0149 others(2): Show |
5 | HG00140.hp1 HG01106.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.4001-1162T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079879 | |||||||
chr11:74079913 | C | T | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-1196G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079913 | |||||||
chr11:74079931 | T | C | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-1214A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079931 | |||||||
chr11:74079993 | C | A | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-1276G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079993 | |||||||
chr11:74080226 | T | A | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4001-1509A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080226 | |||||||
chr11:74080299 | T | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4001-1582A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080299 | |||||||
chr11:74080349 | T | G | 32 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(29): Show |
32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4001-1632A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080349 | |||||||
chr11:74080423 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001-1706A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080423 | |||||||
chr11:74080501 | G | A | 4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001-1784C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080501 | |||||||
chr11:74080700 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4001-1983C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080700 | |||||||
chr11:74080781 | G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4001-2064C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080781 | |||||||
chr11:74081214 | T | C | 1 | a0026c0047t0002g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4001-2497A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081214 | |||||||
chr11:74081268 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4001-2551G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081268 | |||||||
chr11:74081329 | C | G | 2 | a0008c0007t0001g0211 a0008c0007t0001g0212 |
2 | NA18963.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.4001-2612G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081329 | |||||||
chr11:74081482 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4001-2765A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081482 | |||||||
chr11:74081499 | A | C | 2 | a0002c0003t0001g0090 a0002c0003t0001g0091 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4001-2782T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081499 | |||||||
chr11:74081604 | TTCA | T | 200 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(197): Show |
200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.4001-2890_4001-288 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081604 | |||||||
chr11:74081604 | TTCATCA | T | 9 | a0005c0006t0001g0020 a0005c0006t0001g0021 a0005c0006t0001g0022 others(6): Show |
9 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.4001-2893_4001-288 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081604 | |||||||
chr11:74081629 | T | C | 1 | a0005c0027t0001g0012 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4001-2912A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081629 | |||||||
chr11:74081678 | T | C | 209 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4001-2961A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081678 | |||||||
chr11:74081904 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4000+2977A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081904 | |||||||
chr11:74081970 | T | C | 1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4000+2911A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081970 | |||||||
chr11:74081995 | T | A | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4000+2886A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081995 | |||||||
chr11:74082094 | G | A | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4000+2787C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082094 | |||||||
chr11:74082123 | A | AT | 163 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4000+2757dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082123 | |||||||
chr11:74082123 | A | T | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.4000+2758T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082123 | |||||||
chr11:74082172 | G | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4000+2709C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082172 | |||||||
chr11:74082238 | C | G | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4000+2643G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082238 | |||||||
chr11:74082501 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4000+2380A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082501 | |||||||
chr11:74082602 | T | C | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4000+2279A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082602 | |||||||
chr11:74082698 | C | A | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4000+2183G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082698 | |||||||
chr11:74082797 | C | T | 2 | a0002c0003t0001g0090 a0002c0003t0001g0091 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4000+2084G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082797 | |||||||
chr11:74082830 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4000+2051A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082830 | |||||||
chr11:74082865 | C | A | 4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4000+2016G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082865 | |||||||
chr11:74082987 | C | A | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.4000+1894G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082987 | |||||||
chr11:74083024 | G | A | 84 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(81): Show |
84 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.4000+1857C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083024 | |||||||
chr11:74083029 | C | T | 1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4000+1852G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083029 | |||||||
chr11:74083056 | C | T | 1 | a0030c0042t0001g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4000+1825G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083056 | |||||||
chr11:74083107 | A | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4000+1774T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083107 | |||||||
chr11:74083108 | G | GA | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4000+1772dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083108 | |||||||
chr11:74083164 | G | C | 1 | a0010c0010t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4000+1717C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083164 | |||||||
chr11:74083213 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4000+1668A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083213 | |||||||
chr11:74083214 | A | G | 209 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4000+1667T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083214 | |||||||
chr11:74083580 | T | G | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4000+1301A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083580 | |||||||
chr11:74083751 | T | C | 5 | a0004c0004t0001g0037 a0004c0004t0001g0038 a0004c0004t0001g0039 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4000+1130A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083751 | |||||||
chr11:74083886 | G | A | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4000+995C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083886 | |||||||
chr11:74083986 | A | T | 1 | a0017c0044t0001g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4000+895T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083986 | |||||||
chr11:74084006 | C | T | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4000+875G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084006 | |||||||
chr11:74084096 | T | C | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4000+785A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084096 | |||||||
chr11:74084162 | A | C | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4000+719T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084162 | |||||||
chr11:74084261 | C | T | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4000+620G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084261 | |||||||
chr11:74084366 | G | A | 169 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4000+515C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084366 | |||||||
chr11:74084423 | AAAGTAT | A | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4000+452_4000+457d others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084423 | |||||||
chr11:74084432 | TA | T | 169 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(166): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4000+448delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084432 | |||||||
chr11:74084495 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4000+386G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084495 | |||||||
chr11:74084571 | T | C | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4000+310A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084571 | |||||||
chr11:74084615 | TCAA | T | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4000+263_4000+265d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084615 | |||||||
chr11:74084728 | A | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4000+153T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084728 | |||||||
chr11:74084741 | A | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4000+140T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084741 | |||||||
chr11:74084786 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4000+95A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084786 | |||||||
chr11:74085142 | A | AT | 83 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0002c0005t0001g0087 others(80): Show |
84 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.3911-173dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085142 | |||||||
chr11:74085391 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3910+227G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085391 | |||||||
chr11:74085392 | G | A | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3910+226C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085392 | |||||||
chr11:74085563 | T | C | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(311): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.3910+55A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085563 | |||||||
chr11:74085942 | T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3642-56A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74085942 | |||||||
chr11:74086148 | T | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3642-262A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086148 | |||||||
chr11:74086153 | C | G | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3642-267G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086153 | |||||||
chr11:74086202 | A | G | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3642-316T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086202 | |||||||
chr11:74086431 | C | A | 1 | a0029c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3642-545G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086431 | |||||||
chr11:74086450 | C | T | 1 | a0006c0012t0001g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3642-564G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086450 | |||||||
chr11:74086459 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3642-573A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086459 | |||||||
chr11:74086472 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3642-586A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086472 | |||||||
chr11:74086475 | C | T | 144 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.3642-589G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086475 | |||||||
chr11:74086839 | T | C | 4 | a0003c0034t0001g0185 a0011c0015t0001g0001 a0011c0015t0001g0223 others(1): Show |
5 | HG01884.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3642-953A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086839 | |||||||
chr11:74086862 | C | G | 126 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(123): Show |
126 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.3642-976G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086862 | |||||||
chr11:74086942 | T | C | 1 | a0003c0002t0001g0257 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3642-1056A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086942 | |||||||
chr11:74087131 | A | G | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3642-1245T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087131 | |||||||
chr11:74087478 | C | T | 8 | a0005c0006t0001g0021 a0005c0006t0001g0022 a0005c0006t0001g0023 others(5): Show |
8 | HG01106.hp2 HG02145.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3642-1592G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087478 | |||||||
chr11:74087592 | T | G | 3 | a0003c0002t0001g0256 a0003c0002t0001g0262 a0003c0002t0001g0294 |
3 | NA18950.hp1 NA18991.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3642-1706A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087592 | |||||||
chr11:74087721 | A | G | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3642-1835T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087721 | |||||||
chr11:74087723 | C | A | 2 | a0003c0002t0001g0246 a0003c0002t0001g0248 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3642-1837G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087723 | |||||||
chr11:74087814 | A | C | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3642-1928T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087814 | |||||||
chr11:74088255 | C | T | 229 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.3642-2369G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088255 | |||||||
chr11:74088269 | G | C | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3642-2383C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088269 | |||||||
chr11:74088280 | T | G | 144 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.3642-2394A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088280 | |||||||
chr11:74088352 | G | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3641+2461C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088352 | |||||||
chr11:74088394 | A | G | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3641+2419T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088394 | |||||||
chr11:74088849 | G | A | 144 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.3641+1964C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088849 | |||||||
chr11:74088956 | T | C | 135 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(132): Show |
135 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.3641+1857A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088956 | |||||||
chr11:74089034 | G | T | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3641+1779C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089034 | |||||||
chr11:74089046 | A | C | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3641+1767T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089046 | |||||||
chr11:74089067 | G | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.3641+1746C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089067 | |||||||
chr11:74089437 | A | C | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3641+1376T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089437 | |||||||
chr11:74089842 | C | T | 104 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.3641+971G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089842 | |||||||
chr11:74089951 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3641+862T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089951 | |||||||
chr11:74090107 | G | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3641+706C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090107 | |||||||
chr11:74090134 | C | A | 2 | a0003c0002t0001g0246 a0003c0002t0001g0248 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3641+679G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090134 | |||||||
chr11:74090186 | A | G | 1 | a0003c0002t0001g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3641+627T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090186 | |||||||
chr11:74090220 | T | C | 229 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.3641+593A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090220 | |||||||
chr11:74090257 | A | G | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3641+556T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090257 | |||||||
chr11:74090305 | G | C | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3641+508C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090305 | |||||||
chr11:74090315 | G | A | 18 | a0002c0005t0001g0008 a0002c0005t0001g0058 a0002c0005t0001g0066 others(15): Show |
18 | HG00733.hp2 HG02015.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.3641+498C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090315 | |||||||
chr11:74090327 | G | C | 5 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 others(2): Show |
5 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3641+486C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090327 | |||||||
chr11:74090617 | G | C | 212 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(209): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.3641+196C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090617 | |||||||
chr11:74090727 | C | T | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3641+86G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090727 | |||||||
chr11:74090966 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3518-30A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74090966 | |||||||
chr11:74091059 | A | T | 7 | a0002c0003t0001g0197 a0002c0003t0001g0199 a0002c0003t0001g0200 others(4): Show |
7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3518-123T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091059 | |||||||
chr11:74091188 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3518-252G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091188 | |||||||
chr11:74091453 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3518-517G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091453 | |||||||
chr11:74091691 | A | G | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3517+725T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091691 | |||||||
chr11:74091734 | C | A | 1 | a0005c0006t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3517+682G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091734 | |||||||
chr11:74091791 | T | C | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3517+625A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091791 | |||||||
chr11:74091970 | G | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3517+446C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091970 | |||||||
chr11:74092008 | A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3517+408T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092008 | |||||||
chr11:74092032 | A | ATG | 8 | a0002c0003t0001g0061 a0003c0034t0001g0185 a0007c0009t0002g0313 others(5): Show |
9 | HG01884.hp2 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3517+382_3517+383d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092032 | |||||||
chr11:74092060 | A | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0006c0012t0001g0231 others(3): Show |
6 | HG00438.hp1 HG00558.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3517+356T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092060 | |||||||
chr11:74092062 | T | A | 144 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0052 others(141): Show |
145 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3517+354A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092062 | |||||||
chr11:74092095 | C | G | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3517+321G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092095 | |||||||
chr11:74092216 | C | T | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3517+200G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092216 | |||||||
chr11:74092235 | G | A | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3517+181C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092235 | |||||||
chr11:74092243 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3517+173G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092243 | |||||||
chr11:74092244 | G | A | 2 | a0002c0003t0001g0061 a0002c0003t0001g0070 |
2 | NA18980.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.3517+172C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092244 | |||||||
chr11:74092344 | C | T | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3517+72G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092344 | |||||||
chr11:74092350 | C | T | 1 | a0027c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3517+66G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092350 | |||||||
chr11:74092353 | C | T | 136 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(133): Show |
136 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.3517+63G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092353 | |||||||
chr11:74092379 | G | A | 4 | a0003c0034t0001g0185 a0011c0015t0001g0001 a0011c0015t0001g0223 others(1): Show |
5 | HG01884.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3517+37C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092379 | |||||||
chr11:74092775 | C | CCT | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3345-188_3345-187i others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74092775 | |||||||
chr11:74093043 | C | G | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3345-455G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093043 | |||||||
chr11:74093106 | A | G | 4 | a0002c0003t0001g0061 a0002c0003t0001g0070 a0002c0003t0001g0071 others(1): Show |
4 | HG02129.hp1 HG02132.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345-518T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093106 | |||||||
chr11:74093196 | T | C | 1 | a0003c0002t0001g0262 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3345-608A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093196 | |||||||
chr11:74093336 | T | C | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3344+480A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093336 | |||||||
chr11:74093379 | A | G | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3344+437T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093379 | |||||||
chr11:74093464 | C | G | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3344+352G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093464 | |||||||
chr11:74093476 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3344+340C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093476 | |||||||
chr11:74093628 | T | C | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3344+188A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093628 | |||||||
chr11:74094199 | G | GT | 6 | a0001c0001t0001g0117 a0001c0001t0001g0192 a0002c0003t0001g0054 others(3): Show |
6 | HG02559.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3161-201dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094199 | |||||||
chr11:74094199 | GT | G | 92 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0002c0003t0001g0016 others(89): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3161-201delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094199 | |||||||
chr11:74094234 | G | A | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3161-235C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094234 | |||||||
chr11:74094351 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3161-352G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094351 | |||||||
chr11:74094549 | G | A | 1 | a0003c0002t0001g0296 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3161-550C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094549 | |||||||
chr11:74094844 | T | G | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3160+384A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094844 | |||||||
chr11:74094926 | A | G | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3160+302T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094926 | |||||||
chr11:74094939 | T | C | 1 | a0023c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3160+289A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094939 | |||||||
chr11:74094979 | A | T | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3160+249T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094979 | |||||||
chr11:74095152 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3160+76G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74095152 | |||||||
