Item | Value |
---|---|
geneid | 83988 |
ensemblid | ENSG00000104490.18 |
hgncid | 7655 |
symbol | NCALD |
name | neurocalcin delta |
refseq_nuc | NM_032041.3 |
refseq_prot | NP_114430.2 |
ensembl_nuc | ENST00000220931.11 |
ensembl_prot | ENSP00000220931.6 |
mane_status | MANE Select |
chr | chr8 |
start | 101686542 |
end | 101790969 |
strand | - |
ver | v1.2 |
region | chr8:101686542-101790969 |
region5000 | chr8:101681542-101795969 |
regionname0 | NCALD_chr8_101686542_101790969 |
regionname5000 | NCALD_chr8_101681542_101795969 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 579 | 299 | 82 | 50 | 129 | 2 | 34 | NCALD_chr8_101681542_101795969 | NCALD | ATGGG others(574): Show |
chr8 | 101681542 | 101795969 | ||
a0001c0002 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | ATGGG others(574): Show |
chr8 | 101681542 | 101795969 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3476 | 130 | 37 | 28 | 51 | 1 | 13 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0002 | 0/1 | 3476 | 52 | 4 | 11 | 31 | 0 | 5 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0003 | 0/0 | 3476 | 27 | 0 | 4 | 16 | 0 | 7 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0004 | 0/0 | 3476 | 20 | 7 | 2 | 5 | 1 | 5 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0005 | 1/0 | 3476 | 13 | 0 | 0 | 12 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0006 | 0/0 | 3477 | 11 | 2 | 0 | 9 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3472): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0007 | 0/0 | 3476 | 10 | 8 | 0 | 0 | 0 | 2 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0008 | 0/0 | 3476 | 7 | 7 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0009 | 0/0 | 3476 | 6 | 3 | 2 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0010 | 0/0 | 3476 | 3 | 3 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0011 | 0/0 | 3476 | 2 | 0 | 2 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0012 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0013 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0014 | 0/0 | 3476 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0015 | 0/0 | 3476 | 2 | 1 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0016 | 0/0 | 3476 | 2 | 0 | 0 | 2 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0017 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0018 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0019 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0020 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0021 | 0/0 | 3477 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3472): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0022 | 0/0 | 3477 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3472): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0023 | 0/0 | 3477 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3472): Show |
chr8 | 101681542 | 101795969 |
a0001c0001t0024 | 0/0 | 3476 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
a0001c0002t0011 | 0/0 | 3476 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | AAAGG others(3471): Show |
chr8 | 101681542 | 101795969 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0221 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0008g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0011g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0011g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0013g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0014g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0014g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0015g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0016g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0016g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0017g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0018g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0019g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0020g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0021g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0022g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0023g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0001t0024g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
a0001c0002t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00423 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0091 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01069 | hp2 | a0001 | c0001 | t0015 | g0197 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01074 | hp1 | a0001 | c0001 | t0009 | g0248 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01081 | hp2 | a0001 | c0001 | t0011 | g0030 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01106 | hp2 | a0001 | c0001 | t0011 | g0051 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | IBS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0086 | EUR | IBS | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02080 | hp1 | a0001 | c0001 | t0022 | g0069 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CDX | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0111 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0261 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0190 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | KHV | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0109 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02647 | hp1 | a0001 | c0001 | t0024 | g0159 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0268 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0280 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0028 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0285 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0284 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0258 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03098 | hp2 | a0001 | c0001 | t0023 | g0160 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0257 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0282 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03225 | hp2 | a0001 | c0001 | t0020 | g0265 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0251 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0157 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0085 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03669 | hp1 | a0001 | c0001 | t0021 | g0045 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03710 | hp1 | a0001 | c0001 | t0009 | g0218 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0166 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0167 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0056 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18947 | hp2 | a0001 | c0001 | t0016 | g0064 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18953 | hp1 | a0001 | c0001 | t0017 | g0080 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18981 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18984 | hp2 | a0001 | c0002 | t0011 | g0148 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19062 | hp2 | a0001 | c0001 | t0016 | g0063 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19065 | hp2 | a0001 | c0001 | t0019 | g0123 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19080 | hp2 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0004 | AFR | YRI | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ASW | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ASW | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02109 | hp2 | a0001 | c0001 | t0010 | g0112 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0277 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0287 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0281 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | MSL | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0004 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | USA | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0102 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0093 | REF | REF | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0221 | REF | REF | NCALD_chr8_101681542_101795969 | NCALD | chr8 | 101681542 | 101795969 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:101719258 | G | A | 1 | a0001c0002 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.372C>T | p.Ile124Ile | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/4 | 499/3476 | 372/582 | 124/193 | chr8 | 101719258 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:101686827 | C | T | 2 | a0001c0001t0011 a0001c0002t0011 |
3 | HG01081.hp2 HG01106.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2482G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 2482 | chr8 | 101686827 | ||||||
chr8:101687033 | T | C | 1 | a0001c0001t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2276A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 2276 | chr8 | 101687033 | ||||||
chr8:101687490 | T | C | 1 | a0001c0001t0019 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1819A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1819 | chr8 | 101687490 | ||||||
chr8:101687501 | G | T | 2 | a0001c0001t0015 a0001c0001t0023 |
3 | HG01069.hp2 HG03098.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1808C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1808 | chr8 | 101687501 | ||||||
chr8:101687777 | C | T | 1 | a0001c0001t0013 | 2 | HG06807.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1532G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1532 | chr8 | 101687777 | ||||||
chr8:101687938 | G | T | 1 | a0001c0001t0022 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1371 | chr8 | 101687938 | ||||||
chr8:101688002 | C | T | 1 | a0001c0001t0004 | 20 | HG00738.hp1 HG01167.hp2 HG01515.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1307 | chr8 | 101688002 | ||||||
chr8:101688067 | T | C | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(3): Show |
62 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1242A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1242 | chr8 | 101688067 | ||||||
chr8:101688100 | T | C | 6 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0011 others(3): Show |
62 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1209A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1209 | chr8 | 101688100 | ||||||
chr8:101688103 | G | A | 2 | a0001c0001t0003 a0001c0001t0016 |
29 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1206C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1206 | chr8 | 101688103 | ||||||
chr8:101688268 | T | G | 1 | a0001c0001t0014 | 2 | HG02615.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1041A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 1041 | chr8 | 101688268 | ||||||
chr8:101688310 | A | G | 2 | a0001c0001t0007 a0001c0001t0018 |
11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*999T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 999 | chr8 | 101688310 | ||||||
chr8:101688408 | A | T | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0017 others(2): Show |
56 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*901T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 901 | chr8 | 101688408 | ||||||
chr8:101688581 | TTTTTA | T | 3 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0020 |
17 | HG02027.hp1 HG02280.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*727delTAAAA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 723 | chr8 | 101688581 | ||||||
chr8:101688815 | C | G | 1 | a0001c0001t0017 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 494 | chr8 | 101688815 | ||||||
chr8:101688889 | C | T | 2 | a0001c0001t0015 a0001c0001t0023 |
3 | HG01069.hp2 HG03098.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*420G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 420 | chr8 | 101688889 | ||||||
chr8:101688895 | G | A | 2 | a0001c0001t0015 a0001c0001t0023 |
3 | HG01069.hp2 HG03098.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 414 | chr8 | 101688895 | ||||||
chr8:101688908 | T | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
286 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*401A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 401 | chr8 | 101688908 | ||||||
chr8:101688909 | T | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
286 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*400A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 400 | chr8 | 101688909 | ||||||
chr8:101688926 | T | A | 1 | a0001c0001t0016 | 2 | NA18947.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 383 | chr8 | 101688926 | ||||||
chr8:101689101 | C | T | 1 | a0001c0001t0010 | 3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 208 | chr8 | 101689101 | ||||||
chr8:101689138 | G | A | 1 | a0001c0001t0020 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 171 | chr8 | 101689138 | ||||||
chr8:101689203 | C | T | 1 | a0001c0001t0012 | 2 | HG02976.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*106G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 106 | chr8 | 101689203 | ||||||
chr8:101689228 | C | CA | 4 | a0001c0001t0006 a0001c0001t0021 a0001c0001t0022 others(1): Show |
14 | HG00423.hp2 HG02080.hp1 HG02523.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*80dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 80 | chr8 | 101689228 | ||||||
chr8:101689246 | G | A | 1 | a0001c0001t0008 | 7 | HG02258.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*63C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 63 | chr8 | 101689246 | ||||||
chr8:101689293 | T | C | 1 | a0001c0001t0024 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 4/4 | 16 | chr8 | 101689293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:101689460 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.485-54G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689460 | |||||||
chr8:101689641 | C | T | 42 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(39): Show |
42 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.485-235G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689641 | |||||||
chr8:101689683 | A | C | 1 | a0001c0001t0004g0092 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.485-277T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689683 | |||||||
chr8:101689730 | G | T | 32 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(29): Show |
32 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.485-324C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689730 | |||||||
chr8:101689744 | T | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0012 others(55): Show |
59 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.485-338A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689744 | |||||||
chr8:101689822 | G | A | 96 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(93): Show |
97 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.485-416C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689822 | |||||||
chr8:101689933 | G | A | 72 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(69): Show |
75 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.485-527C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689933 | |||||||
chr8:101689950 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.485-544A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689950 | |||||||
chr8:101689959 | C | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(78): Show |
84 | HG00423.hp2 HG00639.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.485-553G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101689959 | |||||||
chr8:101690179 | C | CCTTT | 92 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(89): Show |
93 | HG00423.hp2 HG00639.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.485-774_485-773ins others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690179 | |||||||
chr8:101690379 | A | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(186): Show |
193 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.485-973T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690379 | |||||||
chr8:101690433 | C | T | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.485-1027G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690433 | |||||||
chr8:101690470 | C | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-1064G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690470 | |||||||
chr8:101690509 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
264 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.485-1103T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690509 | |||||||
chr8:101690599 | A | G | 3 | a0001c0001t0007g0277 a0001c0001t0007g0278 a0001c0001t0007g0281 |
3 | HG02055.hp1 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.485-1193T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690599 | |||||||
chr8:101690829 | G | C | 1 | a0001c0001t0002g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.485-1423C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690829 | |||||||
chr8:101690934 | C | T | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.485-1528G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690934 | |||||||
chr8:101690935 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0089 a0001c0001t0001g0147 others(2): Show |
5 | HG01952.hp2 HG02132.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-1529C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101690935 | |||||||
chr8:101691106 | C | A | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+1685G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691106 | |||||||
chr8:101691223 | C | T | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
127 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.484+1568G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691223 | |||||||
chr8:101691250 | A | AC | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0198 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+1540dupG | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691250 | |||||||
chr8:101691254 | C | G | 2 | a0001c0001t0007g0166 a0001c0001t0007g0251 |
2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.484+1537G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691254 | |||||||
chr8:101691452 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0089 |
2 | HG01952.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.484+1339C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691452 | |||||||
chr8:101691588 | T | A | 1 | a0001c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.484+1203A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691588 | |||||||
chr8:101691722 | A | G | 161 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0016 others(158): Show |
163 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.484+1069T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691722 | |||||||
chr8:101691758 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.484+1033A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101691758 | |||||||
chr8:101692014 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.484+777G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692014 | |||||||
chr8:101692278 | C | T | 94 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
96 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.484+513G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692278 | |||||||
chr8:101692302 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.484+489G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692302 | |||||||
chr8:101692328 | C | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(66): Show |
69 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.484+463G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692328 | |||||||
chr8:101692342 | A | G | 81 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(78): Show |
82 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.484+449T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692342 | |||||||
chr8:101692468 | C | A | 2 | a0001c0001t0001g0266 a0001c0001t0007g0290 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.484+323G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692468 | |||||||
chr8:101692610 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.484+181G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692610 | |||||||
chr8:101692644 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.484+147G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692644 | |||||||
chr8:101692737 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0001t0003g0025 others(30): Show |
34 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.484+54G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 3/3 | chr8 | 101692737 | |||||||
chr8:101692957 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0229 others(4): Show |
7 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-61A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101692957 | |||||||
chr8:101693000 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-104G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693000 | |||||||
chr8:101693219 | C | T | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.379-323G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693219 | |||||||
chr8:101693246 | G | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0126 a0001c0001t0001g0220 |
3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-350C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693246 | |||||||
chr8:101693315 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-419C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693315 | |||||||
chr8:101693318 | G | GT | 13 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0174 others(10): Show |
14 | HG00438.hp1 HG01081.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.379-423dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | G | GTT | 24 | a0001c0001t0001g0014 a0001c0001t0002g0012 a0001c0001t0002g0015 others(21): Show |
24 | HG00597.hp2 HG00621.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.379-424_379-423dup others(2): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | G | GTTT | 16 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0049 others(13): Show |
16 | HG00423.hp1 HG01952.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-425_379-423dup others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GT | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0033 others(28): Show |
31 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.379-423delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTT | G | 33 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0047 others(30): Show |
33 | HG01109.hp1 HG01257.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.379-424_379-423del others(2): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTT | G | 60 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.379-425_379-423del others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTTT | G | 8 | a0001c0001t0001g0131 a0001c0001t0001g0224 a0001c0001t0007g0284 others(5): Show |
8 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-426_379-423del others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.379-438_379-423del others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTTTTTT others(10): Show |
G | 35 | a0001c0001t0002g0002 a0001c0001t0002g0164 a0001c0001t0002g0168 others(32): Show |
36 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.379-439_379-423del others(17): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0003g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.379-440_379-423del others(18): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379-441_379-423del others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693318 | GTTTTTTT others(14): Show |
G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp1 HG01069.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.379-443_379-423del others(21): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693318 | |||||||
chr8:101693322 | T | G | 1 | a0001c0001t0008g0001 | 3 | HG03139.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.379-426A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693322 | |||||||
chr8:101693323 | T | G | 3 | a0001c0001t0008g0156 a0001c0001t0008g0259 a0001c0001t0008g0261 |
3 | HG02258.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.379-427A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693323 | |||||||
chr8:101693351 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.379-455A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693351 | |||||||
chr8:101693369 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0007g0290 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-473G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693369 | |||||||
chr8:101693406 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0007g0290 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-510G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693406 | |||||||
chr8:101693418 | C | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0151 others(11): Show |
14 | HG01109.hp2 HG02074.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-522G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101693418 | |||||||
chr8:101694008 | C | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(177): Show |
184 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.379-1112G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694008 | |||||||
chr8:101694012 | A | AC | 187 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(184): Show |
191 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.379-1117_379-1116i others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694012 | |||||||
chr8:101694089 | G | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1193C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694089 | |||||||
chr8:101694219 | G | A | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
103 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.379-1323C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694219 | |||||||
chr8:101694289 | G | A | 1 | a0001c0001t0003g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.379-1393C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694289 | |||||||
chr8:101694336 | C | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(254): Show |
261 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(258): Show |
intron_variant | MODIFIER | c.379-1440G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694336 | |||||||
chr8:101694390 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(167): Show |
172 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.379-1494A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694390 | |||||||
chr8:101694429 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.379-1533T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694429 | |||||||
chr8:101694462 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.379-1566G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694462 | |||||||
chr8:101694593 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0007g0290 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-1697C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694593 | |||||||
chr8:101694754 | C | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(244): Show |
251 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(248): Show |
intron_variant | MODIFIER | c.379-1858G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694754 | |||||||
chr8:101694838 | C | T | 1 | a0001c0001t0008g0268 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.379-1942G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101694838 | |||||||
chr8:101695036 | C | T | 6 | a0001c0001t0001g0266 a0001c0001t0007g0290 a0001c0001t0008g0001 others(3): Show |
8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-2140G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695036 | |||||||
chr8:101695358 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.379-2462A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695358 | |||||||
chr8:101695419 | T | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(8): Show |
11 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.379-2523A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695419 | |||||||
chr8:101695846 | A | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0078 a0001c0001t0001g0126 others(1): Show |
4 | HG04184.hp1 NA18948.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-2950T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695846 | |||||||
chr8:101695967 | T | G | 1 | a0001c0001t0015g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.379-3071A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101695967 | |||||||
chr8:101696080 | C | G | 6 | a0001c0001t0001g0266 a0001c0001t0007g0290 a0001c0001t0008g0001 others(3): Show |
8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-3184G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696080 | |||||||
chr8:101696143 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(158): Show |
163 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.379-3247A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696143 | |||||||
chr8:101696525 | C | T | 1 | a0001c0001t0009g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.379-3629G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696525 | |||||||
chr8:101696526 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.379-3630C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696526 | |||||||
chr8:101696533 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.379-3637C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696533 | |||||||
chr8:101696708 | T | C | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.379-3812A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696708 | |||||||
chr8:101696819 | T | C | 1 | a0001c0001t0023g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.379-3923A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696819 | |||||||
chr8:101696825 | T | TA | 78 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
78 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.379-3930dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696825 | |||||||
chr8:101696927 | G | A | 7 | a0001c0001t0004g0260 a0001c0001t0009g0091 a0001c0001t0009g0218 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-4031C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101696927 | |||||||
chr8:101697183 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.379-4287C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697183 | |||||||
chr8:101697316 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-4420G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697316 | |||||||
chr8:101697374 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.379-4478C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697374 | |||||||
chr8:101697706 | T | G | 7 | a0001c0001t0004g0260 a0001c0001t0009g0091 a0001c0001t0009g0218 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-4810A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697706 | |||||||
