Item | Value |
---|---|
geneid | 8927 |
ensemblid | ENSG00000164061.5 |
hgncid | 1117 |
symbol | BSN |
name | bassoon presynaptic cytomatrix protein |
refseq_nuc | NM_003458.4 |
refseq_prot | NP_003449.2 |
ensembl_nuc | ENST00000296452.5 |
ensembl_prot | ENSP00000296452.4 |
mane_status | MANE Select |
chr | chr3 |
start | 49554477 |
end | 49671549 |
strand | + |
ver | v1.2 |
region | chr3:49554477-49671549 |
region5000 | chr3:49549477-49676549 |
regionname0 | BSN_chr3_49554477_49671549 |
regionname5000 | BSN_chr3_49549477_49676549 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 3926 | 69 | 23 | 17 | 15 | 3 | 10 | 13 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0002 | 0/0 | 3926 | 46 | 13 | 14 | 6 | 7 | 6 | 5 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0003 | 1/0 | 3926 | 31 | 21 | 5 | 0 | 3 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0004 | 0/0 | 3926 | 5 | 1 | 3 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0005 | 0/0 | 3926 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0006 | 0/0 | 3926 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0007 | 0/0 | 3926 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0008 | 0/0 | 3926 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0009 | 0/0 | 3926 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0010 | 0/0 | 3926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0011 | 0/0 | 3926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0012 | 0/0 | 3926 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0013 | 0/0 | 3926 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0014 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0015 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0016 | 0/0 | 3926 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0017 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0018 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0019 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0020 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0021 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0022 | 0/0 | 3926 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0023 | 0/0 | 3926 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0024 | 0/0 | 3926 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
a0025 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | MGNEV others(3921): Show |
chr3 | 49549477 | 49676549 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 11778 | 66 | 23 | 16 | 13 | 3 | 10 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0001c0016 | 0/0 | 11778 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0001c0017 | 0/0 | 11778 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0001c0027 | 0/0 | 11778 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0002c0002 | 0/0 | 11778 | 41 | 11 | 12 | 6 | 6 | 6 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0002c0008 | 0/0 | 11778 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0002c0018 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0002c0019 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0002c0020 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0003c0003 | 0/0 | 11778 | 15 | 14 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0003c0004 | 1/0 | 11778 | 14 | 6 | 3 | 0 | 3 | 1 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0003c0023 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0003c0033 | 0/0 | 11778 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0004c0006 | 0/0 | 11778 | 4 | 1 | 2 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0004c0022 | 0/0 | 11778 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0005c0007 | 0/0 | 11778 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0005c0032 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0005c0034 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0006c0005 | 0/0 | 11778 | 4 | 0 | 0 | 4 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0007c0011 | 0/0 | 11778 | 2 | 0 | 0 | 1 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0008c0014 | 0/0 | 11778 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0009c0012 | 0/0 | 11778 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0010c0015 | 0/0 | 11778 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0011c0013 | 0/0 | 11778 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0012c0009 | 0/0 | 11778 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0013c0010 | 0/0 | 11778 | 2 | 0 | 0 | 2 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0014c0030 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0015c0036 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0016c0026 | 0/0 | 11778 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0017c0037 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0018c0025 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0019c0038 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0020c0024 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0021c0028 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0022c0031 | 0/0 | 11778 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0023c0021 | 0/0 | 11778 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0024c0035 | 0/0 | 11778 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 | ||
a0025c0029 | 0/0 | 11778 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | ATGGG others(11773): Show |
chr3 | 49549477 | 49676549 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 15969 | 25 | 5 | 5 | 9 | 0 | 6 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0003 | 0/1 | 15969 | 21 | 14 | 4 | 0 | 0 | 2 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0007 | 0/0 | 15969 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0009 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0011 | 0/0 | 15965 | 3 | 0 | 1 | 0 | 1 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15960): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0012 | 0/0 | 15969 | 3 | 0 | 1 | 0 | 2 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0015 | 0/0 | 15971 | 2 | 1 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0020 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0021 | 0/0 | 15971 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0022 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0023 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0026 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0029 | 0/0 | 15967 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15962): Show |
chr3 | 49549477 | 49676549 |
a0001c0001t0030 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0016t0003 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0017t0002 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0001c0027t0003 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0002t0001 | 0/0 | 15969 | 35 | 11 | 9 | 4 | 6 | 5 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0002t0005 | 0/0 | 15969 | 4 | 0 | 3 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0002t0018 | 0/0 | 15971 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0002c0002t0019 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0008t0001 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0018t0001 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0019t0001 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0002c0020t0024 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0003c0003t0004 | 0/0 | 15971 | 11 | 10 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0003c0003t0010 | 0/0 | 15971 | 3 | 3 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0003c0003t0016 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0003c0004t0004 | 0/0 | 15971 | 6 | 3 | 3 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0003c0004t0006 | 0/0 | 15971 | 6 | 2 | 0 | 0 | 3 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0003c0004t0014 | 1/0 | 15971 | 2 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0003c0023t0016 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0003c0033t0004 | 0/0 | 15971 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0004c0006t0002 | 0/0 | 15969 | 4 | 1 | 2 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0004c0022t0002 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0005c0007t0007 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0005c0007t0031 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0005c0007t0032 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0005c0032t0007 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0005c0034t0017 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0006c0005t0008 | 0/0 | 15969 | 4 | 0 | 0 | 4 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0007c0011t0001 | 0/0 | 15969 | 2 | 0 | 0 | 1 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0008c0014t0009 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0009c0012t0005 | 0/0 | 15969 | 2 | 0 | 2 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0010c0015t0002 | 0/0 | 15969 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0011c0013t0013 | 0/0 | 15969 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0012c0009t0001 | 0/0 | 15969 | 2 | 2 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0013c0010t0001 | 0/0 | 15969 | 2 | 0 | 0 | 2 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0014c0030t0002 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0015c0036t0001 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0016c0026t0002 | 0/0 | 15969 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0017c0037t0025 | 0/0 | 15971 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15966): Show |
chr3 | 49549477 | 49676549 |
a0018c0025t0028 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0019c0038t0027 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0020c0024t0007 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0021c0028t0003 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0022c0031t0002 | 0/0 | 15969 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0023c0021t0002 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0024c0035t0002 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
a0025c0029t0003 | 0/0 | 15969 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | AGGCG others(15964): Show |
chr3 | 49549477 | 49676549 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0009g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0011g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0012g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0012g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0015g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0020g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0021g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0022g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0023g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0026g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0029g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0001t0030g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0016t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0017t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0001c0027t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0018g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0002t0019g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0008t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0008t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0018t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0019t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0002c0020t0024g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0003t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0006g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0004t0014g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0023t0016g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0003c0033t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0004c0006t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0004c0006t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0004c0006t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0004c0006t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0004c0022t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0005c0007t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0005c0007t0031g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0005c0007t0032g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0005c0032t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0005c0034t0017g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0006c0005t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0006c0005t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0006c0005t0008g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0006c0005t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0007c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0007c0011t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0008c0014t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0008c0014t0009g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0009c0012t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0009c0012t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0010c0015t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0010c0015t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0011c0013t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0011c0013t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0012c0009t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0012c0009t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0013c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0013c0010t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0014c0030t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0015c0036t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0016c0026t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0017c0037t0025g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0018c0025t0028g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0019c0038t0027g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0020c0024t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0021c0028t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0022c0031t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0023c0021t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0024c0035t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
a0025c0029t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0086 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00099 | hp2 | a0014 | c0030 | t0002 | g0142 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00140 | hp1 | a0004 | c0006 | t0002 | g0036 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00140 | hp2 | a0015 | c0036 | t0001 | g0059 | EUR | GBR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00280 | hp1 | a0001 | c0001 | t0012 | g0135 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0058 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0081 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0126 | EUR | FIN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00544 | hp1 | a0001 | c0001 | t0030 | g0143 | EAS | CHS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00544 | hp2 | a0007 | c0011 | t0001 | g0066 | EAS | CHS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00642 | hp1 | a0001 | c0001 | t0012 | g0056 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00733 | hp2 | a0004 | c0006 | t0002 | g0034 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG00735 | hp2 | a0001 | c0001 | t0020 | g0108 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01069 | hp2 | a0003 | c0033 | t0004 | g0025 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01070 | hp1 | a0003 | c0004 | t0004 | g0026 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01070 | hp2 | a0002 | c0008 | t0001 | g0172 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01071 | hp2 | a0002 | c0008 | t0001 | g0168 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01074 | hp1 | a0016 | c0026 | t0002 | g0099 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01074 | hp2 | a0003 | c0003 | t0004 | g0018 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01081 | hp1 | a0002 | c0002 | t0005 | g0073 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01081 | hp2 | a0008 | c0014 | t0009 | g0041 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01106 | hp2 | a0001 | c0001 | t0011 | g0124 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0141 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01167 | hp2 | a0001 | c0027 | t0003 | g0185 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01168 | hp2 | a0002 | c0002 | t0005 | g0061 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01192 | hp1 | a0008 | c0014 | t0009 | g0098 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01192 | hp2 | a0003 | c0004 | t0004 | g0027 | AMR | PUR | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01257 | hp1 | a0009 | c0012 | t0005 | g0083 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01258 | hp1 | a0009 | c0012 | t0005 | g0084 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01433 | hp1 | a0004 | c0022 | t0002 | g0033 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01433 | hp2 | a0002 | c0002 | t0005 | g0074 | AMR | CLM | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0174 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01515 | hp2 | a0001 | c0001 | t0012 | g0115 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01516 | hp1 | a0003 | c0004 | t0006 | g0030 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01516 | hp2 | a0002 | c0019 | t0001 | g0055 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0173 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01517 | hp2 | a0003 | c0004 | t0006 | g0031 | EUR | IBS | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01884 | hp1 | a0003 | c0003 | t0004 | g0023 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01884 | hp2 | a0017 | c0037 | t0025 | g0051 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01891 | hp1 | a0010 | c0015 | t0002 | g0107 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01928 | hp1 | a0001 | c0001 | t0022 | g0091 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01928 | hp2 | a0001 | c0001 | t0009 | g0148 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01981 | hp1 | a0003 | c0004 | t0004 | g0037 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02257 | hp1 | a0003 | c0004 | t0006 | g0032 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02300 | hp1 | a0004 | c0006 | t0002 | g0178 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02300 | hp2 | a0001 | c0001 | t0009 | g0093 | AMR | PEL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02451 | hp2 | a0005 | c0007 | t0032 | g0005 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02572 | hp2 | a0011 | c0013 | t0013 | g0050 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02602 | hp1 | a0018 | c0025 | t0028 | g0100 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02615 | hp2 | a0003 | c0004 | t0006 | g0116 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02622 | hp1 | a0003 | c0003 | t0010 | g0011 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02683 | hp1 | a0019 | c0038 | t0027 | g0004 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02723 | hp2 | a0002 | c0020 | t0024 | g0165 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02735 | hp1 | a0007 | c0011 | t0001 | g0065 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02735 | hp2 | a0001 | c0001 | t0011 | g0097 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0085 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02895 | hp1 | a0005 | c0034 | t0017 | g0002 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02895 | hp2 | a0003 | c0003 | t0010 | g0013 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02896 | hp1 | a0003 | c0003 | t0010 | g0012 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02922 | hp1 | a0011 | c0013 | t0013 | g0049 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02965 | hp1 | a0003 | c0003 | t0004 | g0017 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02970 | hp1 | a0020 | c0024 | t0007 | g0009 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02976 | hp1 | a0003 | c0003 | t0004 | g0021 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02976 | hp2 | a0012 | c0009 | t0001 | g0072 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03041 | hp1 | a0003 | c0003 | t0016 | g0159 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03098 | hp1 | a0003 | c0004 | t0004 | g0028 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03130 | hp2 | a0005 | c0007 | t0007 | g0003 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03139 | hp2 | a0003 | c0003 | t0004 | g0020 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0024 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03225 | hp1 | a0003 | c0004 | t0004 | g0016 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03225 | hp2 | a0002 | c0018 | t0001 | g0010 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03453 | hp2 | a0003 | c0023 | t0016 | g0156 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0019 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03516 | hp2 | a0010 | c0015 | t0002 | g0102 | AFR | ESN | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03654 | hp2 | a0002 | c0002 | t0019 | g0057 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03710 | hp1 | a0021 | c0028 | t0003 | g0149 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03834 | hp2 | a0003 | c0004 | t0006 | g0001 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | BEB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG04115 | hp1 | a0022 | c0031 | t0002 | g0090 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG04115 | hp2 | a0001 | c0001 | t0023 | g0144 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18612 | hp1 | a0001 | c0001 | t0029 | g0120 | EAS | CHB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | CHB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18906 | hp1 | a0003 | c0003 | t0004 | g0045 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | YRI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18951 | hp1 | a0023 | c0021 | t0002 | g0110 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18951 | hp2 | a0006 | c0005 | t0008 | g0063 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18963 | hp1 | a0013 | c0010 | t0001 | g0164 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18979 | hp2 | a0001 | c0016 | t0003 | g0163 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18995 | hp1 | a0001 | c0001 | t0021 | g0092 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA18995 | hp2 | a0024 | c0035 | t0002 | g0133 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19000 | hp1 | a0006 | c0005 | t0008 | g0161 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19003 | hp1 | a0002 | c0002 | t0018 | g0039 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19003 | hp2 | a0001 | c0017 | t0002 | g0105 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19012 | hp1 | a0002 | c0002 | t0005 | g0038 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19030 | hp1 | a0003 | c0004 | t0014 | g0043 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19030 | hp2 | a0003 | c0003 | t0004 | g0014 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19043 | hp1 | a0003 | c0004 | t0004 | g0029 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19043 | hp2 | a0025 | c0029 | t0003 | g0048 | AFR | LWK | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19065 | hp1 | a0013 | c0010 | t0001 | g0064 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19070 | hp1 | a0006 | c0005 | t0008 | g0067 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19079 | hp1 | a0001 | c0001 | t0026 | g0145 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA19079 | hp2 | a0006 | c0005 | t0008 | g0068 | EAS | JPT | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA20129 | hp1 | a0012 | c0009 | t0001 | g0071 | AFR | ASW | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA20129 | hp2 | a0003 | c0003 | t0004 | g0015 | AFR | ASW | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA20752 | hp1 | a0003 | c0004 | t0006 | g0001 | EUR | TSI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0060 | EUR | TSI | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02109 | hp2 | a0004 | c0006 | t0002 | g0035 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02486 | hp1 | a0005 | c0007 | t0031 | g0006 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0022 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
HG06807 | hp2 | a0001 | c0001 | t0015 | g0157 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
NA20300 | hp2 | a0005 | c0032 | t0007 | g0079 | AFR | USA | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0140 | REF | REF | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
homoSapiens | grch38p0 | a0003 | c0004 | t0014 | g0044 | REF | REF | BSN_chr3_49549477_49676549 | BSN | chr3 | 49549477 | 49676549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:49642892 | A | C | 1 | a0017 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1258A>C | p.Met420Leu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/12 | 1384/15971 | 1258/11781 | 420/3926 | chr3 | 49642892 | |||
chr3:49651574 | C | T | 1 | a0015 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.2018C>T | p.Ala673Val | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 2144/15971 | 2018/11781 | 673/3926 | chr3 | 49651574 | |||
chr3:49651777 | G | A | 8 | a0002 a0006 a0007 others(5): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
missense_variant | MODERATE | c.2221G>A | p.Ala741Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 2347/15971 | 2221/11781 | 741/3926 | chr3 | 49651777 | |||
chr3:49652209 | C | T | 1 | a0009 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.2653C>T | p.Pro885Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 2779/15971 | 2653/11781 | 885/3926 | chr3 | 49652209 | |||
chr3:49652590 | C | T | 1 | a0024 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.3034C>T | p.Arg1012Cys | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3160/15971 | 3034/11781 | 1012/3926 | chr3 | 49652590 | |||
chr3:49652816 | G | A | 1 | a0023 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.3260G>A | p.Arg1087Gln | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3386/15971 | 3260/11781 | 1087/3926 | chr3 | 49652816 | |||
chr3:49653187 | C | T | 3 | a0006 a0007 a0013 |
8 | HG00544.hp2 HG02735.hp1 NA18951.hp2 others(5): Show |
missense_variant | MODERATE | c.3631C>T | p.Pro1211Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3757/15971 | 3631/11781 | 1211/3926 | chr3 | 49653187 | |||
chr3:49653194 | G | A | 1 | a0004 | 5 | HG00140.hp1 HG00733.hp2 HG01433.hp1 others(2): Show |
missense_variant | MODERATE | c.3638G>A | p.Gly1213Asp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3764/15971 | 3638/11781 | 1213/3926 | chr3 | 49653194 | |||
chr3:49653251 | C | T | 2 | a0005 a0019 |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
missense_variant | MODERATE | c.3695C>T | p.Thr1232Ile | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3821/15971 | 3695/11781 | 1232/3926 | chr3 | 49653251 | |||
chr3:49653857 | A | G | 1 | a0012 | 2 | HG02976.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.4301A>G | p.Asp1434Gly | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4427/15971 | 4301/11781 | 1434/3926 | chr3 | 49653857 | |||
chr3:49654049 | C | T | 1 | a0011 | 2 | HG02572.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.4493C>T | p.Pro1498Leu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4619/15971 | 4493/11781 | 1498/3926 | chr3 | 49654049 | |||
chr3:49654186 | C | T | 1 | a0022 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.4630C>T | p.Arg1544Cys | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4756/15971 | 4630/11781 | 1544/3926 | chr3 | 49654186 | |||
chr3:49654663 | A | G | 1 | a0025 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.5107A>G | p.Ile1703Val | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 5233/15971 | 5107/11781 | 1703/3926 | chr3 | 49654663 | |||
