Item | Value |
---|---|
geneid | 23013 |
ensemblid | ENSG00000065526.13 |
hgncid | 17575 |
symbol | SPEN |
name | spen family transcriptional repressor |
refseq_nuc | NM_015001.3 |
refseq_prot | NP_055816.2 |
ensembl_nuc | ENST00000375759.8 |
ensembl_prot | ENSP00000364912.3 |
mane_status | MANE Select |
chr | chr1 |
start | 15847707 |
end | 15940456 |
strand | + |
ver | v1.2 |
region | chr1:15847707-15940456 |
region5000 | chr1:15842707-15945456 |
regionname0 | SPEN_chr1_15847707_15940456 |
regionname5000 | SPEN_chr1_15842707_15945456 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 3664 | 126 | 57 | 29 | 10 | 11 | 18 | 5 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0002 | 1/0 | 3664 | 73 | 2 | 13 | 46 | 1 | 10 | 35 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0003 | 0/0 | 3664 | 65 | 3 | 12 | 46 | 0 | 4 | 33 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0004 | 0/0 | 3664 | 10 | 7 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0005 | 0/0 | 3663 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3658): Show |
chr1 | 15842707 | 15945456 |
a0006 | 0/0 | 3664 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0007 | 0/0 | 3664 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0008 | 0/0 | 3664 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0009 | 0/0 | 3664 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0010 | 0/0 | 3664 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0011 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0012 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0013 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0014 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0015 | 0/0 | 3664 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0016 | 0/0 | 3664 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0017 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0018 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0019 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0020 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0021 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0022 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0023 | 0/0 | 3664 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
a0024 | 0/0 | 3664 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | MVRET others(3659): Show |
chr1 | 15842707 | 15945456 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 10992 | 89 | 35 | 22 | 5 | 9 | 17 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0004 | 0/0 | 10992 | 12 | 6 | 2 | 3 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0005 | 0/0 | 10992 | 8 | 6 | 2 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0007 | 0/0 | 10992 | 4 | 4 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0014 | 0/0 | 10992 | 2 | 0 | 1 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0015 | 0/0 | 10992 | 2 | 0 | 0 | 2 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0017 | 0/0 | 10992 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0023 | 0/0 | 10992 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0026 | 0/0 | 10992 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0027 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0028 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0029 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0037 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0001c0038 | 0/0 | 10992 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0002c0002 | 1/0 | 10992 | 72 | 2 | 13 | 45 | 1 | 10 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0002c0018 | 0/0 | 10992 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0003c0003 | 0/0 | 10992 | 65 | 3 | 12 | 46 | 0 | 4 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0004c0006 | 0/0 | 10992 | 7 | 4 | 3 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0004c0009 | 0/0 | 10992 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0005c0011 | 0/0 | 10989 | 3 | 0 | 2 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10984): Show |
chr1 | 15842707 | 15945456 | ||
a0006c0008 | 0/0 | 10992 | 3 | 2 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0007c0012 | 0/0 | 10992 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0008c0010 | 0/0 | 10992 | 3 | 0 | 0 | 3 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0009c0013 | 0/0 | 10992 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0010c0016 | 0/0 | 10992 | 2 | 0 | 0 | 0 | 0 | 2 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0011c0034 | 0/0 | 10992 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0012c0025 | 0/0 | 10992 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0013c0019 | 0/0 | 10992 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0014c0039 | 0/0 | 10992 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0015c0031 | 0/0 | 10992 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0016c0022 | 0/0 | 10992 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0017c0030 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0018c0020 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0019c0024 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0020c0033 | 0/0 | 10992 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0021c0035 | 0/0 | 10992 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0022c0032 | 0/0 | 10992 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0023c0036 | 0/0 | 10992 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 | ||
a0024c0021 | 0/0 | 10992 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | ATGGT others(10987): Show |
chr1 | 15842707 | 15945456 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 12385 | 87 | 34 | 21 | 5 | 9 | 17 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0001t0005 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0001t0006 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0004t0001 | 0/0 | 12385 | 12 | 6 | 2 | 3 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0005t0001 | 0/0 | 12385 | 8 | 6 | 2 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0007t0001 | 0/0 | 12385 | 4 | 4 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0014t0001 | 0/0 | 12385 | 2 | 0 | 1 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0015t0001 | 0/0 | 12385 | 2 | 0 | 0 | 2 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0017t0001 | 0/0 | 12385 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0023t0003 | 0/0 | 12385 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0026t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0027t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0028t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0029t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0037t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0001c0038t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0002c0002t0001 | 1/0 | 12385 | 71 | 2 | 13 | 44 | 1 | 10 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0002c0002t0004 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0002c0018t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0003c0003t0001 | 0/0 | 12385 | 64 | 3 | 12 | 46 | 0 | 3 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0003c0003t0007 | 0/0 | 12385 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0004c0006t0001 | 0/0 | 12385 | 7 | 4 | 3 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0004c0009t0001 | 0/0 | 12385 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0005c0011t0001 | 0/0 | 12382 | 3 | 0 | 2 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12377): Show |
chr1 | 15842707 | 15945456 |
a0006c0008t0001 | 0/0 | 12385 | 3 | 2 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0007c0012t0001 | 0/0 | 12385 | 3 | 3 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0008c0010t0001 | 0/0 | 12385 | 3 | 0 | 0 | 3 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0009c0013t0002 | 0/0 | 12385 | 2 | 2 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0010c0016t0001 | 0/0 | 12385 | 2 | 0 | 0 | 0 | 0 | 2 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0011c0034t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0012c0025t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0013c0019t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0014c0039t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0015c0031t0001 | 0/0 | 12385 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0016c0022t0001 | 0/0 | 12385 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0017c0030t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0018c0020t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0019c0024t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0020c0033t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0021c0035t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0022c0032t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0023c0036t0001 | 0/0 | 12385 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
a0024c0021t0001 | 0/0 | 12385 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | AGTGG others(12380): Show |
chr1 | 15842707 | 15945456 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0005t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0007t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0014t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0014t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0015t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0017t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0017t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0023t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0026t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0027t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0028t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0029t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0037t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0001c0038t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0002c0018t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0003c0003t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0006t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0009t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0009t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0004c0009t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0011t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0011t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0005c0011t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0006c0008t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0006c0008t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0006c0008t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0007c0012t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0007c0012t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0007c0012t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0008c0010t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0008c0010t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0008c0010t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0009c0013t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0009c0013t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0010c0016t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0010c0016t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0011c0034t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0012c0025t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0013c0019t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0014c0039t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0015c0031t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0016c0022t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0017c0030t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0018c0020t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0019c0024t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0020c0033t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0021c0035t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0022c0032t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0023c0036t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