chr8:101697919 | T | C | 78 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
78 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.379-5023A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101697919 | |||||||
chr8:101698048 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.379-5152G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698048 | |||||||
chr8:101698259 | G | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-5363C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698259 | |||||||
chr8:101698318 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-5422G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698318 | |||||||
chr8:101698433 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.379-5537A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698433 | |||||||
chr8:101698481 | G | C | 7 | a0001c0001t0004g0260 a0001c0001t0009g0091 a0001c0001t0009g0218 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-5585C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101698481 | |||||||
chr8:101699079 | G | GA | 254 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(251): Show |
258 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(255): Show |
intron_variant | MODIFIER | c.379-6184dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699079 | |||||||
chr8:101699079 | G | GAA | 16 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0151 others(13): Show |
16 | HG00423.hp2 HG01109.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-6185_379-6184d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699079 | |||||||
chr8:101699100 | G | A | 4 | a0001c0001t0015g0085 a0001c0001t0015g0197 a0001c0001t0023g0160 others(1): Show |
4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-6204C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699100 | |||||||
chr8:101699203 | T | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(270): Show |
277 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(274): Show |
intron_variant | MODIFIER | c.379-6307A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699203 | |||||||
chr8:101699242 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-6346T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699242 | |||||||
chr8:101699353 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379-6457G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699353 | |||||||
chr8:101699416 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(161): Show |
166 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.379-6520A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699416 | |||||||
chr8:101699461 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0041 others(7): Show |
11 | HG01257.hp2 HG01258.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.379-6565A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699461 | |||||||
chr8:101699699 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(165): Show |
170 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.379-6803C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699699 | |||||||
chr8:101699762 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-6866C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699762 | |||||||
chr8:101699789 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379-6893A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699789 | |||||||
chr8:101699969 | G | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(164): Show |
169 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.379-7073C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699969 | |||||||
chr8:101699990 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.379-7094C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101699990 | |||||||
chr8:101700028 | T | TTTTA | 96 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0041 others(93): Show |
98 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.379-7136_379-7133d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700028 | |||||||
chr8:101700028 | TTTTA | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0158 others(5): Show |
8 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-7136_379-7133d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700028 | |||||||
chr8:101700056 | A | ATTTATTT others(1): Show |
8 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0133 others(5): Show |
8 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-7161_379-7160i others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700056 | |||||||
chr8:101700056 | A | T | 7 | a0001c0001t0001g0186 a0001c0001t0001g0266 a0001c0001t0007g0290 others(4): Show |
9 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-7160T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700056 | |||||||
chr8:101700118 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(168): Show |
173 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.379-7222A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700118 | |||||||
chr8:101700412 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379-7516C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700412 | |||||||
chr8:101700439 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.379-7543T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700439 | |||||||
chr8:101700529 | G | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0032 others(66): Show |
70 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.379-7633C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700529 | |||||||
chr8:101700576 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(158): Show |
163 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.379-7680G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700576 | |||||||
chr8:101700587 | G | A | 5 | a0001c0001t0006g0073 a0001c0001t0006g0133 a0001c0001t0006g0138 others(2): Show |
5 | NA18966.hp1 NA18970.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-7691C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700587 | |||||||
chr8:101700646 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(159): Show |
164 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.379-7750T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700646 | |||||||
chr8:101700666 | T | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
259 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.379-7770A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700666 | |||||||
chr8:101700929 | G | T | 4 | a0001c0001t0015g0085 a0001c0001t0015g0197 a0001c0001t0023g0160 others(1): Show |
4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-8033C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101700929 | |||||||
chr8:101701012 | G | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(26): Show |
29 | HG01069.hp2 HG01167.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.379-8116C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701012 | |||||||
chr8:101701068 | T | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
259 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.379-8172A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701068 | |||||||
chr8:101701163 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-8267G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701163 | |||||||
chr8:101701177 | G | A | 8 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0133 others(5): Show |
8 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-8281C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701177 | |||||||
chr8:101701178 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0135 |
2 | NA18956.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.379-8282T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701178 | |||||||
chr8:101701184 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.379-8288C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701184 | |||||||
chr8:101701186 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.379-8290A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701186 | |||||||
chr8:101701242 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.379-8346G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701242 | |||||||
chr8:101701270 | C | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-8374G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701270 | |||||||
chr8:101701308 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0007g0290 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.379-8412A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701308 | |||||||
chr8:101701320 | G | A | 7 | a0001c0001t0004g0260 a0001c0001t0009g0091 a0001c0001t0009g0218 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-8424C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701320 | |||||||
chr8:101701458 | A | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.379-8562T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701458 | |||||||
chr8:101701656 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0126 a0001c0001t0001g0220 |
3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-8760A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701656 | |||||||
chr8:101701657 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0126 a0001c0001t0001g0220 |
3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-8761A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701657 | |||||||
chr8:101701699 | G | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
259 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.379-8803C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101701699 | |||||||
chr8:101702077 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-9181C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702077 | |||||||
chr8:101702108 | A | C | 14 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(11): Show |
16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-9212T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702108 | |||||||
chr8:101702141 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.379-9245T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702141 | |||||||
chr8:101702195 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.379-9299G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702195 | |||||||
chr8:101702201 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.379-9305A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702201 | |||||||
chr8:101702291 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0052 |
2 | HG01257.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.379-9395G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702291 | |||||||
chr8:101702327 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379-9431C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702327 | |||||||
chr8:101702718 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.379-9822C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702718 | |||||||
chr8:101702735 | G | A | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.379-9839C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702735 | |||||||
chr8:101702742 | T | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(260): Show |
267 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(264): Show |
intron_variant | MODIFIER | c.379-9846A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702742 | |||||||
chr8:101702775 | C | G | 14 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(11): Show |
16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.379-9879G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702775 | |||||||
chr8:101702792 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0126 a0001c0001t0001g0220 |
3 | HG04184.hp1 NA18948.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.379-9896A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702792 | |||||||
chr8:101702793 | T | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-9897A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702793 | |||||||
chr8:101702797 | G | A | 1 | a0001c0001t0004g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.379-9901C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702797 | |||||||
chr8:101702820 | T | G | 1 | a0001c0001t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.379-9924A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702820 | |||||||
chr8:101702822 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-9926A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702822 | |||||||
chr8:101702898 | C | A | 1 | a0001c0001t0002g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.379-10002G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101702898 | |||||||
chr8:101703120 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.379-10224G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703120 | |||||||
chr8:101703152 | C | CT | 21 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(18): Show |
23 | HG00639.hp2 HG01243.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.379-10257dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703152 | |||||||
chr8:101703152 | CT | C | 67 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
67 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.379-10257delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703152 | |||||||
chr8:101703165 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.379-10269A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703165 | |||||||
chr8:101703389 | A | ACAGGACA others(8): Show |
4 | a0001c0001t0007g0281 a0001c0001t0009g0280 a0001c0001t0009g0282 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-10508_379-1049 others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703389 | |||||||
chr8:101703413 | G | A | 7 | a0001c0001t0004g0260 a0001c0001t0009g0091 a0001c0001t0009g0218 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.379-10517C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703413 | |||||||
chr8:101703467 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-10571T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703467 | |||||||
chr8:101703517 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.379-10621T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703517 | |||||||
chr8:101703569 | T | C | 7 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-10673A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703569 | |||||||
chr8:101703576 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-10680T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703576 | |||||||
chr8:101703580 | A | C | 1 | a0001c0001t0003g0225 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.379-10684T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703580 | |||||||
chr8:101703703 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-10807C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703703 | |||||||
chr8:101703858 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.379-10962T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703858 | |||||||
chr8:101703981 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.379-11085G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101703981 | |||||||
chr8:101704148 | A | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(74): Show |
77 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.379-11252T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704148 | |||||||
chr8:101704349 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.379-11453G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704349 | |||||||
chr8:101704531 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.379-11635T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704531 | |||||||
chr8:101704691 | C | A | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-11795G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704691 | |||||||
chr8:101704921 | AAAAAAAT | A | 3 | a0001c0001t0001g0195 a0001c0001t0002g0273 a0001c0001t0008g0268 |
3 | HG01167.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.379-12032_379-1202 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101704921 | |||||||
chr8:101705211 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-12315T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705211 | |||||||
chr8:101705224 | A | AAAATAAA others(17): Show |
6 | a0001c0001t0001g0266 a0001c0001t0007g0290 a0001c0001t0008g0001 others(3): Show |
8 | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-12329_379-1232 others(28): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705224 | |||||||
chr8:101705224 | A | AAAATAAA others(21): Show |
4 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0145 others(1): Show |
4 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-12329_379-1232 others(32): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705224 | |||||||
chr8:101705224 | A | AAAATAAA others(25): Show |
3 | a0001c0001t0006g0138 a0001c0001t0006g0191 a0001c0001t0006g0243 |
3 | NA18981.hp1 NA19068.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.379-12329_379-1232 others(36): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705224 | |||||||
chr8:101705232 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.379-12336A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705232 | |||||||
chr8:101705267 | A | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(8): Show |
11 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.379-12371T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705267 | |||||||
chr8:101705340 | T | C | 1 | a0001c0001t0002g0027 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.379-12444A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705340 | |||||||
chr8:101705386 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.379-12490A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705386 | |||||||
chr8:101705517 | G | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0118 |
2 | NA18977.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.379-12621C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705517 | |||||||
chr8:101705525 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.379-12629G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705525 | |||||||
chr8:101705592 | G | T | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.379-12696C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705592 | |||||||
chr8:101705654 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.379-12758G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705654 | |||||||
chr8:101705760 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-12864T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705760 | |||||||
chr8:101705823 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0057 |
2 | HG00738.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.379-12927C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101705823 | |||||||
chr8:101706054 | G | T | 1 | a0001c0001t0008g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.379-13158C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706054 | |||||||
chr8:101706134 | G | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(82): Show |
85 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.378+13118C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706134 | |||||||
chr8:101706229 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+13023A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706229 | |||||||
chr8:101706247 | G | A | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+13005C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706247 | |||||||
chr8:101706317 | T | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(52): Show |
57 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.378+12935A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706317 | |||||||
chr8:101706317 | T | TA | 7 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0250 others(4): Show |
7 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+12934dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706317 | |||||||
chr8:101706317 | T | TAAA | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12932_378+1293 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706317 | |||||||
chr8:101706332 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.378+12920C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706332 | |||||||
chr8:101706369 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12883G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706369 | |||||||
chr8:101706380 | G | A | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12872C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706380 | |||||||
chr8:101706477 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12775T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706477 | |||||||
chr8:101706496 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+12756A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706496 | |||||||
chr8:101706638 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(178): Show |
186 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.378+12614G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706638 | |||||||
chr8:101706880 | AGATAAAT others(5): Show |
A | 73 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(70): Show |
73 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.378+12360_378+1237 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706880 | |||||||
chr8:101706922 | A | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(90): Show |
95 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.378+12330T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101706922 | |||||||
chr8:101707035 | C | T | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(82): Show |
87 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+12217G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707035 | |||||||
chr8:101707092 | G | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(82): Show |
87 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+12160C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707092 | |||||||
chr8:101707344 | G | A | 7 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+11908C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707344 | |||||||
chr8:101707405 | G | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(155): Show |
161 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.378+11847C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707405 | |||||||
chr8:101707544 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.378+11708A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707544 | |||||||
chr8:101707606 | G | C | 1 | a0001c0001t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+11646C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707606 | |||||||
chr8:101707614 | G | A | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11638C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707614 | |||||||
chr8:101707688 | A | G | 46 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(43): Show |
46 | HG00597.hp2 HG00639.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.378+11564T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707688 | |||||||
chr8:101707692 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11560T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707692 | |||||||
chr8:101707736 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02055.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.378+11516G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707736 | |||||||
chr8:101707746 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11506G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707746 | |||||||
chr8:101707827 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11425A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707827 | |||||||
chr8:101707902 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.378+11350T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707902 | |||||||
chr8:101707903 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.378+11349A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707903 | |||||||
chr8:101707903 | TAATA | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11345_378+1134 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101707903 | |||||||
chr8:101708011 | A | G | 4 | a0001c0001t0015g0085 a0001c0001t0015g0197 a0001c0001t0023g0160 others(1): Show |
4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+11241T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708011 | |||||||
chr8:101708035 | G | C | 1 | a0001c0001t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+11217C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708035 | |||||||
chr8:101708068 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.378+11184C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708068 | |||||||
chr8:101708125 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+11127A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708125 | |||||||
chr8:101708133 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.378+11119A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708133 | |||||||
chr8:101708357 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10895A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708357 | |||||||
chr8:101708654 | C | CA | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10597dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708654 | |||||||
chr8:101708658 | A | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10594T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708658 | |||||||
chr8:101708674 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.378+10578G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708674 | |||||||
chr8:101708754 | T | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+10498A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708754 | |||||||
chr8:101708812 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(8): Show |
11 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+10440A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708812 | |||||||
chr8:101708841 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.378+10411C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708841 | |||||||
chr8:101708944 | A | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10308T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708944 | |||||||
chr8:101708977 | C | CT | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10274dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101708977 | |||||||
chr8:101709114 | G | A | 7 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+10138C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709114 | |||||||
chr8:101709148 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.378+10104G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709148 | |||||||
chr8:101709196 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.378+10056C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709196 | |||||||
chr8:101709198 | C | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+10054G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709198 | |||||||
chr8:101709203 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0135 |
2 | NA18956.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.378+10049C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709203 | |||||||
chr8:101709243 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+10009A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709243 | |||||||
chr8:101709362 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9890G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709362 | |||||||
chr8:101709569 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9683G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709569 | |||||||
chr8:101709774 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.378+9478G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709774 | |||||||
chr8:101709838 | G | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9414C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709838 | |||||||
chr8:101709881 | C | CTAA | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9368_378+9370d others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101709881 | |||||||
chr8:101710187 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.378+9065G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710187 | |||||||
chr8:101710252 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+9000T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710252 | |||||||
chr8:101710355 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.378+8897G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710355 | |||||||
chr8:101710369 | G | GTT | 11 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(8): Show |
13 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.378+8881_378+8882d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710369 | |||||||
chr8:101710389 | G | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+8863C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710389 | |||||||
chr8:101710491 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8761A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710491 | |||||||
chr8:101710620 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.378+8632A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710620 | |||||||
chr8:101710730 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.378+8522C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710730 | |||||||
chr8:101710764 | T | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8488A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710764 | |||||||
chr8:101710974 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.378+8278A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710974 | |||||||
chr8:101710974 | T | G | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.378+8278A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710974 | |||||||
chr8:101710975 | G | A | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8277C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101710975 | |||||||
chr8:101711006 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8246T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711006 | |||||||
chr8:101711036 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.378+8216C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711036 | |||||||
chr8:101711099 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0007g0290 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.378+8153G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711099 | |||||||
chr8:101711139 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8113G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711139 | |||||||
chr8:101711141 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.378+8111G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711141 | |||||||