chr3:49655422 | C | T | 1 | a0021 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.5866C>T | p.Arg1956Trp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 5992/15971 | 5866/11781 | 1956/3926 | chr3 | 49655422 | |||
chr3:49655477 | A | C | 1 | a0010 | 2 | HG01891.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.5921A>C | p.Gln1974Pro | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6047/15971 | 5921/11781 | 1974/3926 | chr3 | 49655477 | |||
chr3:49656067 | G | A | 1 | a0020 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.6511G>A | p.Ala2171Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6637/15971 | 6511/11781 | 2171/3926 | chr3 | 49656067 | |||
chr3:49656970 | C | T | 1 | a0008 | 2 | HG01081.hp2 HG01192.hp1 |
missense_variant | MODERATE | c.7414C>T | p.Arg2472Trp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 7540/15971 | 7414/11781 | 2472/3926 | chr3 | 49656970 | |||
chr3:49657006 | C | A | 1 | a0018 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.7450C>A | p.Pro2484Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 7576/15971 | 7450/11781 | 2484/3926 | chr3 | 49657006 | |||
chr3:49658069 | C | T | 1 | a0017 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.8513C>T | p.Thr2838Met | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 8639/15971 | 8513/11781 | 2838/3926 | chr3 | 49658069 | |||
chr3:49660642 | G | A | 1 | a0016 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.8797G>A | p.Val2933Ile | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 8923/15971 | 8797/11781 | 2933/3926 | chr3 | 49660642 | |||
chr3:49660682 | G | A | 1 | a0014 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.8837G>A | p.Arg2946Gln | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 8963/15971 | 8837/11781 | 2946/3926 | chr3 | 49660682 | |||
chr3:49663146 | G | T | 1 | a0007 | 2 | HG00544.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.10988G>T | p.Gly3663Val | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/12 | 11114/15971 | 10988/11781 | 3663/3926 | chr3 | 49663146 | |||
chr3:49663442 | C | A | 1 | a0019 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.11284C>A | p.Pro3762Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/12 | 11410/15971 | 11284/11781 | 3762/3926 | chr3 | 49663442 | |||
chr3:49663647 | G | A | 1 | a0007 | 2 | HG00544.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.11489G>A | p.Gly3830Asp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/12 | 11615/15971 | 11489/11781 | 3830/3926 | chr3 | 49663647 | |||
chr3:49663865 | G | A | 17 | a0001 a0004 a0005 others(14): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
missense_variant | MODERATE | c.11587G>A | p.Ala3863Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 8/12 | 11713/15971 | 11587/11781 | 3863/3926 | chr3 | 49663865 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:49554644 | G | A | 1 | a0001c0016 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.42G>A | p.Gly14Gly | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/12 | 168/15971 | 42/11781 | 14/3926 | chr3 | 49554644 | |||
chr3:49554713 | T | C | 1 | a0001c0017 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.111T>C | p.Pro37Pro | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/12 | 237/15971 | 111/11781 | 37/3926 | chr3 | 49554713 | |||
chr3:49554794 | C | T | 1 | a0019c0038 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.192C>T | p.Gly64Gly | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/12 | 318/15971 | 192/11781 | 64/3926 | chr3 | 49554794 | |||
chr3:49642624 | C | T | 1 | a0019c0038 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.990C>T | p.Thr330Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/12 | 1116/15971 | 990/11781 | 330/3926 | chr3 | 49642624 | |||
chr3:49652736 | G | T | 1 | a0005c0034 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.3180G>T | p.Arg1060Arg | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3306/15971 | 3180/11781 | 1060/3926 | chr3 | 49652736 | |||
chr3:49652766 | G | A | 36 | a0001c0001 a0001c0016 a0001c0017 others(33): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
synonymous_variant | LOW | c.3210G>A | p.Thr1070Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3336/15971 | 3210/11781 | 1070/3926 | chr3 | 49652766 | |||
chr3:49652895 | C | T | 1 | a0002c0020 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.3339C>T | p.Ala1113Ala | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3465/15971 | 3339/11781 | 1113/3926 | chr3 | 49652895 | |||
chr3:49653063 | C | T | 11 | a0002c0002 a0002c0018 a0002c0019 others(8): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
synonymous_variant | LOW | c.3507C>T | p.Ser1169Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3633/15971 | 3507/11781 | 1169/3926 | chr3 | 49653063 | |||
chr3:49653351 | G | A | 1 | a0011c0013 | 2 | HG02572.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.3795G>A | p.Gln1265Gln | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 3921/15971 | 3795/11781 | 1265/3926 | chr3 | 49653351 | |||
chr3:49654242 | A | G | 1 | a0014c0030 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.4686A>G | p.Ala1562Ala | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 4812/15971 | 4686/11781 | 1562/3926 | chr3 | 49654242 | |||
chr3:49655400 | G | A | 1 | a0004c0022 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.5844G>A | p.Glu1948Glu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 5970/15971 | 5844/11781 | 1948/3926 | chr3 | 49655400 | |||
chr3:49655496 | G | A | 1 | a0003c0023 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.5940G>A | p.Leu1980Leu | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6066/15971 | 5940/11781 | 1980/3926 | chr3 | 49655496 | |||
chr3:49655589 | C | T | 1 | a0002c0019 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.6033C>T | p.Asp2011Asp | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 6159/15971 | 6033/11781 | 2011/3926 | chr3 | 49655589 | |||
chr3:49656606 | C | T | 1 | a0003c0033 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.7050C>T | p.Ser2350Ser | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/12 | 7176/15971 | 7050/11781 | 2350/3926 | chr3 | 49656606 | |||
chr3:49661262 | T | C | 1 | a0002c0018 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.9417T>C | p.Arg3139Arg | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 9543/15971 | 9417/11781 | 3139/3926 | chr3 | 49661262 | |||
chr3:49662090 | C | T | 1 | a0005c0032 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.10245C>T | p.Asn3415Asn | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/12 | 10371/15971 | 10245/11781 | 3415/3926 | chr3 | 49662090 | |||
chr3:49664526 | A | G | 1 | a0001c0027 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.11712A>G | p.Ala3904Ala | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 9/12 | 11838/15971 | 11712/11781 | 3904/3926 | chr3 | 49664526 | |||
chr3:49664550 | G | A | 9 | a0002c0002 a0002c0008 a0002c0018 others(6): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
synonymous_variant | LOW | c.11736G>A | p.Thr3912Thr | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 9/12 | 11862/15971 | 11736/11781 | 3912/3926 | chr3 | 49664550 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:49667609 | C | G | 1 | a0005c0007t0032 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 2770 | chr3 | 49667609 | ||||||
chr3:49667832 | C | T | 2 | a0003c0003t0016 a0003c0023t0016 |
2 | HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*347C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 2993 | chr3 | 49667832 | ||||||
chr3:49668054 | C | A | 1 | a0011c0013t0013 | 2 | HG02572.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*569C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3215 | chr3 | 49668054 | ||||||
chr3:49668057 | G | A | 1 | a0005c0034t0017 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*572G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3218 | chr3 | 49668057 | ||||||
chr3:49668079 | T | A | 12 | a0002c0002t0001 a0002c0002t0005 a0002c0002t0018 others(9): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*594T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3240 | chr3 | 49668079 | ||||||
chr3:49668285 | G | A | 1 | a0001c0001t0020 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*800G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3446 | chr3 | 49668285 | ||||||
chr3:49668317 | C | T | 1 | a0002c0002t0019 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3478 | chr3 | 49668317 | ||||||
chr3:49668552 | G | C | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | HG01928.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1067G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 3713 | chr3 | 49668552 | ||||||
chr3:49668916 | T | C | 1 | a0001c0001t0023 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1431T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4077 | chr3 | 49668916 | ||||||
chr3:49669241 | G | A | 1 | a0003c0003t0010 | 3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1756G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4402 | chr3 | 49669241 | ||||||
chr3:49669266 | A | G | 3 | a0002c0002t0005 a0002c0002t0018 a0009c0012t0005 |
7 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1781A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4427 | chr3 | 49669266 | ||||||
chr3:49669303 | G | C | 1 | a0003c0004t0006 | 6 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1818G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4464 | chr3 | 49669303 | ||||||
chr3:49669305 | C | T | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(34): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1820C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4466 | chr3 | 49669305 | ||||||
chr3:49669401 | T | C | 1 | a0001c0001t0026 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1916T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4562 | chr3 | 49669401 | ||||||
chr3:49669799 | C | T | 2 | a0003c0003t0016 a0003c0023t0016 |
2 | HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2314C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 4960 | chr3 | 49669799 | ||||||
chr3:49670132 | C | T | 1 | a0005c0007t0031 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2647C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5293 | chr3 | 49670132 | ||||||
chr3:49670215 | C | T | 59 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(56): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2730C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5376 | chr3 | 49670215 | ||||||
chr3:49670470 | C | T | 2 | a0003c0003t0016 a0003c0023t0016 |
2 | HG03041.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2985C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5631 | chr3 | 49670470 | ||||||
chr3:49670618 | T | G | 2 | a0001c0001t0009 a0008c0014t0009 |
4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3133T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 5779 | chr3 | 49670618 | ||||||
chr3:49670923 | C | T | 1 | a0017c0037t0025 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3438C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6084 | chr3 | 49670923 | ||||||
chr3:49671019 | C | T | 1 | a0001c0001t0030 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3534C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6180 | chr3 | 49671019 | ||||||
chr3:49671069 | G | T | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(26): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3584G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6230 | chr3 | 49671069 | ||||||
chr3:49671110 | T | C | 1 | a0018c0025t0028 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6271 | chr3 | 49671110 | ||||||
chr3:49671149 | C | T | 1 | a0001c0001t0012 | 3 | HG00280.hp1 HG00642.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3664C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6310 | chr3 | 49671149 | ||||||
chr3:49671153 | CGTGCGTG others(5): Show |
C | 1 | a0001c0001t0015 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3672_*3683delCGTG others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6318 | INFO_REALIGN_3_PRIME | chr3 | 49671153 | |||||
chr3:49671155 | TGC | T | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(46): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*3672_*3673delCG | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6318 | INFO_REALIGN_3_PRIME | chr3 | 49671155 | |||||
chr3:49671157 | C | T | 10 | a0001c0001t0021 a0001c0001t0029 a0002c0002t0018 others(7): Show |
32 | HG01069.hp2 HG01070.hp1 HG01074.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3672C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6318 | chr3 | 49671157 | ||||||
chr3:49671336 | T | C | 18 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(15): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3851T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6497 | chr3 | 49671336 | ||||||
chr3:49671370 | TCAAA | T | 2 | a0001c0001t0011 a0001c0001t0029 |
4 | HG00323.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3893_*3896delACAA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6539 | INFO_REALIGN_3_PRIME | chr3 | 49671370 | |||||
chr3:49671465 | C | T | 1 | a0019c0038t0027 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3980C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 12/12 | 6626 | chr3 | 49671465 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:49554951 | C | T | 1 | a0001c0027t0003g0185 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.224+125C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49554951 | |||||||
chr3:49555427 | T | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+601T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555427 | |||||||
chr3:49555534 | G | A | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+708G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555534 | |||||||
chr3:49555976 | A | G | 6 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+1150A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555976 | |||||||
chr3:49555977 | G | T | 6 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+1151G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49555977 | |||||||
chr3:49556165 | G | A | 14 | a0003c0003t0004g0014 a0003c0003t0004g0015 a0003c0003t0004g0017 others(11): Show |
14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.224+1339G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556165 | |||||||
chr3:49556322 | A | G | 1 | a0004c0006t0002g0178 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.224+1496A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556322 | |||||||
chr3:49556627 | T | C | 15 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0004t0004g0028 others(12): Show |
16 | HG00140.hp1 HG00733.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.224+1801T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556627 | |||||||
chr3:49556918 | T | C | 2 | a0002c0002t0005g0038 a0002c0002t0018g0039 |
2 | NA19003.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.224+2092T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556918 | |||||||
chr3:49556927 | G | T | 3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 |
3 | HG02004.hp2 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.224+2101G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49556927 | |||||||
chr3:49557227 | A | G | 1 | a0005c0007t0031g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224+2401A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49557227 | |||||||
chr3:49557307 | C | T | 10 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(7): Show |
10 | HG01074.hp2 HG01884.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+2481C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49557307 | |||||||
chr3:49557558 | T | TGGA | 9 | a0002c0002t0001g0166 a0002c0002t0001g0167 a0002c0002t0001g0169 others(6): Show |
9 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.224+2733_224+2735d others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49557558 | ||||||
chr3:49557575 | G | GT | 14 | a0001c0001t0002g0160 a0001c0001t0003g0152 a0001c0001t0003g0153 others(11): Show |
14 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.224+2769dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49557575 | ||||||
chr3:49557575 | GT | G | 7 | a0001c0001t0003g0040 a0005c0007t0007g0003 a0005c0007t0031g0006 others(4): Show |
7 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+2769delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49557575 | ||||||
chr3:49557992 | C | T | 7 | a0002c0002t0001g0151 a0002c0002t0001g0179 a0002c0002t0001g0180 others(4): Show |
7 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+3166C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49557992 | |||||||
chr3:49558353 | C | T | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+3527C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49558353 | |||||||
chr3:49559029 | C | T | 143 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.224+4203C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559029 | |||||||
chr3:49559160 | C | G | 67 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.224+4334C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559160 | |||||||
chr3:49559227 | G | A | 1 | a0022c0031t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.224+4401G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559227 | |||||||
chr3:49559370 | A | C | 1 | a0001c0001t0002g0150 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.224+4544A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559370 | |||||||
chr3:49559580 | C | T | 62 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+4754C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559580 | |||||||
chr3:49559622 | C | T | 13 | a0001c0016t0003g0163 a0002c0002t0001g0087 a0002c0002t0001g0088 others(10): Show |
13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+4796C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559622 | |||||||
chr3:49559646 | T | A | 1 | a0001c0001t0022g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224+4820T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559646 | |||||||
chr3:49559696 | T | G | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+4870T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559696 | |||||||
chr3:49559797 | C | G | 60 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.224+4971C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559797 | |||||||
chr3:49559880 | G | T | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5054G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559880 | |||||||
chr3:49559881 | A | C | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5055A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559881 | |||||||
chr3:49559882 | G | T | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5056G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559882 | |||||||
chr3:49559886 | A | T | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5060A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559886 | |||||||
chr3:49559888 | T | A | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5062T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559888 | |||||||
chr3:49559889 | G | A | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5063G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559889 | |||||||
chr3:49559892 | G | A | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5066G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559892 | |||||||
chr3:49559894 | C | G | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5068C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559894 | |||||||
chr3:49559895 | T | C | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5069T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559895 | |||||||
chr3:49559906 | A | T | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5080A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559906 | |||||||
chr3:49559931 | G | T | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5105G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559931 | |||||||
chr3:49559944 | G | A | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5118G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559944 | |||||||
chr3:49559945 | G | T | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5119G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559945 | |||||||
chr3:49559948 | A | G | 1 | a0002c0002t0001g0162 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.224+5122A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49559948 | |||||||
chr3:49560075 | T | C | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+5249T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49560075 | |||||||
chr3:49560304 | T | C | 62 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+5478T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49560304 | |||||||
chr3:49560631 | T | C | 143 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.224+5805T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49560631 | |||||||
chr3:49561550 | T | A | 1 | a0002c0002t0005g0038 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.224+6724T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49561550 | |||||||
chr3:49561706 | A | C | 1 | a0003c0003t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.224+6880A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49561706 | |||||||
chr3:49561968 | C | T | 2 | a0001c0001t0003g0158 a0001c0001t0015g0157 |
2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+7142C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49561968 | |||||||
chr3:49562187 | C | T | 2 | a0002c0002t0001g0173 a0002c0002t0001g0174 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.224+7361C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562187 | |||||||
chr3:49562345 | A | G | 1 | a0021c0028t0003g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.224+7519A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562345 | |||||||
chr3:49562440 | TAAATTAG others(45): Show |
T | 1 | a0022c0031t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.224+7616_224+7667d others(54): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49562440 | ||||||
chr3:49562816 | G | A | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+7990G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562816 | |||||||
chr3:49562886 | G | A | 151 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.224+8060G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562886 | |||||||
chr3:49562993 | C | T | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.224+8167C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49562993 | |||||||
chr3:49563396 | A | G | 1 | a0002c0002t0001g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224+8570A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49563396 | |||||||
chr3:49563822 | T | C | 151 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.224+8996T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49563822 | |||||||
chr3:49564014 | C | T | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224+9188C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564014 | |||||||
chr3:49564066 | C | T | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+9240C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564066 | |||||||
chr3:49564556 | C | T | 1 | a0001c0001t0009g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.224+9730C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564556 | |||||||
chr3:49564799 | C | A | 1 | a0001c0001t0007g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.224+9973C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49564799 | |||||||
chr3:49564995 | TA | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+10181delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49564995 | ||||||
chr3:49565144 | C | CT | 58 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0002c0002t0001g0054 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.224+10337dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49565144 | ||||||
chr3:49565148 | T | C | 1 | a0001c0001t0021g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224+10322T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565148 | |||||||
chr3:49565304 | G | C | 3 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 |
3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.224+10478G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565304 | |||||||
chr3:49565313 | AT | A | 140 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(137): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.224+10509delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49565313 | ||||||
chr3:49565359 | C | T | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224+10533C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565359 | |||||||
chr3:49565567 | G | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+10741G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565567 | |||||||
chr3:49565736 | A | G | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224+10910A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565736 | |||||||
chr3:49565800 | C | T | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+10974C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565800 | |||||||
chr3:49565853 | G | A | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224+11027G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565853 | |||||||
chr3:49565856 | C | T | 60 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.224+11030C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565856 | |||||||
chr3:49565995 | G | A | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+11169G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49565995 | |||||||
chr3:49566491 | A | C | 1 | a0003c0004t0004g0037 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.224+11665A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49566491 | |||||||
chr3:49566600 | C | T | 1 | a0003c0023t0016g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224+11774C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49566600 | |||||||
chr3:49566788 | GA | G | 85 | a0001c0001t0002g0101 a0001c0001t0002g0103 a0001c0001t0002g0104 others(82): Show |
85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.224+11984delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49566788 | ||||||
chr3:49566865 | G | GT | 67 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.224+12049dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49566865 | ||||||
chr3:49567301 | GCT | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+12478_224+1247 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49567301 | ||||||
chr3:49567366 | C | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+12540C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49567366 | |||||||
chr3:49567471 | G | A | 143 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(140): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.224+12645G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49567471 | |||||||
chr3:49568116 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224+13290C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568116 | |||||||
chr3:49568755 | A | C | 47 | a0001c0001t0002g0160 a0001c0016t0003g0163 a0002c0002t0001g0052 others(44): Show |
47 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.224+13929A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568755 | |||||||
chr3:49568952 | G | A | 13 | a0001c0001t0012g0056 a0002c0002t0001g0053 a0002c0002t0001g0054 others(10): Show |
13 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.224+14126G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568952 | |||||||
chr3:49568996 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.224+14170C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49568996 | |||||||
chr3:49569542 | C | T | 1 | a0005c0032t0007g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.224+14716C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49569542 | |||||||