a0024c0021t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00280 | hp2 | a0005 | c0011 | t0001 | g0159 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0226 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00323 | hp2 | a0001 | c0014 | t0001 | g0018 | EUR | FIN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0183 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00423 | hp2 | a0003 | c0003 | t0001 | g0167 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0137 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0109 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00558 | hp2 | a0011 | c0034 | t0001 | g0264 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00642 | hp1 | a0012 | c0025 | t0001 | g0043 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | CHS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00735 | hp1 | a0001 | c0026 | t0001 | g0096 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG00741 | hp2 | a0001 | c0038 | t0001 | g0093 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01069 | hp1 | a0001 | c0014 | t0001 | g0033 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0208 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01070 | hp1 | a0004 | c0006 | t0001 | g0112 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01071 | hp1 | a0001 | c0005 | t0001 | g0209 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01071 | hp2 | a0004 | c0006 | t0001 | g0113 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0083 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01099 | hp2 | a0001 | c0004 | t0001 | g0095 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01109 | hp2 | a0004 | c0006 | t0001 | g0117 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01167 | hp1 | a0006 | c0008 | t0001 | g0099 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0172 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01192 | hp1 | a0013 | c0019 | t0001 | g0034 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01192 | hp2 | a0014 | c0039 | t0001 | g0124 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0097 | AMR | PUR | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0173 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01256 | hp2 | a0003 | c0003 | t0001 | g0125 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01346 | hp2 | a0003 | c0003 | t0001 | g0170 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01361 | hp2 | a0003 | c0003 | t0001 | g0130 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0128 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01496 | hp1 | a0005 | c0011 | t0001 | g0003 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01515 | hp2 | a0001 | c0023 | t0003 | g0006 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01516 | hp1 | a0015 | c0031 | t0001 | g0007 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01891 | hp2 | a0001 | c0005 | t0001 | g0210 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0146 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01934 | hp2 | a0005 | c0011 | t0001 | g0175 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0127 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01975 | hp2 | a0016 | c0022 | t0001 | g0013 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0145 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02040 | hp1 | a0003 | c0003 | t0001 | g0144 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02132 | hp1 | a0001 | c0015 | t0001 | g0046 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02132 | hp2 | a0003 | c0003 | t0001 | g0136 | EAS | KHV | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02145 | hp1 | a0017 | c0030 | t0001 | g0080 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CDX | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0212 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02273 | hp1 | a0003 | c0003 | t0001 | g0126 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0168 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0131 | AMR | PEL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02572 | hp1 | a0018 | c0020 | t0001 | g0110 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0270 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02602 | hp2 | a0003 | c0003 | t0007 | g0162 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02615 | hp2 | a0001 | c0027 | t0001 | g0076 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0204 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02630 | hp1 | a0001 | c0005 | t0001 | g0288 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0169 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02647 | hp2 | a0004 | c0006 | t0001 | g0116 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0178 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0141 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02809 | hp1 | a0007 | c0012 | t0001 | g0104 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02818 | hp2 | a0006 | c0008 | t0001 | g0100 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02886 | hp1 | a0009 | c0013 | t0002 | g0054 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02895 | hp2 | a0004 | c0009 | t0001 | g0118 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02896 | hp1 | a0007 | c0012 | t0001 | g0105 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02896 | hp2 | a0001 | c0037 | t0001 | g0197 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02897 | hp1 | a0007 | c0012 | t0001 | g0103 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02922 | hp2 | a0006 | c0008 | t0001 | g0101 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02970 | hp1 | a0004 | c0009 | t0001 | g0114 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02976 | hp2 | a0004 | c0006 | t0001 | g0115 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0177 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0240 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03130 | hp1 | a0001 | c0007 | t0001 | g0294 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03139 | hp1 | a0019 | c0024 | t0001 | g0304 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03225 | hp1 | a0001 | c0017 | t0001 | g0049 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03225 | hp2 | a0001 | c0028 | t0001 | g0088 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03453 | hp2 | a0004 | c0009 | t0001 | g0189 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03486 | hp1 | a0009 | c0013 | t0002 | g0055 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0241 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03516 | hp1 | a0001 | c0017 | t0001 | g0060 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0092 | AFR | ESN | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03579 | hp1 | a0001 | c0005 | t0001 | g0211 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03579 | hp2 | a0001 | c0007 | t0001 | g0295 | AFR | MSL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0227 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0230 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04115 | hp2 | a0010 | c0016 | t0001 | g0222 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04184 | hp2 | a0010 | c0016 | t0001 | g0284 | SAS | BEB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0232 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04204 | hp2 | a0001 | c0004 | t0001 | g0084 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0255 | SAS | STU | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0303 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | CHB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18944 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18954 | hp1 | a0020 | c0033 | t0001 | g0217 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18961 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18977 | hp2 | a0021 | c0035 | t0001 | g0176 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18978 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18987 | hp1 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18995 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19005 | hp2 | a0022 | c0032 | t0001 | g0087 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19007 | hp1 | a0002 | c0002 | t0004 | g0243 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19011 | hp1 | a0023 | c0036 | t0001 | g0164 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19011 | hp2 | a0002 | c0018 | t0001 | g0276 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19030 | hp1 | a0001 | c0005 | t0001 | g0287 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0085 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19054 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19064 | hp1 | a0008 | c0010 | t0001 | g0220 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19067 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19068 | hp1 | a0008 | c0010 | t0001 | g0218 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19079 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19079 | hp2 | a0008 | c0010 | t0001 | g0219 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19087 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19090 | hp1 | a0001 | c0015 | t0001 | g0062 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0090 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA19240 | hp2 | a0001 | c0007 | t0001 | g0293 | AFR | YRI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | ASW | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20129 | hp2 | a0004 | c0006 | t0001 | g0111 | AFR | ASW | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | GIH | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0132 | AMR | CLM | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02486 | hp2 | a0004 | c0006 | t0001 | g0002 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02559 | hp1 | a0001 | c0029 | t0001 | g0094 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
HG06807 | hp2 | a0001 | c0007 | t0001 | g0296 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0064 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | USA | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
NA21309 | hp2 | a0024 | c0021 | t0001 | g0063 | AFR | LWK | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0035 | REF | REF | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0107 | REF | REF | SPEN_chr1_15842707_15945456 | SPEN | chr1 | 15842707 | 15945456 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15876500 | C | T | 1 | a0014 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.703C>T | p.Arg235Trp | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/15 | 1064/12385 | 703/10995 | 235/3664 | chr1 | 15876500 | |||
chr1:15920891 | G | A | 1 | a0009 | 2 | HG02886.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.1657G>A | p.Gly553Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/15 | 2018/12385 | 1657/10995 | 553/3664 | chr1 | 15920891 | |||
chr1:15928591 | G | A | 1 | a0013 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.2351G>A | p.Arg784His | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 2712/12385 | 2351/10995 | 784/3664 | chr1 | 15928591 | |||