chr8:101711142 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8110G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711142 | |||||||
chr8:101711244 | A | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+8008T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711244 | |||||||
chr8:101711259 | C | T | 1 | a0001c0001t0017g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.378+7993G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711259 | |||||||
chr8:101711260 | GA | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+7991delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711260 | |||||||
chr8:101711281 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(271): Show |
279 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(276): Show |
intron_variant | MODIFIER | c.378+7971A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711281 | |||||||
chr8:101711329 | C | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(271): Show |
279 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(276): Show |
intron_variant | MODIFIER | c.378+7923G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711329 | |||||||
chr8:101711365 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+7887A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711365 | |||||||
chr8:101711408 | C | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+7844G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711408 | |||||||
chr8:101711409 | G | A | 4 | a0001c0001t0007g0281 a0001c0001t0009g0280 a0001c0001t0009g0282 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7843C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711409 | |||||||
chr8:101711410 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+7842C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711410 | |||||||
chr8:101711472 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.378+7780G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711472 | |||||||
chr8:101711507 | A | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+7745T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711507 | |||||||
chr8:101711582 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+7670A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711582 | |||||||
chr8:101711730 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.378+7522C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101711730 | |||||||
chr8:101712004 | T | C | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.378+7248A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712004 | |||||||
chr8:101712087 | C | T | 4 | a0001c0001t0007g0281 a0001c0001t0009g0280 a0001c0001t0009g0282 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+7165G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712087 | |||||||
chr8:101712237 | A | G | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+7015T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712237 | |||||||
chr8:101712244 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.378+7008T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712244 | |||||||
chr8:101712323 | G | A | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6929C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712323 | |||||||
chr8:101712415 | T | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6837A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712415 | |||||||
chr8:101712580 | T | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(47): Show |
52 | HG00423.hp1 HG00621.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.378+6672A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712580 | |||||||
chr8:101712587 | C | CA | 77 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(74): Show |
77 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.378+6664dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712587 | C | CAA | 18 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(15): Show |
18 | HG00735.hp2 HG01109.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+6663_378+6664d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712587 | C | CAAAAAAA | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+6658_378+6664d others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712587 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0006g0007 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.378+6655_378+6664d others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712587 | CA | C | 26 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(23): Show |
26 | HG00597.hp2 HG00639.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.378+6664delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712587 | CAA | C | 8 | a0001c0001t0002g0273 a0001c0001t0004g0260 a0001c0001t0009g0091 others(5): Show |
8 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+6663_378+6664d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712587 | CAAAAAAA others(5): Show |
C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(58): Show |
62 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.378+6653_378+6664d others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712587 | |||||||
chr8:101712602 | A | AAG | 12 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(9): Show |
12 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.378+6649_378+6650i others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712602 | |||||||
chr8:101712692 | A | G | 4 | a0001c0001t0001g0195 a0001c0001t0002g0273 a0001c0001t0008g0268 others(1): Show |
5 | HG01167.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+6560T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712692 | |||||||
chr8:101712801 | G | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(233): Show |
239 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.378+6451C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712801 | |||||||
chr8:101712809 | T | G | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6443A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712809 | |||||||
chr8:101712810 | A | G | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+6442T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712810 | |||||||
chr8:101712851 | C | T | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6401G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712851 | |||||||
chr8:101712969 | T | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6283A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101712969 | |||||||
chr8:101713054 | G | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6198C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713054 | |||||||
chr8:101713079 | C | T | 4 | a0001c0001t0004g0260 a0001c0001t0010g0037 a0001c0001t0010g0111 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+6173G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713079 | |||||||
chr8:101713089 | A | AG | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+6162_378+6163i others(3): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713089 | |||||||
chr8:101713293 | T | C | 5 | a0001c0001t0001g0104 a0001c0001t0015g0085 a0001c0001t0015g0197 others(2): Show |
5 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+5959A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713293 | |||||||
chr8:101713323 | A | G | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5929T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713323 | |||||||
chr8:101713340 | G | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5912C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713340 | |||||||
chr8:101713353 | C | G | 35 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0215 others(32): Show |
36 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.378+5899G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713353 | |||||||
chr8:101713454 | C | CA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+5797dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713454 | |||||||
chr8:101713464 | C | A | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5788G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713464 | |||||||
chr8:101713493 | GT | G | 290 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(287): Show |
294 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.378+5758delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713493 | |||||||
chr8:101713717 | A | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5535T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713717 | |||||||
chr8:101713756 | G | A | 43 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0215 others(40): Show |
44 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.378+5496C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713756 | |||||||
chr8:101713782 | A | G | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5470T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713782 | |||||||
chr8:101713819 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.378+5433G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713819 | |||||||
chr8:101713836 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+5416C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713836 | |||||||
chr8:101713898 | A | T | 1 | a0001c0001t0004g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.378+5354T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713898 | |||||||
chr8:101713899 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG00609.hp2 HG02071.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+5353C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713899 | |||||||
chr8:101713899 | G | C | 1 | a0001c0001t0004g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.378+5353C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713899 | |||||||
chr8:101713900 | A | C | 1 | a0001c0001t0004g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.378+5352T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713900 | |||||||
chr8:101713914 | T | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5338A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101713914 | |||||||
chr8:101714039 | C | T | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5213G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714039 | |||||||
chr8:101714075 | T | C | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5177A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714075 | |||||||
chr8:101714112 | G | A | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+5140C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714112 | |||||||
chr8:101714123 | T | C | 1 | a0001c0001t0007g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.378+5129A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714123 | |||||||
chr8:101714177 | A | C | 1 | a0001c0001t0002g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.378+5075T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714177 | |||||||
chr8:101714312 | G | A | 266 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(263): Show |
271 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(268): Show |
intron_variant | MODIFIER | c.378+4940C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714312 | |||||||
chr8:101714508 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.378+4744C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714508 | |||||||
chr8:101714562 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.378+4690A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714562 | |||||||
chr8:101714699 | TAAGAACA others(308): Show |
T | 12 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(9): Show |
14 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.378+4238_378+4552d others(2): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714699 | |||||||
chr8:101714719 | G | A | 8 | a0001c0001t0001g0186 a0001c0001t0004g0260 a0001c0001t0009g0091 others(5): Show |
8 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+4533C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714719 | |||||||
chr8:101714859 | C | T | 8 | a0001c0001t0001g0186 a0001c0001t0004g0260 a0001c0001t0009g0091 others(5): Show |
8 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+4393G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714859 | |||||||
chr8:101714890 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+4362C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714890 | |||||||
chr8:101714891 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.378+4361C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714891 | |||||||
chr8:101714962 | A | C | 1 | a0001c0001t0021g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.378+4290T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714962 | |||||||
chr8:101714998 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0108 |
3 | HG01891.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.378+4254G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101714998 | |||||||
chr8:101715003 | C | CAAAAAAA others(10): Show |
11 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0036 others(8): Show |
11 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.378+4248_378+4249i others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | |||||||
chr8:101715003 | C | CAAAAAAA others(11): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0263 a0001c0001t0006g0246 others(1): Show |
4 | HG01109.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+4248_378+4249i others(20): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | |||||||
chr8:101715003 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0004g0260 a0001c0001t0010g0037 a0001c0001t0010g0111 |
3 | HG02257.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.378+4248_378+4249i others(21): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | |||||||
chr8:101715003 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0009g0218 a0001c0001t0009g0248 a0001c0001t0010g0112 |
3 | HG01074.hp1 HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.378+4248_378+4249i others(22): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | |||||||
chr8:101715003 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0009g0091 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.378+4248_378+4249i others(23): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715003 | |||||||
chr8:101715106 | C | G | 13 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(10): Show |
15 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+4146G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715106 | |||||||
chr8:101715158 | C | G | 2 | a0001c0001t0005g0029 a0001c0001t0005g0090 |
2 | NA19004.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.378+4094G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715158 | |||||||
chr8:101715206 | C | T | 7 | a0001c0001t0001g0266 a0001c0001t0007g0290 a0001c0001t0008g0001 others(4): Show |
9 | HG02258.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+4046G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715206 | |||||||
chr8:101715277 | T | C | 1 | a0001c0001t0005g0153 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.378+3975A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715277 | |||||||
chr8:101715315 | T | C | 2 | a0001c0001t0003g0171 a0001c0001t0003g0172 |
2 | NA18945.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.378+3937A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715315 | |||||||
chr8:101715334 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.378+3918A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715334 | |||||||
chr8:101715441 | A | T | 14 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(11): Show |
16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+3811T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715441 | |||||||
chr8:101715465 | C | CAACACTG others(3): Show |
14 | a0001c0001t0001g0266 a0001c0001t0006g0007 a0001c0001t0006g0073 others(11): Show |
16 | HG00423.hp2 HG02258.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+3786_378+3787i others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715465 | |||||||
chr8:101715479 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.378+3773A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715479 | |||||||
chr8:101715818 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0015g0085 a0001c0001t0015g0197 others(2): Show |
5 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+3434T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715818 | |||||||
chr8:101715819 | C | T | 1 | a0001c0001t0005g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.378+3433G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715819 | |||||||
chr8:101715878 | A | T | 5 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0200 others(2): Show |
5 | HG01106.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+3374T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101715878 | |||||||
chr8:101716008 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+3244G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716008 | |||||||
chr8:101716283 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.378+2969G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716283 | |||||||
chr8:101716348 | T | G | 1 | a0001c0001t0001g0013 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.378+2904A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716348 | |||||||
chr8:101716381 | A | G | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.378+2871T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716381 | |||||||
chr8:101716553 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(237): Show |
243 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.378+2699C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716553 | |||||||
chr8:101716696 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.378+2556C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716696 | |||||||
chr8:101716728 | C | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+2524G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716728 | |||||||
chr8:101716794 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.378+2458C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101716794 | |||||||
chr8:101717175 | T | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
48 | HG00597.hp2 HG01069.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.378+2077A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717175 | |||||||
chr8:101717247 | T | C | 49 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
49 | HG00597.hp2 HG01069.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.378+2005A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717247 | |||||||
chr8:101717701 | CCAGA | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0188 others(6): Show |
9 | HG01109.hp2 HG02074.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+1547_378+1550d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717701 | |||||||
chr8:101717834 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.378+1418A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717834 | |||||||
chr8:101717992 | G | A | 275 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(272): Show |
280 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.378+1260C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101717992 | |||||||
chr8:101718069 | A | C | 20 | a0001c0001t0001g0186 a0001c0001t0003g0077 a0001c0001t0004g0260 others(17): Show |
22 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.378+1183T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718069 | |||||||
chr8:101718178 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.378+1074C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718178 | |||||||
chr8:101718225 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.378+1027G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718225 | |||||||
chr8:101718287 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.378+965G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718287 | |||||||
chr8:101718846 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(4): Show |
7 | HG01109.hp2 HG02074.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+406A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101718846 | |||||||
chr8:101719136 | T | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0061 others(27): Show |
30 | HG00597.hp2 HG01515.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.378+116A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101719136 | |||||||
chr8:101719246 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.378+6T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | 101719246 | |||||||
chr8:101719823 | AAGAT | A | 3 | a0001c0001t0015g0197 a0001c0001t0023g0160 a0001c0001t0024g0159 |
3 | HG01069.hp2 HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-179_-19-176del others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719823 | |||||||
chr8:101719906 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-19-258G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719906 | |||||||
chr8:101719912 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-19-264C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719912 | |||||||
chr8:101719924 | C | T | 66 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(63): Show |
66 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-19-276G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719924 | |||||||
chr8:101719925 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-277C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101719925 | |||||||
chr8:101720020 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-372T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720020 | |||||||
chr8:101720021 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-373T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720021 | |||||||
chr8:101720465 | G | T | 36 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
38 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-19-817C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720465 | |||||||
chr8:101720485 | A | C | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-837T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720485 | |||||||
chr8:101720540 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0052 |
2 | HG01257.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-19-892A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720540 | |||||||
chr8:101720578 | C | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-930G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720578 | |||||||
chr8:101720619 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-19-971A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720619 | |||||||
chr8:101720875 | T | C | 1 | a0001c0001t0005g0182 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-19-1227A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101720875 | |||||||
chr8:101721064 | G | A | 1 | a0001c0001t0004g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-19-1416C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721064 | |||||||
chr8:101721120 | A | G | 4 | a0001c0001t0001g0283 a0001c0001t0007g0284 a0001c0001t0007g0285 others(1): Show |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-1472T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721120 | |||||||
chr8:101721168 | GA | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(208): Show |
216 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.-19-1521delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721168 | |||||||
chr8:101721168 | GAA | G | 64 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(61): Show |
64 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-19-1522_-19-1521d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721168 | |||||||
chr8:101721363 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-19-1715G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721363 | |||||||
chr8:101721541 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19-1893C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721541 | |||||||
chr8:101721635 | C | T | 7 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-1987G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721635 | |||||||
chr8:101721636 | G | A | 1 | a0001c0001t0010g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-1988C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721636 | |||||||
chr8:101721852 | G | A | 7 | a0001c0001t0004g0260 a0001c0001t0009g0091 a0001c0001t0009g0218 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2204C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721852 | |||||||
chr8:101721854 | C | CTT | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 NA18966.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-2208_-19-2207d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721854 | |||||||
chr8:101721854 | CT | C | 72 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0047 others(69): Show |
74 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.-19-2207delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721854 | |||||||
chr8:101721903 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-2255C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101721903 | |||||||
chr8:101722007 | A | T | 7 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-2359T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722007 | |||||||
chr8:101722147 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19-2499G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722147 | |||||||
chr8:101722200 | A | G | 7 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(4): Show |
7 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-2552T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722200 | |||||||
chr8:101722213 | G | A | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-2565C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722213 | |||||||
chr8:101722293 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-2645A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722293 | |||||||
chr8:101722427 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-2779C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722427 | |||||||
chr8:101722451 | T | C | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-2803A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722451 | |||||||
chr8:101722670 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-3022C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722670 | |||||||
chr8:101722839 | G | T | 12 | a0001c0001t0003g0077 a0001c0001t0004g0260 a0001c0001t0008g0001 others(9): Show |
14 | HG00639.hp2 HG01069.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-3191C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722839 | |||||||
chr8:101722876 | T | A | 15 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0239 others(12): Show |
15 | HG00544.hp1 HG01099.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-3228A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101722876 | |||||||
chr8:101723071 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-3423C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723071 | |||||||
chr8:101723157 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
225 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.-19-3509T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723157 | |||||||
chr8:101723177 | G | A | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-3529C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723177 | |||||||
chr8:101723189 | CCAGT | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0263 a0001c0001t0001g0283 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-3545_-19-3542d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723189 | |||||||
chr8:101723335 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0015g0197 a0001c0001t0023g0160 others(1): Show |
4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-3687A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723335 | |||||||
chr8:101723714 | AT | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-4067delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723714 | |||||||
chr8:101723896 | TTTG | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0094 others(13): Show |
16 | HG00544.hp1 HG01099.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-4251_-19-4249d others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723896 | |||||||
chr8:101723984 | G | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0032 others(14): Show |
17 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19-4336C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101723984 | |||||||
chr8:101724011 | C | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-4363G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724011 | |||||||
chr8:101724064 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0015g0197 a0001c0001t0023g0160 others(1): Show |
4 | HG01069.hp2 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-4416G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724064 | |||||||
chr8:101724190 | TCA | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-4544_-19-4543d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724190 | |||||||
chr8:101724369 | C | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0032 others(12): Show |
15 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-4721G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724369 | |||||||
chr8:101724491 | T | C | 8 | a0001c0001t0003g0077 a0001c0001t0004g0260 a0001c0001t0009g0091 others(5): Show |
8 | HG00639.hp2 HG01069.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-4843A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724491 | |||||||
chr8:101724765 | AG | A | 4 | a0001c0001t0004g0260 a0001c0001t0010g0037 a0001c0001t0010g0111 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-5118delC | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724765 | |||||||
chr8:101724785 | G | A | 46 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0186 others(43): Show |
47 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-19-5137C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724785 | |||||||
chr8:101724866 | A | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0263 a0001c0001t0001g0283 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5218T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724866 | |||||||
chr8:101724868 | C | G | 1 | a0001c0001t0011g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19-5220G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724868 | |||||||
chr8:101724969 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0004g0291 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-19-5321G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101724969 | |||||||
chr8:101725059 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-5411A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725059 | |||||||
chr8:101725112 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-19-5464G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725112 | |||||||