chr11:74095430 | CT | C | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2980-23delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095430 | |||||||
chr11:74095433 | G | A | 3 | a0005c0006t0001g0006 a0005c0006t0001g0007 a0005c0006t0001g0013 |
3 | HG00642.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2980-25C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095433 | |||||||
chr11:74095508 | A | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2980-100T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095508 | |||||||
chr11:74095781 | G | A | 16 | a0001c0001t0001g0125 a0001c0001t0001g0164 a0002c0003t0001g0196 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2980-373C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095781 | |||||||
chr11:74095786 | T | A | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2980-378A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095786 | |||||||
chr11:74095997 | T | G | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-589A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095997 | |||||||
chr11:74096196 | G | A | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2980-788C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096196 | |||||||
chr11:74096256 | T | C | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-848A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096256 | |||||||
chr11:74096482 | A | T | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-1074T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096482 | |||||||
chr11:74096485 | GA | G | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-1078delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096485 | |||||||
chr11:74096593 | T | A | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-1185A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096593 | |||||||
chr11:74096812 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2979+1197G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096812 | |||||||
chr11:74096856 | A | T | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2979+1153T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096856 | |||||||
chr11:74096867 | A | G | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2979+1142T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096867 | |||||||
chr11:74096885 | T | C | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2979+1124A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096885 | |||||||
chr11:74096910 | G | C | 80 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2979+1099C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096910 | |||||||
chr11:74096910 | G | T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2979+1099C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096910 | |||||||
chr11:74097149 | G | A | 2 | a0002c0003t0001g0196 a0002c0003t0001g0204 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2979+860C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097149 | |||||||
chr11:74097149 | GA | G | 105 | a0001c0001t0001g0192 a0002c0005t0001g0189 a0003c0002t0001g0241 others(102): Show |
106 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2979+859delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097149 | |||||||
chr11:74097178 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2979+831A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097178 | |||||||
chr11:74097213 | C | T | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2979+796G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097213 | |||||||
chr11:74097659 | T | G | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2979+350A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097659 | |||||||
chr11:74098307 | T | C | 1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2733-52A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74098307 | |||||||
chr11:74098529 | G | A | 1 | a0003c0002t0001g0288 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2733-274C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74098529 | |||||||
chr11:74098748 | G | T | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2733-493C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74098748 | |||||||
chr11:74099011 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2733-756A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099011 | |||||||
chr11:74099043 | T | C | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2733-788A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099043 | |||||||
chr11:74099265 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2733-1010T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099265 | |||||||
chr11:74099518 | T | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.2732+1007A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099518 | |||||||
chr11:74099554 | G | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2732+971C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099554 | |||||||
chr11:74099614 | A | G | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2732+911T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099614 | |||||||
chr11:74099622 | C | T | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2732+903G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099622 | |||||||
chr11:74099667 | C | T | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2732+858G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099667 | |||||||
chr11:74099713 | G | A | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2732+812C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099713 | |||||||
chr11:74099724 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2732+801C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099724 | |||||||
chr11:74099826 | A | G | 84 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(81): Show |
85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2732+699T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099826 | |||||||
chr11:74099851 | G | A | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.2732+674C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099851 | |||||||
chr11:74099852 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2732+673A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099852 | |||||||
chr11:74099895 | CA | C | 80 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(77): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2732+629delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099895 | |||||||
chr11:74099937 | G | T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2732+588C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099937 | |||||||
chr11:74099983 | C | T | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2732+542G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099983 | |||||||
chr11:74100131 | T | C | 1 | a0004c0004t0001g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2732+394A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100131 | |||||||
chr11:74100196 | T | C | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2732+329A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100196 | |||||||
chr11:74100268 | T | G | 1 | a0029c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2732+257A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100268 | |||||||
chr11:74100336 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2732+189A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100336 | |||||||
chr11:74100758 | T | G | 1 | a0002c0005t0001g0066 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2581-82A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100758 | |||||||
chr11:74100898 | G | C | 1 | a0027c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2581-222C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100898 | |||||||
chr11:74100942 | G | T | 63 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(60): Show |
63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.2581-266C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100942 | |||||||
chr11:74100976 | C | T | 2 | a0002c0003t0001g0090 a0002c0003t0001g0091 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2581-300G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100976 | |||||||
chr11:74101290 | A | G | 1 | a0026c0047t0002g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2581-614T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101290 | |||||||
chr11:74101400 | G | A | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2581-724C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101400 | |||||||
chr11:74101911 | C | T | 2 | a0003c0002t0001g0266 a0003c0002t0001g0267 |
2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2580+1220G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101911 | |||||||
chr11:74101973 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2580+1158A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101973 | |||||||
chr11:74101983 | A | G | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2580+1148T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101983 | |||||||
chr11:74102000 | A | T | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2580+1131T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102000 | |||||||
chr11:74102119 | A | C | 81 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2580+1012T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102119 | |||||||
chr11:74102510 | C | T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2580+621G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102510 | |||||||
chr11:74102519 | G | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2580+612C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102519 | |||||||
chr11:74102620 | C | T | 67 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2580+511G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102620 | |||||||
chr11:74102747 | T | C | 1 | a0026c0047t0002g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2580+384A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102747 | |||||||
chr11:74102749 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2580+382G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102749 | |||||||
chr11:74103666 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2086-41A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74103666 | |||||||
chr11:74103906 | A | G | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2086-281T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74103906 | |||||||
chr11:74104102 | T | C | 67 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(64): Show |
68 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2086-477A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104102 | |||||||
chr11:74104263 | A | G | 2 | a0011c0018t0001g0131 a0011c0018t0001g0132 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2086-638T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104263 | |||||||
chr11:74104493 | CA | C | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2086-869delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104493 | |||||||
chr11:74104668 | A | T | 73 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2086-1043T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104668 | |||||||
chr11:74104894 | C | A | 98 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(95): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2086-1269G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104894 | |||||||
chr11:74105124 | T | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2085+1247A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105124 | |||||||
chr11:74105299 | C | T | 37 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(34): Show |
38 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.2085+1072G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105299 | |||||||
chr11:74105381 | G | C | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2085+990C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105381 | |||||||
chr11:74105442 | T | C | 11 | a0002c0003t0001g0196 a0002c0003t0001g0204 a0002c0003t0001g0205 others(8): Show |
11 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.2085+929A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105442 | |||||||
chr11:74105567 | G | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2085+804C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105567 | |||||||
chr11:74105608 | C | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0117 |
3 | NA18970.hp1 NA18984.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2085+763G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105608 | |||||||
chr11:74105728 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+643A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105728 | |||||||
chr11:74105821 | G | A | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2085+550C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105821 | |||||||
chr11:74105886 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2085+485A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105886 | |||||||
chr11:74106200 | C | T | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2085+171G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74106200 | |||||||
chr11:74106931 | A | G | 1 | a0002c0003t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1963-438T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74106931 | |||||||
chr11:74107047 | C | T | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1963-554G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107047 | |||||||
chr11:74107322 | T | TCA | 11 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0174 others(8): Show |
11 | HG01192.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1963-831_1963-830d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCACA | 5 | a0001c0001t0001g0029 a0011c0015t0001g0001 a0011c0015t0001g0223 others(2): Show |
6 | HG01884.hp2 HG02132.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-833_1963-830d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCACACA | 6 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-835_1963-830d others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCACACAC others(3): Show |
1 | a0023c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1963-839_1963-830d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCACACAC others(7): Show |
1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1963-843_1963-830d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCTCACAC others(7): Show |
6 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-830_1963-829i others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCTCACAC others(9): Show |
2 | a0006c0008t0001g0230 a0006c0012t0001g0231 |
2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1963-830_1963-829i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCTCACAC others(11): Show |
8 | a0006c0012t0001g0234 a0006c0012t0001g0235 a0010c0010t0001g0303 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1963-830_1963-829i others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCTCACAC others(13): Show |
5 | a0010c0010t0001g0302 a0010c0010t0001g0306 a0010c0010t0001g0307 others(2): Show |
5 | HG04228.hp2 NA18984.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1963-830_1963-829i others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCTCACAC others(15): Show |
1 | a0006c0012t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1963-830_1963-829i others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | T | TCTCACAC others(19): Show |
1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1963-830_1963-829i others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107322 | TCA | T | 59 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(56): Show |
59 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1963-831_1963-830d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | |||||||
chr11:74107801 | T | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1962+1233A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107801 | |||||||
chr11:74107827 | C | T | 1 | a0006c0012t0001g0231 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1962+1207G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107827 | |||||||
chr11:74107954 | T | C | 21 | a0004c0004t0001g0032 a0004c0004t0001g0034 a0004c0004t0001g0035 others(18): Show |
21 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1962+1080A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107954 | |||||||
chr11:74108105 | C | T | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1962+929G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108105 | |||||||
chr11:74108107 | C | T | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1962+927G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108107 | |||||||
chr11:74108115 | C | T | 3 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0026c0047t0002g0310 |
3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1962+919G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108115 | |||||||
chr11:74108130 | G | A | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1962+904C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108130 | |||||||
chr11:74108144 | CTG | C | 90 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(87): Show |
91 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1962+888_1962+889d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108144 | |||||||
chr11:74108147 | TG | T | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0010c0010t0001g0302 others(8): Show |
11 | HG02280.hp2 HG02886.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+886delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108147 | |||||||
chr11:74108149 | T | C | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0010c0010t0001g0302 others(8): Show |
11 | HG02280.hp2 HG02886.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+885A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108149 | |||||||
chr11:74108150 | C | A | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0010c0010t0001g0302 others(8): Show |
11 | HG02280.hp2 HG02886.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+884G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108150 | |||||||
chr11:74108481 | T | C | 8 | a0002c0003t0001g0197 a0002c0003t0001g0199 a0002c0003t0001g0200 others(5): Show |
8 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1962+553A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108481 | |||||||
chr11:74108527 | T | C | 104 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1962+507A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108527 | |||||||
chr11:74108564 | C | A | 2 | a0003c0016t0001g0242 a0036c0022t0001g0295 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1962+470G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108564 | |||||||
chr11:74109028 | A | T | 1 | a0006c0012t0001g0231 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.1962+6T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74109028 | |||||||
chr11:74109213 | C | T | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1844-61G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109213 | |||||||
chr11:74109653 | A | G | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1844-501T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109653 | |||||||
chr11:74109839 | G | A | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1844-687C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109839 | |||||||
chr11:74109914 | T | C | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1844-762A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109914 | |||||||
chr11:74109919 | C | CA | 5 | a0003c0041t0001g0297 a0011c0015t0001g0001 a0011c0015t0001g0223 others(2): Show |
6 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1844-768dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109919 | |||||||
chr11:74109922 | C | A | 100 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(97): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1844-770G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109922 | |||||||
chr11:74109954 | G | A | 1 | a0002c0003t0001g0060 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1844-802C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109954 | |||||||
chr11:74109954 | G | GCGC | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-803_1844-802i others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109954 | |||||||
chr11:74109956 | C | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-804G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109956 | |||||||
chr11:74109959 | T | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-807A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109959 | |||||||
chr11:74109962 | T | C | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-810A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109962 | |||||||
chr11:74109963 | C | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-811G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109963 | |||||||
chr11:74109964 | C | CTTGGGAG others(9): Show |
8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-813_1844-812i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109964 | |||||||
chr11:74109965 | C | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-813G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109965 | |||||||
chr11:74109966 | A | G | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-814T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109966 | |||||||
chr11:74110005 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00408.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.1844-853C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110005 | |||||||
chr11:74110082 | A | AAAAT | 87 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(84): Show |
87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1844-934_1844-931d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | |||||||
chr11:74110082 | A | AAAATAAA others(5): Show |
3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844-942_1844-931d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | |||||||
chr11:74110082 | A | AAAATAAA others(13): Show |
1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1844-950_1844-931d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | |||||||
chr11:74110082 | A | AAAATAAA others(101): Show |
8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-931_1844-930i others(110): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | |||||||
chr11:74110098 | T | TAAATA | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1844-951_1844-947d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110098 | |||||||
chr11:74110915 | G | C | 4 | a0006c0008t0001g0230 a0006c0008t0001g0238 a0006c0008t0001g0239 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844-1763C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110915 | |||||||
chr11:74111024 | T | G | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1844-1872A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111024 | |||||||
chr11:74111029 | CCAA | C | 3 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 |
3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1844-1880_1844-187 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111029 | |||||||
chr11:74111089 | C | T | 228 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(225): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1844-1937G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111089 | |||||||
chr11:74111264 | C | T | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1844-2112G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111264 | |||||||
chr11:74111634 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1843+2146A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111634 | |||||||
chr11:74111641 | C | T | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1843+2139G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111641 | |||||||
chr11:74111647 | T | C | 99 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(96): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1843+2133A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111647 | |||||||
chr11:74111868 | G | C | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843+1912C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111868 | |||||||
chr11:74111919 | T | TAC | 24 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0095 others(21): Show |
24 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1843+1859_1843+186 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | T | TACAC | 4 | a0001c0001t0001g0139 a0004c0004t0001g0035 a0011c0018t0001g0131 others(1): Show |
4 | HG01169.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843+1857_1843+186 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TAC | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0100 a0001c0001t0001g0102 others(25): Show |
28 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1843+1859_1843+186 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACAC | T | 22 | a0001c0001t0001g0164 a0001c0001t0001g0191 a0002c0003t0001g0016 others(19): Show |