chr1:15928710 | C | T | 1 | a0007 | 3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.2470C>T | p.Arg824Cys | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 2831/12385 | 2470/10995 | 824/3664 | chr1 | 15928710 | |||
chr1:15929149 | C | T | 5 | a0003 a0005 a0014 others(2): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
missense_variant | MODERATE | c.2909C>T | p.Ala970Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3270/12385 | 2909/10995 | 970/3664 | chr1 | 15929149 | |||
chr1:15929259 | C | A | 1 | a0018 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.3019C>A | p.Pro1007Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3380/12385 | 3019/10995 | 1007/3664 | chr1 | 15929259 | |||
chr1:15929304 | G | A | 1 | a0013 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.3064G>A | p.Val1022Met | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3425/12385 | 3064/10995 | 1022/3664 | chr1 | 15929304 | |||
chr1:15929511 | C | G | 1 | a0001 | 8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
missense_variant | MODERATE | c.3271C>G | p.Leu1091Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3632/12385 | 3271/10995 | 1091/3664 | chr1 | 15929511 | |||
chr1:15929512 | T | C | 19 | a0001 a0003 a0004 others(16): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
missense_variant | MODERATE | c.3272T>C | p.Leu1091Pro | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 3633/12385 | 3272/10995 | 1091/3664 | chr1 | 15929512 | |||
chr1:15931150 | T | C | 2 | a0006 a0024 |
4 | HG01167.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.4910T>C | p.Val1637Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5271/12385 | 4910/10995 | 1637/3664 | chr1 | 15931150 | |||
chr1:15931311 | C | T | 1 | a0023 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.5071C>T | p.Pro1691Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5432/12385 | 5071/10995 | 1691/3664 | chr1 | 15931311 | |||
chr1:15931623 | C | T | 1 | a0022 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.5383C>T | p.Pro1795Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5744/12385 | 5383/10995 | 1795/3664 | chr1 | 15931623 | |||
chr1:15931807 | A | G | 1 | a0015 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.5567A>G | p.Asn1856Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 5928/12385 | 5567/10995 | 1856/3664 | chr1 | 15931807 | |||
chr1:15932188 | C | T | 1 | a0018 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.5948C>T | p.Ser1983Leu | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6309/12385 | 5948/10995 | 1983/3664 | chr1 | 15932188 | |||
chr1:15932307 | G | A | 1 | a0016 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.6067G>A | p.Val2023Met | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6428/12385 | 6067/10995 | 2023/3664 | chr1 | 15932307 | |||
chr1:15932413 | C | T | 1 | a0011 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.6173C>T | p.Ala2058Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6534/12385 | 6173/10995 | 2058/3664 | chr1 | 15932413 | |||
chr1:15932440 | C | T | 1 | a0010 | 2 | HG04115.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.6200C>T | p.Pro2067Leu | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6561/12385 | 6200/10995 | 2067/3664 | chr1 | 15932440 | |||
chr1:15932835 | G | T | 1 | a0021 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.6595G>T | p.Ala2199Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6956/12385 | 6595/10995 | 2199/3664 | chr1 | 15932835 | |||
chr1:15932959 | C | T | 2 | a0008 a0020 |
4 | NA18954.hp1 NA19064.hp1 NA19068.hp1 others(1): Show |
missense_variant | MODERATE | c.6719C>T | p.Pro2240Leu | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7080/12385 | 6719/10995 | 2240/3664 | chr1 | 15932959 | |||
chr1:15933152 | TAGC | T | 1 | a0005 | 3 | HG00280.hp2 HG01496.hp1 HG01934.hp2 |
disruptive_inframe_deletion | MODERATE | c.6915_6917delCAG | p.Ser2306del | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7276/12385 | 6915/10995 | 2305/3664 | INFO_REALIGN_3_PRIME | chr1 | 15933152 | ||
chr1:15933318 | A | G | 19 | a0001 a0003 a0004 others(16): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
missense_variant | MODERATE | c.7078A>G | p.Asn2360Asp | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7439/12385 | 7078/10995 | 2360/3664 | chr1 | 15933318 | |||
chr1:15933420 | C | T | 1 | a0017 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.7180C>T | p.Pro2394Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7541/12385 | 7180/10995 | 2394/3664 | chr1 | 15933420 | |||
chr1:15933897 | A | G | 1 | a0006 | 3 | HG01167.hp1 HG02818.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.7657A>G | p.Ser2553Gly | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8018/12385 | 7657/10995 | 2553/3664 | chr1 | 15933897 | |||
chr1:15934018 | A | G | 2 | a0004 a0018 |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
missense_variant | MODERATE | c.7778A>G | p.Asn2593Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8139/12385 | 7778/10995 | 2593/3664 | chr1 | 15934018 | |||
chr1:15934308 | G | A | 1 | a0019 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.8068G>A | p.Val2690Met | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8429/12385 | 8068/10995 | 2690/3664 | chr1 | 15934308 | |||
chr1:15934428 | A | T | 1 | a0020 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.8188A>T | p.Ser2730Cys | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8549/12385 | 8188/10995 | 2730/3664 | chr1 | 15934428 | |||
chr1:15937527 | G | C | 1 | a0012 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.10391G>C | p.Gly3464Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/15 | 10752/12385 | 10391/10995 | 3464/3664 | chr1 | 15937527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15872927 | G | A | 1 | a0002c0018 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.195G>A | p.Ser65Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/15 | 556/12385 | 195/10995 | 65/3664 | chr1 | 15872927 | |||
chr1:15919484 | A | T | 1 | a0001c0017 | 2 | HG03225.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.1602A>T | p.Thr534Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/15 | 1963/12385 | 1602/10995 | 534/3664 | chr1 | 15919484 | |||
chr1:15919487 | A | C | 1 | a0001c0038 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1605A>C | p.Arg535Arg | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/15 | 1966/12385 | 1605/10995 | 535/3664 | chr1 | 15919487 | |||
chr1:15928412 | A | G | 1 | a0001c0037 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.2172A>G | p.Arg724Arg | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 2533/12385 | 2172/10995 | 724/3664 | chr1 | 15928412 | |||
chr1:15930761 | A | G | 3 | a0004c0006 a0004c0009 a0018c0020 |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
synonymous_variant | LOW | c.4521A>G | p.Lys1507Lys | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 4882/12385 | 4521/10995 | 1507/3664 | chr1 | 15930761 | |||
chr1:15932066 | A | T | 1 | a0001c0015 | 2 | HG02132.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.5826A>T | p.Ala1942Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6187/12385 | 5826/10995 | 1942/3664 | chr1 | 15932066 | |||
chr1:15932648 | G | A | 5 | a0001c0007 a0001c0023 a0004c0006 others(2): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(13): Show |
synonymous_variant | LOW | c.6408G>A | p.Gln2136Gln | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 6769/12385 | 6408/10995 | 2136/3664 | chr1 | 15932648 | |||
chr1:15933164 | C | T | 2 | a0001c0029 a0017c0030 |
2 | HG02145.hp1 HG02559.hp1 |
synonymous_variant | LOW | c.6924C>T | p.Thr2308Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7285/12385 | 6924/10995 | 2308/3664 | chr1 | 15933164 | |||
chr1:15933374 | C | T | 1 | a0001c0028 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.7134C>T | p.Pro2378Pro | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 7495/12385 | 7134/10995 | 2378/3664 | chr1 | 15933374 | |||
chr1:15933887 | C | T | 1 | a0001c0027 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.7647C>T | p.Val2549Val | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8008/12385 | 7647/10995 | 2549/3664 | chr1 | 15933887 | |||
chr1:15934421 | C | T | 5 | a0003c0003 a0005c0011 a0014c0039 others(2): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
synonymous_variant | LOW | c.8181C>T | p.Ala2727Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8542/12385 | 8181/10995 | 2727/3664 | chr1 | 15934421 | |||
chr1:15934460 | C | G | 1 | a0001c0026 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.8220C>G | p.Thr2740Thr | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 8581/12385 | 8220/10995 | 2740/3664 | chr1 | 15934460 | |||
chr1:15935319 | C | A | 1 | a0001c0014 | 2 | HG00323.hp2 HG01069.hp1 |
synonymous_variant | LOW | c.9079C>A | p.Arg3027Arg | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 9440/12385 | 9079/10995 | 3027/3664 | chr1 | 15935319 | |||
chr1:15935861 | C | T | 1 | a0004c0006 | 7 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(4): Show |
synonymous_variant | LOW | c.9621C>T | p.Ser3207Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 9982/12385 | 9621/10995 | 3207/3664 | chr1 | 15935861 | |||
chr1:15935909 | C | T | 5 | a0003c0003 a0005c0011 a0014c0039 others(2): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
synonymous_variant | LOW | c.9669C>T | p.Ser3223Ser | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 10030/12385 | 9669/10995 | 3223/3664 | chr1 | 15935909 | |||
chr1:15936224 | T | C | 3 | a0004c0006 a0004c0009 a0018c0020 |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
synonymous_variant | LOW | c.9984T>C | p.Ala3328Ala | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/15 | 10345/12385 | 9984/10995 | 3328/3664 | chr1 | 15936224 | |||
chr1:15937621 | C | T | 1 | a0001c0007 | 4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.10485C>T | p.Pro3495Pro | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/15 | 10846/12385 | 10485/10995 | 3495/3664 | chr1 | 15937621 | |||
chr1:15937835 | C | T | 1 | a0001c0038 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.10533C>T | p.Gly3511Gly | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/15 | 10894/12385 | 10533/10995 | 3511/3664 | chr1 | 15937835 | |||
chr1:15939409 | T | A | 4 | a0001c0004 a0001c0028 a0001c0038 others(1): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
synonymous_variant | LOW | c.10977T>A | p.Ile3659Ile | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 11338/12385 | 10977/10995 | 3659/3664 | chr1 | 15939409 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15847829 | G | C | 1 | a0001c0023t0003 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-239G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/15 | 239 | chr1 | 15847829 | ||||||
chr1:15939688 | C | G | 1 | a0003c0003t0007 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 261 | chr1 | 15939688 | ||||||
chr1:15939812 | G | A | 1 | a0009c0013t0002 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 385 | chr1 | 15939812 | ||||||
chr1:15939858 | C | A | 1 | a0002c0002t0004 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 431 | chr1 | 15939858 | ||||||
chr1:15939938 | T | C | 1 | a0001c0001t0005 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 511 | chr1 | 15939938 | ||||||