chr3:49569595 | G | A | 1 | a0014c0030t0002g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.224+14769G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49569595 | |||||||
chr3:49570519 | C | T | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224+15693C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49570519 | |||||||
chr3:49570691 | G | C | 4 | a0001c0001t0009g0093 a0001c0001t0009g0148 a0008c0014t0009g0041 others(1): Show |
4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+15865G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49570691 | |||||||
chr3:49571479 | G | A | 1 | a0001c0001t0022g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224+16653G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571479 | |||||||
chr3:49571693 | C | T | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+16867C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571693 | |||||||
chr3:49571799 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.224+16973C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571799 | |||||||
chr3:49571870 | C | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+17044C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49571870 | |||||||
chr3:49572006 | G | A | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224+17180G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572006 | |||||||
chr3:49572044 | C | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+17218C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572044 | |||||||
chr3:49572141 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.224+17315A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572141 | |||||||
chr3:49572242 | G | C | 1 | a0016c0026t0002g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.224+17416G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572242 | |||||||
chr3:49572361 | G | T | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+17535G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572361 | |||||||
chr3:49572423 | C | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+17597C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572423 | |||||||
chr3:49572434 | G | A | 7 | a0002c0002t0001g0151 a0002c0002t0001g0179 a0002c0002t0001g0180 others(4): Show |
7 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+17608G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572434 | |||||||
chr3:49572556 | C | T | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+17730C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572556 | |||||||
chr3:49572694 | C | T | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224+17868C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572694 | |||||||
chr3:49572790 | C | T | 61 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224+17964C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49572790 | |||||||
chr3:49573188 | G | A | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+18362G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573188 | |||||||
chr3:49573281 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.224+18455G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573281 | |||||||
chr3:49573524 | C | T | 72 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.224+18698C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573524 | |||||||
chr3:49573656 | G | GT | 3 | a0001c0016t0003g0163 a0002c0002t0001g0052 a0002c0020t0024g0165 |
3 | HG02723.hp2 HG02738.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.224+18830_224+1883 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573656 | |||||||
chr3:49573657 | G | GT | 5 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+18848dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49573657 | ||||||
chr3:49573657 | G | T | 67 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.224+18831G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573657 | |||||||
chr3:49573932 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.224+19106C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573932 | |||||||
chr3:49573986 | G | A | 1 | a0001c0001t0021g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224+19160G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49573986 | |||||||
chr3:49574024 | A | G | 62 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+19198A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574024 | |||||||
chr3:49574061 | C | T | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+19235C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574061 | |||||||
chr3:49574132 | A | ATT | 88 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.224+19321_224+1932 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574132 | ||||||
chr3:49574132 | A | ATTT | 57 | a0001c0001t0002g0134 a0001c0001t0002g0137 a0001c0001t0002g0138 others(54): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.224+19320_224+1932 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574132 | ||||||
chr3:49574132 | A | ATTTT | 9 | a0002c0002t0001g0089 a0002c0002t0001g0162 a0002c0002t0001g0179 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.224+19319_224+1932 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574132 | ||||||
chr3:49574227 | CA | C | 62 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+19404delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574227 | ||||||
chr3:49574233 | T | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+19407T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574233 | |||||||
chr3:49574325 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.224+19499A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574325 | |||||||
chr3:49574630 | CT | C | 136 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.224+19827delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574630 | ||||||
chr3:49574630 | CTT | C | 10 | a0001c0001t0030g0143 a0002c0002t0001g0062 a0002c0002t0001g0080 others(7): Show |
10 | HG00544.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.224+19826_224+1982 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49574630 | ||||||
chr3:49574755 | C | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+19929C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574755 | |||||||
chr3:49574834 | C | T | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+20008C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49574834 | |||||||
chr3:49575035 | G | T | 1 | a0001c0001t0003g0131 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.224+20209G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575035 | |||||||
chr3:49575420 | A | G | 4 | a0002c0002t0001g0052 a0002c0002t0001g0076 a0002c0002t0001g0077 others(1): Show |
4 | HG02055.hp2 HG02602.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+20594A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575420 | |||||||
chr3:49575424 | GTATA | G | 2 | a0002c0002t0001g0052 a0002c0002t0001g0078 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.224+20604_224+2060 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575424 | ||||||
chr3:49575492 | A | G | 2 | a0001c0001t0002g0130 a0001c0001t0002g0137 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.224+20666A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575492 | |||||||
chr3:49575567 | C | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+20741C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575567 | |||||||
chr3:49575601 | A | G | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+20775A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575601 | |||||||
chr3:49575644 | A | ATG | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+20832_224+2083 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575644 | ||||||
chr3:49575658 | GTA | G | 102 | a0001c0001t0002g0123 a0001c0001t0002g0147 a0001c0001t0002g0160 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.224+20851_224+2085 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575658 | ||||||
chr3:49575658 | GTATA | G | 48 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(45): Show |
48 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.224+20849_224+2085 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49575658 | ||||||
chr3:49575662 | A | G | 3 | a0001c0001t0003g0158 a0001c0001t0015g0157 a0017c0037t0025g0051 |
3 | HG01884.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+20836A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575662 | |||||||
chr3:49575745 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.224+20919G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49575745 | |||||||
chr3:49576129 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.224+21303G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49576129 | |||||||
chr3:49577110 | TG | T | 2 | a0001c0001t0012g0115 a0001c0001t0012g0135 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.224+22285delG | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577110 | |||||||
chr3:49577538 | CT | C | 75 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.224+22715delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49577538 | ||||||
chr3:49577541 | T | C | 11 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 others(8): Show |
11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.224+22715T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577541 | |||||||
chr3:49577543 | T | C | 75 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.224+22717T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577543 | |||||||
chr3:49577769 | A | G | 1 | a0002c0002t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.224+22943A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577769 | |||||||
chr3:49577832 | G | A | 1 | a0002c0002t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.224+23006G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577832 | |||||||
chr3:49577884 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.224+23058G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577884 | |||||||
chr3:49577975 | C | T | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224+23149C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49577975 | |||||||
chr3:49578191 | G | T | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+23365G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578191 | |||||||
chr3:49578410 | G | GT | 44 | a0001c0001t0002g0160 a0001c0016t0003g0163 a0002c0002t0001g0062 others(41): Show |
44 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.224+23597dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49578410 | ||||||
chr3:49578410 | G | GTT | 15 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(12): Show |
15 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.224+23596_224+2359 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49578410 | ||||||
chr3:49578410 | GT | G | 71 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.224+23597delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49578410 | ||||||
chr3:49578620 | G | GA | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+23794_224+2379 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578620 | |||||||
chr3:49578621 | T | C | 75 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.224+23795T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578621 | |||||||
chr3:49578630 | T | C | 1 | a0003c0004t0006g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.224+23804T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578630 | |||||||
chr3:49578642 | G | A | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.224+23816G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578642 | |||||||
chr3:49578696 | G | A | 1 | a0002c0002t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.224+23870G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578696 | |||||||
chr3:49578894 | G | A | 1 | a0013c0010t0001g0164 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.224+24068G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49578894 | |||||||
chr3:49579154 | AT | A | 7 | a0002c0002t0001g0062 a0002c0002t0001g0174 a0002c0002t0005g0038 others(4): Show |
7 | HG01070.hp2 HG01081.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+24344delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579154 | ||||||
chr3:49579564 | A | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+24738A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49579564 | |||||||
chr3:49579584 | C | CT | 11 | a0002c0002t0001g0052 a0002c0002t0001g0076 a0002c0002t0001g0077 others(8): Show |
11 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.224+24768dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579584 | ||||||
chr3:49579738 | T | C | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224+24912T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49579738 | |||||||
chr3:49579769 | AT | A | 86 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.224+24950delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579769 | ||||||
chr3:49579796 | ATTGGAAA others(23): Show |
A | 148 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.224+24972_224+2500 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49579796 | ||||||
chr3:49580162 | A | G | 2 | a0001c0001t0002g0096 a0021c0028t0003g0149 |
2 | HG02738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.224+25336A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580162 | |||||||
chr3:49580494 | C | T | 1 | a0003c0004t0004g0037 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.224+25668C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580494 | |||||||
chr3:49580698 | A | G | 1 | a0002c0002t0005g0074 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.224+25872A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580698 | |||||||
chr3:49580831 | G | A | 10 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(7): Show |
10 | HG01074.hp2 HG01884.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+26005G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580831 | |||||||
chr3:49580951 | T | C | 1 | a0005c0032t0007g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.224+26125T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49580951 | |||||||
chr3:49580978 | C | CT | 61 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224+26166dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49580978 | ||||||
chr3:49581074 | C | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+26248C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581074 | |||||||
chr3:49581417 | C | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26591C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581417 | |||||||
chr3:49581419 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26593T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581419 | |||||||
chr3:49581424 | C | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26598C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581424 | |||||||
chr3:49581428 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26602T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581428 | |||||||
chr3:49581429 | A | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26603A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581429 | |||||||
chr3:49581430 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26604T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581430 | |||||||
chr3:49581434 | A | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26608A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581434 | |||||||
chr3:49581437 | A | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26611A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581437 | |||||||
chr3:49581438 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26612T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581438 | |||||||
chr3:49581439 | A | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26613A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581439 | |||||||
chr3:49581441 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26615T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581441 | |||||||
chr3:49581442 | G | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26616G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581442 | |||||||
chr3:49581443 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26617T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581443 | |||||||
chr3:49581446 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26620T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581446 | |||||||
chr3:49581450 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26624T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581450 | |||||||
chr3:49581451 | G | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26625G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581451 | |||||||
chr3:49581452 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26626T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581452 | |||||||
chr3:49581453 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26627T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581453 | |||||||
chr3:49581454 | C | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26628C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581454 | |||||||
chr3:49581455 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26629T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581455 | |||||||
chr3:49581457 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26631T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581457 | |||||||
chr3:49581458 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26632T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581458 | |||||||
chr3:49581459 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26633T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581459 | |||||||
chr3:49581460 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26634T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581460 | |||||||
chr3:49581462 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26636T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581462 | |||||||
chr3:49581463 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26637T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581463 | |||||||
chr3:49581464 | A | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26638A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581464 | |||||||
chr3:49581465 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26639T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581465 | |||||||
chr3:49581466 | T | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26640T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581466 | |||||||
chr3:49581469 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26643T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581469 | |||||||
chr3:49581472 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26646T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581472 | |||||||
chr3:49581473 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26647T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581473 | |||||||
chr3:49581475 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26649T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581475 | |||||||
chr3:49581477 | A | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26651A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581477 | |||||||
chr3:49581478 | A | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26652A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581478 | |||||||
chr3:49581479 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26653T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581479 | |||||||
chr3:49581484 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26658T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581484 | |||||||
chr3:49581485 | A | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26659A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581485 | |||||||
chr3:49581486 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26660T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581486 | |||||||
chr3:49581487 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26661T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581487 | |||||||
chr3:49581492 | C | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26666C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581492 | |||||||
chr3:49581493 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26667T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581493 | |||||||
chr3:49581496 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26670T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581496 | |||||||
chr3:49581497 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26671T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581497 | |||||||
chr3:49581500 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26674T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581500 | |||||||
chr3:49581502 | T | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26676T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581502 | |||||||
chr3:49581510 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26684T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581510 | |||||||
chr3:49581511 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26685T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581511 | |||||||
chr3:49581517 | T | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26691T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581517 | |||||||
chr3:49581518 | A | G | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26692A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581518 | |||||||
chr3:49581519 | G | C | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26693G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581519 | |||||||
chr3:49581520 | G | T | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+26694G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581520 | |||||||
chr3:49581601 | G | A | 1 | a0001c0001t0011g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.224+26775G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581601 | |||||||
chr3:49581752 | A | T | 1 | a0002c0002t0018g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.224+26926A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49581752 | |||||||
chr3:49582060 | C | T | 148 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.224+27234C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582060 | |||||||
chr3:49582218 | T | C | 61 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224+27392T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582218 | |||||||
chr3:49582241 | C | T | 1 | a0002c0002t0005g0038 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.224+27415C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49582241 | |||||||
chr3:49582952 | C | CATTT | 41 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.224+28157_224+2816 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | ||||||
chr3:49582952 | C | CATTTATT others(1): Show |
89 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0103 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.224+28153_224+2816 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | ||||||
chr3:49582952 | C | CATTTATT others(5): Show |
18 | a0001c0001t0002g0101 a0001c0001t0002g0113 a0001c0001t0002g0134 others(15): Show |
18 | HG00323.hp2 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.224+28149_224+2816 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | ||||||
chr3:49582952 | C | CATTTATT others(9): Show |
3 | a0001c0001t0003g0128 a0001c0001t0003g0154 a0001c0001t0003g0155 |
3 | HG02559.hp1 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.224+28145_224+2816 others(20): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | ||||||
chr3:49582952 | CATTT | C | 4 | a0005c0007t0007g0003 a0005c0007t0032g0005 a0005c0034t0017g0002 others(1): Show |
4 | HG02451.hp2 HG02683.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+28157_224+2816 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49582952 | ||||||
chr3:49583337 | A | G | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.224+28511A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583337 | |||||||
chr3:49583615 | AAATAAAA others(12): Show |
A | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224+28792_224+2881 others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49583615 | ||||||
chr3:49583753 | G | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+28927G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583753 | |||||||
chr3:49583864 | G | GATTT | 4 | a0005c0007t0031g0006 a0005c0007t0032g0005 a0005c0034t0017g0002 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+29061_224+2906 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49583864 | ||||||
chr3:49583934 | C | T | 17 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(14): Show |
17 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.224+29108C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583934 | |||||||
chr3:49583979 | T | C | 1 | a0003c0004t0004g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.224+29153T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49583979 | |||||||
chr3:49584087 | G | A | 3 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0033t0004g0025 |
3 | HG01069.hp2 HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.224+29261G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584087 | |||||||
chr3:49584121 | G | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+29295G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584121 | |||||||
chr3:49584285 | A | AT | 165 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(162): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.224+29469dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49584285 | ||||||
chr3:49584285 | A | ATT | 5 | a0001c0001t0002g0130 a0001c0001t0002g0137 a0002c0002t0001g0086 others(2): Show |
5 | HG00099.hp1 HG00140.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.224+29468_224+2946 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49584285 | ||||||
chr3:49584384 | T | G | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+29558T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584384 | |||||||
chr3:49584561 | C | T | 148 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.224+29735C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584561 | |||||||
chr3:49584691 | C | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+29865C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584691 | |||||||
chr3:49584698 | T | C | 1 | a0001c0001t0026g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.224+29872T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584698 | |||||||
chr3:49584716 | G | A | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+29890G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584716 | |||||||
chr3:49584992 | A | G | 1 | a0001c0001t0011g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.224+30166A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49584992 | |||||||
chr3:49585116 | T | G | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+30290T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585116 | |||||||
chr3:49585199 | G | GT | 155 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.224+30383dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49585199 | ||||||
chr3:49585237 | T | C | 1 | a0005c0007t0007g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.224+30411T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585237 | |||||||
chr3:49585439 | G | A | 8 | a0001c0001t0002g0160 a0006c0005t0008g0063 a0006c0005t0008g0067 others(5): Show |
8 | HG00544.hp2 HG02735.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+30613G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585439 | |||||||
chr3:49585565 | C | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+30739C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585565 | |||||||
chr3:49585700 | CTAAT | C | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.224+30876_224+3087 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49585700 | ||||||