chr8:101725144 | A | T | 18 | a0001c0001t0003g0077 a0001c0001t0004g0260 a0001c0001t0006g0007 others(15): Show |
20 | HG00423.hp2 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-5496T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725144 | |||||||
chr8:101725200 | G | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5552C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725200 | |||||||
chr8:101725341 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5693C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725341 | |||||||
chr8:101725368 | G | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5720C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725368 | |||||||
chr8:101725501 | T | C | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-5853A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725501 | |||||||
chr8:101725563 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-5915T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725563 | |||||||
chr8:101725798 | G | A | 11 | a0001c0001t0001g0195 a0001c0001t0001g0256 a0001c0001t0001g0266 others(8): Show |
14 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19-6150C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725798 | |||||||
chr8:101725850 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-19-6202A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725850 | |||||||
chr8:101725858 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-19-6210A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725858 | |||||||
chr8:101725910 | T | G | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-6262A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725910 | |||||||
chr8:101725999 | G | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(147): Show |
153 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-19-6351C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101725999 | |||||||
chr8:101726144 | T | C | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-6496A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726144 | |||||||
chr8:101726440 | A | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(281): Show |
288 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(285): Show |
intron_variant | MODIFIER | c.-19-6792T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726440 | |||||||
chr8:101726451 | G | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0114 |
2 | NA18970.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-19-6803C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726451 | |||||||
chr8:101726632 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19-6984A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726632 | |||||||
chr8:101726678 | A | G | 48 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0186 others(45): Show |
51 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.-19-7030T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726678 | |||||||
chr8:101726724 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-19-7076C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726724 | |||||||
chr8:101726736 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0008g0268 |
2 | HG01167.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-19-7088G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726736 | |||||||
chr8:101726998 | C | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7350G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101726998 | |||||||
chr8:101727336 | C | G | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7688G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727336 | |||||||
chr8:101727390 | A | C | 45 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0186 others(42): Show |
46 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-7742T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727390 | |||||||
chr8:101727490 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(74): Show |
78 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.-19-7842C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727490 | |||||||
chr8:101727508 | A | G | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7860T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727508 | |||||||
chr8:101727606 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(64): Show |
68 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-19-7958C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727606 | |||||||
chr8:101727616 | G | A | 34 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0215 others(31): Show |
35 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19-7968C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101727616 | |||||||
chr8:101728053 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8405C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728053 | |||||||
chr8:101728271 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(63): Show |
67 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19-8623G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728271 | |||||||
chr8:101728280 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-19-8632G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728280 | |||||||
chr8:101728311 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-19-8663T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728311 | |||||||
chr8:101728361 | C | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8713G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728361 | |||||||
chr8:101728366 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(200): Show |
208 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.-19-8718G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728366 | |||||||
chr8:101728575 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19-8927G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728575 | |||||||
chr8:101728591 | T | C | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-8943A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728591 | |||||||
chr8:101728611 | A | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(205): Show |
213 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.-19-8963T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728611 | |||||||
chr8:101728737 | G | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(203): Show |
211 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.-19-9089C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728737 | |||||||
chr8:101728771 | A | G | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9123T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728771 | |||||||
chr8:101728830 | A | AAAAC | 51 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(48): Show |
52 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-19-9186_-19-9183d others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728830 | |||||||
chr8:101728855 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19-9207G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728855 | |||||||
chr8:101728880 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9232C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728880 | |||||||
chr8:101728932 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9284C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728932 | |||||||
chr8:101728995 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0061 others(8): Show |
11 | HG02738.hp1 NA18940.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19-9347C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101728995 | |||||||
chr8:101729283 | GA | G | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9636delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729283 | |||||||
chr8:101729293 | A | C | 10 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-9645T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729293 | |||||||
chr8:101729462 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19-9814A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729462 | |||||||
chr8:101729530 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(7): Show |
10 | HG01069.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-9882C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729530 | |||||||
chr8:101729536 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-9888C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729536 | |||||||
chr8:101729578 | A | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(215): Show |
223 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.-19-9930T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729578 | |||||||
chr8:101729649 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19-10001G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729649 | |||||||
chr8:101729707 | G | T | 37 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(34): Show |
37 | HG00738.hp1 HG01069.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19-10059C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729707 | |||||||
chr8:101729765 | C | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0263 a0001c0001t0001g0283 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10117G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729765 | |||||||
chr8:101729840 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(194): Show |
200 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.-19-10192T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729840 | |||||||
chr8:101729914 | A | C | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10266T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729914 | |||||||
chr8:101729961 | A | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0146 a0001c0001t0001g0174 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-10313T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729961 | |||||||
chr8:101729966 | C | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10318G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729966 | |||||||
chr8:101729976 | C | T | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-10328G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101729976 | |||||||
chr8:101730022 | A | C | 7 | a0001c0001t0001g0010 a0001c0001t0006g0007 a0001c0001t0006g0073 others(4): Show |
7 | HG00423.hp2 HG00597.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-10374T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730022 | |||||||
chr8:101730093 | A | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0179 |
2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-19-10445T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730093 | |||||||
chr8:101730142 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(221): Show |
229 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.-19-10494A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730142 | |||||||
chr8:101730165 | A | G | 46 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0024 others(43): Show |
48 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-19-10517T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730165 | |||||||
chr8:101730253 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(167): Show |
173 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.-19-10605C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730253 | |||||||
chr8:101730340 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(175): Show |
181 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-19-10692C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730340 | |||||||
chr8:101730378 | G | A | 9 | a0001c0001t0001g0228 a0001c0001t0002g0178 a0001c0001t0004g0055 others(6): Show |
9 | HG01167.hp2 HG01515.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-10730C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730378 | |||||||
chr8:101730402 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
188 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.-19-10754A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730402 | |||||||
chr8:101730435 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19-10787C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730435 | |||||||
chr8:101730479 | C | CA | 31 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0035 others(28): Show |
31 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19-10832dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | |||||||
chr8:101730479 | C | CAA | 10 | a0001c0001t0001g0229 a0001c0001t0001g0274 a0001c0001t0001g0292 others(7): Show |
10 | HG00544.hp1 HG01074.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-10833_-19-1083 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | |||||||
chr8:101730479 | C | CAAA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(90): Show |
96 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-19-10834_-19-1083 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | |||||||
chr8:101730479 | C | CAAAA | 38 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0032 others(35): Show |
38 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-19-10835_-19-1083 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | |||||||
chr8:101730479 | C | CAAAAA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(14): Show |
17 | HG00438.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-10836_-19-1083 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | |||||||
chr8:101730479 | C | CAAAAAA | 6 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0245 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-10837_-19-1083 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730479 | |||||||
chr8:101730606 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-10958T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730606 | |||||||
chr8:101730702 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0006g0007 a0001c0001t0006g0073 others(4): Show |
7 | HG00423.hp2 HG00597.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-11054T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730702 | |||||||
chr8:101730738 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-11090A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730738 | |||||||
chr8:101730770 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-19-11122A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730770 | |||||||
chr8:101730803 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(126): Show |
132 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-19-11155T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730803 | |||||||
chr8:101730841 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(132): Show |
138 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-11193C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730841 | |||||||
chr8:101730889 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(125): Show |
131 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-19-11241A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730889 | |||||||
chr8:101730927 | T | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0263 a0001c0001t0001g0283 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11279A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730927 | |||||||
chr8:101730956 | C | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0073 a0001c0001t0006g0138 others(3): Show |
6 | HG00423.hp2 HG02523.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11308G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101730956 | |||||||
chr8:101731014 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-19-11366A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731014 | |||||||
chr8:101731053 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0272 |
2 | HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.-19-11405C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731053 | |||||||
chr8:101731223 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19-11575T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731223 | |||||||
chr8:101731260 | G | A | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11612C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731260 | |||||||
chr8:101731280 | G | A | 54 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0186 others(51): Show |
56 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19-11632C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731280 | |||||||
chr8:101731281 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-11633C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731281 | |||||||
chr8:101731549 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0006g0073 a0001c0001t0006g0191 |
3 | HG00597.hp1 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-19-11901A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731549 | |||||||
chr8:101731555 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-19-11907G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731555 | |||||||
chr8:101731581 | T | C | 4 | a0001c0001t0008g0001 a0001c0001t0008g0156 a0001c0001t0008g0259 others(1): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-11933A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731581 | |||||||
chr8:101731584 | G | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(108): Show |
114 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19-11936C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731584 | |||||||
chr8:101731649 | G | A | 45 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0186 others(42): Show |
46 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-12001C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731649 | |||||||
chr8:101731784 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-12136T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731784 | |||||||
chr8:101731821 | T | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(79): Show |
84 | HG00544.hp1 HG00597.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19-12173A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731821 | |||||||
chr8:101731831 | C | A | 18 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0032 others(15): Show |
18 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-12183G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101731831 | |||||||
chr8:101732003 | T | C | 98 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(95): Show |
98 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.-19-12355A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732003 | |||||||
chr8:101732260 | G | A | 4 | a0001c0001t0003g0129 a0001c0001t0003g0171 a0001c0001t0003g0172 others(1): Show |
4 | HG02071.hp1 NA18945.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-12612C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732260 | |||||||
chr8:101732392 | C | T | 7 | a0001c0001t0001g0195 a0001c0001t0001g0256 a0001c0001t0001g0266 others(4): Show |
8 | HG01167.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-12744G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732392 | |||||||
chr8:101732441 | T | G | 2 | a0001c0001t0023g0160 a0001c0001t0024g0159 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-12793A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732441 | |||||||
chr8:101732493 | G | A | 83 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(80): Show |
85 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.-19-12845C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732493 | |||||||
chr8:101732590 | C | CT | 20 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0067 others(17): Show |
20 | HG00544.hp2 HG01106.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19-12943dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CT | C | 27 | a0001c0001t0001g0035 a0001c0001t0001g0046 a0001c0001t0001g0047 others(24): Show |
27 | HG00738.hp2 HG01257.hp1 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-12943delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CTTT | C | 7 | a0001c0001t0003g0077 a0001c0001t0004g0260 a0001c0001t0009g0218 others(4): Show |
7 | HG00639.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-12945_-19-1294 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CTTTT | C | 9 | a0001c0001t0001g0010 a0001c0001t0006g0007 a0001c0001t0006g0073 others(6): Show |
9 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-12946_-19-1294 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CTTTTT | C | 28 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(25): Show |
28 | HG00423.hp1 HG00597.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19-12947_-19-1294 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CTTTTTT | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(128): Show |
133 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.-19-12948_-19-1294 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CTTTTTTT | C | 12 | a0001c0001t0001g0151 a0001c0001t0001g0176 a0001c0001t0001g0250 others(9): Show |
13 | HG00544.hp1 HG01109.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-12949_-19-1294 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732590 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0036 a0001c0001t0005g0029 a0001c0001t0005g0090 others(11): Show |
16 | HG02074.hp1 HG02083.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-12950_-19-1294 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732590 | |||||||
chr8:101732627 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(133): Show |
137 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-19-12979T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732627 | |||||||
chr8:101732756 | G | A | 20 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0263 others(17): Show |
22 | HG00544.hp1 HG01109.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-13108C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732756 | |||||||
chr8:101732762 | C | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0108 |
3 | HG01891.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-19-13114G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732762 | |||||||
chr8:101732814 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19-13166C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732814 | |||||||
chr8:101732970 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18971.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-19-13322A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732970 | |||||||
chr8:101732971 | C | A | 10 | a0001c0001t0001g0036 a0001c0001t0005g0029 a0001c0001t0005g0090 others(7): Show |
10 | HG00544.hp1 HG02074.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-13323G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101732971 | |||||||
chr8:101733063 | C | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0022 others(72): Show |
77 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-19-13415G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733063 | |||||||
chr8:101733067 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(7): Show |
10 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19-13419G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733067 | |||||||
chr8:101733116 | T | C | 2 | a0001c0001t0023g0160 a0001c0001t0024g0159 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-13468A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733116 | |||||||
chr8:101733123 | G | C | 80 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0022 others(77): Show |
81 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-19-13475C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733123 | |||||||
chr8:101733193 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(99): Show |
104 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-13545G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733193 | |||||||
chr8:101733194 | G | A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(35): Show |
39 | HG00738.hp1 HG01069.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-19-13546C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733194 | |||||||
chr8:101733551 | CT | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(99): Show |
104 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-13904delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733551 | |||||||
chr8:101733574 | G | A | 10 | a0001c0001t0001g0036 a0001c0001t0005g0029 a0001c0001t0005g0090 others(7): Show |
10 | HG00544.hp1 HG02074.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-13926C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733574 | |||||||
chr8:101733699 | T | C | 208 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(205): Show |
211 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.-19-14051A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733699 | |||||||
chr8:101733724 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-14076G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733724 | |||||||
chr8:101733825 | C | G | 1 | a0001c0001t0002g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-19-14177G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733825 | |||||||
chr8:101733856 | T | G | 2 | a0001c0001t0003g0206 a0001c0001t0003g0214 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-19-14208A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733856 | |||||||
chr8:101733907 | G | A | 2 | a0001c0001t0023g0160 a0001c0001t0024g0159 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-14259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733907 | |||||||
chr8:101733911 | T | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(101): Show |
106 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-19-14263A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733911 | |||||||
chr8:101733988 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-19-14340G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733988 | |||||||
chr8:101733995 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(98): Show |
103 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-19-14347G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101733995 | |||||||
chr8:101734026 | C | A | 1 | a0001c0001t0002g0027 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19-14378G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734026 | |||||||
chr8:101734079 | T | C | 1 | a0001c0001t0006g0243 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-19-14431A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734079 | |||||||
chr8:101734091 | A | C | 8 | a0001c0001t0001g0010 a0001c0001t0006g0007 a0001c0001t0006g0073 others(5): Show |
8 | HG00423.hp2 HG00597.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-14443T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734091 | |||||||
chr8:101734108 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0023 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19-14460C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734108 | |||||||
chr8:101734208 | C | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(202): Show |
210 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.-19-14560G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734208 | |||||||
chr8:101734484 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19-14836A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734484 | |||||||
chr8:101734496 | C | A | 1 | a0001c0001t0002g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-19-14848G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734496 | |||||||
chr8:101734944 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(191): Show |
197 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.-19-15296C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101734944 | |||||||
chr8:101735166 | C | T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(41): Show |
46 | HG00597.hp2 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19-15518G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735166 | |||||||
chr8:101735269 | T | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(87): Show |
93 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-19-15621A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735269 | |||||||
chr8:101735385 | G | A | 66 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(63): Show |
68 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-19-15737C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735385 | |||||||
chr8:101735430 | C | T | 2 | a0001c0001t0003g0129 a0001c0001t0003g0227 |
2 | HG02071.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-19-15782G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735430 | |||||||
chr8:101735475 | CCT | C | 4 | a0001c0001t0001g0283 a0001c0001t0007g0284 a0001c0001t0007g0285 others(1): Show |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-15829_-19-1582 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735475 | |||||||
chr8:101735503 | C | A | 2 | a0001c0001t0001g0195 a0001c0001t0008g0268 |
2 | HG01167.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-19-15855G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735503 | |||||||
chr8:101735580 | A | C | 1 | a0001c0001t0018g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-15932T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735580 | |||||||
chr8:101735611 | C | T | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0021 others(95): Show |
99 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19-15963G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735611 | |||||||
chr8:101735653 | A | T | 1 | a0001c0001t0004g0055 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-19-16005T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735653 | |||||||
chr8:101735660 | G | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0046 others(13): Show |
16 | HG00544.hp1 HG01952.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-16012C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735660 | |||||||
chr8:101735801 | T | C | 2 | a0001c0001t0009g0091 a0001c0001t0009g0248 |
2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-19-16153A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735801 | |||||||
chr8:101735831 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-19-16183A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101735831 | |||||||
chr8:101736002 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
178 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-19-16354A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736002 | |||||||
chr8:101736090 | G | A | 2 | a0001c0001t0010g0111 a0001c0001t0010g0112 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-19-16442C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736090 | |||||||
chr8:101736202 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0144 others(2): Show |
5 | HG02056.hp2 HG03669.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-16554A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736202 | |||||||
chr8:101736222 | C | G | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-16574G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736222 | |||||||