chr1:15940413 | T | C | 1 | a0001c0001t0006 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*986T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 15/15 | 986 | chr1 | 15940413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:15848166 | C | G | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+16C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848166 | |||||||
chr1:15848218 | G | T | 1 | a0003c0003t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.83+68G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848218 | |||||||
chr1:15848244 | G | T | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+94G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848244 | |||||||
chr1:15848252 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83+102C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848252 | |||||||
chr1:15848283 | C | G | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+133C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848283 | |||||||
chr1:15848379 | C | A | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+229C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848379 | |||||||
chr1:15848410 | C | G | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83+260C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848410 | |||||||
chr1:15848491 | C | CG | 5 | a0001c0001t0005g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(2): Show |
5 | HG00621.hp1 HG01496.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+345dupG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15848491 | ||||||
chr1:15848510 | G | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+360G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848510 | |||||||
chr1:15848609 | CT | C | 55 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.83+461delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15848609 | ||||||
chr1:15848626 | G | C | 1 | a0015c0031t0001g0007 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.83+476G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848626 | |||||||
chr1:15848668 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+518C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848668 | |||||||
chr1:15848822 | C | T | 106 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(103): Show |
106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.83+672C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848822 | |||||||
chr1:15848896 | A | C | 89 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0007t0001g0293 others(86): Show |
89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.83+746A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848896 | |||||||
chr1:15848903 | C | G | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.83+753C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848903 | |||||||
chr1:15848947 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.83+797G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848947 | |||||||
chr1:15848958 | C | G | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.83+808C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15848958 | |||||||
chr1:15849066 | TGTAGTGC others(10): Show |
T | 1 | a0002c0002t0001g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.83+917_83+933delGT others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849066 | |||||||
chr1:15849100 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.83+950C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849100 | |||||||
chr1:15849309 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.83+1159T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849309 | |||||||
chr1:15849436 | T | C | 1 | a0003c0003t0001g0109 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.83+1286T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849436 | |||||||
chr1:15849556 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.83+1406G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849556 | |||||||
chr1:15849622 | G | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+1472G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15849622 | |||||||
chr1:15850030 | A | C | 1 | a0001c0005t0001g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.83+1880A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850030 | |||||||
chr1:15850225 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.83+2075G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850225 | |||||||
chr1:15850226 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.83+2076C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850226 | |||||||
chr1:15850383 | ATTCTT | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.83+2236_83+2240del others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15850383 | ||||||
chr1:15850400 | GT | G | 224 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.83+2261delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15850400 | ||||||
chr1:15850475 | G | A | 1 | a0002c0002t0001g0195 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.83+2325G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850475 | |||||||
chr1:15850489 | G | C | 11 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(8): Show |
11 | HG01106.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+2339G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850489 | |||||||
chr1:15850514 | G | A | 213 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.83+2364G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850514 | |||||||
chr1:15850678 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.83+2528A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850678 | |||||||
chr1:15850688 | A | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83+2538A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850688 | |||||||
chr1:15850770 | T | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+2620T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850770 | |||||||
chr1:15850790 | A | G | 79 | a0001c0004t0001g0275 a0002c0002t0001g0004 a0002c0002t0001g0005 others(76): Show |
79 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.83+2640A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850790 | |||||||
chr1:15850975 | C | G | 1 | a0002c0002t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.83+2825C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15850975 | |||||||
chr1:15851083 | G | A | 215 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.83+2933G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851083 | |||||||
chr1:15851172 | A | C | 4 | a0001c0005t0001g0210 a0001c0005t0001g0211 a0001c0005t0001g0212 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+3022A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851172 | |||||||
chr1:15851555 | C | T | 1 | a0002c0002t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.83+3405C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851555 | |||||||
chr1:15851575 | T | G | 2 | a0002c0002t0001g0004 a0002c0002t0001g0213 |
2 | HG00621.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.83+3425T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851575 | |||||||
chr1:15851697 | TAAAG | T | 5 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+3549_83+3552del others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15851697 | ||||||
chr1:15851760 | G | A | 82 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(79): Show |
82 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.83+3610G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851760 | |||||||
chr1:15851768 | A | G | 1 | a0015c0031t0001g0007 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.83+3618A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851768 | |||||||
chr1:15851937 | C | T | 3 | a0006c0008t0001g0099 a0006c0008t0001g0100 a0006c0008t0001g0101 |
3 | HG01167.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.83+3787C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15851937 | |||||||
chr1:15852168 | A | C | 1 | a0004c0009t0001g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.83+4018A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852168 | |||||||
chr1:15852289 | C | A | 1 | a0002c0002t0001g0214 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.83+4139C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852289 | |||||||
chr1:15852389 | A | G | 1 | a0001c0015t0001g0062 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.83+4239A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852389 | |||||||
chr1:15852422 | T | C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.83+4272T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852422 | |||||||
chr1:15852613 | T | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+4463T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852613 | |||||||
chr1:15852694 | G | C | 4 | a0001c0005t0001g0210 a0001c0005t0001g0211 a0001c0005t0001g0212 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4544G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15852694 | |||||||
chr1:15853067 | G | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+4917G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853067 | |||||||
chr1:15853100 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83+4950C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853100 | |||||||
chr1:15853219 | T | A | 1 | a0024c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+5069T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853219 | |||||||
chr1:15853290 | A | G | 1 | a0003c0003t0001g0188 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.83+5140A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853290 | |||||||
chr1:15853668 | A | AT | 12 | a0001c0005t0001g0212 a0004c0006t0001g0002 a0004c0006t0001g0111 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+5531dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15853668 | ||||||
chr1:15853688 | G | A | 1 | a0003c0003t0001g0121 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.83+5538G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853688 | |||||||
chr1:15853707 | A | G | 1 | a0001c0001t0006g0097 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+5557A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853707 | |||||||
chr1:15853769 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83+5619A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853769 | |||||||
chr1:15853858 | G | A | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.83+5708G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853858 | |||||||
chr1:15853866 | A | G | 1 | a0002c0002t0001g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.83+5716A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853866 | |||||||
chr1:15853877 | C | T | 9 | a0003c0003t0001g0121 a0003c0003t0001g0180 a0003c0003t0001g0181 others(6): Show |
9 | HG00423.hp1 HG00673.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+5727C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853877 | |||||||
chr1:15853912 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.83+5762G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853912 | |||||||
chr1:15853935 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG00099.hp2 HG01175.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+5785G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15853935 | |||||||
chr1:15854003 | G | A | 19 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
19 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.83+5853G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854003 | |||||||
chr1:15854147 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.83+5997A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854147 | |||||||