chr3:49585880 | G | A | 1 | a0010c0015t0002g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.224+31054G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49585880 | |||||||
chr3:49586013 | A | G | 7 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(4): Show |
7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+31187A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586013 | |||||||
chr3:49586076 | C | G | 1 | a0001c0001t0003g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.224+31250C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586076 | |||||||
chr3:49586130 | T | C | 1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224+31304T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586130 | |||||||
chr3:49586251 | G | C | 4 | a0001c0001t0009g0093 a0001c0001t0009g0148 a0008c0014t0009g0041 others(1): Show |
4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+31425G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586251 | |||||||
chr3:49586326 | C | CTCTA | 64 | a0001c0001t0002g0094 a0001c0001t0002g0104 a0001c0001t0002g0106 others(61): Show |
64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.224+31535_224+3153 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | ||||||
chr3:49586326 | C | CTCTATCT others(1): Show |
56 | a0001c0001t0002g0096 a0001c0001t0002g0101 a0001c0001t0002g0109 others(53): Show |
56 | HG00140.hp1 HG01081.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.224+31531_224+3153 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | ||||||
chr3:49586326 | C | CTCTATCT others(5): Show |
8 | a0001c0001t0002g0112 a0001c0001t0002g0138 a0001c0001t0003g0158 others(5): Show |
8 | HG02735.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+31527_224+3153 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | ||||||
chr3:49586326 | C | CTCTATCT others(9): Show |
4 | a0002c0002t0001g0088 a0002c0002t0001g0183 a0002c0002t0001g0184 others(1): Show |
4 | HG02970.hp2 HG03710.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+31523_224+3153 others(20): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | ||||||
chr3:49586326 | CTCTA | C | 4 | a0001c0001t0009g0148 a0001c0001t0015g0141 a0002c0020t0024g0165 others(1): Show |
4 | HG01109.hp1 HG01928.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.224+31535_224+3153 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49586326 | ||||||
chr3:49586583 | C | T | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.224+31757C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586583 | |||||||
chr3:49586632 | T | C | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.224+31806T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586632 | |||||||
chr3:49586662 | T | G | 171 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.224+31836T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586662 | |||||||
chr3:49586944 | A | C | 62 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.224+32118A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586944 | |||||||
chr3:49586982 | G | A | 1 | a0019c0038t0027g0004 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.224+32156G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49586982 | |||||||
chr3:49587219 | G | A | 14 | a0003c0003t0004g0014 a0003c0003t0004g0015 a0003c0003t0004g0017 others(11): Show |
14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.224+32393G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49587219 | |||||||
chr3:49587376 | C | T | 1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224+32550C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49587376 | |||||||
chr3:49587660 | G | C | 7 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(4): Show |
7 | HG01074.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.224+32834G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49587660 | |||||||
chr3:49587887 | T | TTTTCTTT others(17): Show |
1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.224+33064_224+3306 others(28): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTC | 20 | a0001c0001t0007g0042 a0001c0001t0020g0108 a0001c0016t0003g0163 others(17): Show |
21 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.224+33101_224+3310 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTCTT others(3): Show |
33 | a0001c0001t0002g0112 a0001c0001t0002g0150 a0001c0001t0002g0176 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.224+33096_224+3310 others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTCTT others(8): Show |
34 | a0001c0001t0002g0094 a0001c0001t0002g0103 a0001c0001t0002g0106 others(31): Show |
34 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.224+33091_224+3310 others(19): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTCTT others(13): Show |
30 | a0001c0001t0002g0096 a0001c0001t0002g0104 a0001c0001t0002g0114 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.224+33086_224+3310 others(24): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTCTT others(18): Show |
27 | a0001c0001t0002g0109 a0001c0001t0002g0130 a0001c0001t0002g0132 others(24): Show |
27 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.224+33081_224+3310 others(29): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTCTT others(23): Show |
11 | a0001c0001t0003g0040 a0001c0001t0003g0121 a0001c0001t0003g0125 others(8): Show |
11 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.224+33076_224+3310 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | T | TTTTTCTT others(28): Show |
1 | a0002c0019t0001g0055 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.224+33071_224+3310 others(39): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | TTTTTC | T | 11 | a0002c0002t0001g0151 a0002c0002t0001g0179 a0002c0002t0001g0180 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.224+33101_224+3310 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | TTTTTCTT others(3): Show |
T | 6 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.224+33096_224+3310 others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587887 | TTTTTCTT others(13): Show |
T | 2 | a0001c0001t0003g0158 a0001c0001t0015g0157 |
2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+33086_224+3310 others(24): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587887 | ||||||
chr3:49587928 | T | TTTTCTTT others(22): Show |
1 | a0001c0001t0021g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.224+33105_224+3310 others(33): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49587928 | ||||||
chr3:49588218 | G | A | 1 | a0002c0002t0019g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.224+33392G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588218 | |||||||
chr3:49588500 | A | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.224+33674A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588500 | |||||||
chr3:49588703 | G | T | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+33877G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588703 | |||||||
chr3:49588749 | T | G | 75 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.224+33923T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588749 | |||||||
chr3:49588873 | G | A | 171 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.224+34047G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49588873 | |||||||
chr3:49588919 | G | GT | 7 | a0001c0001t0002g0132 a0001c0001t0029g0120 a0003c0004t0004g0016 others(4): Show |
7 | HG00544.hp2 HG00642.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+34106dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49588919 | ||||||
chr3:49589040 | G | A | 1 | a0001c0001t0022g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224+34214G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589040 | |||||||
chr3:49589082 | A | ATTTTTT | 86 | a0001c0001t0002g0094 a0001c0001t0002g0101 a0001c0001t0002g0103 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.224+34265_224+3427 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589082 | ||||||
chr3:49589082 | A | ATTTTTTT | 58 | a0001c0001t0002g0096 a0001c0001t0002g0130 a0001c0001t0002g0150 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.224+34264_224+3427 others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589082 | ||||||
chr3:49589082 | A | ATTTTTTT others(1): Show |
10 | a0002c0002t0001g0052 a0002c0002t0001g0060 a0002c0002t0001g0077 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.224+34263_224+3427 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589082 | ||||||
chr3:49589167 | C | T | 13 | a0001c0016t0003g0163 a0002c0002t0001g0087 a0002c0002t0001g0088 others(10): Show |
13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+34341C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589167 | |||||||
chr3:49589211 | C | T | 4 | a0001c0001t0002g0160 a0007c0011t0001g0065 a0007c0011t0001g0066 others(1): Show |
4 | HG00544.hp2 HG02735.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+34385C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589211 | |||||||
chr3:49589233 | C | T | 13 | a0001c0016t0003g0163 a0002c0002t0001g0087 a0002c0002t0001g0088 others(10): Show |
13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+34407C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589233 | |||||||
chr3:49589479 | C | T | 1 | a0005c0007t0031g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224+34653C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589479 | |||||||
chr3:49589513 | C | CT | 181 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(178): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.224+34698dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589513 | ||||||
chr3:49589646 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0025c0029t0003g0048 |
3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.224+34820A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49589646 | |||||||
chr3:49589844 | G | GT | 69 | a0001c0001t0002g0160 a0001c0001t0003g0152 a0001c0001t0003g0153 others(66): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.224+35030dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49589844 | ||||||
chr3:49590027 | G | A | 2 | a0002c0002t0001g0080 a0002c0002t0001g0082 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.225-34948G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590027 | |||||||
chr3:49590106 | G | C | 1 | a0019c0038t0027g0004 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225-34869G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590106 | |||||||
chr3:49590135 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225-34840C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590135 | |||||||
chr3:49590327 | AAAAC | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-34644_225-3464 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49590327 | ||||||
chr3:49590420 | G | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0177 |
2 | HG02004.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.225-34555G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590420 | |||||||
chr3:49590564 | C | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-34411C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590564 | |||||||
chr3:49590714 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.225-34261C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590714 | |||||||
chr3:49590722 | CATA | C | 10 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0004t0004g0028 others(7): Show |
11 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-34247_225-3424 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49590722 | ||||||
chr3:49590767 | A | T | 1 | a0002c0002t0001g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225-34208A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49590767 | |||||||
chr3:49591373 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225-33602C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591373 | |||||||
chr3:49591588 | ATTTTTG | A | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 |
3 | HG00323.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.225-33369_225-3336 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49591588 | ||||||
chr3:49591605 | T | G | 1 | a0001c0001t0002g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-33370T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591605 | |||||||
chr3:49591606 | G | T | 1 | a0001c0001t0002g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-33369G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591606 | |||||||
chr3:49591958 | G | A | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-33017G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49591958 | |||||||
chr3:49592122 | A | T | 1 | a0001c0001t0007g0007 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.225-32853A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592122 | |||||||
chr3:49592202 | C | T | 4 | a0001c0001t0002g0160 a0007c0011t0001g0065 a0007c0011t0001g0066 others(1): Show |
4 | HG00544.hp2 HG02735.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-32773C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592202 | |||||||
chr3:49592256 | C | G | 3 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 |
3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.225-32719C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592256 | |||||||
chr3:49592340 | C | A | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-32635C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592340 | |||||||
chr3:49592476 | G | A | 1 | a0001c0016t0003g0163 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.225-32499G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592476 | |||||||
chr3:49592510 | T | C | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-32465T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592510 | |||||||
chr3:49592645 | G | T | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-32330G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49592645 | |||||||
chr3:49593733 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-31242T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593733 | |||||||
chr3:49593734 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-31241C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593734 | |||||||
chr3:49593788 | G | T | 59 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-31187G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593788 | |||||||
chr3:49593805 | G | GT | 7 | a0001c0001t0002g0101 a0001c0001t0002g0134 a0001c0001t0002g0146 others(4): Show |
7 | HG01884.hp2 HG01934.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-31155dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49593805 | ||||||
chr3:49593812 | T | G | 1 | a0003c0003t0004g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-31163T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593812 | |||||||
chr3:49593893 | C | T | 72 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.225-31082C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593893 | |||||||
chr3:49593903 | C | T | 1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225-31072C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593903 | |||||||
chr3:49593960 | G | A | 17 | a0001c0001t0002g0094 a0001c0001t0002g0104 a0001c0001t0002g0106 others(14): Show |
17 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.225-31015G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49593960 | |||||||
chr3:49594152 | G | A | 13 | a0001c0016t0003g0163 a0002c0002t0001g0087 a0002c0002t0001g0088 others(10): Show |
13 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-30823G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594152 | |||||||
chr3:49594227 | G | A | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-30748G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594227 | |||||||
chr3:49594236 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.225-30739G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594236 | |||||||
chr3:49594257 | A | G | 1 | a0003c0003t0004g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-30718A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594257 | |||||||
chr3:49594521 | C | T | 1 | a0002c0002t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225-30454C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594521 | |||||||
chr3:49594876 | G | A | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-30099G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594876 | |||||||
chr3:49594883 | T | A | 1 | a0003c0003t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-30092T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49594883 | |||||||
chr3:49594890 | A | AT | 147 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.225-30070dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49594890 | ||||||
chr3:49595089 | C | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-29886C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49595089 | |||||||
chr3:49595192 | A | AT | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-29766dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49595192 | ||||||
chr3:49595194 | T | TC | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-29781_225-2978 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49595194 | |||||||
chr3:49595195 | T | C | 144 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.225-29780T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49595195 | |||||||
chr3:49596239 | C | T | 1 | a0001c0001t0030g0143 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-28736C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49596239 | |||||||
chr3:49596670 | A | G | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-28305A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49596670 | |||||||
chr3:49596679 | C | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0025c0029t0003g0048 |
3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.225-28296C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49596679 | |||||||
chr3:49597161 | T | C | 7 | a0002c0002t0005g0038 a0002c0002t0005g0061 a0002c0002t0005g0073 others(4): Show |
7 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-27814T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597161 | |||||||
chr3:49597263 | G | A | 61 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-27712G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597263 | |||||||
chr3:49597273 | C | T | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-27702C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597273 | |||||||
chr3:49597402 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0025c0029t0003g0048 |
3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.225-27573C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597402 | |||||||
chr3:49597435 | A | G | 1 | a0001c0001t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225-27540A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597435 | |||||||
chr3:49597601 | G | C | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-27374G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597601 | |||||||
chr3:49597921 | G | A | 60 | a0001c0001t0002g0160 a0001c0001t0012g0056 a0001c0016t0003g0163 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.225-27054G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597921 | |||||||
chr3:49597923 | G | A | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-27052G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597923 | |||||||
chr3:49597923 | G | C | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-27052G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49597923 | |||||||
chr3:49598114 | A | T | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-26861A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49598114 | |||||||
chr3:49598512 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.225-26463C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49598512 | |||||||
chr3:49598801 | G | C | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-26174G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49598801 | |||||||
chr3:49599468 | G | A | 3 | a0002c0002t0001g0169 a0002c0002t0001g0173 a0002c0002t0001g0174 |
3 | HG01515.hp1 HG01517.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.225-25507G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599468 | |||||||
chr3:49599544 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.225-25431G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599544 | |||||||
chr3:49599616 | C | G | 4 | a0001c0001t0011g0097 a0001c0001t0011g0124 a0001c0001t0011g0126 others(1): Show |
4 | HG00323.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-25359C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599616 | |||||||
chr3:49599666 | A | C | 8 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-25309A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599666 | |||||||
chr3:49599951 | G | A | 8 | a0001c0001t0002g0160 a0006c0005t0008g0063 a0006c0005t0008g0067 others(5): Show |
8 | HG00544.hp2 HG02735.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.225-25024G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49599951 | |||||||
chr3:49600067 | G | C | 2 | a0001c0001t0002g0160 a0003c0003t0004g0045 |
2 | NA18906.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.225-24908G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600067 | |||||||
chr3:49600068 | C | G | 1 | a0001c0001t0002g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.225-24907C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600068 | |||||||
chr3:49600609 | C | T | 3 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0002c0018t0001g0010 |
3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.225-24366C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600609 | |||||||
chr3:49600651 | AAAATT | A | 64 | a0001c0001t0002g0160 a0001c0001t0007g0007 a0001c0001t0007g0008 others(61): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.225-24322_225-2431 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49600651 | ||||||
chr3:49600667 | G | T | 1 | a0003c0003t0004g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.225-24308G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49600667 | |||||||
chr3:49601380 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.225-23595G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49601380 | |||||||
chr3:49601689 | T | G | 2 | a0001c0001t0007g0007 a0001c0001t0007g0008 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.225-23286T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49601689 | |||||||
chr3:49601927 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.225-23048A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49601927 | |||||||
chr3:49602020 | A | T | 2 | a0002c0002t0001g0062 a0002c0002t0001g0069 |
2 | HG01167.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.225-22955A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602020 | |||||||
chr3:49602102 | T | C | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-22873T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602102 | |||||||
chr3:49602173 | G | C | 2 | a0001c0001t0012g0115 a0001c0001t0012g0135 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-22802G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602173 | |||||||
chr3:49602370 | G | T | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.225-22605G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602370 | |||||||
chr3:49602377 | G | T | 1 | a0003c0003t0004g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-22598G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602377 | |||||||
chr3:49602442 | T | A | 1 | a0001c0001t0007g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.225-22533T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602442 | |||||||
chr3:49602445 | A | AT | 6 | a0001c0001t0022g0091 a0001c0001t0030g0143 a0001c0027t0003g0185 others(3): Show |
6 | HG00544.hp1 HG01167.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-22511dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49602445 | ||||||
chr3:49602445 | A | T | 1 | a0001c0001t0007g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.225-22530A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602445 | |||||||
chr3:49602445 | AT | A | 11 | a0001c0001t0003g0127 a0002c0002t0001g0062 a0002c0002t0001g0089 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-22511delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49602445 | ||||||
chr3:49602532 | G | A | 1 | a0019c0038t0027g0004 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225-22443G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602532 | |||||||
chr3:49602780 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.225-22195C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602780 | |||||||
chr3:49602941 | G | A | 3 | a0001c0001t0002g0101 a0001c0001t0002g0113 a0001c0001t0002g0134 |
3 | HG02055.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.225-22034G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602941 | |||||||
chr3:49602994 | C | T | 3 | a0001c0001t0002g0114 a0001c0001t0002g0132 a0001c0001t0002g0139 |
3 | HG00642.hp2 HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.225-21981C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49602994 | |||||||
chr3:49603114 | GGGCCCCT others(22): Show |
G | 6 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-21849_225-2182 others(33): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49603114 | ||||||
chr3:49603160 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0023g0144 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.225-21815C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49603160 | |||||||
chr3:49603616 | G | A | 7 | a0002c0002t0005g0038 a0002c0002t0005g0061 a0002c0002t0005g0073 others(4): Show |
7 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-21359G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49603616 | |||||||
chr3:49604594 | C | T | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.225-20381C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604594 | |||||||
chr3:49604643 | G | A | 2 | a0001c0001t0012g0115 a0001c0001t0012g0135 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-20332G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604643 | |||||||
chr3:49604703 | C | G | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20272C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604703 | |||||||
chr3:49604704 | A | C | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20271A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604704 | |||||||
chr3:49604705 | G | A | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20270G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604705 | |||||||
chr3:49604944 | T | C | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-20031T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604944 | |||||||
chr3:49604997 | C | T | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-19978C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49604997 | |||||||
chr3:49605264 | T | A | 1 | a0002c0002t0001g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225-19711T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605264 | |||||||
chr3:49605303 | A | C | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-19672A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605303 | |||||||
chr3:49605307 | A | T | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19668A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605307 | |||||||
chr3:49605308 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19667T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605308 | |||||||
chr3:49605313 | TTA | T | 14 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0002c0002t0001g0169 others(11): Show |
14 | HG01515.hp1 HG01517.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-19650_225-1964 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605313 | ||||||
chr3:49605327 | T | A | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-19648T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605327 | |||||||
chr3:49605405 | T | A | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-19570T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605405 | |||||||
chr3:49605436 | TATTATAT others(113): Show |