chr8:101736417 | A | G | 1 | a0001c0001t0007g0281 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-19-16769T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736417 | |||||||
chr8:101736528 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-16880G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736528 | |||||||
chr8:101736582 | G | A | 11 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0270 others(8): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19-16934C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736582 | |||||||
chr8:101736583 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0007g0031 |
2 | HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-19-16935T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736583 | |||||||
chr8:101736714 | C | T | 2 | a0001c0001t0003g0171 a0001c0001t0003g0172 |
2 | NA18945.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.-19-17066G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736714 | |||||||
chr8:101736751 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-17103C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736751 | |||||||
chr8:101736855 | C | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0004g0253 others(4): Show |
7 | HG01074.hp1 HG01515.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-17207G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101736855 | |||||||
chr8:101737018 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-19-17370C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737018 | |||||||
chr8:101737171 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0032 others(55): Show |
59 | HG00621.hp1 HG00738.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.-19-17523A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737171 | |||||||
chr8:101737180 | G | A | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-17532C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737180 | |||||||
chr8:101737340 | C | A | 172 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
175 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.-19-17692G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737340 | |||||||
chr8:101737376 | T | A | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0161 |
3 | HG01081.hp1 HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-19-17728A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737376 | |||||||
chr8:101737454 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-17806A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737454 | |||||||
chr8:101737500 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19-17852A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737500 | |||||||
chr8:101737542 | C | T | 148 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(145): Show |
149 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-19-17894G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737542 | |||||||
chr8:101737558 | G | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
202 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.-19-17910C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737558 | |||||||
chr8:101737804 | T | C | 149 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(146): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-19-18156A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101737804 | |||||||
chr8:101738163 | T | C | 164 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(161): Show |
167 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-19-18515A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738163 | |||||||
chr8:101738266 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0041 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-18618C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738266 | |||||||
chr8:101738281 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-19-18633A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738281 | |||||||
chr8:101738320 | G | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-19-18672C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738320 | |||||||
chr8:101738369 | C | T | 16 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0001g0256 others(13): Show |
18 | HG01074.hp1 HG01109.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-18721G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738369 | |||||||
chr8:101738519 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0041 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-18871C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738519 | |||||||
chr8:101738552 | C | CA | 6 | a0001c0001t0001g0212 a0001c0001t0002g0006 a0001c0001t0002g0162 others(3): Show |
6 | HG01981.hp2 HG02273.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-18905dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | |||||||
chr8:101738552 | CAA | C | 57 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
59 | HG00621.hp1 HG00735.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.-19-18906_-19-1890 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | |||||||
chr8:101738552 | CAAAA | C | 22 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0094 others(19): Show |
22 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-18908_-19-1890 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | |||||||
chr8:101738552 | CAAAAA | C | 158 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(155): Show |
161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.-19-18909_-19-1890 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738552 | |||||||
chr8:101738562 | A | T | 1 | a0001c0001t0008g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19-18914T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738562 | |||||||
chr8:101738636 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-18988G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738636 | |||||||
chr8:101738637 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-18989C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738637 | |||||||
chr8:101738799 | C | T | 2 | a0001c0001t0003g0230 a0001c0001t0005g0231 |
2 | NA18950.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-19-19151G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101738799 | |||||||
chr8:101739240 | A | T | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-19592T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739240 | |||||||
chr8:101739261 | T | C | 199 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(196): Show |
202 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.-19-19613A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739261 | |||||||
chr8:101739277 | C | A | 7 | a0001c0001t0001g0250 a0001c0001t0001g0266 a0001c0001t0001g0267 others(4): Show |
7 | HG00738.hp1 HG01192.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-19629G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739277 | |||||||
chr8:101739377 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-19-19729C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739377 | |||||||
chr8:101739381 | A | G | 1 | a0001c0001t0006g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19-19733T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739381 | |||||||
chr8:101739499 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0279 |
2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19-19851C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739499 | |||||||
chr8:101739526 | T | C | 1 | a0001c0001t0013g0004 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-19878A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739526 | |||||||
chr8:101739652 | G | GA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0061 others(82): Show |
88 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.-19-20005dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739652 | |||||||
chr8:101739729 | C | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0270 a0001c0001t0001g0288 others(3): Show |
6 | HG01346.hp1 HG01433.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-20081G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739729 | |||||||
chr8:101739778 | T | C | 9 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(6): Show |
9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-20130A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739778 | |||||||
chr8:101739866 | A | G | 7 | a0001c0001t0001g0078 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-20218T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739866 | |||||||
chr8:101739935 | C | A | 7 | a0001c0001t0001g0078 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-20287G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739935 | |||||||
chr8:101739954 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-19-20306G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739954 | |||||||
chr8:101739956 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-19-20308A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101739956 | |||||||
chr8:101740069 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-20421A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740069 | |||||||
chr8:101740180 | C | A | 1 | a0001c0001t0008g0268 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-19-20532G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740180 | |||||||
chr8:101740188 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-19-20540C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740188 | |||||||
chr8:101740306 | G | T | 1 | a0001c0001t0003g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-20658C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740306 | |||||||
chr8:101740307 | A | T | 1 | a0001c0001t0003g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-20659T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740307 | |||||||
chr8:101740325 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-19-20677T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740325 | |||||||
chr8:101740355 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-19-20707G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740355 | |||||||
chr8:101740725 | A | G | 15 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(12): Show |
15 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-21077T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740725 | |||||||
chr8:101740871 | C | T | 2 | a0001c0001t0010g0111 a0001c0001t0010g0112 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-19-21223G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101740871 | |||||||
chr8:101741112 | C | A | 9 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(6): Show |
9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-21464G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741112 | |||||||
chr8:101741151 | C | G | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-21503G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741151 | |||||||
chr8:101741151 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-21503G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741151 | |||||||
chr8:101741165 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-19-21517G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741165 | |||||||
chr8:101741181 | A | T | 1 | a0001c0001t0007g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-21533T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741181 | |||||||
chr8:101741182 | C | T | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-21534G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741182 | |||||||
chr8:101741354 | C | T | 224 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(221): Show |
228 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.-19-21706G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741354 | |||||||
chr8:101741375 | C | A | 1 | a0001c0001t0003g0232 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-19-21727G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741375 | |||||||
chr8:101741472 | G | A | 1 | a0001c0001t0002g0006 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-19-21824C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741472 | |||||||
chr8:101741634 | GA | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-21987delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741634 | |||||||
chr8:101741634 | GAA | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0041 others(76): Show |
82 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.-19-21988_-19-2198 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741634 | |||||||
chr8:101741637 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-19-21989T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741637 | |||||||
chr8:101741678 | G | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0229 others(12): Show |
15 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-22030C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741678 | |||||||
chr8:101741725 | G | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-22077C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741725 | |||||||
chr8:101741763 | C | CA | 7 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0212 others(4): Show |
7 | HG01069.hp2 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-22116dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | |||||||
chr8:101741763 | CA | C | 126 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0024 others(123): Show |
127 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-19-22116delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | |||||||
chr8:101741763 | CAA | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0139 others(5): Show |
8 | HG00735.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-22117_-19-2211 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | |||||||
chr8:101741763 | CAAAAAAA | C | 13 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(10): Show |
13 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-22122_-19-2211 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | |||||||
chr8:101741763 | CAAAAAAA others(1): Show |
C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(59): Show |
65 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.-19-22123_-19-2211 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741763 | |||||||
chr8:101741895 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0004g0157 others(1): Show |
4 | HG00738.hp2 HG02622.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-22247G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741895 | |||||||
chr8:101741923 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0279 others(1): Show |
4 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-22275G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741923 | |||||||
chr8:101741936 | C | CA | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
140 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-19-22289dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741936 | |||||||
chr8:101741936 | CA | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(53): Show |
59 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.-19-22289delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741936 | |||||||
chr8:101741936 | CAA | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0188 others(24): Show |
27 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-22290_-19-2228 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741936 | |||||||
chr8:101741954 | G | A | 2 | a0001c0001t0004g0095 a0001c0001t0004g0105 |
2 | NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-19-22306C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741954 | |||||||
chr8:101741955 | A | G | 1 | a0001c0001t0004g0105 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-19-22307T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741955 | |||||||
chr8:101741959 | G | A | 2 | a0001c0001t0004g0095 a0001c0001t0004g0105 |
2 | NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-19-22311C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741959 | |||||||
chr8:101741959 | G | GAA | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-22313_-19-2231 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741959 | |||||||
chr8:101741959 | GA | G | 16 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0229 others(13): Show |
16 | HG01346.hp1 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-22312delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741959 | |||||||
chr8:101741996 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-22348C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101741996 | |||||||
chr8:101742089 | T | A | 1 | a0001c0001t0023g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19-22441A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742089 | |||||||
chr8:101742090 | G | GA | 19 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(16): Show |
19 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19-22443dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742090 | |||||||
chr8:101742090 | GA | G | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-22443delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742090 | |||||||
chr8:101742135 | C | A | 2 | a0001c0001t0001g0175 a0001c0001t0005g0005 |
2 | HG02027.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-19-22487G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742135 | |||||||
chr8:101742230 | GA | G | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-22583delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742230 | |||||||
chr8:101742238 | A | G | 1 | a0001c0001t0020g0265 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19-22590T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742238 | |||||||
chr8:101742256 | G | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-22608C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742256 | |||||||
chr8:101742358 | TTC | T | 14 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(11): Show |
14 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-22712_-19-2271 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742358 | |||||||
chr8:101742420 | T | G | 1 | a0001c0001t0003g0118 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-19-22772A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742420 | |||||||
chr8:101742510 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-22862T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742510 | |||||||
chr8:101742577 | T | C | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-22929A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742577 | |||||||
chr8:101742646 | C | A | 141 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(138): Show |
142 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-19-22998G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742646 | |||||||
chr8:101742664 | A | AT | 9 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(6): Show |
9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-23017dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742664 | |||||||
chr8:101742694 | G | A | 159 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(156): Show |
160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.-19-23046C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742694 | |||||||
chr8:101742932 | T | C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0229 others(14): Show |
17 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19-23284A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742932 | |||||||
chr8:101742995 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-23347T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101742995 | |||||||
chr8:101743031 | C | T | 160 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(157): Show |
161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.-19-23383G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743031 | |||||||
chr8:101743267 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19-23619T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743267 | |||||||
chr8:101743282 | CA | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-23635delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743282 | |||||||
chr8:101743378 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-19-23730T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743378 | |||||||
chr8:101743412 | C | T | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-23764G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743412 | |||||||
chr8:101743413 | A | G | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-23765T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743413 | |||||||
chr8:101743758 | G | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
144 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-24110C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743758 | |||||||
chr8:101743870 | T | C | 1 | a0001c0001t0014g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19-24222A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101743870 | |||||||
chr8:101744122 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-19-24474G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744122 | |||||||
chr8:101744140 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-24492T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744140 | |||||||
chr8:101744374 | A | G | 20 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(17): Show |
22 | HG01109.hp2 HG01891.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-24726T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744374 | |||||||
chr8:101744462 | G | T | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-24814C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744462 | |||||||
chr8:101744623 | A | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-24975T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744623 | |||||||
chr8:101744636 | A | G | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-24988T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744636 | |||||||
chr8:101744658 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-19-25010T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744658 | |||||||
chr8:101744679 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-25031C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744679 | |||||||
chr8:101744784 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-25136T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744784 | |||||||
chr8:101744791 | A | T | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-25143T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744791 | |||||||
chr8:101744833 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19-25185C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101744833 | |||||||
chr8:101745126 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0198 a0001c0001t0001g0245 others(2): Show |
5 | HG01069.hp2 HG01243.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-25478A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745126 | |||||||
chr8:101745341 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0229 others(12): Show |
15 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-25693C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745341 | |||||||
chr8:101745385 | T | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-25737A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745385 | |||||||
chr8:101745466 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-25818C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745466 | |||||||
chr8:101745540 | C | T | 179 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(176): Show |
182 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.-19-25892G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745540 | |||||||
chr8:101745615 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(39): Show |
43 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-25967G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745615 | |||||||
chr8:101745668 | G | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-26020C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745668 | |||||||
chr8:101745727 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-19-26079T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745727 | |||||||
chr8:101745754 | C | T | 1 | a0001c0001t0005g0154 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-26106G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745754 | |||||||
chr8:101745835 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-26187G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745835 | |||||||
chr8:101745868 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-26220A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101745868 | |||||||
chr8:101746302 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-26654G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746302 | |||||||
chr8:101746334 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0002g0040 others(1): Show |
4 | NA18956.hp1 NA18956.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-26686C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746334 | |||||||
chr8:101746335 | C | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0002g0040 others(1): Show |
4 | NA18956.hp1 NA18956.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-26687G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746335 | |||||||
chr8:101746377 | A | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-26729T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746377 | |||||||
chr8:101746451 | CAT | C | 41 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(38): Show |
43 | HG01109.hp2 HG01346.hp1 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.-19-26805_-19-2680 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746451 | |||||||
chr8:101746507 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18940.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-19-26859A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746507 | |||||||
chr8:101746704 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0149 a0001c0001t0017g0080 |
3 | HG03239.hp2 NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-19-27056C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746704 | |||||||
chr8:101746741 | T | C | 2 | a0001c0001t0002g0103 a0001c0001t0004g0086 |
2 | HG00639.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-19-27093A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746741 | |||||||
chr8:101746782 | A | G | 3 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0187 |
3 | NA18952.hp1 NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-19-27134T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746782 | |||||||
chr8:101746816 | A | T | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
140 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-19-27168T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101746816 | |||||||
chr8:101747002 | A | G | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
140 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-19-27354T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747002 | |||||||
chr8:101747003 | TTA | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-27357_-19-2735 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747003 | |||||||
chr8:101747047 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-19-27399A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747047 | |||||||
chr8:101747055 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0146 a0001c0001t0002g0002 |
4 | NA18747.hp2 NA18944.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-27407T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747055 | |||||||
chr8:101747159 | A | C | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-27511T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747159 | |||||||
chr8:101747193 | TCTC | T | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
140 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-19-27548_-19-2754 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747193 | |||||||
chr8:101747208 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-19-27560A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747208 | |||||||
chr8:101747446 | G | A | 9 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(6): Show |
9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-27798C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747446 | |||||||
chr8:101747468 | G | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-27820C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747468 | |||||||
chr8:101747501 | C | T | 26 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(23): Show |
28 | HG01109.hp2 HG01346.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19-27853G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747501 | |||||||
chr8:101747718 | A | AT | 13 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
13 | HG01346.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-28071dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747718 | |||||||
chr8:101747718 | AT | A | 6 | a0001c0001t0001g0084 a0001c0001t0002g0209 a0001c0001t0008g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-28071delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747718 | |||||||
chr8:101747718 | ATT | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-28072_-19-2807 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747718 | |||||||
chr8:101747809 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(29): Show |
33 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19-28161G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747809 | |||||||
chr8:101747907 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-28259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747907 | |||||||
chr8:101747916 | C | T | 1 | a0001c0001t0013g0004 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-28268G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101747916 | |||||||
chr8:101748030 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-28382T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748030 | |||||||
chr8:101748214 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(28): Show |
32 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-19-28566A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748214 | |||||||
chr8:101748257 | T | G | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-19-28609A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748257 | |||||||
chr8:101748330 | C | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(31): Show |
35 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19-28682G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748330 | |||||||
chr8:101748421 | C | T | 2 | a0001c0001t0004g0167 a0001c0001t0007g0166 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-19-28773G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748421 | |||||||