chr1:15854473 | A | T | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+6323A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854473 | |||||||
chr1:15854509 | C | T | 1 | a0003c0003t0001g0179 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.83+6359C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854509 | |||||||
chr1:15854544 | A | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+6394A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854544 | |||||||
chr1:15854556 | C | G | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.83+6406C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854556 | |||||||
chr1:15854566 | C | T | 7 | a0001c0005t0001g0208 a0001c0005t0001g0209 a0001c0005t0001g0210 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+6416C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854566 | |||||||
chr1:15854665 | G | A | 1 | a0024c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+6515G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854665 | |||||||
chr1:15854906 | C | G | 2 | a0003c0003t0001g0177 a0003c0003t0001g0178 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.83+6756C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15854906 | |||||||
chr1:15855416 | T | C | 35 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(32): Show |
35 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.83+7266T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855416 | |||||||
chr1:15855484 | T | C | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.83+7334T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855484 | |||||||
chr1:15855577 | C | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83+7427C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855577 | |||||||
chr1:15855989 | A | AC | 189 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.83+7840dupC | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15855989 | ||||||
chr1:15855990 | C | CCT | 36 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0037 others(33): Show |
36 | HG00639.hp2 HG00735.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.83+7840_83+7841ins others(2): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855990 | |||||||
chr1:15855991 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0198 others(1): Show |
4 | HG01081.hp2 HG01167.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+7841T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15855991 | |||||||
chr1:15856016 | G | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.83+7866G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856016 | |||||||
chr1:15856115 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83+7965A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856115 | |||||||
chr1:15856208 | T | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+8058T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856208 | |||||||
chr1:15856318 | A | G | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.83+8168A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856318 | |||||||
chr1:15856535 | T | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+8385T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856535 | |||||||
chr1:15856542 | G | C | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+8392G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856542 | |||||||
chr1:15856558 | C | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+8408C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856558 | |||||||
chr1:15856565 | C | CT | 8 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0007t0001g0293 others(5): Show |
8 | HG00741.hp2 HG02145.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+8435dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15856565 | ||||||
chr1:15856565 | CT | C | 157 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.83+8435delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15856565 | ||||||
chr1:15856693 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+8543G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856693 | |||||||
chr1:15856749 | A | G | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.83+8599A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856749 | |||||||
chr1:15856775 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.83+8625C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15856775 | |||||||
chr1:15857050 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.83+8900C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857050 | |||||||
chr1:15857061 | C | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.83+8911C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857061 | |||||||
chr1:15857317 | G | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.83+9167G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857317 | |||||||
chr1:15857470 | C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+9320C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857470 | |||||||
chr1:15857637 | G | A | 106 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(103): Show |
106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.83+9487G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857637 | |||||||
chr1:15857660 | A | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+9510A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857660 | |||||||
chr1:15857689 | G | GT | 212 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.83+9547dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15857689 | ||||||
chr1:15857689 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.83+9539G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857689 | |||||||
chr1:15857703 | C | T | 21 | a0001c0001t0001g0098 a0001c0001t0006g0097 a0001c0004t0001g0064 others(18): Show |
21 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+9553C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857703 | |||||||
chr1:15857745 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83+9595C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15857745 | |||||||
chr1:15858021 | G | C | 2 | a0002c0002t0001g0215 a0002c0002t0001g0216 |
2 | NA18941.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.83+9871G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858021 | |||||||
chr1:15858145 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(17): Show |
20 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.83+9995G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858145 | |||||||
chr1:15858252 | C | CA | 206 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.83+10115dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858252 | ||||||
chr1:15858252 | C | CAA | 9 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0005g0001 others(6): Show |
9 | HG01074.hp2 HG02071.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+10114_83+10115d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858252 | ||||||
chr1:15858252 | CA | C | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+10115delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858252 | ||||||
chr1:15858481 | A | G | 2 | a0001c0004t0001g0064 a0001c0004t0001g0092 |
2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.83+10331A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858481 | |||||||
chr1:15858490 | A | C | 1 | a0003c0003t0001g0122 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.83+10340A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858490 | |||||||
chr1:15858572 | A | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.83+10422A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858572 | |||||||
chr1:15858628 | T | C | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.83+10478T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858628 | |||||||
chr1:15858647 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.83+10497A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858647 | |||||||
chr1:15858658 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.83+10508A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858658 | |||||||
chr1:15858800 | C | G | 1 | a0024c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+10650C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858800 | |||||||
chr1:15858811 | G | T | 2 | a0001c0029t0001g0094 a0017c0030t0001g0080 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.83+10661G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858811 | |||||||
chr1:15858861 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+10711T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858861 | |||||||
chr1:15858946 | AAAAC | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+10808_83+10811d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15858946 | ||||||
chr1:15858969 | A | G | 3 | a0007c0012t0001g0103 a0007c0012t0001g0104 a0007c0012t0001g0105 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.83+10819A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858969 | |||||||
chr1:15858997 | A | C | 14 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(11): Show |
14 | HG01106.hp2 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+10847A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15858997 | |||||||
chr1:15859110 | A | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.83+10960A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859110 | |||||||
chr1:15859126 | G | A | 1 | a0010c0016t0001g0222 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+10976G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859126 | |||||||
chr1:15859140 | G | GT | 32 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.83+11006dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | ||||||
chr1:15859140 | G | GTT | 170 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(167): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.83+11005_83+11006d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | ||||||
chr1:15859140 | G | GTTT | 20 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.83+11004_83+11006d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | ||||||
chr1:15859140 | G | GTTTT | 12 | a0001c0005t0001g0287 a0004c0006t0001g0002 a0004c0006t0001g0111 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+11003_83+11006d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | ||||||
chr1:15859140 | GT | G | 11 | a0003c0003t0001g0122 a0003c0003t0001g0123 a0003c0003t0001g0125 others(8): Show |
11 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+11006delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859140 | ||||||
chr1:15859260 | A | G | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.83+11110A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859260 | |||||||
chr1:15859340 | CTGTTTTC others(1): Show |
C | 3 | a0001c0004t0001g0089 a0001c0004t0001g0090 a0001c0004t0001g0091 |
3 | HG02486.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.83+11192_83+11199d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859340 | ||||||
chr1:15859358 | C | CT | 126 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(123): Show |
126 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.83+11225dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859358 | ||||||
chr1:15859358 | C | CTT | 9 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0001g0199 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+11224_83+11225d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859358 | ||||||
chr1:15859358 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+11208C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859358 | |||||||