T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19536_225-1941 others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605436 | ||||||
chr3:49605439 | T | TATATATA others(23): Show |
3 | a0003c0003t0010g0011 a0003c0003t0010g0012 a0003c0003t0010g0013 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.225-19483_225-1945 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605439 | ||||||
chr3:49605439 | TATATATA others(23): Show |
T | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-19483_225-1945 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605439 | ||||||
chr3:49605447 | T | A | 63 | a0001c0001t0012g0056 a0001c0001t0015g0157 a0001c0017t0002g0105 others(60): Show |
63 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.225-19528T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605447 | |||||||
chr3:49605454 | A | T | 2 | a0001c0001t0015g0157 a0001c0017t0002g0105 |
2 | HG06807.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19521A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605454 | |||||||
chr3:49605461 | TTA | T | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-19507_225-1950 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605461 | ||||||
chr3:49605469 | A | T | 58 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.225-19506A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605469 | |||||||
chr3:49605476 | A | ATTATATA others(87): Show |
1 | a0001c0001t0003g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19492_225-1949 others(98): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605476 | ||||||
chr3:49605477 | T | A | 4 | a0007c0011t0001g0065 a0007c0011t0001g0066 a0013c0010t0001g0064 others(1): Show |
4 | HG00544.hp2 HG02735.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19498T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605477 | |||||||
chr3:49605477 | T | TTATATAA others(39): Show |
8 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(5): Show |
8 | HG01074.hp2 HG01884.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-19454_225-1945 others(50): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605477 | ||||||
chr3:49605477 | T | TTATATAT others(39): Show |
1 | a0003c0003t0004g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-19492_225-1949 others(50): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605477 | ||||||
chr3:49605477 | T | TTATATAT others(64): Show |
1 | a0001c0001t0002g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.225-19492_225-1949 others(75): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605477 | ||||||
chr3:49605479 | A | ATATAATA others(31): Show |
1 | a0003c0004t0004g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-19484_225-1948 others(42): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605479 | ||||||
chr3:49605484 | A | T | 83 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.225-19491A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605484 | |||||||
chr3:49605491 | T | A | 1 | a0001c0017t0002g0105 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.225-19484T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605491 | |||||||
chr3:49605491 | T | TTATATAT others(4): Show |
1 | a0003c0003t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-19477_225-1947 others(15): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605491 | ||||||
chr3:49605492 | T | A | 79 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.225-19483T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605492 | |||||||
chr3:49605493 | ATATATAA others(7): Show |
A | 1 | a0003c0023t0016g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-19467_225-1945 others(18): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605493 | ||||||
chr3:49605499 | A | T | 3 | a0007c0011t0001g0065 a0013c0010t0001g0064 a0013c0010t0001g0164 |
3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19476A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605499 | |||||||
chr3:49605500 | A | T | 78 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.225-19475A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605500 | |||||||
chr3:49605507 | T | A | 3 | a0001c0017t0002g0105 a0002c0002t0001g0070 a0007c0011t0001g0066 |
3 | HG00544.hp2 HG02615.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19468T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605507 | |||||||
chr3:49605513 | A | ATATTTTA others(24): Show |
2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-19462_225-1946 others(35): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605513 | |||||||
chr3:49605513 | A | T | 1 | a0003c0023t0016g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-19462A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605513 | |||||||
chr3:49605513 | AAT | A | 129 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.225-19452_225-1945 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605513 | ||||||
chr3:49605513 | AATATAT | A | 4 | a0006c0005t0008g0063 a0006c0005t0008g0067 a0006c0005t0008g0068 others(1): Show |
4 | NA18951.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19456_225-1945 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605513 | ||||||
chr3:49605514 | A | T | 10 | a0001c0001t0002g0137 a0001c0001t0007g0007 a0001c0001t0007g0008 others(7): Show |
10 | HG00544.hp2 HG01074.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-19461A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605514 | |||||||
chr3:49605515 | T | TA | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-19459dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605515 | ||||||
chr3:49605515 | T | TATATA | 6 | a0001c0001t0002g0137 a0001c0001t0007g0007 a0001c0001t0007g0008 others(3): Show |
6 | HG01074.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-19459_225-1945 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605515 | ||||||
chr3:49605516 | A | ATATAT | 2 | a0002c0002t0001g0070 a0007c0011t0001g0066 |
2 | HG00544.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.225-19458_225-1945 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605516 | ||||||
chr3:49605516 | A | ATATATAA others(90): Show |
1 | a0001c0001t0003g0095 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.225-19453_225-1945 others(101): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605516 | ||||||
chr3:49605516 | A | T | 1 | a0001c0001t0003g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19459A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605516 | |||||||
chr3:49605518 | A | AATATATA others(12): Show |
1 | a0001c0001t0002g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225-19457_225-1945 others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605518 | |||||||
chr3:49605524 | A | AT | 2 | a0001c0001t0002g0150 a0002c0020t0024g0165 |
2 | HG02723.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.225-19451_225-1945 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605524 | |||||||
chr3:49605524 | A | T | 5 | a0007c0011t0001g0065 a0011c0013t0013g0049 a0011c0013t0013g0050 others(2): Show |
5 | HG02572.hp2 HG02735.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19451A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605524 | |||||||
chr3:49605525 | A | T | 2 | a0002c0002t0001g0070 a0007c0011t0001g0066 |
2 | HG00544.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.225-19450A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605525 | |||||||
chr3:49605531 | A | T | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-19444A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605531 | |||||||
chr3:49605532 | A | T | 3 | a0001c0001t0002g0138 a0001c0001t0003g0095 a0001c0017t0002g0105 |
3 | HG03942.hp1 HG04228.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19443A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605532 | |||||||
chr3:49605539 | TTA | T | 64 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0152 others(61): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.225-19428_225-1942 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605539 | ||||||
chr3:49605540 | T | TATATATA others(26): Show |
1 | a0007c0011t0001g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-19428_225-1942 others(37): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605540 | ||||||
chr3:49605544 | T | TA | 3 | a0007c0011t0001g0065 a0013c0010t0001g0064 a0013c0010t0001g0164 |
3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19430dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605544 | ||||||
chr3:49605545 | A | AT | 2 | a0001c0001t0012g0115 a0001c0001t0012g0135 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-19429dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605545 | ||||||
chr3:49605547 | AT | A | 14 | a0003c0003t0004g0014 a0003c0003t0004g0015 a0003c0003t0004g0017 others(11): Show |
14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-19424delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605547 | ||||||
chr3:49605549 | T | A | 6 | a0001c0001t0012g0115 a0001c0001t0012g0135 a0002c0002t0001g0070 others(3): Show |
6 | HG00280.hp1 HG01515.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-19426T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605549 | |||||||
chr3:49605550 | T | A | 7 | a0001c0001t0002g0138 a0001c0017t0002g0105 a0007c0011t0001g0065 others(4): Show |
7 | HG00544.hp2 HG02683.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-19425T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605550 | |||||||
chr3:49605550 | T | TA | 4 | a0001c0001t0003g0095 a0001c0001t0003g0119 a0011c0013t0013g0049 others(1): Show |
4 | HG02572.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19425_225-1942 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605550 | |||||||
chr3:49605551 | T | A | 2 | a0001c0001t0012g0115 a0001c0001t0012g0135 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-19424T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605551 | |||||||
chr3:49605556 | A | ATTT | 2 | a0001c0001t0002g0138 a0001c0017t0002g0105 |
2 | HG03942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19419_225-1941 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605556 | |||||||
chr3:49605556 | A | T | 1 | a0007c0011t0001g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-19419A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605556 | |||||||
chr3:49605557 | A | T | 1 | a0007c0011t0001g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-19418A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605557 | |||||||
chr3:49605558 | T | C | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19417T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605558 | |||||||
chr3:49605564 | T | A | 3 | a0001c0001t0002g0138 a0001c0017t0002g0105 a0007c0011t0001g0066 |
3 | HG00544.hp2 HG03942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19411T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605564 | |||||||
chr3:49605564 | T | TAATATAT others(127): Show |
4 | a0001c0001t0003g0040 a0001c0001t0003g0121 a0001c0001t0003g0127 others(1): Show |
4 | HG02622.hp2 HG02896.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-19411_225-1941 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605564 | |||||||
chr3:49605564 | T | TAATATAT others(25): Show |
1 | a0002c0002t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.225-19411_225-1941 others(36): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605564 | |||||||
chr3:49605565 | T | A | 2 | a0001c0001t0003g0136 a0001c0001t0015g0141 |
2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.225-19410T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605565 | |||||||
chr3:49605569 | TA | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19405delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605569 | |||||||
chr3:49605571 | T | G | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19404T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605571 | |||||||
chr3:49605571 | T | TA | 2 | a0001c0001t0002g0112 a0001c0001t0002g0150 |
2 | NA18973.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.225-19404_225-1940 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605571 | |||||||
chr3:49605571 | T | TTA | 6 | a0003c0003t0004g0017 a0003c0003t0004g0018 a0003c0003t0004g0019 others(3): Show |
6 | HG01074.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-19396_225-1939 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605571 | ||||||
chr3:49605572 | T | A | 2 | a0001c0001t0003g0136 a0001c0001t0015g0141 |
2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.225-19403T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605572 | |||||||
chr3:49605572 | T | TTTATATA | 3 | a0007c0011t0001g0065 a0013c0010t0001g0064 a0013c0010t0001g0164 |
3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19403_225-1940 others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605572 | |||||||
chr3:49605573 | ATATATAT | A | 54 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(51): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.225-19393_225-1938 others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605573 | ||||||
chr3:49605579 | A | T | 6 | a0001c0001t0003g0040 a0001c0001t0003g0121 a0001c0001t0003g0127 others(3): Show |
6 | HG00544.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-19396A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605579 | |||||||
chr3:49605580 | T | A | 13 | a0001c0001t0002g0138 a0001c0001t0003g0040 a0001c0001t0003g0121 others(10): Show |
13 | HG00544.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-19395T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605580 | |||||||
chr3:49605580 | T | TTA | 37 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0106 others(34): Show |
37 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.225-19389_225-1938 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(94): Show |
27 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0103 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.225-19388_225-1938 others(105): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(127): Show |
2 | a0001c0001t0002g0109 a0001c0001t0002g0132 |
2 | HG00642.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.225-19388_225-1938 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(61): Show |
1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225-19388_225-1938 others(72): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(94): Show |
7 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(4): Show |
7 | HG00323.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-19388_225-1938 others(105): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(127): Show |
2 | a0001c0001t0007g0007 a0001c0001t0007g0008 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.225-19388_225-1938 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(159): Show |
2 | a0001c0001t0003g0046 a0025c0029t0003g0048 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.225-19388_225-1938 others(170): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(160): Show |
1 | a0001c0001t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225-19388_225-1938 others(171): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(92): Show |
1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-19388_225-1938 others(103): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(2): Show |
3 | a0007c0011t0001g0065 a0013c0010t0001g0064 a0013c0010t0001g0164 |
3 | HG02735.hp1 NA18963.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.225-19387_225-1938 others(13): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTATATAT others(68): Show |
1 | a0001c0001t0011g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.225-19387_225-1938 others(79): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTTATATA others(19): Show |
3 | a0001c0001t0003g0095 a0011c0013t0013g0049 a0011c0013t0013g0050 |
3 | HG02572.hp2 HG02922.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.225-19394_225-1939 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605580 | T | TTTATATA others(52): Show |
1 | a0001c0001t0003g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19394_225-1939 others(63): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605580 | ||||||
chr3:49605585 | T | C | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19390T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605585 | |||||||
chr3:49605588 | T | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19387T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605588 | |||||||
chr3:49605589 | T | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-19386T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605589 | |||||||
chr3:49605591 | T | C | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19384T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605591 | |||||||
chr3:49605597 | A | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19378A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605597 | |||||||
chr3:49605602 | TA | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19372delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605602 | |||||||
chr3:49605603 | A | G | 1 | a0002c0002t0001g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.225-19372A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605603 | |||||||
chr3:49605604 | T | A | 4 | a0001c0001t0003g0136 a0001c0001t0015g0141 a0002c0002t0001g0087 others(1): Show |
4 | HG01109.hp1 HG03139.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-19371T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605604 | |||||||
chr3:49605604 | T | G | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19371T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605604 | |||||||
chr3:49605604 | T | TTATATAT others(52): Show |
1 | a0019c0038t0027g0004 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(63): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605604 | ||||||
chr3:49605611 | T | TAATATAT others(127): Show |
1 | a0004c0006t0002g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-19364_225-1936 others(138): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605611 | |||||||
chr3:49605612 | T | A | 21 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0106 others(18): Show |
21 | HG00544.hp1 HG01081.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.225-19363T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605612 | |||||||
chr3:49605617 | A | ATATTTAT others(95): Show |
3 | a0001c0001t0002g0138 a0001c0001t0022g0091 a0001c0017t0002g0105 |
3 | HG01928.hp1 HG03942.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.225-19356_225-1935 others(106): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605617 | A | ATATTTAT others(124): Show |
1 | a0001c0001t0030g0143 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(135): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605617 | A | ATATTTAT others(86): Show |
1 | a0001c0001t0026g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(97): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605617 | A | ATATTTAT others(128): Show |
1 | a0001c0001t0003g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.225-19356_225-1935 others(139): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605617 | A | ATATTTAT others(128): Show |
26 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0106 others(23): Show |
26 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.225-19356_225-1935 others(139): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605617 | A | ATATTTAT others(194): Show |
1 | a0001c0001t0003g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(205): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605617 | A | ATATTTAT others(159): Show |
1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-19356_225-1935 others(170): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605617 | ||||||
chr3:49605620 | A | C | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19355A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605620 | |||||||
chr3:49605620 | A | T | 35 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0106 others(32): Show |
35 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.225-19355A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605620 | |||||||
chr3:49605626 | AT | A | 4 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19348delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605626 | |||||||
chr3:49605633 | TTAC | T | 4 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19341_225-1933 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605633 | |||||||
chr3:49605634 | T | A | 4 | a0001c0001t0002g0138 a0001c0001t0003g0125 a0003c0004t0004g0016 others(1): Show |
4 | HG00639.hp2 HG02109.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-19341T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605634 | |||||||
chr3:49605636 | C | A | 37 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0106 others(34): Show |
37 | HG00544.hp1 HG00639.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.225-19339C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605636 | |||||||
chr3:49605636 | C | CATATATG others(29): Show |
5 | a0001c0001t0002g0132 a0004c0006t0002g0034 a0004c0006t0002g0036 others(2): Show |
5 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-19306_225-1930 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605636 | ||||||
chr3:49605636 | C | CATATATG others(29): Show |
1 | a0001c0001t0003g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.225-19304_225-1930 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605636 | ||||||
chr3:49605637 | A | G | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19338A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605637 | |||||||
chr3:49605642 | TG | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19332delG | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605642 | |||||||
chr3:49605643 | G | T | 9 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0152 others(6): Show |
9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-19332G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605643 | |||||||
chr3:49605645 | A | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19330A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605645 | |||||||
chr3:49605652 | ATTAT | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19322_225-1931 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605652 | |||||||
chr3:49605658 | TATA | T | 4 | a0003c0004t0006g0001 a0003c0004t0006g0030 a0003c0004t0006g0031 others(1): Show |
5 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19313_225-1931 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605658 | ||||||
chr3:49605660 | T | A | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19315T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605660 | |||||||
chr3:49605661 | A | T | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19314A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605661 | |||||||
chr3:49605663 | T | C | 5 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-19312T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605663 | |||||||
chr3:49605670 | T | A | 41 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0106 others(38): Show |
41 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.225-19305T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605670 | |||||||
chr3:49605670 | T | TAAATATA others(29): Show |
28 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0103 others(25): Show |
28 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.225-19304_225-1930 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605670 | ||||||
chr3:49605672 | C | A | 148 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.225-19303C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605672 | |||||||
chr3:49605672 | C | CATATATG others(29): Show |
2 | a0001c0001t0002g0130 a0001c0001t0011g0097 |
2 | HG02735.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.225-19296_225-1926 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605672 | ||||||
chr3:49605672 | C | CATATATG others(65): Show |
2 | a0001c0001t0011g0124 a0001c0001t0011g0126 |
2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.225-19270_225-1926 others(76): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605672 | ||||||
chr3:49605691 | A | ATATATAA others(29): Show |
2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-19270_225-1926 others(40): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605691 | ||||||
chr3:49605729 | T | G | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-19246T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605729 | |||||||
chr3:49605740 | AATAT | A | 59 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-19229_225-1922 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605740 | ||||||
chr3:49605767 | A | T | 1 | a0001c0001t0002g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.225-19208A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605767 | |||||||
chr3:49605785 | AATATATA others(11): Show |
A | 1 | a0001c0001t0022g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.225-19173_225-1915 others(22): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605785 | ||||||
chr3:49605869 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19106T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605869 | |||||||
chr3:49605872 | T | TTATATAT others(23): Show |
57 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(54): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.225-19078_225-1907 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605872 | ||||||
chr3:49605872 | T | TTATATAT others(24): Show |
1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-19078_225-1907 others(35): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605872 | ||||||
chr3:49605884 | A | ATAAATAT others(25): Show |
1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-19078_225-1907 others(36): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605884 | ||||||
chr3:49605898 | G | A | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.225-19077G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605898 | |||||||
chr3:49605906 | A | ATATAGAT others(22): Show |
1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19069_225-1906 others(33): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605906 | |||||||
chr3:49605909 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19066T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605909 | |||||||
chr3:49605912 | A | T | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-19063A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605912 | |||||||
chr3:49605913 | T | C | 1 | a0001c0001t0022g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.225-19062T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605913 | |||||||
chr3:49605923 | T | G | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-19052T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605923 | |||||||
chr3:49605925 | T | TA | 99 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(96): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.225-19046dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49605925 | ||||||
chr3:49605929 | ATCT | A | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.225-19045_225-1904 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605929 | |||||||
chr3:49605932 | T | A | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-19043T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605932 | |||||||
chr3:49605935 | T | C | 82 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.225-19040T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605935 | |||||||
chr3:49605938 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-19037T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605938 | |||||||
chr3:49605939 | A | G | 2 | a0002c0002t0001g0080 a0002c0002t0001g0082 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.225-19036A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49605939 | |||||||
chr3:49606018 | ATATATT | A | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-18951_225-1894 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606018 | ||||||