chr8:101748609 | C | T | 1 | a0001c0001t0006g0007 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19-28961G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748609 | |||||||
chr8:101748907 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
231 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.-19-29259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748907 | |||||||
chr8:101748946 | G | A | 9 | a0001c0001t0001g0114 a0001c0001t0001g0126 a0001c0001t0002g0115 others(6): Show |
9 | HG01081.hp1 HG01952.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-29298C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748946 | |||||||
chr8:101748947 | C | G | 1 | a0001c0001t0004g0262 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-19-29299G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748947 | |||||||
chr8:101748999 | C | T | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-29351G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101748999 | |||||||
chr8:101749104 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
231 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(228): Show |
intron_variant | MODIFIER | c.-19-29456C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749104 | |||||||
chr8:101749142 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-19-29494T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749142 | |||||||
chr8:101749171 | C | T | 1 | a0001c0001t0006g0243 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-19-29523G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749171 | |||||||
chr8:101749387 | A | T | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19-29739T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749387 | |||||||
chr8:101749494 | G | T | 10 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0002g0196 others(7): Show |
10 | HG01074.hp2 HG01261.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19-29846C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749494 | |||||||
chr8:101749591 | G | A | 9 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(6): Show |
9 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-29943C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749591 | |||||||
chr8:101749603 | C | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
220 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-19-29955G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749603 | |||||||
chr8:101749754 | G | A | 165 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(162): Show |
166 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-19-30106C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749754 | |||||||
chr8:101749846 | G | A | 162 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(159): Show |
163 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-19-30198C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101749846 | |||||||
chr8:101750130 | A | G | 165 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(162): Show |
166 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-19-30482T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750130 | |||||||
chr8:101750222 | TC | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
219 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.-19-30575delG | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750222 | |||||||
chr8:101750229 | C | G | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-30581G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750229 | |||||||
chr8:101750299 | A | G | 1 | a0001c0001t0021g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-19-30651T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750299 | |||||||
chr8:101750308 | A | T | 168 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(165): Show |
169 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-19-30660T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750308 | |||||||
chr8:101750568 | A | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(222): Show |
229 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.-19-30920T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750568 | |||||||
chr8:101750661 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-31013A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750661 | |||||||
chr8:101750696 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19-31048G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750696 | |||||||
chr8:101750785 | A | G | 171 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(168): Show |
172 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-19-31137T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750785 | |||||||
chr8:101750786 | C | A | 171 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(168): Show |
172 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-19-31138G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750786 | |||||||
chr8:101750891 | T | C | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-31243A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750891 | |||||||
chr8:101750906 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19-31258C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750906 | |||||||
chr8:101750953 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0279 a0001c0001t0007g0031 |
3 | HG02257.hp1 HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19-31305C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101750953 | |||||||
chr8:101751011 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG02080.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-19-31363G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751011 | |||||||
chr8:101751113 | G | A | 1 | a0001c0001t0015g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19-31465C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751113 | |||||||
chr8:101751126 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-31478G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751126 | |||||||
chr8:101751174 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-31526G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751174 | |||||||
chr8:101751277 | C | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-31629G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751277 | |||||||
chr8:101751319 | G | A | 1 | a0001c0001t0006g0133 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-19-31671C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751319 | |||||||
chr8:101751345 | G | A | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-19-31697C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751345 | |||||||
chr8:101751415 | C | A | 3 | a0001c0001t0001g0235 a0001c0001t0002g0237 a0001c0001t0004g0236 |
3 | HG02083.hp1 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-19-31767G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751415 | |||||||
chr8:101751416 | T | A | 3 | a0001c0001t0001g0235 a0001c0001t0002g0237 a0001c0001t0004g0236 |
3 | HG02083.hp1 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-19-31768A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751416 | |||||||
chr8:101751475 | G | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(17): Show |
21 | HG00621.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19-31827C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751475 | |||||||
chr8:101751515 | G | T | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-31867C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751515 | |||||||
chr8:101751603 | G | A | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-19-31955C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751603 | |||||||
chr8:101751773 | C | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-32125G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751773 | |||||||
chr8:101751775 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-32127C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751775 | |||||||
chr8:101751780 | T | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-32132A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751780 | |||||||
chr8:101751782 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-19-32134G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751782 | |||||||
chr8:101751805 | T | G | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-19-32157A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751805 | |||||||
chr8:101751810 | G | T | 11 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(8): Show |
11 | HG02083.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-32162C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751810 | |||||||
chr8:101751829 | T | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-32181A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751829 | |||||||
chr8:101751889 | C | T | 4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
4 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-32241G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751889 | |||||||
chr8:101751906 | C | G | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-32258G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751906 | |||||||
chr8:101751907 | G | A | 2 | a0001c0001t0023g0160 a0001c0001t0024g0159 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-32259C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101751907 | |||||||
chr8:101752185 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19-32537A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752185 | |||||||
chr8:101752257 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-32609A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752257 | |||||||
chr8:101752358 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19-32710T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752358 | |||||||
chr8:101752526 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-19-32878A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752526 | |||||||
chr8:101752629 | A | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0033 others(33): Show |
37 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.-19-32981T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752629 | |||||||
chr8:101752718 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(217): Show |
224 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.-19-33070G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752718 | |||||||
chr8:101752832 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-33184G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752832 | |||||||
chr8:101752957 | T | C | 1 | a0001c0001t0011g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19-33309A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752957 | |||||||
chr8:101752957 | T | TGTATTTT others(319): Show |
7 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(4): Show |
7 | HG02647.hp2 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-33310_-19-3330 others(330): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752957 | |||||||
chr8:101752957 | T | TGTATTTT others(321): Show |
1 | a0001c0001t0001g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19-33310_-19-3330 others(332): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101752957 | |||||||
chr8:101753075 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-19-33427C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753075 | |||||||
chr8:101753402 | A | T | 2 | a0001c0001t0001g0252 a0001c0001t0004g0254 |
2 | HG01891.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-19-33754T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753402 | |||||||
chr8:101753654 | T | C | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-34006A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753654 | |||||||
chr8:101753720 | G | A | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-34072C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753720 | |||||||
chr8:101753724 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-34076C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753724 | |||||||
chr8:101753777 | G | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-34129C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753777 | |||||||
chr8:101753948 | T | A | 150 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-19-34300A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753948 | |||||||
chr8:101753956 | T | A | 2 | a0001c0001t0004g0095 a0001c0001t0004g0105 |
2 | NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-19-34308A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101753956 | |||||||
chr8:101754014 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
184 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.-19-34366C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754014 | |||||||
chr8:101754076 | T | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-34428A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754076 | |||||||
chr8:101754144 | G | C | 1 | a0001c0001t0004g0086 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-19-34496C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754144 | |||||||
chr8:101754237 | C | G | 9 | a0001c0001t0001g0256 a0001c0001t0001g0263 a0001c0001t0004g0260 others(6): Show |
11 | HG01109.hp2 HG02258.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-34589G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754237 | |||||||
chr8:101754285 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-34637T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754285 | |||||||
chr8:101754309 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-19-34661G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754309 | |||||||
chr8:101754311 | T | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-34663A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754311 | |||||||
chr8:101754311 | T | G | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-34663A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754311 | |||||||
chr8:101754337 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-19-34689C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754337 | |||||||
chr8:101754369 | G | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-19-34721C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754369 | |||||||
chr8:101754499 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-34851G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754499 | |||||||
chr8:101754521 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-19-34873C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754521 | |||||||
chr8:101754776 | A | G | 152 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(149): Show |
153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-19-35128T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754776 | |||||||
chr8:101754799 | G | A | 188 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(185): Show |
190 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.-19-35151C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754799 | |||||||
chr8:101754866 | GAATA | G | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19-35222_-19-3521 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754866 | |||||||
chr8:101754870 | A | G | 1 | a0001c0001t0007g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19-35222T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101754870 | |||||||
chr8:101755005 | C | G | 1 | a0001c0001t0019g0123 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-19-35357G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755005 | |||||||
chr8:101755024 | T | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(184): Show |
189 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.-19-35376A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755024 | |||||||
chr8:101755161 | T | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-35513A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755161 | |||||||
chr8:101755251 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-35603C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755251 | |||||||
chr8:101755324 | ATTCCCGT | A | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+35531_-20+3553 others(11): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755324 | |||||||
chr8:101755377 | T | C | 1 | a0001c0001t0004g0223 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-20+35485A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755377 | |||||||
chr8:101755429 | T | C | 147 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-20+35433A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755429 | |||||||
chr8:101755435 | C | T | 147 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-20+35427G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755435 | |||||||
chr8:101755490 | C | A | 176 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
179 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.-20+35372G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755490 | |||||||
chr8:101755612 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-20+35250C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755612 | |||||||
chr8:101755652 | T | C | 1 | a0001c0001t0006g0191 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-20+35210A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755652 | |||||||
chr8:101755770 | G | T | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+35092C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755770 | |||||||
chr8:101755836 | T | C | 1 | a0001c0001t0005g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-20+35026A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755836 | |||||||
chr8:101755839 | T | G | 149 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(146): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-20+35023A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101755839 | |||||||
chr8:101756039 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-20+34823C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756039 | |||||||
chr8:101756078 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-20+34784G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756078 | |||||||
chr8:101756084 | CT | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
182 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.-20+34777delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756084 | |||||||
chr8:101756160 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-20+34702C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756160 | |||||||
chr8:101756246 | T | G | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+34616A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756246 | |||||||
chr8:101756481 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-20+34381C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756481 | |||||||
chr8:101756561 | C | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0002g0049 others(3): Show |
6 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+34301G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756561 | |||||||
chr8:101756611 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+34251T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756611 | |||||||
chr8:101756750 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-20+34112G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101756750 | |||||||
chr8:101757102 | C | G | 1 | a0001c0001t0002g0168 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-20+33760G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757102 | |||||||
chr8:101757156 | C | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(191): Show |
196 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.-20+33706G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757156 | |||||||
chr8:101757279 | T | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(212): Show |
219 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.-20+33583A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757279 | |||||||
chr8:101757302 | C | G | 2 | a0001c0001t0006g0190 a0001c0001t0006g0191 |
2 | HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+33560G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757302 | |||||||
chr8:101757321 | T | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+33541A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757321 | |||||||
chr8:101757372 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0041 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+33490G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757372 | |||||||
chr8:101757381 | G | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(37): Show |
41 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.-20+33481C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757381 | |||||||
chr8:101757531 | T | C | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-20+33331A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757531 | |||||||
chr8:101757609 | T | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(187): Show |
192 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.-20+33253A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757609 | |||||||
chr8:101757679 | T | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
143 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-20+33183A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757679 | |||||||
chr8:101757715 | T | C | 1 | a0001c0001t0004g0262 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+33147A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757715 | |||||||
chr8:101757726 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(38): Show |
42 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.-20+33136G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757726 | |||||||
chr8:101757874 | A | C | 3 | a0001c0001t0001g0235 a0001c0001t0002g0237 a0001c0001t0004g0236 |
3 | HG02083.hp1 NA19060.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-20+32988T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757874 | |||||||
chr8:101757877 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG01069.hp1 HG01952.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+32985C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757877 | |||||||
chr8:101757878 | AG | A | 7 | a0001c0001t0001g0041 a0001c0001t0002g0179 a0001c0001t0005g0180 others(4): Show |
7 | HG00621.hp1 HG02083.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+32983delC | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757878 | |||||||
chr8:101757899 | T | A | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+32963A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757899 | |||||||
chr8:101757910 | A | G | 2 | a0001c0001t0006g0190 a0001c0001t0006g0191 |
2 | HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+32952T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101757910 | |||||||
chr8:101758127 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-20+32735A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758127 | |||||||
chr8:101758236 | T | C | 27 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(24): Show |
29 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.-20+32626A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758236 | |||||||
chr8:101758308 | C | T | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+32554G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758308 | |||||||
chr8:101758378 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+32484G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758378 | |||||||
chr8:101758466 | A | G | 2 | a0001c0001t0004g0167 a0001c0001t0007g0166 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-20+32396T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758466 | |||||||
chr8:101758625 | C | T | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+32237G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758625 | |||||||
chr8:101758674 | C | T | 3 | a0001c0001t0010g0037 a0001c0001t0010g0111 a0001c0001t0010g0112 |
3 | HG02109.hp2 HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-20+32188G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758674 | |||||||
chr8:101758750 | C | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+32112G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758750 | |||||||
chr8:101758826 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(222): Show |
229 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.-20+32036A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758826 | |||||||
chr8:101758831 | T | C | 149 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(146): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-20+32031A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758831 | |||||||
chr8:101758833 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-20+32029G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758833 | |||||||
chr8:101758833 | CT | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
147 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-20+32028delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758833 | |||||||
chr8:101758938 | A | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+31924T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758938 | |||||||
chr8:101758939 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+31923G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101758939 | |||||||
chr8:101759001 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-20+31861G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759001 | |||||||
chr8:101759012 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0174 others(26): Show |
30 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+31850A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759012 | |||||||
chr8:101759065 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+31797C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759065 | |||||||
chr8:101759100 | C | A | 1 | a0001c0001t0007g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-20+31762G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759100 | |||||||
chr8:101759170 | G | A | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+31692C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759170 | |||||||
chr8:101759340 | CA | C | 7 | a0001c0001t0001g0114 a0001c0001t0002g0115 a0001c0001t0002g0119 others(4): Show |
7 | HG01081.hp1 HG01952.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+31521delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759340 | |||||||
chr8:101759455 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+31407A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759455 | |||||||
chr8:101759637 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+31225C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759637 | |||||||
chr8:101759743 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0002g0164 |
2 | HG00735.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+31119C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759743 | |||||||
chr8:101759821 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0041 others(42): Show |
46 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-20+31041C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759821 | |||||||
chr8:101759828 | C | G | 12 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+31034G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759828 | |||||||
chr8:101759952 | G | A | 19 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(16): Show |
21 | HG01099.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.-20+30910C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759952 | |||||||
chr8:101759994 | C | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0279 a0001c0001t0007g0031 |
3 | HG02257.hp1 HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-20+30868G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101759994 | |||||||
chr8:101760207 | T | A | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+30655A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760207 | |||||||
chr8:101760558 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-20+30304A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760558 | |||||||
chr8:101760618 | T | C | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+30244A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760618 | |||||||
chr8:101760658 | A | T | 287 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(284): Show |
292 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(289): Show |
intron_variant | MODIFIER | c.-20+30204T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760658 | |||||||
chr8:101760729 | G | C | 2 | a0001c0001t0007g0277 a0001c0001t0007g0278 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-20+30133C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760729 | |||||||
chr8:101760744 | A | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0163 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+30118T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101760744 | |||||||
chr8:101761156 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+29706G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761156 | |||||||
chr8:101761260 | C | T | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(227): Show |
234 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.-20+29602G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761260 | |||||||
chr8:101761492 | A | G | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+29370T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761492 | |||||||
chr8:101761501 | A | G | 1 | a0001c0001t0007g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+29361T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761501 | |||||||
chr8:101761675 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+29187C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761675 | |||||||
chr8:101761685 | T | C | 137 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(134): Show |
138 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-20+29177A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761685 | |||||||
chr8:101761717 | T | C | 4 | a0001c0001t0001g0283 a0001c0001t0007g0284 a0001c0001t0007g0285 others(1): Show |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+29145A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761717 | |||||||
chr8:101761817 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20+29045C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101761817 | |||||||
chr8:101762157 | T | C | 1 | a0001c0001t0004g0223 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-20+28705A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762157 | |||||||
chr8:101762163 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0009g0248 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-20+28699G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762163 | |||||||