23 | HG01123.hp1 HG01169.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1843+1857_1843+186 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACAC | T | 41 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0175 others(38): Show |
41 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1843+1855_1843+186 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACACA others(1): Show |
T | 44 | a0002c0003t0001g0050 a0002c0003t0001g0051 a0002c0003t0001g0052 others(41): Show |
44 | HG00639.hp1 HG01074.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.1843+1853_1843+186 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACACA others(3): Show |
T | 6 | a0002c0003t0001g0196 a0002c0003t0001g0204 a0002c0005t0001g0008 others(3): Show |
6 | HG00733.hp2 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1843+1851_1843+186 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACACA others(5): Show |
T | 13 | a0002c0003t0001g0197 a0002c0005t0001g0049 a0003c0034t0001g0185 others(10): Show |
13 | HG00738.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1843+1849_1843+186 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACACA others(7): Show |
T | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1843+1847_1843+186 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACACA others(11): Show |
T | 2 | a0002c0003t0001g0081 a0002c0003t0001g0187 |
2 | HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1843+1843_1843+186 others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111919 | TACACACA others(27): Show |
T | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1843+1827_1843+186 others(38): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | |||||||
chr11:74111921 | C | T | 74 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1843+1859G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111921 | |||||||
chr11:74111931 | C | T | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1843+1849G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111931 | |||||||
chr11:74111933 | C | T | 7 | a0003c0034t0001g0185 a0006c0012t0001g0235 a0010c0010t0001g0302 others(4): Show |
7 | HG02615.hp1 HG03098.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.1843+1847G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111933 | |||||||
chr11:74111935 | C | T | 9 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1843+1845G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111935 | |||||||
chr11:74111955 | CACACACA others(9): Show |
C | 8 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(5): Show |
8 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843+1809_1843+182 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111955 | |||||||
chr11:74111957 | CACACACA others(7): Show |
C | 3 | a0003c0002t0001g0282 a0003c0002t0001g0291 a0026c0047t0002g0310 |
3 | HG00609.hp1 HG02717.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1843+1809_1843+182 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111957 | |||||||
chr11:74111959 | CACACACA others(5): Show |
C | 20 | a0003c0002t0001g0241 a0003c0002t0001g0250 a0003c0002t0001g0251 others(17): Show |
20 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.1843+1809_1843+182 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111959 | |||||||
chr11:74111959 | CACACACA others(7): Show |
C | 1 | a0003c0002t0001g0271 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1843+1807_1843+182 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111959 | |||||||
chr11:74111961 | CACACACA others(3): Show |
C | 28 | a0003c0002t0001g0246 a0003c0002t0001g0247 a0003c0002t0001g0248 others(25): Show |
28 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1843+1809_1843+181 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111961 | |||||||
chr11:74111963 | CACACACA others(1): Show |
C | 11 | a0002c0003t0001g0090 a0002c0003t0001g0091 a0003c0002t0001g0243 others(8): Show |
11 | HG02647.hp1 HG02896.hp1 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.1843+1809_1843+181 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111963 | |||||||
chr11:74111965 | CACACAT | C | 4 | a0003c0002t0001g0288 a0003c0002t0001g0289 a0003c0002t0001g0290 others(1): Show |
4 | HG02056.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843+1809_1843+181 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111965 | |||||||
chr11:74111971 | T | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0146 a0001c0001t0001g0151 others(13): Show |
16 | HG01099.hp2 HG01433.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1843+1809A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111971 | |||||||
chr11:74112101 | A | C | 2 | a0003c0002t0001g0269 a0003c0002t0001g0270 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1843+1679T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74112101 | |||||||
chr11:74112486 | T | C | 1 | a0003c0002t0003g0004 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1843+1294A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74112486 | |||||||
chr11:74112514 | G | A | 8 | a0003c0002t0001g0247 a0003c0002t0001g0258 a0003c0002t0001g0263 others(5): Show |
8 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843+1266C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74112514 | |||||||
chr11:74113094 | T | C | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1843+686A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113094 | |||||||
chr11:74113404 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0175 others(1): Show |
4 | HG02040.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843+376G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113404 | |||||||
chr11:74113500 | G | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843+280C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113500 | |||||||
chr11:74113636 | C | T | 2 | a0008c0007t0001g0177 a0020c0033t0001g0178 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1843+144G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113636 | |||||||
chr11:74113659 | G | A | 10 | a0004c0004t0001g0033 a0004c0004t0001g0034 a0004c0004t0001g0035 others(7): Show |
10 | HG02622.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1843+121C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113659 | |||||||
chr11:74113659 | G | T | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1843+121C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113659 | |||||||
chr11:74113679 | C | CA | 6 | a0001c0001t0001g0123 a0002c0005t0001g0188 a0003c0002t0001g0246 others(3): Show |
6 | HG02145.hp2 HG02622.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1843+100dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113679 | |||||||
chr11:74113679 | CA | C | 12 | a0001c0001t0001g0151 a0002c0003t0001g0078 a0003c0016t0001g0242 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1843+100delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113679 | |||||||
chr11:74114103 | T | C | 1 | a0002c0003t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1731-211A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/32 | chr11 | 74114103 | |||||||
chr11:74114212 | ATACT | A | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1730+168_1730+171d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/32 | chr11 | 74114212 | |||||||
chr11:74114244 | G | C | 1 | a0032c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1730+140C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/32 | chr11 | 74114244 | |||||||
chr11:74114707 | T | C | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1521-114A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114707 | |||||||
chr11:74114708 | A | T | 1 | a0009c0011t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1521-115T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114708 | |||||||
chr11:74114843 | A | G | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1521-250T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114843 | |||||||
chr11:74114895 | T | C | 12 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(9): Show |
12 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1521-302A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114895 | |||||||
chr11:74115013 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1521-420G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115013 | |||||||
chr11:74115100 | A | T | 3 | a0004c0004t0001g0036 a0004c0004t0001g0041 a0004c0004t0001g0046 |
3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1521-507T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115100 | |||||||
chr11:74115195 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0160 |
2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1521-602G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115195 | |||||||
chr11:74115319 | C | T | 4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-726G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115319 | |||||||
chr11:74115693 | C | A | 6 | a0009c0011t0001g0053 a0009c0011t0001g0063 a0009c0011t0001g0064 others(3): Show |
6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1521-1100G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115693 | |||||||
chr11:74115708 | T | A | 6 | a0009c0011t0001g0053 a0009c0011t0001g0063 a0009c0011t0001g0064 others(3): Show |
6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1521-1115A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115708 | |||||||
chr11:74115964 | A | C | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1521-1371T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115964 | |||||||
chr11:74116237 | C | T | 2 | a0003c0002t0001g0266 a0003c0002t0001g0267 |
2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1521-1644G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116237 | |||||||
chr11:74116272 | T | C | 1 | a0021c0037t0001g0273 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1521-1679A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116272 | |||||||
chr11:74116366 | A | G | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-1773T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116366 | |||||||
chr11:74116769 | CATATATG others(241): Show |
C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1211_1520+145 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116769 | |||||||
chr11:74116819 | CAT | C | 73 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1520+1407_1520+140 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116819 | |||||||
chr11:74116828 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1520+1400C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116828 | |||||||
chr11:74116836 | A | ATATATAC others(13): Show |
1 | a0024c0024t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1520+1372_1520+139 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116836 | |||||||
chr11:74116841 | T | TACACGTG others(35): Show |
1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1520+1345_1520+138 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116841 | |||||||
chr11:74116846 | G | A | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1520+1382C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116846 | |||||||
chr11:74116848 | GTA | G | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+1378_1520+137 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116848 | |||||||
chr11:74116854 | GTGTATAT others(11): Show |
G | 1 | a0008c0007t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1520+1356_1520+137 others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116854 | |||||||
chr11:74116856 | GTATATAC others(13): Show |
G | 1 | a0002c0003t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1520+1352_1520+137 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116856 | |||||||
chr11:74116876 | A | G | 16 | a0003c0002t0001g0252 a0003c0002t0001g0253 a0003c0002t0001g0254 others(13): Show |
16 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.1520+1352T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116876 | |||||||
chr11:74116887 | C | T | 2 | a0003c0002t0001g0254 a0003c0002t0001g0255 |
2 | NA18941.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1520+1341G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116887 | |||||||
chr11:74116908 | A | ATG | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1520+1318_1520+131 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116908 | |||||||
chr11:74116917 | T | C | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1311A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116917 | |||||||
chr11:74116917 | T | TACATATA others(13): Show |
1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1520+1291_1520+131 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116917 | |||||||
chr11:74116927 | C | CGTGTATA others(21): Show |
1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1520+1273_1520+130 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116927 | |||||||
chr11:74116927 | CGTGTATA others(21): Show |
C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1520+1273_1520+130 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116927 | |||||||
chr11:74116935 | T | TACACATA others(31): Show |
1 | a0023c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1520+1255_1520+129 others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116935 | |||||||
chr11:74116943 | TAC | T | 24 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(21): Show |
24 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1520+1283_1520+128 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116943 | |||||||
chr11:74116945 | C | T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1520+1283G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116945 | |||||||
chr11:74116948 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1520+1280C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116948 | |||||||
chr11:74116950 | A | G | 26 | a0002c0003t0001g0215 a0003c0034t0001g0185 a0006c0008t0001g0229 others(23): Show |
26 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1520+1278T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116950 | |||||||
chr11:74116958 | G | A | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0003c0034t0001g0185 others(24): Show |
27 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1520+1270C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116958 | |||||||
chr11:74116965 | C | T | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1263G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116965 | |||||||
chr11:74116973 | C | T | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1255G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116973 | |||||||
chr11:74116978 | A | G | 26 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(23): Show |
26 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1520+1250T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116978 | |||||||
chr11:74116984 | A | G | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1244T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116984 | |||||||
chr11:74116985 | C | T | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1243G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116985 | |||||||
chr11:74116987 | C | CATATACG others(21): Show |
6 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0152 others(3): Show |
6 | HG01109.hp2 HG01358.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520+1213_1520+124 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116987 | |||||||
chr11:74116987 | C | T | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1241G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116987 | |||||||
chr11:74116998 | A | G | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1230T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116998 | |||||||
chr11:74117000 | A | G | 26 | a0002c0003t0001g0071 a0003c0034t0001g0185 a0006c0008t0001g0229 others(23): Show |
26 | HG01884.hp1 HG02055.hp1 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.1520+1228T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117000 | |||||||
chr11:74117021 | C | G | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1207G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117021 | |||||||
chr11:74117024 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1204C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117024 | |||||||
chr11:74117026 | A | AT | 10 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(7): Show |
10 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1201dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117026 | |||||||
chr11:74117026 | A | G | 3 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1520+1202T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117026 | |||||||
chr11:74117028 | A | G | 61 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1520+1200T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117028 | |||||||
chr11:74117030 | GTATATAT others(79): Show |
G | 2 | a0003c0016t0001g0242 a0036c0022t0001g0295 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1520+1112_1520+119 others(90): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117030 | |||||||
chr11:74117031 | T | TATATATA others(3): Show |
3 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0164 |
3 | HG02109.hp2 HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1196_1520+119 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117031 | |||||||
chr11:74117031 | TATATATA others(37): Show |
T | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1520+1153_1520+119 others(48): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117031 | |||||||
chr11:74117039 | C | CACAT | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1188_1520+118 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117039 | |||||||
chr11:74117039 | CGT | C | 16 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(13): Show |
16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1520+1187_1520+118 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117039 | |||||||
chr11:74117039 | CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0138 |
2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1179_1520+118 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117039 | |||||||
chr11:74117040 | G | A | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1188C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117040 | |||||||
chr11:74117042 | G | A | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1186C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117042 | |||||||
chr11:74117044 | G | A | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0133 others(9): Show |
12 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1520+1184C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117044 | |||||||
chr11:74117045 | T | C | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1183A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117045 | |||||||
chr11:74117046 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0164 |
3 | HG02109.hp2 HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1182C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117046 | |||||||
chr11:74117046 | G | GTATATAT others(3): Show |
1 | a0006c0012t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1520+1181_1520+118 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117046 | |||||||
chr11:74117046 | GTGTATAT others(49): Show |
G | 2 | a0003c0034t0001g0185 a0031c0025t0001g0222 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1520+1126_1520+118 others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117046 | |||||||
chr11:74117047 | T | TATATATA others(149): Show |
1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1520+1180_1520+118 others(160): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117047 | |||||||
chr11:74117047 | TGTATATA others(21): Show |
T | 6 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(3): Show |
6 | HG02280.hp2 HG04228.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520+1153_1520+118 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117047 | |||||||
chr11:74117048 | G | A | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1520+1180C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | G | GTATATAT others(35): Show |
1 | a0004c0004t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1520+1179_1520+118 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(33): Show |
G | 5 | a0001c0001t0001g0155 a0002c0003t0001g0016 a0002c0003t0001g0017 others(2): Show |
5 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1140_1520+117 others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(47): Show |
G | 17 | a0001c0001t0001g0096 a0001c0001t0001g0154 a0002c0003t0001g0018 others(14): Show |
17 | HG02083.hp1 HG02083.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1520+1126_1520+117 others(58): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(61): Show |
G | 12 | a0002c0003t0001g0057 a0002c0003t0001g0206 a0002c0003t0001g0208 others(9): Show |
13 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1520+1112_1520+117 others(72): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(75): Show |
G | 66 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(63): Show |
66 | HG00423.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1520+1098_1520+117 others(86): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(89): Show |
G | 51 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(48): Show |
51 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1520+1084_1520+117 others(100): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(103): Show |
G | 23 | a0003c0041t0001g0297 a0005c0006t0001g0006 a0005c0006t0001g0007 others(20): Show |
23 | HG01099.hp1 HG01106.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1520+1070_1520+117 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117048 | GTATATAT others(131): Show |
G | 1 | a0005c0006t0001g0013 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1520+1042_1520+117 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | |||||||
chr11:74117049 | T | A | 1 | a0006c0012t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1520+1179A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117049 | |||||||
chr11:74117049 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1520+1153_1520+117 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117049 | |||||||
chr11:74117049 | TATATATA others(19): Show |
T | 3 | a0003c0002t0001g0253 a0007c0017t0001g0194 a0022c0032t0001g0176 |
3 | HG00597.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1520+1153_1520+117 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117049 | |||||||
chr11:74117051 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0138 |
2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1177A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117051 | |||||||
chr11:74117054 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1174T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117054 | |||||||
chr11:74117057 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1171A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117057 | |||||||
chr11:74117058 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1520+1170T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117058 | |||||||
chr11:74117059 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0138 others(1): Show |
4 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1169A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117059 | |||||||
chr11:74117059 | TGA | T | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1167_1520+116 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117059 | |||||||
chr11:74117060 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1168C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117060 | |||||||
chr11:74117061 | A | T | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0133 others(2): Show |
5 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1167T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117061 | |||||||
chr11:74117061 | AATATATA others(21): Show |
A | 1 | a0007c0017t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1520+1139_1520+116 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117061 | |||||||
chr11:74117062 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0133 a0001c0001t0001g0138 |
3 | HG00140.hp1 HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1520+1166T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117062 | |||||||
chr11:74117063 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1520+1153_1520+116 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117063 | |||||||
chr11:74117063 | T | TATATATA others(47): Show |
1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1520+1164_1520+116 others(58): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117063 | |||||||
chr11:74117063 | TATATATA others(5): Show |
T | 8 | a0001c0001t0001g0095 a0003c0002t0001g0254 a0003c0002t0001g0255 others(5): Show |
8 | HG01074.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520+1153_1520+116 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117063 | |||||||
chr11:74117065 | T | C | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1163A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117065 | |||||||
chr11:74117066 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1162T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117066 | |||||||