chr3:49606019 | T | A | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-18956T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606019 | |||||||
chr3:49606032 | A | C | 1 | a0003c0004t0006g0116 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225-18943A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606032 | |||||||
chr3:49606040 | T | A | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18935T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606040 | |||||||
chr3:49606041 | T | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18934T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606041 | |||||||
chr3:49606060 | A | AATAATAA others(12): Show |
1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18912_225-1891 others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606060 | ||||||
chr3:49606071 | TA | T | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-18899delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606071 | ||||||
chr3:49606074 | A | T | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18901A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606074 | |||||||
chr3:49606082 | A | T | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18893A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606082 | |||||||
chr3:49606083 | AT | A | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-18886delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606083 | ||||||
chr3:49606085 | T | A | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18890T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606085 | |||||||
chr3:49606087 | T | A | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18888T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606087 | |||||||
chr3:49606096 | A | T | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18879A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606096 | |||||||
chr3:49606097 | A | T | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18878A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606097 | |||||||
chr3:49606098 | C | T | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18877C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606098 | |||||||
chr3:49606098 | CATATA | C | 59 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-18871_225-1886 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606098 | ||||||
chr3:49606108 | A | T | 1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18867A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606108 | |||||||
chr3:49606111 | A | T | 1 | a0001c0001t0003g0131 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.225-18864A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606111 | |||||||
chr3:49606118 | C | A | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18857C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606118 | |||||||
chr3:49606118 | C | CGTATAAT others(26): Show |
1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18852_225-1885 others(37): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | ||||||
chr3:49606118 | C | CGTATATA others(25): Show |
30 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0114 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.225-18841_225-1884 others(36): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | ||||||
chr3:49606118 | C | CGTATATA others(57): Show |
1 | a0001c0001t0007g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.225-18841_225-1884 others(68): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | ||||||
chr3:49606118 | C | CGTATATA others(57): Show |
2 | a0001c0001t0007g0007 a0001c0001t0007g0008 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.225-18841_225-1884 others(68): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606118 | ||||||
chr3:49606118 | C | T | 3 | a0003c0003t0004g0014 a0010c0015t0002g0102 a0010c0015t0002g0107 |
3 | HG01891.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.225-18857C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606118 | |||||||
chr3:49606119 | G | C | 1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18856G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606119 | |||||||
chr3:49606120 | T | A | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18855T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606120 | |||||||
chr3:49606121 | A | T | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18854A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606121 | |||||||
chr3:49606126 | T | TTA | 14 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(11): Show |
14 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-18842_225-1884 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606126 | ||||||
chr3:49606133 | T | A | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18842T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606133 | |||||||
chr3:49606133 | T | TAA | 117 | a0001c0001t0002g0101 a0001c0001t0002g0103 a0001c0001t0002g0104 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.225-18841_225-1884 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606133 | ||||||
chr3:49606134 | A | AAATATAT others(27): Show |
1 | a0001c0027t0003g0185 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.225-18841_225-1884 others(38): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606134 | |||||||
chr3:49606135 | C | T | 119 | a0001c0001t0002g0101 a0001c0001t0002g0103 a0001c0001t0002g0104 others(116): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.225-18840C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606135 | |||||||
chr3:49606148 | T | C | 3 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0033t0004g0025 |
3 | HG01069.hp2 HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.225-18827T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606148 | |||||||
chr3:49606150 | T | C | 1 | a0003c0003t0004g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.225-18825T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606150 | |||||||
chr3:49606163 | T | G | 4 | a0006c0005t0008g0063 a0006c0005t0008g0067 a0006c0005t0008g0068 others(1): Show |
4 | NA18951.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-18812T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606163 | |||||||
chr3:49606167 | T | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18808T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606167 | |||||||
chr3:49606172 | T | A | 1 | a0001c0001t0003g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.225-18803T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606172 | |||||||
chr3:49606179 | GTA | G | 94 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0112 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.225-18788_225-1878 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606179 | ||||||
chr3:49606181 | A | ATATATTA others(21): Show |
33 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0002g0111 others(30): Show |
33 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.225-18789_225-1878 others(32): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | ||||||
chr3:49606181 | A | ATATATTA others(136): Show |
1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-18789_225-1878 others(147): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | ||||||
chr3:49606181 | A | ATATATTA others(51): Show |
6 | a0001c0001t0002g0101 a0001c0001t0002g0104 a0001c0001t0002g0109 others(3): Show |
6 | HG02055.hp1 HG02258.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-18789_225-1878 others(62): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | ||||||
chr3:49606181 | A | ATATATTA others(81): Show |
3 | a0001c0001t0003g0118 a0001c0001t0003g0122 a0016c0026t0002g0099 |
3 | HG01074.hp1 HG01257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.225-18789_225-1878 others(92): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606181 | ||||||
chr3:49606187 | A | T | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18788A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606187 | |||||||
chr3:49606187 | ATT | A | 2 | a0008c0014t0009g0041 a0008c0014t0009g0098 |
2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.225-18787_225-1878 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606187 | |||||||
chr3:49606188 | T | A | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18787T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606188 | |||||||
chr3:49606191 | T | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18784T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606191 | |||||||
chr3:49606193 | T | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18782T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606193 | |||||||
chr3:49606193 | T | TA | 39 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18781dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606193 | ||||||
chr3:49606195 | T | A | 39 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18780T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606195 | |||||||
chr3:49606196 | AC | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18778delC | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606196 | |||||||
chr3:49606197 | C | T | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18778C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606197 | |||||||
chr3:49606199 | T | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18776T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606199 | |||||||
chr3:49606202 | AT | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18771delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606202 | ||||||
chr3:49606203 | T | A | 2 | a0012c0009t0001g0071 a0017c0037t0025g0051 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.225-18772T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606203 | |||||||
chr3:49606203 | T | TTATATAT others(18): Show |
2 | a0001c0001t0002g0146 a0001c0001t0029g0120 |
2 | HG02683.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.225-18766_225-1874 others(29): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606203 | ||||||
chr3:49606204 | T | A | 39 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18771T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606204 | |||||||
chr3:49606209 | AT | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18765delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606209 | |||||||
chr3:49606211 | G | A | 42 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(39): Show |
42 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.225-18764G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606211 | |||||||
chr3:49606211 | G | GTA | 3 | a0003c0004t0006g0030 a0003c0004t0006g0031 a0003c0004t0006g0032 |
3 | HG01516.hp1 HG01517.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.225-18758_225-1875 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606211 | ||||||
chr3:49606211 | G | T | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18764G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606211 | |||||||
chr3:49606212 | T | A | 1 | a0012c0009t0001g0071 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.225-18763T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606212 | |||||||
chr3:49606213 | A | T | 39 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18762A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606213 | |||||||
chr3:49606214 | T | A | 40 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(37): Show |
40 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.225-18761T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606214 | |||||||
chr3:49606216 | T | A | 39 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18759T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606216 | |||||||
chr3:49606218 | T | A | 39 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.225-18757T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606218 | |||||||
chr3:49606219 | T | A | 3 | a0003c0003t0004g0045 a0008c0014t0009g0041 a0008c0014t0009g0098 |
3 | HG01081.hp2 HG01192.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-18756T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606219 | |||||||
chr3:49606221 | T | A | 3 | a0002c0002t0001g0087 a0002c0002t0001g0089 a0002c0020t0024g0165 |
3 | HG02723.hp2 NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18754T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606221 | |||||||
chr3:49606223 | T | A | 3 | a0002c0002t0001g0087 a0002c0002t0001g0089 a0002c0020t0024g0165 |
3 | HG02723.hp2 NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18752T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606223 | |||||||
chr3:49606223 | T | TATAAA | 22 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18749_225-1874 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606223 | ||||||
chr3:49606224 | A | AT | 32 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(29): Show |
32 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.225-18750dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606224 | ||||||
chr3:49606224 | A | ATATTAAA others(76): Show |
1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-18749_225-1874 others(87): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606224 | ||||||
chr3:49606225 | T | TA | 7 | a0002c0002t0001g0151 a0002c0002t0001g0179 a0002c0002t0001g0180 others(4): Show |
7 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-18749dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606225 | ||||||
chr3:49606225 | TAC | T | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18748_225-1874 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606225 | ||||||
chr3:49606227 | C | T | 64 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(61): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.225-18748C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606227 | |||||||
chr3:49606233 | T | A | 23 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.225-18742T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606233 | |||||||
chr3:49606235 | ATATATG | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18734_225-1872 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606235 | ||||||
chr3:49606236 | T | A | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18739T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606236 | |||||||
chr3:49606238 | T | A | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18737T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606238 | |||||||
chr3:49606240 | T | TTAAAA | 22 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18735_225-1873 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606240 | |||||||
chr3:49606240 | TGTATATA others(5): Show |
T | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-18734_225-1872 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606240 | |||||||
chr3:49606241 | G | A | 63 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(60): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.225-18734G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606241 | |||||||
chr3:49606248 | T | A | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18727T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | |||||||
chr3:49606248 | T | TATTATAT others(302): Show |
1 | a0003c0004t0004g0028 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.225-18727_225-1872 others(313): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | |||||||
chr3:49606248 | T | TATTATAT others(302): Show |
1 | a0003c0004t0004g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.225-18727_225-1872 others(313): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | |||||||
chr3:49606248 | T | TATTATAT others(272): Show |
1 | a0003c0004t0004g0037 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.225-18727_225-1872 others(283): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606248 | |||||||
chr3:49606250 | ATATAT | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-18724_225-1872 others(9): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606250 | |||||||
chr3:49606254 | A | AT | 3 | a0003c0004t0004g0028 a0003c0004t0004g0029 a0003c0004t0004g0037 |
3 | HG01981.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.225-18720dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(247): Show |
1 | a0003c0003t0004g0019 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(258): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(215): Show |
1 | a0003c0004t0004g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(226): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(217): Show |
2 | a0003c0003t0004g0020 a0003c0003t0004g0024 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(228): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(242): Show |
1 | a0003c0003t0004g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(253): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(249): Show |
3 | a0003c0003t0010g0011 a0003c0003t0010g0012 a0003c0003t0010g0013 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(260): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(333): Show |
1 | a0003c0004t0004g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(344): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(303): Show |
1 | a0003c0033t0004g0025 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(314): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(88): Show |
1 | a0001c0001t0002g0112 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(99): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(87): Show |
1 | a0001c0001t0002g0114 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(98): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(247): Show |
2 | a0003c0003t0004g0017 a0003c0003t0004g0018 |
2 | HG01074.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(258): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(307): Show |
1 | a0003c0003t0004g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(318): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(335): Show |
1 | a0003c0004t0014g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(346): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(331): Show |
3 | a0003c0004t0006g0030 a0003c0004t0006g0031 a0003c0004t0006g0032 |
3 | HG01516.hp1 HG01517.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.225-18719_225-1871 others(342): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606254 | A | ATACATAT others(277): Show |
1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(288): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606254 | ||||||
chr3:49606255 | T | TACATATA others(260): Show |
1 | a0003c0004t0004g0026 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(271): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TACATATA others(269): Show |
1 | a0003c0003t0004g0023 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(280): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TACATATA others(268): Show |
1 | a0003c0003t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(279): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TACATATA others(231): Show |
1 | a0003c0023t0016g0156 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(242): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TACATATA others(323): Show |
1 | a0003c0004t0006g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.225-18719_225-1871 others(334): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TACATATA others(293): Show |
1 | a0003c0004t0006g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.225-18719_225-1871 others(304): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TATTA | 22 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18719_225-1871 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606255 | ||||||
chr3:49606255 | T | TTA | 41 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.225-18720_225-1871 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606255 | |||||||
chr3:49606258 | A | T | 2 | a0003c0004t0004g0026 a0003c0023t0016g0156 |
2 | HG01070.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-18717A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606258 | |||||||
chr3:49606267 | A | ATATATTA others(53): Show |
1 | a0001c0001t0011g0124 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.225-18708_225-1870 others(64): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606267 | |||||||
chr3:49606267 | A | T | 45 | a0001c0001t0002g0112 a0001c0001t0002g0114 a0002c0002t0001g0062 others(42): Show |
45 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.225-18708A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606267 | |||||||
chr3:49606280 | A | AT | 46 | a0001c0001t0002g0112 a0001c0001t0002g0114 a0001c0001t0011g0124 others(43): Show |
46 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.225-18695_225-1869 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606280 | |||||||
chr3:49606280 | A | ATATATAT others(58): Show |
5 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0139 others(2): Show |
5 | HG00642.hp2 HG01168.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-18695_225-1869 others(69): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606280 | |||||||
chr3:49606289 | T | A | 75 | a0001c0001t0002g0112 a0001c0001t0002g0114 a0001c0001t0002g0130 others(72): Show |
76 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.225-18686T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606289 | |||||||
chr3:49606289 | T | TATATATA others(60): Show |
1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.225-18672_225-1867 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | ||||||
chr3:49606289 | T | TATATATA others(60): Show |
6 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0002c0002t0001g0058 others(3): Show |
6 | HG00280.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-18643_225-1864 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | ||||||
chr3:49606289 | T | TATATATA others(59): Show |
64 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.225-18651_225-1865 others(70): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | ||||||
chr3:49606289 | T | TATATATA others(125): Show |
2 | a0003c0003t0004g0021 a0003c0003t0004g0045 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-18665_225-1866 others(136): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | ||||||
chr3:49606289 | T | TATATATA others(16): Show |
22 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.225-18673_225-1867 others(27): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606289 | ||||||
chr3:49606311 | A | AATATATA others(60): Show |
2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-18643_225-1864 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606311 | ||||||
chr3:49606322 | A | AAATATAT others(57): Show |
1 | a0001c0001t0015g0141 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.225-18651_225-1865 others(68): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606322 | ||||||
chr3:49606326 | T | A | 2 | a0001c0001t0015g0141 a0020c0024t0007g0009 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.225-18649T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606326 | |||||||
chr3:49606326 | T | TATATATT others(60): Show |
9 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0003g0154 others(6): Show |
9 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-18643_225-1864 others(71): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49606326 | ||||||
chr3:49606415 | T | G | 1 | a0002c0002t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.225-18560T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606415 | |||||||
chr3:49606498 | G | T | 2 | a0009c0012t0005g0083 a0009c0012t0005g0084 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.225-18477G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606498 | |||||||
chr3:49606550 | A | G | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-18425A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606550 | |||||||
chr3:49606579 | C | T | 59 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.225-18396C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606579 | |||||||
chr3:49606592 | C | T | 1 | a0002c0002t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.225-18383C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606592 | |||||||
chr3:49606635 | A | T | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.225-18340A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606635 | |||||||
chr3:49606743 | G | A | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-18232G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606743 | |||||||
chr3:49606760 | T | C | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-18215T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49606760 | |||||||
chr3:49607254 | G | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-17721G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607254 | |||||||
chr3:49607383 | G | A | 2 | a0001c0001t0002g0096 a0021c0028t0003g0149 |
2 | HG02738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.225-17592G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607383 | |||||||
chr3:49607469 | T | C | 1 | a0007c0011t0001g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.225-17506T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607469 | |||||||
chr3:49607776 | C | T | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.225-17199C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607776 | |||||||
chr3:49607828 | G | A | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-17147G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49607828 | |||||||
chr3:49608025 | A | G | 157 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.225-16950A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608025 | |||||||
chr3:49608069 | C | T | 6 | a0001c0001t0003g0040 a0001c0001t0003g0121 a0001c0001t0003g0127 others(3): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-16906C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608069 | |||||||
chr3:49608278 | A | T | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-16697A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608278 | |||||||
chr3:49608359 | C | T | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-16616C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608359 | |||||||
chr3:49608387 | G | T | 1 | a0001c0001t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.225-16588G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608387 | |||||||
chr3:49608567 | C | T | 5 | a0002c0002t0005g0061 a0002c0002t0005g0073 a0002c0002t0005g0074 others(2): Show |
5 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-16408C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608567 | |||||||
chr3:49608717 | A | G | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.225-16258A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608717 | |||||||
chr3:49608766 | T | C | 1 | a0001c0017t0002g0105 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.225-16209T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608766 | |||||||
chr3:49608773 | A | T | 4 | a0001c0001t0011g0097 a0001c0001t0011g0124 a0001c0001t0011g0126 others(1): Show |
4 | HG00323.hp2 HG01106.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-16202A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608773 | |||||||
chr3:49608829 | G | GA | 4 | a0001c0001t0023g0144 a0006c0005t0008g0161 a0012c0009t0001g0071 others(1): Show |
4 | HG04115.hp2 NA18951.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-16146_225-1614 others(5): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608829 | |||||||
chr3:49608830 | G | A | 172 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.225-16145G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608830 | |||||||
chr3:49608883 | G | C | 1 | a0016c0026t0002g0099 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.225-16092G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49608883 | |||||||
chr3:49609089 | C | CT | 14 | a0001c0001t0012g0056 a0002c0002t0001g0077 a0002c0002t0001g0078 others(11): Show |
14 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-15863dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49609089 | ||||||
chr3:49609089 | CT | C | 72 | a0001c0001t0002g0094 a0001c0001t0002g0101 a0001c0001t0002g0103 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.225-15863delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49609089 | ||||||