chr8:101762213 | A | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+28649T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762213 | |||||||
chr8:101762279 | A | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+28583T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762279 | |||||||
chr8:101762279 | A | G | 1 | a0001c0001t0003g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20+28583T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762279 | |||||||
chr8:101762295 | T | C | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+28567A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762295 | |||||||
chr8:101762352 | G | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(214): Show |
219 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.-20+28510C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762352 | |||||||
chr8:101762457 | T | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+28405A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762457 | |||||||
chr8:101762591 | C | CT | 9 | a0001c0001t0001g0212 a0001c0001t0001g0292 a0001c0001t0002g0006 others(6): Show |
9 | HG00738.hp1 HG01192.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+28270dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762591 | |||||||
chr8:101762591 | CT | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(56): Show |
62 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-20+28270delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762591 | |||||||
chr8:101762608 | T | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(16): Show |
21 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20+28254A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762608 | |||||||
chr8:101762633 | G | A | 1 | a0001c0001t0002g0237 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-20+28229C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762633 | |||||||
chr8:101762718 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-20+28144G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762718 | |||||||
chr8:101762816 | C | T | 1 | a0001c0001t0007g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+28046G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762816 | |||||||
chr8:101762822 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+28040A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762822 | |||||||
chr8:101762864 | G | A | 1 | a0001c0001t0004g0092 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-20+27998C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762864 | |||||||
chr8:101762948 | A | G | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+27914T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101762948 | |||||||
chr8:101763124 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-20+27738A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763124 | |||||||
chr8:101763218 | C | T | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+27644G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763218 | |||||||
chr8:101763256 | C | A | 8 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(5): Show |
8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+27606G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763256 | |||||||
chr8:101763432 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0006g0133 |
2 | NA18945.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-20+27430G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763432 | |||||||
chr8:101763497 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+27365A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763497 | |||||||
chr8:101763506 | G | T | 6 | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0002g0237 others(3): Show |
6 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+27356C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763506 | |||||||
chr8:101763518 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+27344G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763518 | |||||||
chr8:101763630 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
36 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-20+27232G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763630 | |||||||
chr8:101763732 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-20+27130C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763732 | |||||||
chr8:101763877 | G | A | 1 | a0001c0001t0007g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20+26985C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763877 | |||||||
chr8:101763921 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-20+26941G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763921 | |||||||
chr8:101763952 | T | TTCTCTCT others(1): Show |
4 | a0001c0001t0001g0263 a0001c0001t0004g0262 a0001c0001t0012g0257 others(1): Show |
4 | HG01109.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26902_-20+2690 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763952 | |||||||
chr8:101763952 | T | TTCTCTCT others(3): Show |
3 | a0001c0001t0001g0252 a0001c0001t0004g0254 a0001c0001t0004g0255 |
3 | HG01891.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-20+26900_-20+2690 others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763952 | |||||||
chr8:101763965 | T | TC | 3 | a0001c0001t0001g0185 a0001c0001t0002g0164 a0001c0001t0003g0165 |
3 | HG00735.hp1 HG03491.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+26896dupG | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763965 | |||||||
chr8:101763966 | C | CCA | 4 | a0001c0001t0001g0014 a0001c0001t0001g0107 a0001c0001t0001g0128 others(1): Show |
4 | HG02165.hp2 HG04199.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | C | CCCTCTCT others(3): Show |
1 | a0001c0001t0002g0187 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20+26895_-20+2689 others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | C | CT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+26895_-20+2689 others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | C | CTCTCTCT others(5): Show |
5 | a0001c0001t0004g0253 a0001c0001t0004g0260 a0001c0001t0008g0001 others(2): Show |
7 | HG02145.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+26895_-20+2689 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+26895_-20+2689 others(18): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | CCA | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0269 a0001c0001t0002g0015 others(3): Show |
6 | HG01069.hp2 HG02080.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | CCACA | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
12 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20+26892_-20+2689 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763966 | CCACACA | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0274 a0001c0001t0005g0207 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26890_-20+2689 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763966 | |||||||
chr8:101763967 | C | CCTCT | 5 | a0001c0001t0001g0163 a0001c0001t0001g0175 a0001c0001t0003g0171 others(2): Show |
5 | HG02027.hp1 HG03669.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763967 | |||||||
chr8:101763967 | C | CCTCTCT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0176 others(15): Show |
19 | HG00621.hp1 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20+26894_-20+2689 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763967 | |||||||
chr8:101763967 | C | T | 4 | a0001c0001t0001g0263 a0001c0001t0004g0262 a0001c0001t0012g0257 others(1): Show |
4 | HG01109.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26895G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763967 | |||||||
chr8:101763968 | A | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0174 others(24): Show |
28 | HG00621.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-20+26894T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763968 | |||||||
chr8:101763968 | A | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG00735.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+26894T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763968 | |||||||
chr8:101763969 | C | T | 5 | a0001c0001t0001g0163 a0001c0001t0001g0175 a0001c0001t0003g0171 others(2): Show |
5 | HG02027.hp1 HG03669.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26893G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763969 | |||||||
chr8:101763970 | A | C | 5 | a0001c0001t0001g0163 a0001c0001t0001g0175 a0001c0001t0003g0171 others(2): Show |
5 | HG02027.hp1 HG03669.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26892T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763970 | |||||||
chr8:101763970 | A | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(6): Show |
9 | HG00735.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+26892T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763970 | |||||||
chr8:101763971 | C | CT | 3 | a0001c0001t0001g0185 a0001c0001t0002g0164 a0001c0001t0003g0165 |
3 | HG00735.hp1 HG03491.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+26890_-20+2689 others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763971 | |||||||
chr8:101763972 | A | C | 3 | a0001c0001t0001g0185 a0001c0001t0002g0164 a0001c0001t0003g0165 |
3 | HG00735.hp1 HG03491.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-20+26890T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763972 | |||||||
chr8:101763972 | A | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+26890T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763972 | |||||||
chr8:101763973 | CA | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+26888delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763973 | |||||||
chr8:101763974 | A | T | 1 | a0001c0001t0001g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+26888T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763974 | |||||||
chr8:101763976 | A | T | 1 | a0001c0001t0001g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+26886T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763976 | |||||||
chr8:101763990 | ACACACAC others(19): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+26846_-20+2687 others(30): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763990 | |||||||
chr8:101763998 | ACACACAC others(11): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20+26846_-20+2686 others(22): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101763998 | |||||||
chr8:101764000 | ACACACAC others(9): Show |
A | 1 | a0001c0001t0001g0053 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-20+26846_-20+2686 others(20): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764000 | |||||||
chr8:101764002 | ACACACAC others(7): Show |
A | 5 | a0001c0001t0001g0235 a0001c0001t0002g0237 a0001c0001t0004g0236 others(2): Show |
5 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(18): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764002 | |||||||
chr8:101764004 | ACACACAC others(5): Show |
A | 2 | a0001c0001t0001g0188 a0001c0001t0017g0080 |
2 | NA18953.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764004 | |||||||
chr8:101764006 | ACACACAC others(3): Show |
A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01081.hp2 HG01257.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(14): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764006 | |||||||
chr8:101764006 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0149 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-20+26844_-20+2685 others(16): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764006 | |||||||
chr8:101764008 | ACACACAC others(1): Show |
A | 30 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0058 others(27): Show |
30 | HG00609.hp2 HG01106.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(12): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764008 | |||||||
chr8:101764010 | ACACACC | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0036 others(60): Show |
63 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2685 others(10): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764010 | |||||||
chr8:101764012 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-20+26850T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764012 | |||||||
chr8:101764012 | ACACC | A | 40 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0052 others(37): Show |
40 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2684 others(8): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764012 | |||||||
chr8:101764012 | ACACCC | A | 3 | a0001c0001t0001g0011 a0001c0001t0006g0138 a0001c0001t0013g0004 |
3 | HG06807.hp2 NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-20+26845_-20+2684 others(9): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764012 | |||||||
chr8:101764014 | ACC | A | 44 | a0001c0001t0001g0065 a0001c0001t0001g0083 a0001c0001t0001g0099 others(41): Show |
44 | HG00597.hp2 HG00609.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-20+26846_-20+2684 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764014 | |||||||
chr8:101764014 | ACCC | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0140 others(4): Show |
7 | HG03831.hp2 NA18983.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+26845_-20+2684 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764014 | |||||||
chr8:101764016 | C | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0106 others(40): Show |
44 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.-20+26846G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764016 | |||||||
chr8:101764079 | A | T | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+26783T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764079 | |||||||
chr8:101764090 | G | A | 6 | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0002g0237 others(3): Show |
6 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+26772C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764090 | |||||||
chr8:101764108 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+26754A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764108 | |||||||
chr8:101764189 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+26673T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764189 | |||||||
chr8:101764200 | T | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
51 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-20+26662A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764200 | |||||||
chr8:101764286 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+26576T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764286 | |||||||
chr8:101764297 | A | G | 7 | a0001c0001t0001g0094 a0001c0001t0001g0229 a0001c0001t0001g0235 others(4): Show |
7 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+26565T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764297 | |||||||
chr8:101764504 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0006g0190 others(1): Show |
4 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26358G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764504 | |||||||
chr8:101764607 | T | C | 36 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(33): Show |
38 | HG00738.hp1 HG01109.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.-20+26255A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764607 | |||||||
chr8:101764691 | T | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+26171A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764691 | |||||||
chr8:101764805 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-20+26057A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101764805 | |||||||
chr8:101765059 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+25803C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765059 | |||||||
chr8:101765089 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0005g0153 |
2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-20+25773G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765089 | |||||||
chr8:101765115 | C | T | 8 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(5): Show |
8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+25747G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765115 | |||||||
chr8:101765200 | G | T | 1 | a0001c0001t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-20+25662C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765200 | |||||||
chr8:101765275 | A | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
59 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-20+25587T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765275 | |||||||
chr8:101765327 | T | A | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+25535A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765327 | |||||||
chr8:101765430 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+25432A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765430 | |||||||
chr8:101765535 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-20+25327A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765535 | |||||||
chr8:101765659 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-20+25203C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765659 | |||||||
chr8:101765728 | T | G | 8 | a0001c0001t0001g0188 a0001c0001t0001g0264 a0001c0001t0001g0266 others(5): Show |
8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+25134A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101765728 | |||||||
chr8:101766086 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0002g0040 |
3 | NA18946.hp2 NA18969.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-20+24776G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766086 | |||||||
chr8:101766372 | T | TA | 237 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(234): Show |
241 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(238): Show |
intron_variant | MODIFIER | c.-20+24489dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766372 | |||||||
chr8:101766488 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+24374C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766488 | |||||||
chr8:101766524 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20+24338A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766524 | |||||||
chr8:101766754 | T | A | 6 | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0002g0237 others(3): Show |
6 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+24108A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766754 | |||||||
chr8:101766834 | C | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(8): Show |
11 | HG01346.hp1 HG01433.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+24028G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766834 | |||||||
chr8:101766935 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+23927C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101766935 | |||||||
chr8:101767043 | T | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+23819A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767043 | |||||||
chr8:101767054 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-20+23808C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767054 | |||||||
chr8:101767136 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(3): Show |
6 | HG02630.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+23726G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767136 | |||||||
chr8:101767225 | T | C | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+23637A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767225 | |||||||
chr8:101767461 | A | G | 1 | a0001c0001t0007g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+23401T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767461 | |||||||
chr8:101767729 | C | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(20): Show |
24 | HG00621.hp1 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-20+23133G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767729 | |||||||
chr8:101767882 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-20+22980G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767882 | |||||||
chr8:101767908 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0274 a0001c0001t0001g0279 |
3 | HG02257.hp1 HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-20+22954C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101767908 | |||||||
chr8:101768091 | G | T | 4 | a0001c0001t0007g0031 a0001c0001t0010g0037 a0001c0001t0010g0111 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+22771C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768091 | |||||||
chr8:101768335 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20+22527T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768335 | |||||||
chr8:101768389 | GGGC | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
215 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.-20+22470_-20+2247 others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768389 | |||||||
chr8:101768641 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-20+22221C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768641 | |||||||
chr8:101768720 | A | AAC | 33 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(30): Show |
34 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20+22141_-20+2214 others(6): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768720 | |||||||
chr8:101768723 | C | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(30): Show |
34 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-20+22139G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768723 | |||||||
chr8:101768723 | C | CA | 176 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
177 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.-20+22138dupT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101768723 | |||||||
chr8:101769221 | G | T | 161 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-20+21641C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769221 | |||||||
chr8:101769268 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(232): Show |
239 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.-20+21594G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769268 | |||||||
chr8:101769402 | A | G | 6 | a0001c0001t0001g0114 a0001c0001t0002g0115 a0001c0001t0002g0117 others(3): Show |
6 | NA18948.hp2 NA18971.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+21460T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769402 | |||||||
chr8:101769491 | C | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0007g0251 others(2): Show |
6 | HG01074.hp1 HG01515.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+21371G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769491 | |||||||
chr8:101769493 | G | A | 161 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-20+21369C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769493 | |||||||
chr8:101769655 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-20+21207G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769655 | |||||||
chr8:101769681 | C | T | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+21181G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769681 | |||||||
chr8:101769703 | T | C | 7 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+21159A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769703 | |||||||
chr8:101769876 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0279 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+20986T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769876 | |||||||
chr8:101769880 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(42): Show |
46 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-20+20982A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769880 | |||||||
chr8:101769948 | C | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+20914G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769948 | |||||||
chr8:101769962 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20+20900G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769962 | |||||||
chr8:101769984 | A | G | 1 | a0001c0001t0007g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+20878T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101769984 | |||||||
chr8:101770257 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20+20605T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770257 | |||||||
chr8:101770312 | G | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(38): Show |
44 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.-20+20550C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770312 | |||||||
chr8:101770332 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0279 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+20530A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770332 | |||||||
chr8:101770355 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-20+20507A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770355 | |||||||
chr8:101770539 | C | T | 1 | a0001c0001t0014g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+20323G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770539 | |||||||
chr8:101770589 | A | G | 158 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(155): Show |
159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.-20+20273T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770589 | |||||||
chr8:101770876 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-20+19986G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101770876 | |||||||
chr8:101771178 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20+19684C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101771178 | |||||||
chr8:101771297 | GT | G | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+19564delA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101771297 | |||||||
chr8:101771946 | A | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+18916T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101771946 | |||||||
chr8:101772089 | A | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+18773T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772089 | |||||||
chr8:101772205 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+18657G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772205 | |||||||
chr8:101772315 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+18547G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772315 | |||||||
chr8:101772339 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+18523C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772339 | |||||||
chr8:101772442 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-20+18420T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772442 | |||||||
chr8:101772552 | A | G | 11 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0002g0196 others(8): Show |
11 | HG00438.hp2 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+18310T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772552 | |||||||
chr8:101772658 | A | G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0245 a0001c0001t0002g0273 others(2): Show |
5 | HG01069.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+18204T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101772658 | |||||||
chr8:101773018 | T | A | 1 | a0001c0001t0006g0246 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-20+17844A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773018 | |||||||
chr8:101773084 | G | T | 1 | a0001c0001t0004g0157 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-20+17778C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773084 | |||||||
chr8:101773310 | C | T | 1 | a0001c0001t0011g0030 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-20+17552G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773310 | |||||||
chr8:101773360 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-20+17502A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773360 | |||||||
chr8:101773809 | C | T | 1 | a0001c0001t0003g0238 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-20+17053G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773809 | |||||||
chr8:101773822 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-20+17040C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773822 | |||||||
chr8:101773832 | A | C | 7 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(4): Show |
7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+17030T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773832 | |||||||
chr8:101773999 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(4): Show |
7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+16863G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101773999 | |||||||
chr8:101774103 | G | C | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+16759C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774103 | |||||||
chr8:101774189 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+16673G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774189 | |||||||
chr8:101774190 | T | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+16672A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774190 | |||||||
chr8:101774266 | T | C | 7 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(4): Show |
7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+16596A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774266 | |||||||
chr8:101774275 | G | T | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+16587C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774275 | |||||||
chr8:101774355 | A | G | 1 | a0001c0001t0005g0029 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-20+16507T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774355 | |||||||
chr8:101774459 | T | C | 1 | a0001c0001t0006g0133 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-20+16403A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774459 | |||||||
chr8:101774619 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-20+16243C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774619 | |||||||
chr8:101774676 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-20+16186G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774676 | |||||||
chr8:101774690 | G | A | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+16172C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774690 | |||||||
chr8:101774805 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-20+16057A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101774805 | |||||||
chr8:101775101 | C | T | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+15761G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775101 | |||||||
chr8:101775369 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-20+15493C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775369 | |||||||
chr8:101775559 | A | G | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
61 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-20+15303T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775559 | |||||||