chr11:74117068 | A | G | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(10): Show |
13 | HG00140.hp1 HG00741.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1520+1160T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117068 | |||||||
chr11:74117070 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
9 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+1158T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117070 | |||||||
chr11:74117072 | A | G | 12 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0137 others(9): Show |
12 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1520+1156T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117072 | |||||||
chr11:74117073 | T | A | 3 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0234 |
3 | HG02723.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+1155A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117073 | |||||||
chr11:74117074 | G | A | 3 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0234 |
3 | HG02723.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+1154C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117074 | |||||||
chr11:74117075 | A | AAT | 27 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(24): Show |
27 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1520+1151_1520+115 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0099 a0001c0001t0001g0109 a0001c0001t0001g0147 |
3 | HG01109.hp2 HG01192.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1520+1139_1520+115 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | A | AATATATA others(35): Show |
1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1520+1111_1520+115 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | A | T | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0136 others(11): Show |
14 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1520+1153T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | AATATATA others(7): Show |
A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0102 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.1520+1139_1520+115 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | AATATATA others(21): Show |
A | 15 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0122 others(12): Show |
15 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1520+1125_1520+115 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | AATATATA others(35): Show |
A | 10 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0104 others(7): Show |
10 | HG00673.hp2 HG01099.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1111_1520+115 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117075 | AATATATA others(49): Show |
A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0160 others(1): Show |
4 | HG01952.hp1 NA18970.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1097_1520+115 others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | |||||||
chr11:74117079 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0138 |
2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1149A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117079 | |||||||
chr11:74117080 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0138 |
2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1148T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117080 | |||||||
chr11:74117082 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0138 |
2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1146T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117082 | |||||||
chr11:74117084 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0138 others(1): Show |
4 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1144T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117084 | |||||||
chr11:74117086 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1520+1142C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117086 | |||||||
chr11:74117087 | A | T | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0133 others(2): Show |
5 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1141T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117087 | |||||||
chr11:74117087 | AATATATA others(23): Show |
A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0163 |
2 | HG00597.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1520+1111_1520+114 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117087 | |||||||
chr11:74117088 | A | G | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0133 others(2): Show |
5 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1140T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117088 | |||||||
chr11:74117089 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1520+1139A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117089 | |||||||
chr11:74117089 | T | TATATATA others(5): Show |
2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1520+1127_1520+113 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117089 | |||||||
chr11:74117101 | AAT | A | 23 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0136 others(20): Show |
23 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1520+1125_1520+112 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117101 | |||||||
chr11:74117101 | AATATATA others(9): Show |
A | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1520+1111_1520+112 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117101 | |||||||
chr11:74117114 | G | A | 3 | a0004c0004t0001g0036 a0004c0004t0001g0041 a0004c0004t0001g0046 |
3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1114C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117114 | |||||||
chr11:74117115 | A | T | 3 | a0004c0004t0001g0036 a0004c0004t0001g0041 a0004c0004t0001g0046 |
3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1113T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117115 | |||||||
chr11:74117115 | AAT | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0138 others(2): Show |
5 | HG00140.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1111_1520+111 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117115 | |||||||
chr11:74117115 | AATATATA others(23): Show |
A | 1 | a0023c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1520+1083_1520+111 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117115 | |||||||
chr11:74117116 | A | G | 3 | a0004c0004t0001g0036 a0004c0004t0001g0041 a0004c0004t0001g0046 |
3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1112T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117116 | |||||||
chr11:74117117 | T | A | 3 | a0004c0004t0001g0036 a0004c0004t0001g0041 a0004c0004t0001g0046 |
3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1111A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | |||||||
chr11:74117117 | T | TATATATA others(5): Show |
3 | a0004c0004t0001g0044 a0004c0004t0001g0045 a0030c0042t0001g0304 |
3 | HG02922.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1520+1099_1520+111 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | |||||||
chr11:74117117 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1520+1085_1520+111 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | |||||||
chr11:74117117 | T | TATATATA others(3): Show |
4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0014c0020t0004g0218 others(1): Show |
4 | HG02723.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1110_1520+111 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | |||||||
chr11:74117117 | TATATATA others(89): Show |
T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1520+1015_1520+111 others(100): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | |||||||
chr11:74117119 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1520+1109A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117119 | |||||||
chr11:74117129 | AAT | A | 10 | a0001c0001t0001g0114 a0004c0004t0001g0037 a0004c0004t0001g0038 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1097_1520+109 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117129 | |||||||
chr11:74117129 | AATATATA others(9): Show |
A | 1 | a0001c0030t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1520+1083_1520+109 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117129 | |||||||
chr11:74117129 | AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1520+1069_1520+109 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117129 | |||||||
chr11:74117131 | T | TATATATA others(3): Show |
1 | a0006c0012t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1520+1096_1520+109 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117131 | |||||||
chr11:74117131 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1520+1085_1520+109 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117131 | |||||||
chr11:74117143 | A | AAT | 3 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 |
3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1520+1083_1520+108 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | |||||||
chr11:74117143 | AAT | A | 4 | a0003c0016t0001g0249 a0003c0034t0001g0185 a0004c0004t0001g0048 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+1083_1520+108 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | |||||||
chr11:74117143 | AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1520+1055_1520+108 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | |||||||
chr11:74117143 | AATATATA others(37): Show |
A | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1520+1041_1520+108 others(48): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | |||||||
chr11:74117145 | T | TATATATA others(5): Show |
2 | a0004c0004t0001g0044 a0004c0004t0001g0045 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1520+1071_1520+108 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117145 | T | TATATATA others(19): Show |
1 | a0004c0004t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1520+1057_1520+108 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117145 | T | TATATATA others(33): Show |
4 | a0004c0004t0001g0033 a0004c0004t0001g0034 a0004c0004t0001g0042 others(1): Show |
4 | HG02809.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1043_1520+108 others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117145 | T | TATATATA others(47): Show |
1 | a0004c0004t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1520+1029_1520+108 others(58): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117145 | T | TATATATA others(115): Show |
1 | a0004c0004t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1520+1082_1520+108 others(126): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117145 | T | TATATATA others(3): Show |
4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0234 others(1): Show |
4 | HG02615.hp1 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+1082_1520+108 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117145 | TATATATA others(5): Show |
T | 1 | a0028c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1520+1071_1520+108 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | |||||||
chr11:74117157 | AAT | A | 14 | a0001c0001t0001g0157 a0003c0034t0001g0185 a0004c0004t0001g0040 others(11): Show |
14 | HG02055.hp1 HG02280.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1520+1069_1520+107 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117157 | |||||||
chr11:74117159 | T | TATATATA others(5): Show |
2 | a0006c0012t0001g0235 a0030c0042t0001g0304 |
2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1520+1057_1520+106 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117159 | |||||||
chr11:74117159 | T | TATATATA others(3): Show |
3 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0234 |
3 | HG02723.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+1068_1520+106 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117159 | |||||||
chr11:74117168 | A | T | 10 | a0002c0003t0001g0090 a0002c0003t0001g0091 a0008c0007t0001g0082 others(7): Show |
10 | HG02083.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1060T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117168 | |||||||
chr11:74117175 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1520+1053A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117175 | |||||||
chr11:74117182 | A | T | 6 | a0002c0003t0001g0166 a0002c0003t0001g0167 a0002c0003t0001g0169 others(3): Show |
6 | HG01192.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520+1046T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117182 | |||||||
chr11:74117185 | A | AAT | 4 | a0006c0008t0001g0230 a0011c0015t0001g0001 a0011c0015t0001g0223 others(1): Show |
5 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1041_1520+104 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117185 | |||||||
chr11:74117190 | A | G | 2 | a0006c0008t0001g0239 a0006c0008t0001g0240 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1520+1038T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117190 | |||||||
chr11:74117191 | T | A | 2 | a0006c0008t0001g0239 a0006c0008t0001g0240 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1520+1037A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117191 | |||||||
chr11:74117196 | A | T | 74 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(71): Show |
74 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1520+1032T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117196 | |||||||
chr11:74117199 | A | AATATATA others(11): Show |
3 | a0006c0008t0001g0229 a0006c0008t0001g0236 a0006c0008t0001g0237 |
3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1520+1028_1520+102 others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117199 | |||||||
chr11:74117208 | A | G | 3 | a0006c0008t0001g0239 a0006c0008t0001g0240 a0028c0045t0001g0224 |
3 | HG01884.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1520+1020T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117208 | |||||||
chr11:74117209 | T | A | 3 | a0006c0008t0001g0239 a0006c0008t0001g0240 a0028c0045t0001g0224 |
3 | HG01884.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1520+1019A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117209 | |||||||
chr11:74117211 | TGA | T | 3 | a0006c0008t0001g0239 a0006c0008t0001g0240 a0028c0045t0001g0224 |
3 | HG01884.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1520+1015_1520+101 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117211 | |||||||
chr11:74117213 | A | AAT | 37 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0003c0034t0001g0185 others(34): Show |
38 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.1520+1013_1520+101 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117213 | |||||||
chr11:74117217 | T | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1520+1011A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117217 | |||||||
chr11:74117242 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0149 |
3 | HG00140.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1520+986C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117242 | |||||||
chr11:74117243 | T | G | 2 | a0013c0013t0001g0226 a0013c0013t0001g0227 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1520+985A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117243 | |||||||
chr11:74117291 | C | G | 1 | a0030c0042t0001g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1520+937G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117291 | |||||||
chr11:74117361 | A | AAT | 4 | a0001c0001t0001g0097 a0002c0003t0001g0018 a0011c0018t0001g0131 others(1): Show |
4 | HG02965.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+865_1520+866d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATAT | 4 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0144 others(1): Show |
4 | HG01258.hp1 HG01261.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+863_1520+866d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATAT | 4 | a0002c0003t0001g0075 a0002c0028t0001g0011 a0005c0006t0001g0014 others(1): Show |
4 | HG01099.hp1 HG01433.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+861_1520+866d others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(1): Show |
35 | a0002c0003t0001g0050 a0002c0003t0001g0060 a0002c0003t0001g0090 others(32): Show |
35 | HG01106.hp2 HG01192.hp1 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.1520+859_1520+866d others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(3): Show |
21 | a0002c0003t0001g0051 a0002c0003t0001g0059 a0002c0003t0001g0062 others(18): Show |
21 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1520+857_1520+866d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(5): Show |
12 | a0002c0003t0001g0187 a0002c0003t0001g0205 a0002c0003t0001g0207 others(9): Show |
12 | HG01109.hp1 HG02630.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1520+855_1520+866d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(7): Show |
15 | a0002c0003t0001g0031 a0002c0003t0001g0052 a0002c0003t0001g0209 others(12): Show |
15 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1520+853_1520+866d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(9): Show |
3 | a0002c0003t0001g0056 a0002c0003t0001g0206 a0008c0007t0001g0211 |
3 | HG00280.hp2 HG02809.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1520+851_1520+866d others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(11): Show |
10 | a0002c0003t0001g0030 a0002c0003t0001g0208 a0002c0003t0001g0210 others(7): Show |
10 | HG00639.hp2 HG01516.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+849_1520+866d others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(13): Show |
8 | a0002c0003t0001g0054 a0002c0003t0001g0055 a0002c0003t0001g0057 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1520+847_1520+866d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(15): Show |
2 | a0002c0003t0001g0199 a0002c0003t0001g0202 |
2 | HG01123.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1520+845_1520+866d others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(17): Show |
2 | a0002c0003t0001g0201 a0018c0029t0001g0198 |
2 | HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1520+843_1520+866d others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(19): Show |
1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1520+841_1520+866d others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(21): Show |
1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1520+839_1520+866d others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(23): Show |
1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1520+837_1520+866d others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(27): Show |
3 | a0002c0003t0001g0061 a0002c0003t0001g0070 a0002c0003t0001g0071 |
3 | HG02132.hp1 NA18980.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1520+866_1520+867i others(36): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | AATATATA others(33): Show |
1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1520+866_1520+867i others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | A | ATATATAT others(8): Show |
1 | a0002c0003t0001g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1520+866_1520+867i others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | AAT | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(58): Show |
61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1520+865_1520+866d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | AATATATA others(1): Show |
A | 3 | a0001c0001t0001g0161 a0014c0020t0004g0218 a0014c0020t0004g0219 |
3 | HG02723.hp2 HG03041.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1520+859_1520+866d others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117361 | AATATATA others(5): Show |
A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1520+855_1520+866d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | |||||||
chr11:74117472 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1520+756T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117472 | |||||||
chr11:74117563 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1520+665T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117563 | |||||||
chr11:74117576 | T | C | 1 | a0003c0002t0001g0296 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1520+652A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117576 | |||||||
chr11:74117645 | G | A | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1520+583C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117645 | |||||||
chr11:74117731 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1520+497A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117731 | |||||||
chr11:74117846 | G | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1520+382C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117846 | |||||||
chr11:74117900 | C | T | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1520+328G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117900 | |||||||
chr11:74117913 | C | CA | 6 | a0001c0001t0001g0094 a0001c0001t0001g0129 a0001c0001t0001g0148 others(3): Show |
6 | HG01255.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520+314dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117913 | |||||||
chr11:74117913 | CA | C | 9 | a0004c0004t0001g0042 a0007c0009t0002g0311 a0007c0009t0002g0312 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1520+314delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117913 | |||||||
chr11:74118182 | A | G | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1520+46T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74118182 | |||||||
chr11:74118187 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1520+41G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74118187 | |||||||
chr11:74118640 | C | T | 1 | a0024c0024t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1366-258G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118640 | |||||||
chr11:74118666 | T | C | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1366-284A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118666 | |||||||
chr11:74118715 | A | C | 3 | a0002c0003t0001g0200 a0002c0003t0001g0201 a0002c0003t0001g0202 |
3 | HG01123.hp1 HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1366-333T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118715 | |||||||
chr11:74118736 | G | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1366-354C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118736 | |||||||
chr11:74118905 | A | AT | 106 | a0001c0001t0001g0096 a0001c0001t0001g0109 a0001c0001t0001g0119 others(103): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1366-524dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118905 | |||||||
chr11:74118905 | A | ATT | 11 | a0001c0001t0001g0142 a0003c0002t0001g0246 a0003c0002t0001g0284 others(8): Show |
11 | HG02074.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1366-525_1366-524d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118905 | |||||||
chr11:74118905 | AT | A | 12 | a0001c0001t0001g0103 a0004c0004t0001g0032 a0004c0004t0001g0033 others(9): Show |
12 | HG00639.hp1 HG01975.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366-524delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118905 | |||||||
chr11:74118906 | T | A | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1366-524A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118906 | |||||||
chr11:74119498 | C | T | 1 | a0002c0003t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1366-1116G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119498 | |||||||
chr11:74119635 | CT | C | 14 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0002c0003t0001g0199 others(11): Show |
14 | HG02015.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1366-1254delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119635 | |||||||
chr11:74119705 | C | T | 104 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(101): Show |
104 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1366-1323G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119705 | |||||||
chr11:74119712 | T | C | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1366-1330A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119712 | |||||||
chr11:74119784 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1366-1402A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119784 | |||||||
chr11:74119855 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0139 |
2 | HG01169.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1366-1473G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119855 | |||||||
chr11:74119987 | C | A | 78 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(75): Show |
78 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.1366-1605G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119987 | |||||||
chr11:74120093 | G | C | 3 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 |
3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1366-1711C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120093 | |||||||
chr11:74120264 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1366-1882G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120264 | |||||||
chr11:74120402 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1366-2020G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120402 | |||||||
chr11:74120777 | T | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1365+2211A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120777 | |||||||