chr3:49609236 | G | A | 155 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-15739G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609236 | |||||||
chr3:49609268 | A | AT | 6 | a0001c0001t0002g0177 a0002c0002t0001g0052 a0002c0002t0018g0039 others(3): Show |
6 | HG01433.hp1 HG02738.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-15692dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49609268 | ||||||
chr3:49609340 | C | T | 1 | a0002c0002t0001g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.225-15635C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609340 | |||||||
chr3:49609548 | T | C | 157 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.225-15427T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609548 | |||||||
chr3:49609971 | T | A | 155 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.225-15004T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49609971 | |||||||
chr3:49610354 | G | A | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-14621G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610354 | |||||||
chr3:49610388 | G | T | 82 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.225-14587G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610388 | |||||||
chr3:49610451 | G | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-14524G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610451 | |||||||
chr3:49610557 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.225-14418C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610557 | |||||||
chr3:49610559 | G | A | 1 | a0002c0002t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225-14416G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49610559 | |||||||
chr3:49610584 | C | CA | 44 | a0001c0001t0007g0008 a0001c0001t0012g0056 a0002c0002t0001g0052 others(41): Show |
44 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.225-14369dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | ||||||
chr3:49610584 | C | CAA | 23 | a0001c0001t0007g0007 a0001c0001t0007g0042 a0001c0001t0011g0126 others(20): Show |
23 | HG00323.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.225-14370_225-1436 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | ||||||
chr3:49610584 | C | CAAA | 67 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0103 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.225-14371_225-1436 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | ||||||
chr3:49610584 | C | CAAAA | 14 | a0001c0001t0002g0101 a0001c0001t0002g0134 a0001c0001t0002g0150 others(11): Show |
14 | HG01106.hp2 HG01109.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-14372_225-1436 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49610584 | ||||||
chr3:49611054 | A | G | 1 | a0003c0003t0004g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.225-13921A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611054 | |||||||
chr3:49611279 | A | C | 1 | a0001c0001t0002g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.225-13696A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611279 | |||||||
chr3:49611334 | C | T | 4 | a0005c0007t0007g0003 a0005c0007t0032g0005 a0005c0032t0007g0079 others(1): Show |
4 | HG02451.hp2 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-13641C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611334 | |||||||
chr3:49611475 | G | C | 1 | a0002c0002t0001g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.225-13500G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611475 | |||||||
chr3:49611638 | C | T | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.225-13337C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49611638 | |||||||
chr3:49612001 | C | A | 13 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(10): Show |
13 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-12974C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612001 | |||||||
chr3:49612139 | A | AT | 68 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-12822dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49612139 | ||||||
chr3:49612139 | A | ATT | 78 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(75): Show |
78 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.225-12823_225-1282 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49612139 | ||||||
chr3:49612139 | A | ATTT | 7 | a0001c0001t0002g0111 a0001c0001t0002g0150 a0001c0001t0002g0176 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-12824_225-1282 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49612139 | ||||||
chr3:49612159 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.225-12816A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612159 | |||||||
chr3:49612293 | G | C | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-12682G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612293 | |||||||
chr3:49612388 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.225-12587G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612388 | |||||||
chr3:49612440 | A | G | 5 | a0003c0004t0006g0001 a0003c0004t0006g0030 a0003c0004t0006g0031 others(2): Show |
6 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-12535A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612440 | |||||||
chr3:49612454 | C | T | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.225-12521C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612454 | |||||||
chr3:49612556 | C | G | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-12419C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612556 | |||||||
chr3:49612962 | G | A | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-12013G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49612962 | |||||||
chr3:49613275 | T | TTA | 90 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(87): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.225-11685_225-1168 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613275 | ||||||
chr3:49613292 | C | T | 1 | a0001c0001t0011g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11683C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613292 | |||||||
chr3:49613300 | G | C | 1 | a0001c0001t0011g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11675G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613300 | |||||||
chr3:49613303 | C | A | 1 | a0001c0001t0011g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11672C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613303 | |||||||
chr3:49613303 | C | CAAGAGAG others(15): Show |
1 | a0004c0006t0002g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-11672_225-1167 others(26): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613303 | |||||||
chr3:49613303 | C | CAAGAGAG others(19): Show |
1 | a0004c0022t0002g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.225-11672_225-1167 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613303 | |||||||
chr3:49613303 | C | CGA | 7 | a0001c0001t0015g0157 a0002c0002t0001g0076 a0002c0002t0001g0077 others(4): Show |
7 | HG02055.hp2 HG02698.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-11627_225-1162 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGA | 5 | a0002c0002t0001g0052 a0003c0004t0004g0029 a0003c0004t0014g0043 others(2): Show |
5 | HG01069.hp2 HG02738.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-11629_225-1162 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGA | 12 | a0001c0001t0002g0096 a0001c0001t0002g0123 a0001c0001t0011g0124 others(9): Show |
12 | HG00280.hp2 HG00642.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.225-11631_225-1162 others(10): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(1): Show |
14 | a0001c0001t0002g0146 a0001c0001t0003g0122 a0001c0001t0007g0007 others(11): Show |
14 | HG00323.hp1 HG01070.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.225-11633_225-1162 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(3): Show |
16 | a0001c0001t0002g0150 a0001c0001t0002g0177 a0001c0001t0003g0119 others(13): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.225-11635_225-1162 others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(5): Show |
17 | a0001c0001t0002g0130 a0001c0001t0003g0040 a0001c0001t0003g0118 others(14): Show |
17 | HG00544.hp2 HG01257.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.225-11637_225-1162 others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(7): Show |
22 | a0001c0001t0002g0112 a0001c0001t0002g0137 a0001c0001t0002g0138 others(19): Show |
22 | HG00099.hp2 HG00733.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.225-11639_225-1162 others(18): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(9): Show |
18 | a0001c0001t0002g0094 a0001c0001t0002g0114 a0001c0001t0002g0139 others(15): Show |
18 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.225-11641_225-1162 others(20): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(11): Show |
11 | a0001c0001t0002g0111 a0001c0001t0003g0121 a0001c0001t0020g0108 others(8): Show |
11 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-11643_225-1162 others(22): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(13): Show |
9 | a0001c0001t0002g0104 a0001c0001t0002g0132 a0001c0001t0002g0176 others(6): Show |
9 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-11645_225-1162 others(24): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(15): Show |
12 | a0001c0001t0002g0106 a0001c0001t0009g0093 a0001c0001t0009g0148 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.225-11647_225-1162 others(26): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(17): Show |
5 | a0001c0001t0002g0147 a0001c0001t0003g0095 a0002c0002t0001g0086 others(2): Show |
5 | HG00099.hp1 HG00140.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-11649_225-1162 others(28): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(19): Show |
4 | a0001c0001t0002g0103 a0001c0001t0002g0109 a0001c0001t0012g0115 others(1): Show |
4 | HG01515.hp2 HG02698.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-11651_225-1162 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(21): Show |
1 | a0004c0006t0002g0034 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.225-11653_225-1162 others(32): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGAGAG others(23): Show |
1 | a0001c0001t0003g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.225-11655_225-1162 others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGCGAG others(19): Show |
2 | a0001c0001t0002g0101 a0001c0001t0002g0134 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.225-11669_225-1166 others(30): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | C | CGAGCGAG others(21): Show |
1 | a0001c0001t0002g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.225-11669_225-1166 others(32): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | CGA | C | 5 | a0002c0002t0005g0061 a0002c0002t0005g0073 a0002c0002t0005g0074 others(2): Show |
5 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-11627_225-1162 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613303 | CGAGAGAG others(1): Show |
C | 2 | a0002c0020t0024g0165 a0017c0037t0025g0051 |
2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.225-11633_225-1162 others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613303 | ||||||
chr3:49613305 | A | C | 1 | a0001c0001t0011g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.225-11670A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613305 | |||||||
chr3:49613307 | A | AGAGAGAG others(6): Show |
1 | a0001c0001t0030g0143 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-11667_225-1165 others(17): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613307 | ||||||
chr3:49613349 | A | AGAGAGAG others(4): Show |
1 | a0001c0001t0003g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.225-11626_225-1162 others(15): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613349 | |||||||
chr3:49613349 | A | AGAGAGAG others(16): Show |
1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.225-11626_225-1162 others(27): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613349 | |||||||
chr3:49613351 | G | A | 1 | a0024c0035t0002g0133 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.225-11624G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613351 | |||||||
chr3:49613499 | A | T | 4 | a0001c0001t0002g0123 a0001c0001t0002g0147 a0013c0010t0001g0164 others(1): Show |
4 | HG02970.hp1 HG03710.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-11476A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613499 | |||||||
chr3:49613502 | A | T | 144 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.225-11473A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613502 | |||||||
chr3:49613505 | T | A | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-11470T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613505 | |||||||
chr3:49613666 | C | CT | 88 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.225-11296dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49613666 | ||||||
chr3:49613777 | G | A | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-11198G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49613777 | |||||||
chr3:49614024 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.225-10951G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614024 | |||||||
chr3:49614051 | C | CT | 68 | a0001c0001t0002g0096 a0001c0001t0002g0113 a0001c0001t0002g0130 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-10900dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | ||||||
chr3:49614051 | C | CTT | 9 | a0001c0001t0009g0148 a0002c0002t0001g0052 a0002c0002t0001g0054 others(6): Show |
9 | HG00639.hp1 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-10901_225-1090 others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | ||||||
chr3:49614051 | C | CTTT | 5 | a0002c0002t0001g0169 a0002c0002t0001g0173 a0002c0002t0001g0174 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-10902_225-1090 others(7): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | ||||||
chr3:49614051 | C | CTTTT | 6 | a0002c0002t0001g0087 a0002c0002t0001g0088 a0002c0002t0001g0089 others(3): Show |
6 | HG00733.hp1 HG00735.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-10903_225-1090 others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49614051 | ||||||
chr3:49614101 | C | T | 12 | a0002c0002t0001g0087 a0002c0002t0001g0088 a0002c0002t0001g0089 others(9): Show |
12 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.225-10874C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614101 | |||||||
chr3:49614113 | G | T | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-10862G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614113 | |||||||
chr3:49614128 | C | T | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-10847C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614128 | |||||||
chr3:49614170 | C | T | 7 | a0001c0001t0002g0103 a0004c0006t0002g0034 a0004c0006t0002g0035 others(4): Show |
7 | HG00140.hp1 HG00733.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-10805C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614170 | |||||||
chr3:49614208 | C | T | 1 | a0004c0022t0002g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.225-10767C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614208 | |||||||
chr3:49614522 | C | T | 1 | a0003c0004t0004g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-10453C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614522 | |||||||
chr3:49614537 | C | G | 9 | a0002c0002t0001g0166 a0002c0002t0001g0167 a0002c0002t0001g0169 others(6): Show |
9 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-10438C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614537 | |||||||
chr3:49614715 | T | C | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.225-10260T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614715 | |||||||
chr3:49614723 | C | T | 87 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.225-10252C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614723 | |||||||
chr3:49614840 | A | G | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0025c0029t0003g0048 |
3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.225-10135A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614840 | |||||||
chr3:49614902 | G | T | 1 | a0002c0002t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225-10073G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49614902 | |||||||
chr3:49615164 | C | G | 5 | a0004c0006t0002g0034 a0004c0006t0002g0035 a0004c0006t0002g0036 others(2): Show |
5 | HG00140.hp1 HG00733.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-9811C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49615164 | |||||||
chr3:49615945 | A | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.225-9030A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49615945 | |||||||
chr3:49616024 | C | T | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.225-8951C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49616024 | |||||||
chr3:49616508 | C | A | 2 | a0010c0015t0002g0102 a0010c0015t0002g0107 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.225-8467C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49616508 | |||||||
chr3:49617184 | G | A | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-7791G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49617184 | |||||||
chr3:49617210 | A | G | 1 | a0001c0001t0029g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.225-7765A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49617210 | |||||||
chr3:49617277 | AATACATT others(10): Show |
A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.225-7694_225-7678d others(19): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617277 | ||||||
chr3:49617277 | AATACATT others(14): Show |
A | 55 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(52): Show |
55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.225-7694_225-7674d others(23): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617277 | ||||||
chr3:49617277 | AATACATT others(16): Show |
A | 4 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 others(1): Show |
4 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-7694_225-7672d others(25): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617277 | ||||||
chr3:49617283 | T | TTA | 3 | a0003c0004t0004g0037 a0003c0004t0014g0043 a0003c0033t0004g0025 |
3 | HG01069.hp2 HG01981.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.225-7657_225-7656d others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | T | TTATA | 2 | a0003c0003t0004g0014 a0003c0003t0004g0045 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.225-7659_225-7656d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | T | TTATATAT others(3): Show |
2 | a0003c0004t0004g0029 a0003c0004t0006g0031 |
2 | HG01517.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.225-7665_225-7656d others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | T | TTATATAT others(5): Show |
3 | a0003c0004t0004g0026 a0003c0004t0006g0030 a0003c0004t0006g0032 |
3 | HG01070.hp1 HG01516.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.225-7667_225-7656d others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | T | TTATATAT others(7): Show |
3 | a0003c0004t0006g0001 a0003c0004t0006g0116 a0003c0023t0016g0156 |
3 | HG02615.hp2 HG03453.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.225-7669_225-7656d others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | T | TTATATAT others(25): Show |
1 | a0003c0004t0006g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.225-7687_225-7656d others(34): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | TTA | T | 4 | a0003c0003t0004g0023 a0005c0007t0007g0003 a0005c0032t0007g0079 others(1): Show |
4 | HG01884.hp1 HG02683.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-7657_225-7656d others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | TTATA | T | 9 | a0003c0003t0004g0015 a0003c0003t0004g0019 a0003c0003t0004g0020 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-7659_225-7656d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | TTATATA | T | 4 | a0003c0003t0004g0022 a0003c0003t0010g0011 a0003c0003t0010g0012 others(1): Show |
4 | HG02622.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-7661_225-7656d others(8): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | TTATATAT others(5): Show |
T | 1 | a0003c0003t0004g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.225-7667_225-7656d others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | TTATATAT others(7): Show |
T | 4 | a0001c0001t0002g0130 a0011c0013t0013g0049 a0011c0013t0013g0050 others(1): Show |
4 | HG02572.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-7669_225-7656d others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617283 | TTATATAT others(9): Show |
T | 83 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.225-7671_225-7656d others(18): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49617283 | ||||||
chr3:49617430 | C | A | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG01257.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.225-7545C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49617430 | |||||||
chr3:49618278 | C | T | 2 | a0002c0002t0005g0038 a0002c0002t0018g0039 |
2 | NA19003.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.225-6697C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618278 | |||||||
chr3:49618494 | T | A | 11 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0004t0004g0028 others(8): Show |
12 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.225-6481T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618494 | |||||||
chr3:49618570 | A | G | 7 | a0002c0002t0001g0062 a0002c0002t0001g0069 a0002c0002t0001g0070 others(4): Show |
7 | HG01167.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-6405A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618570 | |||||||
chr3:49618610 | A | G | 2 | a0001c0001t0002g0106 a0024c0035t0002g0133 |
2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.225-6365A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49618610 | |||||||
chr3:49619094 | T | A | 1 | a0002c0002t0019g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.225-5881T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619094 | |||||||
chr3:49619097 | CTGAA | C | 170 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.225-5864_225-5861d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49619097 | ||||||
chr3:49619132 | G | A | 1 | a0018c0025t0028g0100 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.225-5843G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619132 | |||||||
chr3:49619356 | G | T | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.225-5619G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619356 | |||||||
chr3:49619729 | C | A | 1 | a0022c0031t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.225-5246C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619729 | |||||||
chr3:49619776 | G | C | 2 | a0001c0001t0003g0125 a0001c0001t0003g0131 |
2 | HG00639.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.225-5199G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619776 | |||||||
chr3:49619983 | CT | C | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.225-4991delT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49619983 | |||||||
chr3:49620008 | A | G | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.225-4967A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620008 | |||||||
chr3:49620038 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.225-4937A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620038 | |||||||
chr3:49620192 | C | T | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-4783C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620192 | |||||||
chr3:49620288 | G | A | 1 | a0022c0031t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.225-4687G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620288 | |||||||
chr3:49620419 | C | T | 72 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.225-4556C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620419 | |||||||
chr3:49620651 | A | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.225-4324A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620651 | |||||||
chr3:49620722 | C | T | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.225-4253C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620722 | |||||||
chr3:49620805 | C | T | 1 | a0002c0002t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.225-4170C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620805 | |||||||
chr3:49620943 | A | G | 1 | a0001c0001t0002g0176 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.225-4032A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49620943 | |||||||
chr3:49621104 | A | C | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225-3871A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49621104 | |||||||
chr3:49621745 | T | C | 2 | a0002c0002t0001g0087 a0002c0002t0001g0089 |
2 | NA18612.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.225-3230T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49621745 | |||||||
chr3:49622324 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.225-2651G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622324 | |||||||
chr3:49622375 | A | G | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.225-2600A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622375 | |||||||
chr3:49622562 | C | G | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.225-2413C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622562 | |||||||
chr3:49622584 | C | T | 1 | a0002c0002t0018g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.225-2391C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49622584 | |||||||
chr3:49623079 | T | A | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.225-1896T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49623079 | |||||||
chr3:49623209 | G | A | 2 | a0002c0008t0001g0168 a0002c0008t0001g0172 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.225-1766G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49623209 | |||||||
chr3:49623636 | C | T | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.225-1339C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49623636 | |||||||
chr3:49624028 | T | G | 1 | a0003c0003t0004g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-947T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624028 | |||||||
chr3:49624201 | C | T | 9 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0004t0004g0037 others(6): Show |
10 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-774C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624201 | |||||||
chr3:49624299 | C | CATTTTTT others(6): Show |
1 | a0001c0001t0002g0109 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.225-676_225-675ins others(13): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624299 | |||||||
chr3:49624300 | C | CTTTTTTT others(4): Show |
1 | a0011c0013t0013g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.225-668_225-658dup others(11): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | ||||||
chr3:49624300 | C | CTTTTTTT others(5): Show |
23 | a0001c0001t0012g0056 a0002c0002t0001g0054 a0002c0002t0001g0060 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.225-669_225-658dup others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | ||||||
chr3:49624300 | C | CTTTTTTT others(6): Show |
72 | a0001c0001t0002g0101 a0001c0001t0002g0103 a0001c0001t0002g0106 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.225-670_225-658dup others(13): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | ||||||
chr3:49624300 | C | CTTTTTTT others(7): Show |
44 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0104 others(41): Show |
44 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.225-671_225-658dup others(14): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | ||||||
chr3:49624300 | C | CTTTTTTT others(8): Show |
9 | a0001c0001t0002g0114 a0001c0001t0002g0147 a0001c0001t0003g0095 others(6): Show |