chr8:101775625 | C | A | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-20+15237G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775625 | |||||||
chr8:101775664 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-20+15198G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775664 | |||||||
chr8:101775767 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+15095G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775767 | |||||||
chr8:101775801 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-20+15061C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775801 | |||||||
chr8:101775876 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-20+14986T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101775876 | |||||||
chr8:101776058 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-20+14804G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776058 | |||||||
chr8:101776072 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0174 others(28): Show |
32 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-20+14790A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776072 | |||||||
chr8:101776094 | T | C | 1 | a0001c0001t0004g0110 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-20+14768A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776094 | |||||||
chr8:101776186 | C | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+14676G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776186 | |||||||
chr8:101776228 | A | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+14634T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776228 | |||||||
chr8:101776234 | C | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(71): Show |
77 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.-20+14628G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776234 | |||||||
chr8:101776448 | C | G | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-20+14414G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776448 | |||||||
chr8:101776457 | A | AT | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+14404dupA | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776457 | |||||||
chr8:101776706 | G | A | 5 | a0001c0001t0002g0027 a0001c0001t0002g0135 a0001c0001t0003g0136 others(2): Show |
5 | NA18956.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+14156C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776706 | |||||||
chr8:101776812 | C | G | 1 | a0001c0001t0009g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+14050G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776812 | |||||||
chr8:101776814 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-20+14048A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776814 | |||||||
chr8:101776851 | G | A | 8 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
8 | HG02451.hp2 NA18950.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+14011C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776851 | |||||||
chr8:101776870 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+13992T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101776870 | |||||||
chr8:101777032 | C | A | 7 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(4): Show |
7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+13830G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777032 | |||||||
chr8:101777044 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+13818G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777044 | |||||||
chr8:101777139 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG02080.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-20+13723G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777139 | |||||||
chr8:101777304 | T | C | 2 | a0001c0001t0007g0277 a0001c0001t0007g0278 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-20+13558A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777304 | |||||||
chr8:101777479 | T | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+13383A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777479 | |||||||
chr8:101777571 | G | A | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+13291C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777571 | |||||||
chr8:101777641 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-20+13221C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777641 | |||||||
chr8:101777762 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
76 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.-20+13100A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777762 | |||||||
chr8:101777763 | G | A | 1 | a0001c0001t0004g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+13099C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777763 | |||||||
chr8:101777859 | T | C | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+13003A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777859 | |||||||
chr8:101777978 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+12884A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101777978 | |||||||
chr8:101778103 | C | A | 2 | a0001c0001t0010g0111 a0001c0001t0010g0112 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-20+12759G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778103 | |||||||
chr8:101778144 | T | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+12718A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778144 | |||||||
chr8:101778482 | T | G | 51 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(48): Show |
52 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-20+12380A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778482 | |||||||
chr8:101778666 | G | A | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+12196C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778666 | |||||||
chr8:101778892 | A | T | 5 | a0001c0001t0001g0235 a0001c0001t0002g0237 a0001c0001t0004g0236 others(2): Show |
5 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+11970T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101778892 | |||||||
chr8:101779100 | T | C | 1 | a0001c0001t0009g0287 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20+11762A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779100 | |||||||
chr8:101779115 | A | G | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+11747T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779115 | |||||||
chr8:101779134 | C | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0279 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+11728G>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779134 | |||||||
chr8:101779134 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+11728G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779134 | |||||||
chr8:101779167 | A | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+11695T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779167 | |||||||
chr8:101779177 | A | T | 1 | a0001c0001t0003g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-20+11685T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779177 | |||||||
chr8:101779238 | TAATCCAG others(34): Show |
T | 1 | a0001c0001t0002g0027 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-20+11583_-20+1162 others(45): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779238 | |||||||
chr8:101779388 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0279 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-20+11474A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779388 | |||||||
chr8:101779618 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-20+11244C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779618 | |||||||
chr8:101779739 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-20+11123C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779739 | |||||||
chr8:101779783 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+11079G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101779783 | |||||||
chr8:101780304 | A | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+10558T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780304 | |||||||
chr8:101780484 | G | C | 1 | a0001c0001t0004g0262 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-20+10378C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780484 | |||||||
chr8:101780530 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+10332T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780530 | |||||||
chr8:101780539 | A | G | 2 | a0001c0001t0006g0190 a0001c0001t0006g0191 |
2 | HG02523.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-20+10323T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780539 | |||||||
chr8:101780592 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+10270T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780592 | |||||||
chr8:101780690 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-20+10172C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780690 | |||||||
chr8:101780694 | A | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+10168T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780694 | |||||||
chr8:101780726 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(230): Show |
237 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.-20+10136G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780726 | |||||||
chr8:101780791 | T | C | 1 | a0001c0001t0013g0004 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+10071A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780791 | |||||||
chr8:101780844 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0174 others(48): Show |
54 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20+10018T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780844 | |||||||
chr8:101780960 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0002g0294 others(1): Show |
4 | HG02132.hp2 NA18612.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+9902C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101780960 | |||||||
chr8:101781044 | G | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9818C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781044 | |||||||
chr8:101781183 | AAT | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(229): Show |
236 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.-20+9677_-20+9678d others(4): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781183 | |||||||
chr8:101781257 | G | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9605C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781257 | |||||||
chr8:101781443 | G | A | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9419C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781443 | |||||||
chr8:101781482 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-20+9380G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781482 | |||||||
chr8:101781661 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-20+9201C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781661 | |||||||
chr8:101781726 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-20+9136C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781726 | |||||||
chr8:101781893 | A | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0174 others(28): Show |
32 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-20+8969T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781893 | |||||||
chr8:101781908 | T | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
224 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.-20+8954A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781908 | |||||||
chr8:101781922 | A | G | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0007g0277 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+8940T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781922 | |||||||
chr8:101781961 | T | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8901A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781961 | |||||||
chr8:101781995 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8867G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781995 | |||||||
chr8:101781997 | TA | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8864delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101781997 | |||||||
chr8:101782007 | T | C | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+8855A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782007 | |||||||
chr8:101782040 | T | TG | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8821dupC | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782040 | |||||||
chr8:101782071 | ATATTG | A | 155 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(152): Show |
156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-20+8786_-20+8790d others(7): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782071 | |||||||
chr8:101782076 | G | A | 28 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(25): Show |
28 | HG00738.hp1 HG01099.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20+8786C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782076 | |||||||
chr8:101782111 | T | TATATATT others(10): Show |
9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8750_-20+8751i others(19): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782111 | |||||||
chr8:101782272 | C | A | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8590G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782272 | |||||||
chr8:101782294 | A | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(10): Show |
13 | HG00738.hp1 HG01192.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+8568T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782294 | |||||||
chr8:101782314 | C | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0235 a0001c0001t0002g0237 others(3): Show |
6 | HG02083.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+8548G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782314 | |||||||
chr8:101782394 | A | C | 7 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(4): Show |
7 | HG02083.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+8468T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782394 | |||||||
chr8:101782646 | A | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8216T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782646 | |||||||
chr8:101782847 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+8015G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101782847 | |||||||
chr8:101783035 | T | C | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+7827A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783035 | |||||||
chr8:101783044 | T | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+7818A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783044 | |||||||
chr8:101783071 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-20+7791C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783071 | |||||||
chr8:101783249 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-20+7613C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783249 | |||||||
chr8:101783451 | T | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+7411A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783451 | |||||||
chr8:101783688 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-20+7174G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101783688 | |||||||
chr8:101784006 | T | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6856A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784006 | |||||||
chr8:101784077 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-20+6785T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784077 | |||||||
chr8:101784164 | C | T | 9 | a0001c0001t0001g0188 a0001c0001t0001g0283 a0001c0001t0007g0281 others(6): Show |
9 | HG02559.hp1 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+6698G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784164 | |||||||
chr8:101784342 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+6520T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784342 | |||||||
chr8:101784344 | T | C | 3 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 |
3 | HG00738.hp1 HG01192.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-20+6518A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784344 | |||||||
chr8:101784392 | G | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 others(55): Show |
61 | HG00621.hp1 HG00735.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.-20+6470C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784392 | |||||||
chr8:101784534 | T | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6328A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784534 | |||||||
chr8:101784627 | A | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6235T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784627 | |||||||
chr8:101784651 | T | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(27): Show |
30 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.-20+6211A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784651 | |||||||
chr8:101784790 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+6072T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784790 | |||||||
chr8:101784825 | A | G | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6037T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784825 | |||||||
chr8:101784851 | G | C | 2 | a0001c0001t0001g0152 a0001c0001t0005g0153 |
2 | HG00544.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-20+6011C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784851 | |||||||
chr8:101784862 | G | T | 5 | a0001c0001t0001g0235 a0001c0001t0002g0237 a0001c0001t0004g0236 others(2): Show |
5 | HG02083.hp1 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+6000C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784862 | |||||||
chr8:101784934 | CA | C | 9 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0001g0279 others(6): Show |
9 | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+5927delT | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784934 | |||||||
chr8:101784971 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+5891T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101784971 | |||||||
chr8:101785000 | A | G | 8 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(5): Show |
8 | HG02280.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+5862T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785000 | |||||||
chr8:101785091 | A | G | 2 | a0001c0001t0023g0160 a0001c0001t0024g0159 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-20+5771T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785091 | |||||||
chr8:101785263 | C | A | 1 | a0001c0001t0005g0154 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-20+5599G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785263 | |||||||
chr8:101785402 | T | G | 4 | a0001c0001t0001g0234 a0001c0001t0003g0230 a0001c0001t0003g0232 others(1): Show |
4 | HG02074.hp2 NA18950.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+5460A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785402 | |||||||
chr8:101785489 | C | T | 148 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(145): Show |
149 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-20+5373G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785489 | |||||||
chr8:101785513 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+5349A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785513 | |||||||
chr8:101785515 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0008g0156 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-20+5347C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785515 | |||||||
chr8:101785541 | G | T | 15 | a0001c0001t0001g0279 a0001c0001t0001g0283 a0001c0001t0001g0288 others(12): Show |
15 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+5321C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785541 | |||||||
chr8:101785585 | A | T | 13 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(10): Show |
15 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+5277T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785585 | |||||||
chr8:101785675 | A | G | 14 | a0001c0001t0001g0283 a0001c0001t0001g0288 a0001c0001t0001g0289 others(11): Show |
14 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+5187T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785675 | |||||||
chr8:101785702 | C | T | 14 | a0001c0001t0001g0283 a0001c0001t0001g0288 a0001c0001t0001g0289 others(11): Show |
14 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+5160G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785702 | |||||||
chr8:101785752 | A | C | 2 | a0001c0001t0001g0249 a0001c0001t0009g0248 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-20+5110T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785752 | |||||||
chr8:101785769 | G | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0174 others(27): Show |
31 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20+5093C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785769 | |||||||
chr8:101785869 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20+4993T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101785869 | |||||||
chr8:101786126 | A | G | 14 | a0001c0001t0001g0283 a0001c0001t0001g0288 a0001c0001t0001g0289 others(11): Show |
14 | HG00738.hp1 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+4736T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786126 | |||||||
chr8:101786337 | G | A | 149 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(146): Show |
150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-20+4525C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786337 | |||||||
chr8:101786351 | T | G | 1 | a0001c0001t0004g0157 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-20+4511A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786351 | |||||||
chr8:101786486 | C | A | 1 | a0001c0001t0001g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20+4376G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786486 | |||||||
chr8:101786511 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-20+4351C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786511 | |||||||
chr8:101786527 | T | C | 7 | a0001c0001t0001g0235 a0001c0001t0001g0274 a0001c0001t0002g0237 others(4): Show |
7 | HG02083.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+4335A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786527 | |||||||
chr8:101786548 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-20+4314A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786548 | |||||||
chr8:101786663 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+4199T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786663 | |||||||
chr8:101786701 | G | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+4161C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786701 | |||||||
chr8:101786987 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-20+3875G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101786987 | |||||||
chr8:101787098 | A | G | 12 | a0001c0001t0001g0283 a0001c0001t0001g0292 a0001c0001t0004g0291 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+3764T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787098 | |||||||
chr8:101787266 | C | T | 150 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-20+3596G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787266 | |||||||
chr8:101787341 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20+3521G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787341 | |||||||
chr8:101787362 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-20+3500G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787362 | |||||||
chr8:101787396 | G | A | 6 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG01099.hp1 HG01192.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+3466C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787396 | |||||||
chr8:101787526 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20+3336C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787526 | |||||||
chr8:101787809 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-20+3053C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787809 | |||||||
chr8:101787909 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+2953T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101787909 | |||||||
chr8:101788005 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-20+2857A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788005 | |||||||
chr8:101788074 | T | A | 12 | a0001c0001t0001g0283 a0001c0001t0001g0292 a0001c0001t0004g0291 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+2788A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788074 | |||||||
chr8:101788157 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0004g0253 a0001c0001t0004g0254 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+2705G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788157 | |||||||
chr8:101788164 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+2698C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788164 | |||||||
chr8:101788231 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2631G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788231 | |||||||
chr8:101788252 | T | C | 12 | a0001c0001t0001g0283 a0001c0001t0001g0292 a0001c0001t0004g0291 others(9): Show |
12 | HG00738.hp1 HG01192.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+2610A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788252 | |||||||
chr8:101788383 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+2479G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788383 | |||||||
chr8:101788435 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2427A>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788435 | |||||||
chr8:101788436 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2426A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788436 | |||||||
chr8:101788437 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2425C>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788437 | |||||||
chr8:101788438 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2424A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788438 | |||||||
chr8:101788440 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2422C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788440 | |||||||
chr8:101788443 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2419C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788443 | |||||||
chr8:101788445 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2417A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788445 | |||||||
chr8:101788446 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2416T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788446 | |||||||
chr8:101788447 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2415A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788447 | |||||||
chr8:101788448 | C | A | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-20+2414G>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788448 | |||||||
chr8:101788499 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-20+2363A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788499 | |||||||
chr8:101788622 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(5): Show |
8 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2240G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788622 | |||||||
chr8:101788838 | T | A | 1 | a0001c0001t0001g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-20+2024A>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788838 | |||||||
chr8:101788876 | T | C | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0007g0251 others(2): Show |
6 | HG01074.hp1 HG01515.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+1986A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788876 | |||||||
chr8:101788939 | GGTT | G | 21 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0263 others(18): Show |
23 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-20+1920_-20+1922d others(5): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101788939 | |||||||
chr8:101789005 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-20+1857C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789005 | |||||||
chr8:101789135 | A | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(6): Show |
9 | HG00423.hp2 HG00597.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+1727T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789135 | |||||||
chr8:101789135 | A | T | 14 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(11): Show |
14 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+1727T>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789135 | |||||||
chr8:101789142 | A | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1720T>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789142 | |||||||
chr8:101789348 | A | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+1514T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789348 | |||||||
chr8:101789497 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-20+1365A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789497 | |||||||
chr8:101789525 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-20+1337G>A | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789525 | |||||||
chr8:101789567 | A | G | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1295T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789567 | |||||||
chr8:101789809 | G | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1053C>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789809 | |||||||
chr8:101789812 | G | A | 14 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(11): Show |
14 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+1050C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789812 | |||||||
chr8:101789859 | A | G | 1 | a0001c0001t0002g0006 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-20+1003T>C | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789859 | |||||||
chr8:101789905 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01346.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-20+957C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789905 | |||||||
chr8:101789921 | T | C | 4 | a0001c0001t0001g0292 a0001c0001t0004g0291 a0001c0001t0004g0293 others(1): Show |
4 | HG00738.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+941A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789921 | |||||||
chr8:101789978 | A | ATCCAGAG others(21): Show |
1 | a0001c0001t0005g0005 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-20+856_-20+883dup others(28): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101789978 | |||||||
chr8:101790601 | G | A | 1 | a0001c0001t0002g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-20+261C>T | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101790601 | |||||||
chr8:101790725 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-20+137A>G | NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | 101790725 |