chr11:74120805 | G | A | 1 | a0018c0029t0001g0198 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1365+2183C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120805 | |||||||
chr11:74120915 | T | C | 1 | a0006c0008t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1365+2073A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120915 | |||||||
chr11:74120993 | C | A | 1 | a0002c0003t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1365+1995G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120993 | |||||||
chr11:74120995 | G | GA | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1365+1992dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120995 | |||||||
chr11:74121166 | T | C | 105 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(102): Show |
105 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.1365+1822A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121166 | |||||||
chr11:74121169 | A | G | 1 | a0003c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1365+1819T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121169 | |||||||
chr11:74121263 | A | G | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1365+1725T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121263 | |||||||
chr11:74121298 | G | A | 1 | a0021c0037t0001g0273 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1365+1690C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121298 | |||||||
chr11:74121418 | C | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1365+1570G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121418 | |||||||
chr11:74121608 | C | CA | 70 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0143 others(67): Show |
70 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1365+1379dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121608 | |||||||
chr11:74121608 | C | CAA | 10 | a0003c0002t0001g0244 a0003c0002t0001g0270 a0007c0009t0002g0311 others(7): Show |
10 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1365+1378_1365+137 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121608 | |||||||
chr11:74121608 | CAAAAAAA others(5): Show |
C | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1365+1368_1365+137 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121608 | |||||||
chr11:74121708 | C | T | 85 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1365+1280G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121708 | |||||||
chr11:74121833 | G | A | 7 | a0003c0002t0001g0243 a0003c0002t0001g0244 a0003c0002t0001g0245 others(4): Show |
7 | HG00558.hp2 NA18980.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+1155C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121833 | |||||||
chr11:74121995 | C | T | 2 | a0003c0016t0001g0242 a0036c0022t0001g0295 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1365+993G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121995 | |||||||
chr11:74122153 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02040.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1365+835G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122153 | |||||||
chr11:74122276 | T | C | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1365+712A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122276 | |||||||
chr11:74122348 | C | T | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1365+640G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122348 | |||||||
chr11:74122622 | T | G | 3 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 |
3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1365+366A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122622 | |||||||
chr11:74122899 | G | A | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1365+89C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122899 | |||||||
chr11:74122912 | C | CTGTCTGG others(7): Show |
229 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1365+75_1365+76ins others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122912 | |||||||
chr11:74122946 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1365+42T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122946 | |||||||
chr11:74123400 | A | G | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-265T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123400 | |||||||
chr11:74123460 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1218-325A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123460 | |||||||
chr11:74123665 | TA | T | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0104 others(6): Show |
9 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-531delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123665 | |||||||
chr11:74123729 | G | T | 8 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(5): Show |
8 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-594C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123729 | |||||||
chr11:74123737 | CT | C | 167 | a0001c0001t0001g0128 a0002c0003t0001g0016 a0002c0003t0001g0017 others(164): Show |
168 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(165): Show |
intron_variant | MODIFIER | c.1218-603delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123737 | |||||||
chr11:74123771 | T | A | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-636A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123771 | |||||||
chr11:74123865 | A | G | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-730T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123865 | |||||||
chr11:74123866 | G | A | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-731C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123866 | |||||||
chr11:74123911 | G | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1218-776C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123911 | |||||||
chr11:74123971 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-836A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123971 | |||||||
chr11:74124251 | A | G | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1218-1116T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74124251 | |||||||
chr11:74124525 | G | A | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1218-1390C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74124525 | |||||||
chr11:74124775 | A | G | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1218-1640T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74124775 | |||||||
chr11:74125017 | T | A | 15 | a0005c0006t0001g0006 a0005c0006t0001g0007 a0005c0006t0001g0013 others(12): Show |
15 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1218-1882A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74125017 | |||||||
chr11:74125040 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1218-1905G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74125040 | |||||||
chr11:74125479 | T | G | 8 | a0003c0002t0001g0257 a0003c0002t0001g0266 a0003c0002t0001g0267 others(5): Show |
8 | HG00438.hp2 HG03654.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-2344A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74125479 | |||||||
chr11:74126006 | ACT | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0149 others(2): Show |
5 | HG00140.hp1 HG01106.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218-2873_1218-287 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126006 | |||||||
chr11:74126305 | T | C | 6 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0013c0013t0001g0225 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218-3170A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126305 | |||||||
chr11:74126517 | C | T | 1 | a0002c0003t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1218-3382G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126517 | |||||||
chr11:74126560 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1218-3425G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126560 | |||||||
chr11:74126636 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1218-3501G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126636 | |||||||
chr11:74126637 | G | A | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1218-3502C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126637 | |||||||
chr11:74126774 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-3639A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126774 | |||||||
chr11:74126791 | T | C | 2 | a0003c0002t0001g0246 a0003c0002t0001g0248 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1218-3656A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126791 | |||||||
chr11:74126852 | T | G | 1 | a0002c0003t0001g0075 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1218-3717A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126852 | |||||||
chr11:74126946 | T | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1218-3811A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126946 | |||||||
chr11:74126986 | A | G | 3 | a0003c0002t0003g0002 a0003c0002t0003g0003 a0003c0002t0003g0004 |
3 | HG00642.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1218-3851T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126986 | |||||||
chr11:74127044 | A | G | 229 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1218-3909T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127044 | |||||||
chr11:74127111 | G | A | 2 | a0003c0002t0001g0269 a0003c0002t0001g0270 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1218-3976C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127111 | |||||||
chr11:74127119 | T | C | 230 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(227): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1218-3984A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127119 | |||||||
chr11:74127222 | G | A | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1218-4087C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127222 | |||||||
chr11:74127357 | A | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0175 others(1): Show |
4 | HG02040.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218-4222T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127357 | |||||||
chr11:74127476 | A | AT | 15 | a0001c0001t0001g0129 a0001c0030t0001g0190 a0002c0003t0001g0167 others(12): Show |
15 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1218-4342dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127476 | |||||||
chr11:74127534 | T | G | 1 | a0001c0030t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1218-4399A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127534 | |||||||
chr11:74127559 | G | A | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1218-4424C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127559 | |||||||
chr11:74127791 | G | A | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1218-4656C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127791 | |||||||
chr11:74127827 | A | G | 1 | a0007c0009t0002g0311 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1218-4692T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127827 | |||||||
chr11:74127886 | G | A | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1218-4751C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127886 | |||||||
chr11:74127926 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1218-4791C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127926 | |||||||
chr11:74128106 | G | A | 1 | a0002c0003t0001g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1217+4738C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128106 | |||||||
chr11:74128142 | C | T | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1217+4702G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128142 | |||||||
chr11:74128168 | G | T | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1217+4676C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128168 | |||||||
chr11:74128534 | TTTTA | T | 3 | a0003c0002t0001g0280 a0003c0002t0001g0281 a0022c0032t0001g0176 |
3 | HG02109.hp1 NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1217+4306_1217+430 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128534 | |||||||
chr11:74128589 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1217+4255C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128589 | |||||||
chr11:74128646 | A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+4198T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128646 | |||||||
chr11:74128725 | A | G | 119 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(116): Show |
119 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.1217+4119T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128725 | |||||||
chr11:74128735 | G | T | 2 | a0002c0003t0001g0090 a0002c0003t0001g0091 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1217+4109C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128735 | |||||||
chr11:74128744 | A | C | 99 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(96): Show |
99 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1217+4100T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128744 | |||||||
chr11:74128752 | C | G | 125 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(122): Show |
125 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(122): Show |
intron_variant | MODIFIER | c.1217+4092G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128752 | |||||||
chr11:74128785 | A | G | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1217+4059T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128785 | |||||||
chr11:74128797 | ACCGCCCT others(4): Show |
A | 1 | a0003c0002t0001g0286 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1217+4036_1217+404 others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128797 | |||||||
chr11:74128800 | G | A | 1 | a0005c0006t0001g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1217+4044C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128800 | |||||||
chr11:74128803 | C | T | 100 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(97): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1217+4041G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128803 | |||||||
chr11:74128824 | T | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+4020A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128824 | |||||||
chr11:74128889 | A | G | 1 | a0002c0003t0001g0030 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1217+3955T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128889 | |||||||
chr11:74128906 | G | A | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1217+3938C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128906 | |||||||
chr11:74128952 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1217+3892G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128952 | |||||||
chr11:74129041 | G | A | 1 | a0002c0003t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1217+3803C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129041 | |||||||
chr11:74129074 | C | G | 1 | a0003c0002t0001g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1217+3770G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129074 | |||||||
chr11:74129075 | A | G | 1 | a0003c0002t0001g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1217+3769T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129075 | |||||||
chr11:74129082 | TGGCCGGG others(30): Show |
T | 20 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(17): Show |
20 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1217+3725_1217+376 others(41): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129082 | |||||||
chr11:74129119 | C | A | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1217+3725G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129119 | |||||||
chr11:74129123 | C | T | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+3721G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129123 | |||||||
chr11:74129170 | G | T | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1217+3674C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129170 | |||||||
chr11:74129173 | A | G | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1217+3671T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129173 | |||||||
chr11:74129183 | T | C | 2 | a0008c0007t0001g0076 a0008c0007t0001g0217 |
2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1217+3661A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129183 | |||||||
chr11:74129200 | G | A | 4 | a0002c0003t0001g0206 a0002c0003t0001g0208 a0002c0003t0001g0209 others(1): Show |
4 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+3644C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129200 | |||||||
chr11:74129216 | G | A | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1217+3628C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129216 | |||||||
chr11:74129279 | C | T | 1 | a0003c0041t0001g0297 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1217+3565G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129279 | |||||||
chr11:74129301 | G | A | 1 | a0003c0002t0001g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1217+3543C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129301 | |||||||
chr11:74129359 | G | A | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1217+3485C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129359 | |||||||
chr11:74129367 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1217+3477A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129367 | |||||||
chr11:74129377 | C | T | 1 | a0006c0008t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1217+3467G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129377 | |||||||
chr11:74129379 | G | C | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1217+3465C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129379 | |||||||
chr11:74129384 | C | T | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1217+3460G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129384 | |||||||
chr11:74129436 | G | A | 1 | a0028c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1217+3408C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129436 | |||||||
chr11:74129537 | C | T | 7 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(4): Show |
7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1217+3307G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129537 | |||||||
chr11:74129585 | TCCAGACT others(69): Show |
T | 10 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(7): Show |
10 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1217+3183_1217+325 others(80): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129585 | |||||||
chr11:74129612 | A | C | 114 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(111): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1217+3232T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129612 | |||||||
chr11:74129628 | C | T | 58 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(55): Show |
58 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1217+3216G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129628 | |||||||
chr11:74129661 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1217+3183G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129661 | |||||||
chr11:74129667 | C | CG | 9 | a0001c0001t0001g0109 a0002c0003t0001g0166 a0003c0002t0001g0244 others(6): Show |
9 | HG01099.hp1 HG01978.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1217+3176dupC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129667 | |||||||
chr11:74129680 | G | A | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1217+3164C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129680 | |||||||
chr11:74129754 | T | G | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1217+3090A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129754 | |||||||
chr11:74129760 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1217+3084C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129760 | |||||||
chr11:74129765 | T | G | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1217+3079A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129765 | |||||||
chr11:74129796 | C | A | 124 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(121): Show |
125 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1217+3048G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129796 | |||||||
chr11:74129803 | G | A | 4 | a0010c0010t0001g0305 a0010c0010t0001g0306 a0010c0010t0001g0307 others(1): Show |
4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+3041C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129803 | |||||||
chr11:74129822 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+3022G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129822 | |||||||
chr11:74129848 | G | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+2996C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129848 | |||||||
chr11:74129852 | C | T | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+2992G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129852 | |||||||
chr11:74129858 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+2986G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129858 | |||||||
chr11:74129965 | T | G | 63 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(60): Show |
63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1217+2879A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129965 | |||||||
chr11:74129985 | A | G | 1 | a0002c0005t0001g0088 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1217+2859T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129985 | |||||||
chr11:74130077 | C | T | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+2767G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130077 | |||||||
chr11:74130078 | G | A | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1217+2766C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130078 | |||||||
chr11:74130122 | G | GGGGAGA | 11 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0006c0012t0001g0231 others(8): Show |
11 | HG02717.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1217+2716_1217+272 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130122 | |||||||
chr11:74130122 | G | GGGGAGAG others(5): Show |
6 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 others(3): Show |
6 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217+2710_1217+272 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130122 | |||||||
chr11:74130140 | A | AGGGAGAG others(6): Show |
7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+2703_1217+270 others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130140 | |||||||
chr11:74130153 | AG | A | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1217+2690delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130153 | |||||||
chr11:74130226 | CT | C | 9 | a0001c0001t0001g0029 a0001c0001t0001g0115 a0001c0001t0001g0133 others(6): Show |
9 | HG01169.hp1 HG01517.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+2617delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130226 | |||||||
chr11:74130281 | G | A | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1217+2563C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130281 | |||||||
chr11:74130352 | A | G | 1 | a0002c0003t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1217+2492T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130352 | |||||||
chr11:74130535 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1217+2309T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130535 | |||||||
chr11:74130683 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1217+2161G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130683 | |||||||
chr11:74130704 | G | A | 1 | a0003c0002t0001g0284 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1217+2140C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130704 | |||||||
chr11:74130838 | A | G | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1217+2006T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130838 | |||||||
chr11:74130846 | G | T | 229 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1217+1998C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130846 | |||||||
chr11:74131094 | G | C | 73 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1217+1750C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131094 | |||||||
chr11:74131322 | C | CA | 9 | a0001c0001t0001g0146 a0003c0002t0001g0284 a0010c0010t0001g0302 others(6): Show |
9 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(6): Show |
intron_variant | MODIFIER | c.1217+1521dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131322 | |||||||
chr11:74131322 | CA | C | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+1521delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131322 | |||||||
chr11:74131439 | A | G | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1217+1405T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131439 | |||||||
chr11:74131536 | T | C | 6 | a0003c0002t0001g0241 a0003c0002t0001g0252 a0003c0002t0001g0253 others(3): Show |
6 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217+1308A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131536 | |||||||
chr11:74131564 | T | A | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+1280A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131564 | |||||||