9 | HG00735.hp1 HG01109.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-672_225-658dup others(15): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | ||||||
chr3:49624300 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0015g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.225-673_225-658dup others(16): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 49624300 | ||||||
chr3:49624300 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.225-675C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 1/11 | chr3 | 49624300 | |||||||
chr3:49625856 | G | A | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.633+473G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49625856 | |||||||
chr3:49626261 | G | A | 3 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 |
3 | HG02257.hp2 HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.633+878G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626261 | |||||||
chr3:49626357 | G | C | 1 | a0001c0001t0002g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.633+974G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626357 | |||||||
chr3:49626456 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0137 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.633+1073T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626456 | |||||||
chr3:49626555 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.633+1172T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49626555 | |||||||
chr3:49627013 | T | G | 1 | a0002c0002t0005g0061 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.633+1630T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627013 | |||||||
chr3:49627020 | T | C | 1 | a0001c0001t0021g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.633+1637T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627020 | |||||||
chr3:49627047 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.633+1664G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627047 | |||||||
chr3:49627334 | A | G | 60 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.633+1951A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627334 | |||||||
chr3:49627409 | T | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0025c0029t0003g0048 |
3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.633+2026T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627409 | |||||||
chr3:49627843 | T | C | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.633+2460T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627843 | |||||||
chr3:49627957 | G | A | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.633+2574G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49627957 | |||||||
chr3:49628179 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.633+2796A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49628179 | |||||||
chr3:49628541 | G | T | 2 | a0001c0001t0002g0146 a0001c0001t0023g0144 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.633+3158G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49628541 | |||||||
chr3:49628543 | T | G | 60 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.633+3160T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49628543 | |||||||
chr3:49629109 | G | A | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+3726G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629109 | |||||||
chr3:49629531 | C | A | 59 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.633+4148C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629531 | |||||||
chr3:49629741 | C | A | 1 | a0001c0001t0002g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.633+4358C>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629741 | |||||||
chr3:49629753 | C | T | 3 | a0003c0003t0010g0011 a0003c0003t0010g0012 a0003c0003t0010g0013 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.633+4370C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629753 | |||||||
chr3:49629909 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.633+4526G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629909 | |||||||
chr3:49629980 | A | T | 1 | a0001c0001t0002g0111 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.633+4597A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49629980 | |||||||
chr3:49630258 | T | C | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.633+4875T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49630258 | |||||||
chr3:49630443 | A | G | 1 | a0001c0001t0002g0150 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.633+5060A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49630443 | |||||||
chr3:49631170 | C | T | 1 | a0013c0010t0001g0164 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.633+5787C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631170 | |||||||
chr3:49631316 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0137 |
2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.633+5933G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631316 | |||||||
chr3:49631346 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.633+5963A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631346 | |||||||
chr3:49631377 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.633+5994G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631377 | |||||||
chr3:49631500 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.633+6117A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631500 | |||||||
chr3:49631541 | G | GAGTA | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0025c0029t0003g0048 |
3 | HG02258.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.633+6161_633+6164d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49631541 | ||||||
chr3:49631557 | C | CA | 13 | a0001c0001t0002g0103 a0001c0001t0003g0046 a0001c0001t0003g0047 others(10): Show |
13 | HG01074.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.633+6192dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49631557 | ||||||
chr3:49631557 | CA | C | 10 | a0002c0002t0001g0076 a0002c0002t0001g0151 a0002c0002t0001g0179 others(7): Show |
10 | HG01081.hp2 HG01257.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.633+6192delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49631557 | ||||||
chr3:49631633 | T | C | 2 | a0001c0001t0002g0146 a0001c0001t0023g0144 |
2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.633+6250T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631633 | |||||||
chr3:49631657 | G | T | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.633+6274G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49631657 | |||||||
chr3:49632515 | G | A | 11 | a0001c0001t0002g0094 a0001c0001t0002g0147 a0001c0001t0003g0117 others(8): Show |
11 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.633+7132G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49632515 | |||||||
chr3:49632696 | C | T | 4 | a0001c0001t0009g0093 a0001c0001t0009g0148 a0008c0014t0009g0041 others(1): Show |
4 | HG01081.hp2 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+7313C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49632696 | |||||||
chr3:49633217 | G | A | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.633+7834G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633217 | |||||||
chr3:49633301 | C | CA | 8 | a0001c0001t0002g0150 a0002c0002t0001g0151 a0002c0002t0001g0179 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.633+7932dupA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49633301 | ||||||
chr3:49633604 | G | A | 13 | a0001c0001t0012g0056 a0002c0002t0001g0053 a0002c0002t0001g0054 others(10): Show |
13 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.633+8221G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633604 | |||||||
chr3:49633753 | C | T | 93 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.633+8370C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633753 | |||||||
chr3:49633791 | T | C | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.633+8408T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49633791 | |||||||
chr3:49634002 | C | T | 1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634-8266C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49634002 | |||||||
chr3:49634221 | A | C | 81 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.634-8047A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49634221 | |||||||
chr3:49634413 | T | A | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-7855T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49634413 | |||||||
chr3:49635633 | T | C | 3 | a0003c0003t0010g0011 a0003c0003t0010g0012 a0003c0003t0010g0013 |
3 | HG02622.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.634-6635T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635633 | |||||||
chr3:49635833 | C | T | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-6435C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635833 | |||||||
chr3:49635852 | G | C | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.634-6416G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635852 | |||||||
chr3:49635937 | G | C | 1 | a0001c0001t0002g0112 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.634-6331G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49635937 | |||||||
chr3:49636229 | A | G | 9 | a0003c0004t0004g0026 a0003c0004t0004g0027 a0003c0004t0004g0037 others(6): Show |
10 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.634-6039A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636229 | |||||||
chr3:49636422 | G | C | 1 | a0001c0001t0011g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.634-5846G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636422 | |||||||
chr3:49636714 | C | G | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.634-5554C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636714 | |||||||
chr3:49636817 | A | G | 2 | a0001c0001t0003g0158 a0001c0001t0015g0157 |
2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.634-5451A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636817 | |||||||
chr3:49636910 | C | T | 170 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.634-5358C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49636910 | |||||||
chr3:49637002 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.634-5266A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637002 | |||||||
chr3:49637025 | A | G | 61 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.634-5243A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637025 | |||||||
chr3:49637425 | G | A | 1 | a0020c0024t0007g0009 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.634-4843G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637425 | |||||||
chr3:49637642 | G | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0123 a0021c0028t0003g0149 |
3 | HG02738.hp2 HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.634-4626G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637642 | |||||||
chr3:49637709 | T | A | 87 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.634-4559T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637709 | |||||||
chr3:49637901 | C | G | 60 | a0001c0001t0012g0056 a0002c0002t0001g0052 a0002c0002t0001g0053 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.634-4367C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49637901 | |||||||
chr3:49638038 | A | G | 1 | a0025c0029t0003g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.634-4230A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638038 | |||||||
chr3:49638075 | G | A | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.634-4193G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638075 | |||||||
chr3:49638124 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634-4144G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638124 | |||||||
chr3:49638189 | C | G | 1 | a0001c0001t0002g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.634-4079C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638189 | |||||||
chr3:49638296 | A | G | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-3972A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638296 | |||||||
chr3:49638404 | G | A | 1 | a0001c0001t0022g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.634-3864G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638404 | |||||||
chr3:49638442 | G | C | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.634-3826G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638442 | |||||||
chr3:49638531 | ATGCTGGG others(8): Show |
A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634-3734_634-3720d others(17): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49638531 | ||||||
chr3:49638665 | G | A | 1 | a0011c0013t0013g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634-3603G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49638665 | |||||||
chr3:49639199 | C | CT | 61 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.634-3052dupT | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49639199 | ||||||
chr3:49639464 | C | T | 1 | a0014c0030t0002g0142 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.634-2804C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639464 | |||||||
chr3:49639487 | G | C | 1 | a0001c0001t0012g0056 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.634-2781G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639487 | |||||||
chr3:49639633 | G | T | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-2635G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639633 | |||||||
chr3:49639646 | A | G | 3 | a0003c0004t0004g0016 a0003c0004t0004g0028 a0003c0004t0004g0029 |
3 | HG03098.hp1 HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.634-2622A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639646 | |||||||
chr3:49639675 | GAGGC | G | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.634-2589_634-2586d others(6): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 49639675 | ||||||
chr3:49639859 | C | G | 94 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.634-2409C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49639859 | |||||||
chr3:49640044 | C | CAT | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.634-2224_634-2223i others(4): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640044 | |||||||
chr3:49640062 | G | A | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.634-2206G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640062 | |||||||
chr3:49640164 | A | G | 1 | a0001c0027t0003g0185 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.634-2104A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640164 | |||||||
chr3:49640644 | G | A | 82 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.634-1624G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640644 | |||||||
chr3:49640780 | G | A | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634-1488G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640780 | |||||||
chr3:49640874 | A | T | 58 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.634-1394A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49640874 | |||||||
chr3:49641218 | A | G | 60 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.634-1050A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641218 | |||||||
chr3:49641280 | A | G | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-988A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641280 | |||||||
chr3:49641639 | G | A | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.634-629G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641639 | |||||||
chr3:49641979 | G | A | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.634-289G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 2/11 | chr3 | 49641979 | |||||||
chr3:49643540 | G | A | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1518+388G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49643540 | |||||||
chr3:49643875 | C | T | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1518+723C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49643875 | |||||||
chr3:49643910 | G | A | 1 | a0001c0001t0030g0143 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1518+758G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49643910 | |||||||
chr3:49644187 | G | T | 6 | a0001c0001t0003g0040 a0001c0001t0003g0121 a0001c0001t0003g0127 others(3): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1518+1035G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644187 | |||||||
chr3:49644271 | A | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1518+1119A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644271 | |||||||
chr3:49644294 | C | T | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1518+1142C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644294 | |||||||
chr3:49644545 | C | T | 3 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 |
3 | HG02257.hp2 HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1518+1393C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644545 | |||||||
chr3:49644781 | C | G | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1518+1629C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644781 | |||||||
chr3:49644878 | G | A | 60 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1518+1726G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49644878 | |||||||
chr3:49645531 | T | A | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1518+2379T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49645531 | |||||||
chr3:49645540 | C | T | 1 | a0022c0031t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1518+2388C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49645540 | |||||||
chr3:49646093 | G | A | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1518+2941G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646093 | |||||||
chr3:49646175 | T | A | 12 | a0003c0003t0004g0015 a0003c0003t0004g0017 a0003c0003t0004g0018 others(9): Show |
12 | HG01074.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1518+3023T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646175 | |||||||
chr3:49646542 | T | C | 1 | a0002c0002t0005g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1518+3390T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646542 | |||||||
chr3:49646786 | T | A | 4 | a0001c0001t0003g0158 a0001c0001t0015g0157 a0003c0003t0016g0159 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1518+3634T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49646786 | |||||||
chr3:49647314 | T | C | 1 | a0003c0003t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1519-3298T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49647314 | |||||||
chr3:49647484 | C | G | 60 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1519-3128C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49647484 | |||||||
chr3:49647640 | G | A | 73 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1519-2972G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49647640 | |||||||
chr3:49648073 | A | G | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1519-2539A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648073 | |||||||
chr3:49648159 | A | G | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1519-2453A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648159 | |||||||
chr3:49648188 | A | G | 1 | a0001c0001t0011g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1519-2424A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648188 | |||||||
chr3:49648783 | CA | C | 3 | a0003c0003t0004g0018 a0003c0003t0004g0019 a0003c0003t0004g0024 |
3 | HG01074.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1519-1828delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648783 | |||||||
chr3:49648880 | A | T | 2 | a0001c0001t0012g0115 a0001c0001t0012g0135 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1519-1732A>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49648880 | |||||||
chr3:49649215 | T | G | 1 | a0001c0001t0011g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1519-1397T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649215 | |||||||
chr3:49649249 | T | C | 60 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1519-1363T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649249 | |||||||
chr3:49649610 | T | C | 156 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1519-1002T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649610 | |||||||
chr3:49649615 | G | C | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1519-997G>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649615 | |||||||
chr3:49649681 | T | C | 1 | a0002c0020t0024g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1519-931T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49649681 | |||||||
chr3:49650053 | C | T | 5 | a0003c0004t0006g0001 a0003c0004t0006g0030 a0003c0004t0006g0031 others(2): Show |
6 | HG01516.hp1 HG01517.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1519-559C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650053 | |||||||
chr3:49650272 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1519-340G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650272 | |||||||
chr3:49650346 | T | G | 154 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1519-266T>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650346 | |||||||
chr3:49650348 | G | A | 1 | a0017c0037t0025g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1519-264G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650348 | |||||||
chr3:49650425 | T | C | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1519-187T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650425 | |||||||
chr3:49650466 | G | T | 1 | a0002c0002t0001g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1519-146G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 3/11 | chr3 | 49650466 | |||||||
chr3:49651240 | G | A | 3 | a0001c0001t0002g0114 a0001c0001t0002g0132 a0001c0001t0002g0139 |
3 | HG00642.hp2 HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1986+161G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 4/11 | chr3 | 49651240 | |||||||
chr3:49651394 | G | A | 2 | a0001c0001t0002g0106 a0024c0035t0002g0133 |
2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1987-149G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 4/11 | chr3 | 49651394 | |||||||
chr3:49651497 | G | A | 4 | a0001c0001t0007g0007 a0001c0001t0007g0008 a0001c0001t0007g0042 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987-46G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 4/11 | chr3 | 49651497 | |||||||
chr3:49658237 | C | T | 1 | a0001c0001t0009g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.8640+41C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658237 | |||||||
chr3:49658239 | G | A | 3 | a0002c0002t0005g0061 a0002c0002t0005g0073 a0002c0002t0005g0074 |
3 | HG01081.hp1 HG01168.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.8640+43G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658239 | |||||||
chr3:49658364 | C | G | 1 | a0003c0003t0004g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8640+168C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658364 | |||||||
chr3:49658657 | A | C | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8640+461A>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658657 | |||||||
chr3:49658742 | C | T | 1 | a0001c0001t0012g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.8640+546C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658742 | |||||||
chr3:49658762 | T | C | 1 | a0002c0002t0001g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8640+566T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49658762 | |||||||
chr3:49659200 | C | G | 98 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.8640+1004C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659200 | |||||||
chr3:49659225 | G | T | 1 | a0022c0031t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8640+1029G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659225 | |||||||
chr3:49659364 | A | G | 54 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(51): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.8641-1122A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659364 | |||||||
chr3:49659572 | A | G | 1 | a0003c0004t0004g0026 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.8641-914A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659572 | |||||||
chr3:49659810 | G | A | 6 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.8641-676G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659810 | |||||||
chr3:49659857 | G | T | 6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.8641-629G>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49659857 | |||||||
chr3:49660026 | G | A | 62 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.8641-460G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49660026 | |||||||
chr3:49660289 | C | G | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.8641-197C>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 5/11 | chr3 | 49660289 | |||||||
chr3:49662646 | C | T | 1 | a0002c0002t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.10717+84C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 6/11 | chr3 | 49662646 | |||||||
chr3:49663715 | A | G | 1 | a0002c0002t0019g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.11508+49A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 7/11 | chr3 | 49663715 | |||||||
chr3:49664224 | T | C | 1 | a0002c0002t0001g0075 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.11609-199T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 8/11 | chr3 | 49664224 | |||||||
chr3:49664680 | T | C | 6 | a0001c0001t0003g0040 a0001c0001t0003g0121 a0001c0001t0003g0127 others(3): Show |
6 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.11741-119T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 9/11 | chr3 | 49664680 | |||||||
chr3:49664897 | C | T | 2 | a0003c0003t0016g0159 a0003c0023t0016g0156 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*14+44C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 10/11 | chr3 | 49664897 | |||||||
chr3:49665051 | T | C | 58 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.*15-178T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 10/11 | chr3 | 49665051 | |||||||
chr3:49666643 | G | A | 2 | a0011c0013t0013g0049 a0011c0013t0013g0050 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.*105-947G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666643 | |||||||
chr3:49666644 | A | G | 100 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.*105-946A>G | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666644 | |||||||
chr3:49666649 | G | A | 1 | a0001c0001t0009g0093 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.*105-941G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666649 | |||||||
chr3:49666684 | G | A | 1 | a0003c0003t0004g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*105-906G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666684 | |||||||
chr3:49666784 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*105-806G>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49666784 | |||||||
chr3:49666899 | G | GGGCTTCC others(3): Show |
6 | a0005c0007t0007g0003 a0005c0007t0031g0006 a0005c0007t0032g0005 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.*105-683_*105-674d others(12): Show |
BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 49666899 | ||||||
chr3:49667208 | C | T | 1 | a0002c0002t0001g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.*105-382C>T | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49667208 | |||||||
chr3:49667296 | T | A | 98 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(95): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.*105-294T>A | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49667296 | |||||||
chr3:49667308 | CA | C | 92 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.*105-264delA | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 49667308 | ||||||
chr3:49667554 | T | C | 86 | a0001c0001t0002g0094 a0001c0001t0002g0096 a0001c0001t0002g0101 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.*105-36T>C | BSN | ENSG00000164061.5 | transcript | ENST00000296452.5 | protein_coding | 11/11 | chr3 | 49667554 |