chr1:15859358 | CT | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0301 others(4): Show |
7 | HG01167.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+11225delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859358 | ||||||
chr1:15859363 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.83+11213T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859363 | |||||||
chr1:15859396 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+11246C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859396 | |||||||
chr1:15859443 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+11293C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859443 | |||||||
chr1:15859450 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83+11300T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859450 | |||||||
chr1:15859658 | T | C | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.83+11508T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859658 | |||||||
chr1:15859660 | T | C | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.83+11510T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859660 | |||||||
chr1:15859665 | G | A | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.83+11515G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859665 | |||||||
chr1:15859905 | C | CTT | 12 | a0001c0001t0001g0016 a0001c0001t0001g0198 a0001c0005t0001g0288 others(9): Show |
12 | HG00323.hp1 HG00323.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.83+11778_83+11779d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTT | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.83+11777_83+11779d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTT | 31 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0031 others(28): Show |
31 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.83+11776_83+11779d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTTT | 47 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(44): Show |
47 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.83+11775_83+11779d others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTTTT | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00621.hp2 HG01515.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+11774_83+11779d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0006g0097 a0001c0004t0001g0083 a0001c0004t0001g0084 others(3): Show |
6 | HG00741.hp2 HG01074.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+11772_83+11779d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTTTTT others(3): Show |
5 | a0001c0004t0001g0086 a0001c0004t0001g0091 a0001c0004t0001g0095 others(2): Show |
5 | HG01099.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+11770_83+11779d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTTTTT others(4): Show |
4 | a0001c0004t0001g0064 a0001c0028t0001g0088 a0006c0008t0001g0099 others(1): Show |
4 | HG01167.hp1 HG03225.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+11769_83+11779d others(13): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859905 | C | CTTTTTTT others(5): Show |
1 | a0006c0008t0001g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.83+11768_83+11779d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15859905 | ||||||
chr1:15859942 | T | C | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.83+11792T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15859942 | |||||||
chr1:15860112 | T | C | 1 | a0001c0007t0001g0293 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+11962T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860112 | |||||||
chr1:15860201 | G | A | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0029t0001g0094 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+12051G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860201 | |||||||
chr1:15860227 | G | A | 105 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(102): Show |
105 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.83+12077G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860227 | |||||||
chr1:15860378 | G | GGT | 93 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
93 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.83+12267_83+12268d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGT | 33 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0044 others(30): Show |
33 | HG00558.hp2 HG01099.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+12265_83+12268d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGT | 17 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0290 others(14): Show |
17 | HG00741.hp2 HG01243.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.83+12263_83+12268d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0057 a0001c0001t0001g0298 a0001c0004t0001g0084 others(3): Show |
6 | HG00642.hp2 HG01516.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+12261_83+12268d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(3): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0098 |
3 | HG00099.hp1 HG00621.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83+12259_83+12268d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(5): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0017t0001g0060 others(1): Show |
4 | HG02074.hp1 HG02145.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+12257_83+12268d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(7): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0017t0001g0049 |
3 | HG00544.hp1 HG03225.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.83+12255_83+12268d others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.83+12253_83+12268d others(18): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(11): Show |
2 | a0001c0001t0001g0050 a0001c0004t0001g0085 |
2 | HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.83+12251_83+12268d others(20): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | G | GGTGTGTG others(15): Show |
1 | a0024c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83+12247_83+12268d others(24): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | GGT | G | 16 | a0001c0001t0001g0019 a0001c0001t0001g0191 a0001c0001t0001g0192 others(13): Show |
16 | HG01099.hp1 HG01346.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+12267_83+12268d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | GGTGT | G | 17 | a0001c0001t0001g0066 a0001c0001t0001g0205 a0001c0001t0001g0206 others(14): Show |
17 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.83+12265_83+12268d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | GGTGTGT | G | 6 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+12263_83+12268d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | GGTGTGTG others(1): Show |
G | 3 | a0004c0009t0001g0114 a0004c0009t0001g0118 a0004c0009t0001g0189 |
3 | HG02895.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.83+12261_83+12268d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | GGTGTGTG others(3): Show |
G | 11 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+12259_83+12268d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860378 | GGTGTGTG others(5): Show |
G | 1 | a0018c0020t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.83+12257_83+12268d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860378 | ||||||
chr1:15860442 | A | AGT | 53 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(50): Show |
53 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.83+12325_83+12326d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | ||||||
chr1:15860442 | A | AGTGT | 54 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(51): Show |
54 | HG00621.hp1 HG00639.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.83+12323_83+12326d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | ||||||
chr1:15860442 | A | AGTGTGT | 10 | a0001c0001t0001g0071 a0001c0001t0001g0102 a0001c0007t0001g0295 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+12321_83+12326d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | ||||||
chr1:15860442 | AGT | A | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.83+12325_83+12326d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | ||||||
chr1:15860442 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.83+12317_83+12326d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15860442 | ||||||
chr1:15860546 | C | G | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-12270C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860546 | |||||||
chr1:15860548 | T | C | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-12268T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860548 | |||||||
chr1:15860549 | C | T | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-12267C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860549 | |||||||
chr1:15860964 | G | C | 1 | a0003c0003t0001g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.84-11852G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15860964 | |||||||
chr1:15861130 | G | A | 82 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(79): Show |
82 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.84-11686G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861130 | |||||||
chr1:15861134 | CT | C | 8 | a0001c0001t0001g0011 a0001c0004t0001g0275 a0001c0014t0001g0018 others(5): Show |
8 | HG00323.hp2 HG01168.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-11666delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15861134 | ||||||
chr1:15861265 | A | G | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84-11551A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861265 | |||||||
chr1:15861287 | A | T | 1 | a0002c0002t0001g0273 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.84-11529A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861287 | |||||||
chr1:15861346 | C | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-11470C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861346 | |||||||
chr1:15861432 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.84-11384G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861432 | |||||||
chr1:15861505 | A | C | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-11311A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861505 | |||||||
chr1:15861625 | T | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-11191T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861625 | |||||||
chr1:15861652 | G | T | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.84-11164G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861652 | |||||||
chr1:15861706 | T | G | 1 | a0002c0002t0001g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.84-11110T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861706 | |||||||
chr1:15861825 | A | T | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-10991A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861825 | |||||||
chr1:15861850 | G | A | 8 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-10966G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861850 | |||||||
chr1:15861964 | C | A | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10852C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861964 | |||||||
chr1:15861966 | T | C | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10850T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861966 | |||||||
chr1:15861967 | G | T | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10849G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861967 | |||||||