chr11:74131588 | C | CT | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1217+1255dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131588 | |||||||
chr11:74131677 | C | T | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1217+1167G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131677 | |||||||
chr11:74133078 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0152 |
2 | HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1089-106A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/32 | chr11 | 74133078 | |||||||
chr11:74133182 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-210A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/32 | chr11 | 74133182 | |||||||
chr11:74133389 | A | G | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1088+36T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/32 | chr11 | 74133389 | |||||||
chr11:74133571 | A | G | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.956-14T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74133571 | |||||||
chr11:74133919 | C | T | 1 | a0002c0003t0001g0051 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.956-362G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74133919 | |||||||
chr11:74133964 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.956-407G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74133964 | |||||||
chr11:74134133 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956-576G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134133 | |||||||
chr11:74134281 | T | G | 2 | a0011c0018t0001g0131 a0011c0018t0001g0132 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.956-724A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134281 | |||||||
chr11:74134502 | G | A | 4 | a0010c0010t0001g0305 a0010c0010t0001g0306 a0010c0010t0001g0307 others(1): Show |
4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-945C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134502 | |||||||
chr11:74134527 | T | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956-970A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134527 | |||||||
chr11:74134537 | C | G | 1 | a0006c0012t0001g0235 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.956-980G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134537 | |||||||
chr11:74134800 | G | A | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956-1243C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134800 | |||||||
chr11:74134844 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.956-1287C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134844 | |||||||
chr11:74134858 | T | C | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-1301A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134858 | |||||||
chr11:74134976 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956-1419G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134976 | |||||||
chr11:74135099 | T | C | 2 | a0004c0004t0001g0033 a0004c0004t0001g0034 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956-1542A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135099 | |||||||
chr11:74135269 | C | CT | 8 | a0002c0005t0001g0087 a0006c0008t0001g0229 a0006c0008t0001g0230 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.956-1713dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135269 | |||||||
chr11:74135269 | CTTTTT | C | 6 | a0003c0002t0001g0246 a0003c0002t0001g0248 a0003c0002t0001g0276 others(3): Show |
6 | NA18948.hp2 NA18963.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-1717_956-1713d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135269 | |||||||
chr11:74135326 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.956-1769C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135326 | |||||||
chr11:74135531 | G | A | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.956-1974C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135531 | |||||||
chr11:74135745 | C | T | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.956-2188G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135745 | |||||||
chr11:74135800 | C | G | 230 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(227): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.956-2243G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135800 | |||||||
chr11:74136148 | T | G | 2 | a0015c0019t0001g0025 a0015c0019t0001g0028 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.955+2572A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136148 | |||||||
chr11:74136275 | G | A | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.955+2445C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136275 | |||||||
chr11:74136446 | G | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+2274C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136446 | |||||||
chr11:74136548 | A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.955+2172T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136548 | |||||||
chr11:74136643 | T | C | 2 | a0004c0004t0001g0042 a0004c0004t0001g0043 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.955+2077A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136643 | |||||||
chr11:74136654 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+2066G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136654 | |||||||
chr11:74136724 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+1996A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136724 | |||||||
chr11:74136772 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.955+1948C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136772 | |||||||
chr11:74136805 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.955+1915T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136805 | |||||||
chr11:74136816 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.955+1904C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136816 | |||||||
chr11:74136964 | TA | T | 85 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.955+1755delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136964 | |||||||
chr11:74137033 | T | C | 1 | a0002c0003t0001g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.955+1687A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137033 | |||||||
chr11:74137327 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.955+1393A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137327 | |||||||
chr11:74137417 | T | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.955+1303A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137417 | |||||||
chr11:74137508 | G | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+1212C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137508 | |||||||
chr11:74137535 | G | GTA | 85 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.955+1183_955+1184d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137535 | |||||||
chr11:74137535 | GTA | G | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+1183_955+1184d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137535 | |||||||
chr11:74137567 | T | TTA | 6 | a0002c0003t0001g0171 a0008c0007t0001g0082 a0008c0007t0001g0221 others(3): Show |
7 | HG01358.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.955+1151_955+1152d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137567 | |||||||
chr11:74137581 | A | T | 21 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(18): Show |
21 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.955+1139T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137581 | |||||||
chr11:74137620 | C | T | 1 | a0009c0011t0001g0063 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.955+1100G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137620 | |||||||
chr11:74137866 | G | A | 106 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(103): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.955+854C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137866 | |||||||
chr11:74137944 | T | A | 1 | a0011c0015t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.955+776A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137944 | |||||||
chr11:74137946 | T | G | 1 | a0011c0015t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.955+774A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137946 | |||||||
chr11:74138282 | A | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+438T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138282 | |||||||
chr11:74138421 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.955+299C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138421 | |||||||
chr11:74138664 | C | T | 1 | a0012c0014t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.955+56G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138664 | |||||||
chr11:74138709 | T | C | 3 | a0002c0003t0001g0050 a0002c0003t0001g0051 a0002c0003t0001g0062 |
3 | HG02300.hp1 HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.955+11A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138709 | |||||||
chr11:74139173 | G | A | 6 | a0009c0011t0001g0053 a0009c0011t0001g0063 a0009c0011t0001g0064 others(3): Show |
6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.708-206C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139173 | |||||||
chr11:74139199 | C | T | 2 | a0005c0006t0001g0026 a0005c0006t0001g0027 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.708-232G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139199 | |||||||
chr11:74139448 | A | C | 1 | a0002c0003t0001g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.707+157T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139448 | |||||||
chr11:74139595 | T | A | 4 | a0003c0034t0001g0185 a0013c0013t0001g0225 a0013c0013t0001g0226 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+10A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139595 | |||||||
chr11:74139873 | T | C | 3 | a0004c0004t0001g0035 a0004c0004t0001g0044 a0004c0004t0001g0045 |
3 | HG02922.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.484-45A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139873 | |||||||
chr11:74139909 | T | TAATGTCC others(24): Show |
10 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(7): Show |
10 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(29): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | T | TAATGTCC others(55): Show |
8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | T | TAATGTCC others(55): Show |
4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | T | TAATGTCC others(86): Show |
3 | a0003c0016t0001g0242 a0025c0040t0001g0301 a0036c0022t0001g0295 |
3 | HG02622.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.484-82_484-81insCC others(91): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | T | TAATGTCC others(115): Show |
49 | a0003c0002t0001g0241 a0003c0002t0001g0246 a0003c0002t0001g0247 others(46): Show |
49 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(120): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | T | TAATGTCC others(146): Show |
10 | a0003c0002t0001g0243 a0003c0002t0001g0244 a0003c0002t0001g0245 others(7): Show |
10 | HG02074.hp1 HG02818.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(151): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | T | TAATGTCC others(177): Show |
1 | a0003c0002t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.484-82_484-81insCC others(182): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139909 | TAATGTCC others(24): Show |
T | 3 | a0008c0007t0001g0211 a0008c0007t0001g0212 a0008c0007t0001g0216 |
3 | NA18956.hp1 NA18963.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.484-112_484-82delC others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | |||||||
chr11:74139921 | T | C | 3 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 |
3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.484-93A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139921 | |||||||
chr11:74139928 | C | G | 17 | a0003c0016t0001g0249 a0007c0009t0002g0311 a0007c0009t0002g0312 others(14): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.484-100G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139928 | |||||||
chr11:74139928 | CAGGATTG others(24): Show |
C | 2 | a0002c0003t0001g0078 a0024c0024t0001g0203 |
2 | HG02615.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.484-131_484-101del others(31): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139928 | |||||||
chr11:74139959 | G | C | 92 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(89): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.484-131C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | |||||||
chr11:74139959 | G | GAGGATTG others(24): Show |
4 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-132_484-131ins others(31): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | |||||||
chr11:74139959 | G | GAGGATTG others(87): Show |
1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-132_484-131ins others(94): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | |||||||
chr11:74139959 | GAGGATTG others(55): Show |
G | 5 | a0002c0003t0001g0061 a0002c0003t0001g0070 a0002c0003t0001g0071 others(2): Show |
5 | HG02129.hp1 HG02132.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-193_484-132del others(62): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | |||||||
chr11:74139990 | G | C | 266 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(263): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.484-162C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139990 | |||||||
chr11:74139990 | G | GAGGATTG others(86): Show |
1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484-163_484-162ins others(93): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139990 | |||||||
chr11:74140052 | G | C | 112 | a0001c0001t0001g0141 a0001c0001t0001g0163 a0002c0003t0001g0061 others(109): Show |
112 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.484-224C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | |||||||
chr11:74140052 | G | GAGGATTG others(210): Show |
2 | a0011c0015t0001g0001 a0011c0015t0001g0223 |
3 | HG01884.hp2 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.484-225_484-224ins others(217): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | |||||||
chr11:74140052 | G | GAGGATTG others(241): Show |
1 | a0028c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.484-225_484-224ins others(248): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | |||||||
chr11:74140052 | GAGGATTG others(24): Show |
G | 116 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(113): Show |
116 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.484-255_484-225del others(31): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | |||||||
chr11:74140060 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.484-232A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140060 | |||||||
chr11:74140083 | C | G | 5 | a0002c0005t0001g0049 a0008c0007t0001g0211 a0008c0007t0001g0212 others(2): Show |
5 | HG00738.hp1 NA18956.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-255G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140083 | |||||||
chr11:74140093 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.484-265T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140093 | |||||||
chr11:74140387 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.484-559A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140387 | |||||||
chr11:74140419 | T | C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-591A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140419 | |||||||
chr11:74140830 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0159 |
2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.484-1002C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140830 | |||||||
chr11:74141004 | A | G | 1 | a0004c0004t0001g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.484-1176T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141004 | |||||||
chr11:74141043 | G | C | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.484-1215C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141043 | |||||||
chr11:74141342 | A | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-1514T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141342 | |||||||
chr11:74141384 | T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.484-1556A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141384 | |||||||
chr11:74141770 | G | A | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-1942C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141770 | |||||||
chr11:74141840 | T | A | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.484-2012A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141840 | |||||||
chr11:74142038 | C | T | 2 | a0002c0003t0001g0090 a0002c0003t0001g0091 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.484-2210G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142038 | |||||||
chr11:74142059 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-2231A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142059 | |||||||
chr11:74142185 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-2357A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142185 | |||||||
chr11:74142194 | A | T | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.484-2366T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142194 | |||||||
chr11:74142379 | A | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-2551T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142379 | |||||||
chr11:74142651 | TAAA | T | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-2826_484-2824d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142651 | |||||||
chr11:74142703 | G | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-2875C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142703 | |||||||
chr11:74142728 | C | T | 1 | a0003c0002t0001g0299 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.484-2900G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142728 | |||||||
chr11:74142838 | C | T | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-3010G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142838 | |||||||
chr11:74143049 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-3221A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143049 | |||||||
chr11:74143093 | C | T | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-3265G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143093 | |||||||
chr11:74143244 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.484-3416T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143244 | |||||||
chr11:74143423 | A | G | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-3595T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143423 | |||||||
chr11:74143455 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.484-3627A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143455 | |||||||
chr11:74143535 | T | TTA | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-3709_484-3708d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143535 | |||||||
chr11:74143703 | G | A | 86 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.484-3875C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143703 | |||||||
chr11:74143822 | T | G | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.484-3994A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143822 | |||||||
chr11:74144344 | C | T | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.484-4516G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144344 | |||||||
chr11:74144432 | T | C | 1 | a0001c0030t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.484-4604A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144432 | |||||||
chr11:74144444 | CT | C | 10 | a0003c0002t0001g0282 a0005c0006t0001g0020 a0005c0006t0001g0021 others(7): Show |
10 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-4617delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144444 | |||||||
chr11:74144474 | G | A | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-4646C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144474 | |||||||
chr11:74144617 | A | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-4789T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144617 | |||||||
chr11:74144723 | G | A | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.484-4895C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144723 | |||||||
chr11:74144803 | T | C | 1 | a0016c0023t0001g0130 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.484-4975A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144803 | |||||||
chr11:74144841 | G | A | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-5013C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144841 | |||||||
chr11:74144973 | T | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-5145A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144973 | |||||||
chr11:74145133 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.484-5305G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74145133 | |||||||
chr11:74145497 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-5669A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74145497 | |||||||
chr11:74145872 | G | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-6044C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74145872 | |||||||
chr11:74146350 | G | A | 1 | a0006c0008t0001g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.484-6522C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146350 | |||||||
chr11:74146393 | T | C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-6565A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146393 | |||||||
chr11:74146539 | T | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-6711A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146539 | |||||||
chr11:74146572 | T | C | 4 | a0003c0034t0001g0185 a0013c0013t0001g0225 a0013c0013t0001g0226 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-6744A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146572 | |||||||
chr11:74146710 | C | CACACACA others(16): Show |
1 | a0024c0024t0001g0203 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.484-6883_484-6882i others(25): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | C | CCA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0103 others(5): Show |
8 | HG01192.hp2 HG01975.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.484-6884_484-6883d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | C | CCACACAC others(5): Show |
59 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(56): Show |
59 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.484-6883_484-6882i others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | C | CCACACAC others(7): Show |
1 | a0003c0002t0001g0296 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.484-6883_484-6882i others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | C | CCACACAC others(9): Show |
4 | a0003c0002t0001g0272 a0003c0016t0001g0242 a0021c0037t0001g0273 others(1): Show |
4 | HG02015.hp2 HG02886.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-6883_484-6882i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | C | CCACACAC others(19): Show |
1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-6883_484-6882i others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | C | CCCCACAC others(5): Show |
1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.484-6883_484-6882i others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | CCA | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0095 others(32): Show |
35 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.484-6884_484-6883d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | CCACA | C | 4 | a0001c0001t0001g0094 a0001c0001t0001g0133 a0001c0001t0001g0152 others(1): Show |
4 | HG01255.hp2 HG01358.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-6886_484-6883d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146710 | CCACACAC others(7): Show |
C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-6896_484-6883d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | |||||||
chr11:74146711 | C | CACACACA others(3): Show |
4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-6884_484-6883i others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146711 | |||||||
chr11:74146713 | C | CACACACA others(1): Show |
7 | a0003c0016t0001g0249 a0007c0009t0002g0312 a0007c0009t0002g0313 others(4): Show |
7 | HG02145.hp2 HG03041.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-6886_484-6885i others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146713 | |||||||
chr11:74146715 | C | CACACAT | 15 | a0007c0009t0002g0311 a0007c0009t0002g0316 a0007c0009t0002g0317 others(12): Show |
16 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.484-6888_484-6887i others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146715 | |||||||
chr11:74146717 | C | CACAT | 11 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(8): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-6890_484-6889i others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146717 | |||||||
chr11:74146747 | C | CACACACA others(21): Show |
1 | a0002c0003t0001g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.484-6920_484-6919i others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(17): Show |
2 | a0002c0003t0001g0090 a0002c0003t0001g0210 |
2 | HG01516.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.484-6920_484-6919i others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(15): Show |
5 | a0002c0003t0001g0083 a0002c0003t0001g0196 a0002c0003t0001g0199 others(2): Show |
5 | HG01081.hp1 HG01169.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(13): Show |
11 | a0002c0003t0001g0197 a0002c0003t0001g0204 a0002c0003t0001g0208 others(8): Show |
11 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(11): Show |
22 | a0002c0003t0001g0050 a0002c0003t0001g0051 a0002c0003t0001g0075 others(19): Show |
22 | HG01109.hp1 HG01123.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(9): Show |
10 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0003t0001g0201 others(7): Show |
10 | HG00280.hp2 HG01361.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(7): Show |
18 | a0002c0003t0001g0052 a0002c0003t0001g0059 a0002c0003t0001g0060 others(15): Show |
18 | HG00642.hp1 HG01192.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(5): Show |
24 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(21): Show |
24 | HG00738.hp1 HG01106.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(3): Show |
6 | a0002c0003t0001g0062 a0005c0006t0001g0006 a0005c0006t0001g0007 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACACACA others(1): Show |
3 | a0004c0004t0001g0040 a0017c0044t0001g0089 a0019c0043t0001g0084 |
3 | HG01099.hp2 HG01261.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.484-6920_484-6919i others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CACAT | 5 | a0004c0004t0001g0037 a0004c0004t0001g0038 a0004c0004t0001g0039 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | CAT | 15 | a0004c0004t0001g0032 a0004c0004t0001g0034 a0004c0004t0001g0035 others(12): Show |
15 | HG01074.hp2 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146747 | C | T | 106 | a0002c0028t0001g0011 a0003c0002t0001g0241 a0003c0002t0001g0243 others(103): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.484-6919G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | |||||||
chr11:74146850 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-7022G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146850 | |||||||
chr11:74146911 | G | A | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-7083C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146911 | |||||||
chr11:74146912 | G | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-7084C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146912 | |||||||
chr11:74146948 | G | A | 2 | a0011c0018t0001g0131 a0011c0018t0001g0132 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.484-7120C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146948 | |||||||
chr11:74146982 | C | T | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.484-7154G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146982 | |||||||
chr11:74147052 | A | AAAAAT | 60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.484-7229_484-7225d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147052 | |||||||
chr11:74147052 | A | AAAAATAA others(3): Show |
3 | a0003c0002t0001g0246 a0003c0016t0001g0242 a0036c0022t0001g0295 |
3 | HG02886.hp2 NA18963.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.484-7234_484-7225d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147052 | |||||||
chr11:74147242 | T | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-7414A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147242 | |||||||
chr11:74147288 | C | T | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-7460G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147288 | |||||||
chr11:74147318 | G | A | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.484-7490C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147318 | |||||||
chr11:74147412 | G | A | 12 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-7584C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147412 | |||||||
chr11:74147444 | C | A | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-7616G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147444 | |||||||
chr11:74147548 | C | G | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-7720G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147548 | |||||||
chr11:74147685 | C | T | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-7857G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147685 | |||||||
chr11:74147792 | T | G | 85 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.484-7964A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147792 | |||||||
chr11:74147844 | C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-8016G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147844 | |||||||
chr11:74148020 | TAAATTTT others(20): Show |
T | 10 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(7): Show |
10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-8219_484-8193d others(29): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148020 | |||||||
chr11:74148148 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-8320A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148148 | |||||||
chr11:74148414 | T | C | 1 | a0008c0007t0001g0082 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.484-8586A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148414 | |||||||
chr11:74148744 | G | C | 38 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(35): Show |
39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.484-8916C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148744 | |||||||
chr11:74148956 | TCAAA | T | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-9132_484-9129d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148956 | |||||||
chr11:74149027 | C | T | 1 | a0003c0002t0001g0257 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.484-9199G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149027 | |||||||
chr11:74149058 | G | T | 1 | a0027c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484-9230C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149058 | |||||||
chr11:74149059 | T | C | 1 | a0002c0003t0001g0210 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.484-9231A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149059 | |||||||
chr11:74149089 | T | C | 85 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.484-9261A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149089 | |||||||
chr11:74149277 | A | T | 37 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(34): Show |
38 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.484-9449T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149277 | |||||||
chr11:74149297 | AC | A | 3 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0026c0047t0002g0310 |
3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.484-9470delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149297 | |||||||
chr11:74149310 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.484-9482A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149310 | |||||||
chr11:74149312 | C | T | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-9484G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149312 | |||||||
chr11:74149358 | TA | T | 229 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(226): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.484-9531delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149358 | |||||||
chr11:74149368 | A | T | 4 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 others(1): Show |
5 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-9540T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149368 | |||||||
chr11:74149425 | T | C | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-9597A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149425 | |||||||
chr11:74149431 | G | A | 4 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(1): Show |
4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-9603C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149431 | |||||||
chr11:74149586 | G | A | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-9758C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149586 | |||||||
chr11:74149597 | CT | C | 20 | a0002c0005t0001g0093 a0003c0034t0001g0185 a0004c0004t0001g0042 others(17): Show |
21 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.484-9770delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149597 | |||||||
chr11:74149630 | C | G | 25 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(22): Show |
25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-9802G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149630 | |||||||
chr11:74149713 | G | A | 2 | a0006c0012t0001g0235 a0025c0040t0001g0301 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.484-9885C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149713 | |||||||
chr11:74149714 | G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-9886C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149714 | |||||||
chr11:74149828 | G | A | 61 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(58): Show |
61 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.484-10000C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149828 | |||||||
chr11:74149829 | G | A | 61 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(58): Show |
61 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.484-10001C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149829 | |||||||
chr11:74149903 | G | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-10075C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149903 | |||||||
chr11:74150121 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.484-10293G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150121 | |||||||
chr11:74150155 | T | TA | 78 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(75): Show |
78 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.484-10328dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150155 | |||||||
chr11:74150155 | TA | T | 8 | a0001c0001t0001g0109 a0001c0001t0001g0174 a0004c0004t0001g0033 others(5): Show |
8 | HG02717.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.484-10328delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150155 | |||||||
chr11:74150206 | G | A | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484-10378C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150206 | |||||||
chr11:74150220 | G | C | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484-10392C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150220 | |||||||
chr11:74150492 | C | CA | 68 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0110 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.484-10665dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | |||||||
chr11:74150492 | C | CAA | 34 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0102 others(31): Show |
34 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.484-10666_484-1066 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | |||||||
chr11:74150492 | C | CAAA | 14 | a0001c0001t0001g0096 a0001c0001t0001g0104 a0001c0001t0001g0105 others(11): Show |
14 | HG00544.hp2 HG02040.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.484-10667_484-1066 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | |||||||
chr11:74150492 | C | CAAAA | 9 | a0001c0001t0001g0122 a0001c0001t0001g0152 a0003c0002t0001g0283 others(6): Show |
9 | HG00438.hp2 HG00558.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-10668_484-1066 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | |||||||
chr11:74150492 | C | CAAAAA | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0153 others(6): Show |
9 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-10669_484-1066 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | |||||||
chr11:74150492 | C | CAAAAAAA others(5): Show |
1 | a0003c0002t0001g0286 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.484-10676_484-1066 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | |||||||
chr11:74150501 | AAAAAAAA others(19): Show |
A | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-10699_484-1067 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150501 | |||||||
chr11:74150505 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.484-10677T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150505 | |||||||
chr11:74150505 | AAAAAAAA others(4): Show |
A | 1 | a0007c0009t0002g0311 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.484-10688_484-1067 others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150505 | |||||||
chr11:74150505 | AAAAAAAA others(15): Show |
A | 5 | a0002c0005t0001g0066 a0002c0005t0001g0067 a0002c0005t0001g0068 others(2): Show |
5 | HG02615.hp2 NA18945.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-10699_484-1067 others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150505 | |||||||
chr11:74150506 | AAAAAAAA others(3): Show |
A | 3 | a0007c0009t0002g0312 a0026c0047t0002g0310 a0032c0046t0002g0309 |
3 | HG02717.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.484-10688_484-1067 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150506 | |||||||
chr11:74150506 | AAAAAAAA others(14): Show |
A | 80 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.484-10699_484-1067 others(25): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150506 | |||||||
chr11:74150507 | AAAAAAAA others(13): Show |
A | 6 | a0002c0003t0001g0061 a0002c0003t0001g0090 a0002c0003t0001g0213 others(3): Show |
6 | HG02647.hp1 HG02895.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-10699_484-1068 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150507 | |||||||
chr11:74150509 | AAAAAAAC | A | 8 | a0004c0004t0001g0181 a0006c0008t0001g0229 a0006c0008t0001g0236 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.484-10688_484-1068 others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150509 | |||||||
chr11:74150511 | AAAAACAA others(9): Show |
A | 3 | a0003c0002t0001g0256 a0011c0015t0001g0001 a0011c0015t0001g0223 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-10699_484-1068 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150511 | |||||||
chr11:74150512 | AAAACAAA others(8): Show |
A | 2 | a0003c0002t0001g0294 a0028c0045t0001g0224 |
2 | HG03209.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.484-10699_484-1068 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150512 | |||||||
chr11:74150515 | AC | A | 7 | a0003c0016t0001g0249 a0005c0006t0001g0020 a0005c0006t0001g0027 others(4): Show |
7 | HG02886.hp1 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-10688delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150515 | |||||||
chr11:74150516 | C | A | 176 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(173): Show |
176 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.484-10688G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150516 | |||||||
chr11:74150517 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.484-10689T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150517 | |||||||
chr11:74150527 | C | A | 106 | a0001c0030t0001g0190 a0003c0002t0001g0241 a0003c0002t0001g0243 others(103): Show |
106 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.484-10699G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150527 | |||||||
chr11:74150528 | A | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-10700T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150528 | |||||||
chr11:74150546 | T | TTTTATTA others(7): Show |
102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-10719_484-1071 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150546 | |||||||
chr11:74150560 | A | C | 11 | a0002c0003t0001g0196 a0002c0003t0001g0204 a0002c0003t0001g0205 others(8): Show |
11 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-10732T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150560 | |||||||
chr11:74150561 | A | C | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.484-10733T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150561 | |||||||
chr11:74150604 | G | A | 1 | a0029c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.484-10776C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150604 | |||||||
chr11:74150605 | C | G | 1 | a0029c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.484-10777G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150605 | |||||||
chr11:74150896 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.483+10503G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150896 | |||||||
chr11:74151171 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.483+10228C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151171 | |||||||
chr11:74151305 | C | CTTTA | 6 | a0002c0003t0001g0083 a0005c0006t0001g0014 a0006c0008t0001g0229 others(3): Show |
6 | HG01169.hp2 HG02074.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+10090_483+1009 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | |||||||
chr11:74151305 | C | CTTTATTT others(1): Show |
14 | a0002c0003t0001g0051 a0006c0008t0001g0230 a0006c0008t0001g0238 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.483+10086_483+1009 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | |||||||
chr11:74151305 | C | CTTTATTT others(5): Show |
16 | a0003c0016t0001g0242 a0003c0016t0001g0249 a0003c0034t0001g0185 others(13): Show |
16 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.483+10082_483+1009 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | |||||||
chr11:74151305 | C | CTTTATTT others(9): Show |
1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+10078_483+1009 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | |||||||
chr11:74151305 | C | CTTTATTT others(13): Show |
1 | a0007c0009t0002g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483+10074_483+1009 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | |||||||
chr11:74151305 | C | CTTTATTT others(17): Show |
1 | a0007c0009t0002g0317 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.483+10070_483+1009 others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | |||||||
chr11:74151312 | T | TATTTATT others(1): Show |
60 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(57): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.483+10086_483+1008 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151312 | |||||||
chr11:74151319 | T | TTATTTAT others(5): Show |
7 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(4): Show |
7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+10079_483+1008 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151319 | |||||||
chr11:74151591 | T | A | 1 | a0008c0007t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.483+9808A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151591 | |||||||
chr11:74151712 | T | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+9687A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151712 | |||||||
chr11:74152089 | T | C | 1 | a0003c0002t0001g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.483+9310A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152089 | |||||||
chr11:74152366 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+9033G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152366 | |||||||
chr11:74152570 | A | G | 1 | a0007c0009t0002g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.483+8829T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152570 | |||||||
chr11:74152635 | T | C | 1 | a0004c0004t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.483+8764A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152635 | |||||||
chr11:74152650 | C | T | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+8749G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152650 | |||||||
chr11:74152873 | C | T | 5 | a0006c0012t0001g0231 a0006c0012t0001g0232 a0006c0012t0001g0233 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+8526G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152873 | |||||||
chr11:74152911 | A | G | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.483+8488T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152911 | |||||||
chr11:74152949 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG00408.hp2 HG00423.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.483+8450G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152949 | |||||||
chr11:74153095 | G | A | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+8304C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153095 | |||||||
chr11:74153105 | T | C | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+8294A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153105 | |||||||
chr11:74153184 | G | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+8215C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153184 | |||||||
chr11:74153210 | A | AAAAAC | 90 | a0001c0001t0001g0105 a0002c0003t0001g0016 a0002c0003t0001g0017 others(87): Show |
90 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.483+8184_483+8188d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | |||||||
chr11:74153210 | A | AAAAACAA others(3): Show |
16 | a0002c0003t0001g0050 a0002c0003t0001g0055 a0002c0003t0001g0056 others(13): Show |
16 | HG00642.hp1 HG01123.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.483+8179_483+8188d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | |||||||
chr11:74153210 | A | AAAAACAA others(8): Show |
2 | a0002c0003t0001g0054 a0005c0027t0001g0012 |
2 | HG02735.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.483+8174_483+8188d others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | |||||||
chr11:74153210 | AAAAAC | A | 79 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0029 others(76): Show |
79 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.483+8184_483+8188d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | |||||||
chr11:74153210 | AAAAACAA others(3): Show |
A | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.483+8179_483+8188d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | |||||||
chr11:74153210 | AAAAACAA others(8): Show |
A | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0104 others(6): Show |
9 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+8174_483+8188d others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | |||||||
chr11:74153228 | A | AACAAG | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+8170_483+8171i others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153228 | |||||||
chr11:74153334 | C | T | 2 | a0002c0003t0001g0196 a0002c0003t0001g0204 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.483+8065G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153334 | |||||||
chr11:74153591 | T | A | 17 | a0003c0034t0001g0185 a0006c0008t0001g0229 a0006c0008t0001g0230 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+7808A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153591 | |||||||
chr11:74153666 | TTTTTTAT others(5): Show |
T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+7721_483+7732d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153666 | |||||||
chr11:74153721 | T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+7678A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153721 | |||||||
chr11:74153952 | T | G | 7 | a0002c0003t0001g0197 a0002c0003t0001g0199 a0002c0003t0001g0200 others(4): Show |
7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+7447A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153952 | |||||||
chr11:74154016 | GA | G | 8 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(5): Show |
8 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+7382delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154016 | |||||||
chr11:74154129 | G | A | 1 | a0002c0003t0001g0172 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.483+7270C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154129 | |||||||
chr11:74154475 | G | T | 1 | a0002c0003t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.483+6924C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154475 | |||||||
chr11:74154711 | T | C | 1 | a0003c0002t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.483+6688A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154711 | |||||||
chr11:74154733 | A | G | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+6666T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154733 | |||||||
chr11:74154737 | C | A | 230 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(227): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.483+6662G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154737 | |||||||
chr11:74154936 | T | C | 1 | a0027c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.483+6463A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154936 | |||||||
chr11:74154993 | A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+6406T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154993 | |||||||
chr11:74154995 | G | A | 3 | a0003c0002t0001g0288 a0003c0002t0001g0289 a0003c0002t0001g0290 |
3 | HG02056.hp1 HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.483+6404C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154995 | |||||||
chr11:74155038 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+6361G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155038 | |||||||