chr1:15861998 | C | T | 1 | a0003c0003t0001g0171 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.84-10818C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15861998 | |||||||
chr1:15862014 | C | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG01175.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84-10802C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862014 | |||||||
chr1:15862060 | A | T | 2 | a0003c0003t0001g0166 a0003c0003t0001g0174 |
2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.84-10756A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862060 | |||||||
chr1:15862094 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.84-10722G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862094 | |||||||
chr1:15862186 | G | A | 215 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.84-10630G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862186 | |||||||
chr1:15862211 | C | T | 1 | a0002c0002t0001g0281 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.84-10605C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862211 | |||||||
chr1:15862566 | T | C | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84-10250T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862566 | |||||||
chr1:15862766 | C | CT | 11 | a0001c0001t0001g0056 a0001c0001t0001g0301 a0001c0001t0001g0302 others(8): Show |
11 | HG02895.hp1 HG02897.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-10037dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15862766 | ||||||
chr1:15862828 | C | T | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.84-9988C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862828 | |||||||
chr1:15862836 | A | G | 1 | a0002c0002t0001g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.84-9980A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862836 | |||||||
chr1:15862873 | T | A | 1 | a0002c0002t0001g0261 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.84-9943T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15862873 | |||||||
chr1:15863123 | A | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0029t0001g0094 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-9693A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863123 | |||||||
chr1:15863185 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.84-9631G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863185 | |||||||
chr1:15863474 | A | G | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.84-9342A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863474 | |||||||
chr1:15863695 | G | C | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-9121G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863695 | |||||||
chr1:15863746 | T | TA | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-9069dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15863746 | ||||||
chr1:15863766 | G | C | 79 | a0001c0004t0001g0275 a0002c0002t0001g0004 a0002c0002t0001g0005 others(76): Show |
79 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.84-9050G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863766 | |||||||
chr1:15863782 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG01175.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84-9034A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15863782 | |||||||
chr1:15864105 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.84-8711A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864105 | |||||||
chr1:15864167 | C | CT | 16 | a0003c0003t0001g0165 a0003c0003t0001g0174 a0003c0003t0001g0188 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-8630dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864167 | ||||||
chr1:15864167 | CTTTTTTT others(2): Show |
C | 214 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(211): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.84-8638_84-8630del others(9): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864167 | ||||||
chr1:15864231 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-8585C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864231 | |||||||
chr1:15864293 | C | T | 2 | a0001c0001t0001g0196 a0001c0037t0001g0197 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.84-8523C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864293 | |||||||
chr1:15864419 | C | T | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8397C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864419 | |||||||
chr1:15864470 | G | GT | 76 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(73): Show |
76 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.84-8327dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864470 | ||||||
chr1:15864470 | G | GTT | 49 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.84-8328_84-8327dup others(2): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864470 | ||||||
chr1:15864470 | GT | G | 9 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(6): Show |
9 | HG01168.hp2 HG01256.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-8327delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864470 | ||||||
chr1:15864474 | T | TG | 14 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(11): Show |
14 | HG01106.hp2 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.84-8342_84-8341ins others(1): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864474 | |||||||
chr1:15864489 | T | A | 1 | a0004c0006t0001g0111 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.84-8327T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864489 | |||||||
chr1:15864607 | G | GT | 20 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0019 others(17): Show |
20 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.84-8188dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864607 | ||||||
chr1:15864607 | GT | G | 171 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(168): Show |
171 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.84-8188delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15864607 | ||||||
chr1:15864717 | G | A | 1 | a0002c0002t0001g0228 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.84-8099G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864717 | |||||||
chr1:15864752 | C | T | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.84-8064C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864752 | |||||||
chr1:15864867 | G | C | 1 | a0001c0005t0001g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84-7949G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864867 | |||||||
chr1:15864886 | G | A | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.84-7930G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15864886 | |||||||
chr1:15865024 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84-7792T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865024 | |||||||
chr1:15865050 | CTTAATT | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(18): Show |
21 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.84-7757_84-7752del others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15865050 | ||||||
chr1:15865213 | G | A | 1 | a0001c0029t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.84-7603G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865213 | |||||||
chr1:15865242 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-7574G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865242 | |||||||
chr1:15865264 | A | G | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84-7552A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865264 | |||||||
chr1:15865420 | G | GT | 30 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0070 others(27): Show |
30 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.84-7377dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15865420 | ||||||
chr1:15865420 | GT | G | 105 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(102): Show |
105 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.84-7377delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15865420 | ||||||
chr1:15865472 | G | C | 1 | a0002c0018t0001g0276 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.84-7344G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865472 | |||||||
chr1:15865584 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-7232G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865584 | |||||||
chr1:15865701 | CAGGT | C | 106 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(103): Show |
106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.84-7114_84-7111del others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865701 | |||||||
chr1:15865722 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-7094A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865722 | |||||||
chr1:15865785 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-7031G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865785 | |||||||
chr1:15865868 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.84-6948G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865868 | |||||||
chr1:15865889 | T | G | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-6927T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865889 | |||||||
chr1:15865895 | T | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-6921T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865895 | |||||||
chr1:15865899 | A | G | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84-6917A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15865899 | |||||||
chr1:15866385 | ACT | A | 3 | a0001c0005t0001g0208 a0001c0005t0001g0209 a0001c0005t0001g0288 |
3 | HG01069.hp2 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.84-6428_84-6427del others(2): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15866385 | ||||||
chr1:15866423 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84-6393G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866423 | |||||||
chr1:15866446 | C | T | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-6370C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866446 | |||||||
chr1:15866555 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-6261A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866555 | |||||||
chr1:15866829 | A | T | 1 | a0003c0003t0001g0125 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84-5987A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866829 | |||||||
chr1:15866830 | T | G | 1 | a0003c0003t0001g0125 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84-5986T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866830 | |||||||
chr1:15866831 | G | C | 1 | a0003c0003t0001g0125 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.84-5985G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866831 | |||||||
chr1:15866994 | A | T | 1 | a0001c0004t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.84-5822A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15866994 | |||||||
chr1:15867052 | T | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-5764T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867052 | |||||||
chr1:15867502 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.84-5314C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867502 | |||||||
chr1:15867710 | G | C | 1 | a0003c0003t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.84-5106G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867710 | |||||||
chr1:15867712 | C | CT | 6 | a0001c0001t0001g0042 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG00099.hp1 HG01346.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.84-5090dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15867712 | ||||||