chr11:74155217 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.483+6182C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155217 | |||||||
chr11:74155321 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.483+6078C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155321 | |||||||
chr11:74155677 | C | T | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+5722G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155677 | |||||||
chr11:74155958 | T | C | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+5441A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155958 | |||||||
chr11:74155968 | C | A | 7 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+5431G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155968 | |||||||
chr11:74156025 | C | T | 1 | a0003c0002t0001g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.483+5374G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156025 | |||||||
chr11:74156417 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.483+4982G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156417 | |||||||
chr11:74156440 | G | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+4959C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156440 | |||||||
chr11:74156459 | C | CA | 28 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(25): Show |
29 | HG00609.hp1 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.483+4939dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | |||||||
chr11:74156459 | C | G | 1 | a0009c0011t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.483+4940G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | |||||||
chr11:74156459 | CA | C | 17 | a0001c0001t0001g0103 a0002c0003t0001g0016 a0002c0005t0001g0058 others(14): Show |
17 | HG01975.hp1 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+4939delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | |||||||
chr11:74156459 | CAAAAAAA others(6): Show |
C | 1 | a0005c0006t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483+4927_483+4939d others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | |||||||
chr11:74156654 | G | C | 1 | a0005c0006t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.483+4745C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156654 | |||||||
chr11:74156937 | C | G | 2 | a0003c0002t0001g0246 a0003c0002t0001g0248 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.483+4462G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156937 | |||||||
chr11:74156941 | A | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG00408.hp2 HG00423.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.483+4458T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156941 | |||||||
chr11:74156946 | G | A | 1 | a0004c0004t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483+4453C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156946 | |||||||
chr11:74157020 | C | A | 79 | a0002c0003t0001g0030 a0002c0003t0001g0031 a0002c0003t0001g0050 others(76): Show |
79 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.483+4379G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157020 | |||||||
chr11:74157268 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483+4131G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157268 | |||||||
chr11:74157567 | T | C | 1 | a0003c0016t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.483+3832A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157567 | |||||||
chr11:74157648 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+3751A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157648 | |||||||
chr11:74157782 | C | T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+3617G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157782 | |||||||
chr11:74157787 | A | G | 7 | a0002c0003t0001g0197 a0002c0003t0001g0199 a0002c0003t0001g0200 others(4): Show |
7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+3612T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157787 | |||||||
chr11:74157806 | G | A | 1 | a0029c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.483+3593C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157806 | |||||||
chr11:74157925 | GTA | G | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+3472_483+3473d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157925 | |||||||
chr11:74158225 | A | G | 1 | a0033c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+3174T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158225 | |||||||
chr11:74158506 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+2893G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158506 | |||||||
chr11:74158667 | A | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+2732T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158667 | |||||||
chr11:74158670 | C | T | 1 | a0011c0015t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.483+2729G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158670 | |||||||
chr11:74158709 | C | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+2690G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158709 | |||||||
chr11:74158722 | CA | C | 94 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(91): Show |
95 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.483+2676delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158722 | |||||||
chr11:74159000 | G | A | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+2399C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159000 | |||||||
chr11:74159056 | G | C | 63 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(60): Show |
63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.483+2343C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159056 | |||||||
chr11:74159061 | T | C | 1 | a0003c0002t0001g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.483+2338A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159061 | |||||||
chr11:74159103 | C | T | 1 | a0003c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.483+2296G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159103 | |||||||
chr11:74159217 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.483+2182T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159217 | |||||||
chr11:74159382 | G | A | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+2017C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159382 | |||||||
chr11:74159511 | T | C | 2 | a0006c0008t0001g0239 a0006c0008t0001g0240 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.483+1888A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159511 | |||||||
chr11:74159628 | TTTAA | T | 4 | a0003c0034t0001g0185 a0013c0013t0001g0225 a0013c0013t0001g0226 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1767_483+1770d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159628 | |||||||
chr11:74159642 | C | T | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.483+1757G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159642 | |||||||
chr11:74159651 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.483+1748T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159651 | |||||||
chr11:74159657 | TA | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+1741delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159657 | |||||||
chr11:74159764 | G | A | 2 | a0003c0016t0001g0242 a0036c0022t0001g0295 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.483+1635C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159764 | |||||||
chr11:74159968 | G | A | 15 | a0005c0006t0001g0006 a0005c0006t0001g0007 a0005c0006t0001g0013 others(12): Show |
15 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.483+1431C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159968 | |||||||
chr11:74160063 | T | G | 4 | a0010c0010t0001g0305 a0010c0010t0001g0306 a0010c0010t0001g0307 others(1): Show |
4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1336A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160063 | |||||||
chr11:74160171 | C | T | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+1228G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160171 | |||||||
chr11:74160176 | G | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+1223C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160176 | |||||||
chr11:74160314 | C | G | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.483+1085G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160314 | |||||||
chr11:74160387 | G | A | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+1012C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160387 | |||||||
chr11:74160400 | T | C | 1 | a0020c0033t0001g0178 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.483+999A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160400 | |||||||
chr11:74160406 | T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+993A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160406 | |||||||
chr11:74160424 | T | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.483+975A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160424 | |||||||
chr11:74160870 | C | T | 1 | a0009c0011t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.483+529G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160870 | |||||||
chr11:74160916 | T | C | 8 | a0002c0005t0001g0085 a0002c0005t0001g0086 a0002c0005t0001g0087 others(5): Show |
8 | NA18942.hp2 NA18948.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+483A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160916 | |||||||
chr11:74161047 | C | T | 8 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(5): Show |
8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+352G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161047 | |||||||
chr11:74161116 | GATTA | G | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+279_483+282del others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161116 | |||||||
chr11:74161221 | G | A | 3 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0026c0047t0002g0310 |
3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.483+178C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161221 | |||||||
chr11:74161316 | A | T | 1 | a0010c0010t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.483+83T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161316 | |||||||
chr11:74161623 | T | C | 2 | a0001c0001t0001g0173 a0017c0044t0001g0089 |
2 | HG01099.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.326-67A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161623 | |||||||
chr11:74161706 | G | A | 2 | a0005c0006t0001g0026 a0005c0006t0001g0027 |
2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.326-150C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161706 | |||||||
chr11:74161723 | A | G | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.326-167T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161723 | |||||||
chr11:74161794 | C | T | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.326-238G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161794 | |||||||
chr11:74161813 | C | CT | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0002c0003t0001g0050 others(5): Show |
8 | HG01109.hp1 HG02300.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-258dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161813 | |||||||
chr11:74161813 | CT | C | 14 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0002c0003t0001g0090 others(11): Show |
14 | HG02647.hp1 HG02717.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.326-258delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161813 | |||||||
chr11:74161816 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.326-260A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161816 | |||||||
chr11:74161971 | A | G | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.326-415T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161971 | |||||||
chr11:74161992 | T | C | 102 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(99): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.326-436A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161992 | |||||||
chr11:74162074 | C | T | 3 | a0003c0002t0001g0243 a0003c0002t0001g0244 a0003c0002t0001g0245 |
3 | NA19011.hp2 NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.326-518G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162074 | |||||||
chr11:74162091 | C | T | 3 | a0002c0003t0001g0197 a0002c0003t0001g0199 a0018c0029t0001g0198 |
3 | HG01169.hp2 HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.326-535G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162091 | |||||||
chr11:74162395 | G | C | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-839C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162395 | |||||||
chr11:74162689 | G | C | 3 | a0007c0009t0002g0313 a0007c0009t0002g0314 a0007c0009t0002g0315 |
3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.326-1133C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162689 | |||||||
chr11:74162691 | C | A | 100 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(97): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.326-1135G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162691 | |||||||
chr11:74162707 | T | C | 1 | a0002c0003t0001g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.326-1151A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162707 | |||||||
chr11:74162764 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.326-1208T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162764 | |||||||
chr11:74163046 | T | A | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.326-1490A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163046 | |||||||
chr11:74163051 | A | C | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-1495T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163051 | |||||||
chr11:74163229 | G | A | 1 | a0022c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.326-1673C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163229 | |||||||
chr11:74163243 | A | G | 7 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(4): Show |
7 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-1687T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163243 | |||||||
chr11:74163482 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA18943.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.326-1926G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163482 | |||||||
chr11:74163508 | C | T | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.326-1952G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163508 | |||||||
chr11:74163636 | G | T | 9 | a0007c0009t0002g0311 a0007c0009t0002g0312 a0007c0009t0002g0313 others(6): Show |
9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-2080C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163636 | |||||||
chr11:74163655 | TTG | T | 3 | a0013c0013t0001g0225 a0013c0013t0001g0226 a0013c0013t0001g0227 |
3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.326-2101_326-2100d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163655 | |||||||
chr11:74164030 | T | C | 4 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-2474A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164030 | |||||||
chr11:74164148 | T | C | 73 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.326-2592A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164148 | |||||||
chr11:74164258 | C | G | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.326-2702G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164258 | |||||||
chr11:74164271 | C | T | 97 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(94): Show |
97 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.326-2715G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164271 | |||||||
chr11:74164309 | A | C | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.326-2753T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164309 | |||||||
chr11:74164425 | C | T | 1 | a0003c0002t0001g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.326-2869G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164425 | |||||||
chr11:74164463 | G | A | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-2907C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164463 | |||||||
chr11:74164502 | G | C | 24 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(21): Show |
24 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.326-2946C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164502 | |||||||
chr11:74164527 | C | G | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.326-2971G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164527 | |||||||
chr11:74164539 | C | G | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.326-2983G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164539 | |||||||
chr11:74164572 | C | T | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326-3016G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164572 | |||||||
chr11:74164695 | T | C | 2 | a0008c0007t0001g0177 a0020c0033t0001g0178 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.326-3139A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164695 | |||||||
chr11:74164872 | C | T | 22 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(19): Show |
22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.326-3316G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164872 | |||||||
chr11:74165139 | T | C | 9 | a0005c0006t0001g0020 a0005c0006t0001g0021 a0005c0006t0001g0022 others(6): Show |
9 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.325+3205A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165139 | |||||||
chr11:74165314 | C | T | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+3030G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165314 | |||||||
chr11:74165337 | G | A | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+3007C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165337 | |||||||
chr11:74165461 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0193 |
3 | NA18943.hp1 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.325+2883C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165461 | |||||||
chr11:74165488 | T | C | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.325+2856A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165488 | |||||||
chr11:74165580 | C | T | 3 | a0011c0015t0001g0001 a0011c0015t0001g0223 a0028c0045t0001g0224 |
4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+2764G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165580 | |||||||
chr11:74165608 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.325+2736A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165608 | |||||||
chr11:74165654 | C | A | 1 | a0004c0004t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325+2690G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165654 | |||||||
chr11:74165783 | T | C | 1 | a0034c0031t0001g0184 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.325+2561A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165783 | |||||||
chr11:74165805 | C | T | 2 | a0002c0003t0001g0030 a0002c0003t0001g0031 |
2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.325+2539G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165805 | |||||||
chr11:74166033 | G | A | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325+2311C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166033 | |||||||
chr11:74166045 | T | C | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+2299A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166045 | |||||||
chr11:74166082 | G | A | 2 | a0007c0017t0001g0194 a0007c0017t0001g0195 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.325+2262C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166082 | |||||||
chr11:74166126 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325+2218G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166126 | |||||||
chr11:74166173 | C | G | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+2171G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166173 | |||||||
chr11:74166274 | G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325+2070C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166274 | |||||||
chr11:74166316 | T | TA | 12 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(9): Show |
12 | HG01109.hp1 HG01433.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.325+2027dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166316 | |||||||
chr11:74166316 | TA | T | 65 | a0002c0003t0001g0196 a0003c0002t0001g0241 a0003c0002t0001g0243 others(62): Show |
66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.325+2027delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166316 | |||||||
chr11:74166335 | AC | A | 22 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(19): Show |
22 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.325+2008delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166335 | |||||||
chr11:74166457 | C | G | 1 | a0003c0016t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.325+1887G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166457 | |||||||
chr11:74166673 | A | G | 2 | a0014c0020t0004g0218 a0014c0020t0004g0219 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.325+1671T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166673 | |||||||
chr11:74167179 | T | C | 64 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(61): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.325+1165A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167179 | |||||||
chr11:74167415 | C | G | 100 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(97): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.325+929G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167415 | |||||||
chr11:74167463 | T | C | 1 | a0025c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.325+881A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167463 | |||||||
chr11:74167467 | T | A | 24 | a0006c0008t0001g0229 a0006c0008t0001g0230 a0006c0008t0001g0236 others(21): Show |
24 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.325+877A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167467 | |||||||
chr11:74167482 | A | G | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.325+862T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167482 | |||||||
chr11:74167639 | G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325+705C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167639 | |||||||
chr11:74167643 | G | A | 21 | a0002c0003t0001g0196 a0002c0003t0001g0197 a0002c0003t0001g0199 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.325+701C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167643 | |||||||
chr11:74167796 | T | C | 73 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.325+548A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167796 | |||||||
chr11:74167857 | A | G | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+487T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167857 | |||||||
chr11:74167885 | T | C | 1 | a0008c0007t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.325+459A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167885 | |||||||
chr11:74168079 | C | CA | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+264dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74168079 | |||||||
chr11:74168670 | T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.56-57A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168670 | |||||||
chr11:74168702 | A | C | 20 | a0002c0003t0001g0016 a0002c0003t0001g0017 a0002c0003t0001g0018 others(17): Show |
20 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.56-89T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168702 | |||||||
chr11:74168753 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.56-140G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168753 | |||||||
chr11:74168792 | C | A | 7 | a0010c0010t0001g0302 a0010c0010t0001g0303 a0010c0010t0001g0305 others(4): Show |
7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-179G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168792 | |||||||
chr11:74168843 | A | C | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.56-230T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168843 | |||||||
chr11:74169194 | A | C | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.56-581T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74169194 | |||||||
chr11:74169651 | G | T | 2 | a0005c0006t0001g0006 a0005c0006t0001g0007 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.56-1038C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74169651 | |||||||
chr11:74170135 | A | G | 1 | a0031c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+603T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170135 | |||||||
chr11:74170335 | T | C | 2 | a0008c0007t0001g0221 a0023c0021t0001g0220 |
2 | HG02523.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.55+403A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170335 | |||||||
chr11:74170535 | T | A | 101 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(98): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.55+203A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170535 | |||||||
chr11:74170716 | A | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.55+22T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170716 |