chr1:15867713 | T | C | 1 | a0003c0003t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.84-5103T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867713 | |||||||
chr1:15867812 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-5004C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15867812 | |||||||
chr1:15868163 | T | A | 25 | a0001c0001t0001g0098 a0001c0001t0001g0299 a0001c0001t0001g0300 others(22): Show |
25 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.84-4653T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868163 | |||||||
chr1:15868438 | C | CT | 30 | a0001c0001t0001g0098 a0001c0001t0001g0298 a0001c0001t0001g0299 others(27): Show |
30 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.84-4364dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15868438 | ||||||
chr1:15868506 | C | T | 2 | a0001c0029t0001g0094 a0017c0030t0001g0080 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.84-4310C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868506 | |||||||
chr1:15868527 | C | T | 1 | a0003c0003t0001g0163 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.84-4289C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868527 | |||||||
chr1:15868623 | A | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-4193A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868623 | |||||||
chr1:15868714 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.84-4102G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868714 | |||||||
chr1:15868764 | C | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-4052C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868764 | |||||||
chr1:15868980 | T | G | 1 | a0002c0002t0001g0238 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.84-3836T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15868980 | |||||||
chr1:15869155 | C | T | 2 | a0001c0029t0001g0094 a0017c0030t0001g0080 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.84-3661C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869155 | |||||||
chr1:15869232 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-3584G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869232 | |||||||
chr1:15869352 | G | A | 13 | a0003c0003t0001g0123 a0003c0003t0001g0139 a0003c0003t0001g0140 others(10): Show |
13 | HG00423.hp2 NA18612.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.84-3464G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869352 | |||||||
chr1:15869380 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
7 | HG00639.hp1 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-3436G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869380 | |||||||
chr1:15869580 | G | GTATT | 73 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(70): Show |
73 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.84-3204_84-3201dup others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | ||||||
chr1:15869580 | G | GTATTTAT others(1): Show |
99 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0070 others(96): Show |
99 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.84-3208_84-3201dup others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | ||||||
chr1:15869580 | G | GTATTTAT others(5): Show |
16 | a0001c0001t0001g0192 a0001c0001t0001g0202 a0001c0004t0001g0064 others(13): Show |
16 | HG00323.hp1 HG01934.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-3212_84-3201dup others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | ||||||
chr1:15869580 | G | GTATTTAT others(9): Show |
2 | a0001c0038t0001g0093 a0002c0002t0001g0249 |
2 | HG00741.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.84-3216_84-3201dup others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15869580 | ||||||
chr1:15869989 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-2827C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15869989 | |||||||
chr1:15870023 | C | G | 2 | a0001c0004t0001g0081 a0002c0002t0001g0082 |
2 | NA18952.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.84-2793C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870023 | |||||||
chr1:15870058 | G | A | 2 | a0009c0013t0002g0054 a0009c0013t0002g0055 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.84-2758G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870058 | |||||||
chr1:15870122 | G | C | 1 | a0002c0002t0001g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.84-2694G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870122 | |||||||
chr1:15870217 | A | C | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-2599A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870217 | |||||||
chr1:15870240 | A | T | 1 | a0001c0001t0001g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.84-2576A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870240 | |||||||
chr1:15870253 | T | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-2563T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870253 | |||||||
chr1:15870264 | A | G | 106 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(103): Show |
106 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.84-2552A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870264 | |||||||
chr1:15870304 | G | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.84-2512G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870304 | |||||||
chr1:15870901 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-1915C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15870901 | |||||||
chr1:15871086 | A | C | 19 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
19 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.84-1730A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871086 | |||||||
chr1:15871260 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.84-1556G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871260 | |||||||
chr1:15871443 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.84-1373C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871443 | |||||||
chr1:15871524 | G | T | 1 | a0001c0007t0001g0296 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.84-1292G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871524 | |||||||
chr1:15871563 | G | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-1253G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871563 | |||||||
chr1:15871747 | A | C | 1 | a0001c0028t0001g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.84-1069A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871747 | |||||||
chr1:15871917 | A | G | 2 | a0001c0004t0001g0089 a0001c0004t0001g0091 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.84-899A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871917 | |||||||
chr1:15871939 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-877G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15871939 | |||||||
chr1:15872145 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-671C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872145 | |||||||
chr1:15872189 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.84-627C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872189 | |||||||
chr1:15872222 | C | CA | 14 | a0001c0001t0001g0031 a0001c0001t0001g0199 a0001c0001t0001g0202 others(11): Show |
14 | HG01109.hp2 HG02040.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.84-572dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872222 | ||||||
chr1:15872222 | CA | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0036 others(79): Show |
82 | HG00544.hp1 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.84-572delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872222 | ||||||
chr1:15872222 | CAA | C | 8 | a0001c0001t0001g0075 a0001c0001t0001g0102 a0001c0004t0001g0084 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-573_84-572delAA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872222 | ||||||
chr1:15872318 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84-498C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872318 | |||||||
chr1:15872320 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.84-496C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872320 | |||||||
chr1:15872359 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0005g0001 |
3 | HG03041.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.84-457A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872359 | |||||||
chr1:15872369 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-447G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872369 | |||||||
chr1:15872462 | T | C | 1 | a0002c0002t0001g0261 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.84-354T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872462 | |||||||
chr1:15872556 | T | C | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.84-260T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872556 | |||||||
chr1:15872558 | C | T | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.84-258C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872558 | |||||||
chr1:15872587 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.84-229G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872587 | |||||||
chr1:15872599 | C | CA | 22 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0045 others(19): Show |
22 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.84-201dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872599 | ||||||
chr1:15872599 | CAAAAA | C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.84-205_84-201delAA others(3): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 15872599 | ||||||
chr1:15872661 | G | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.84-155G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872661 | |||||||
chr1:15872664 | A | C | 1 | a0002c0002t0001g0272 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.84-152A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 1/14 | chr1 | 15872664 | |||||||
chr1:15873269 | G | A | 1 | a0003c0003t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.404+133G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873269 | |||||||
chr1:15873668 | A | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.404+532A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873668 | |||||||
chr1:15873734 | C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404+598C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873734 | |||||||
chr1:15873896 | A | G | 1 | a0003c0003t0001g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.404+760A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15873896 | |||||||
chr1:15874769 | G | A | 2 | a0001c0014t0001g0018 a0001c0014t0001g0033 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.405-1433G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15874769 | |||||||
chr1:15874845 | T | C | 14 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(11): Show |
14 | HG01106.hp2 HG01175.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.405-1357T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15874845 | |||||||
chr1:15874980 | T | C | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-1222T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15874980 | |||||||
chr1:15875007 | G | T | 29 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
29 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.405-1195G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875007 | |||||||
chr1:15875169 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-1033G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875169 | |||||||
chr1:15875217 | C | T | 4 | a0002c0002t0001g0226 a0002c0002t0001g0232 a0002c0002t0001g0250 others(1): Show |
4 | HG00323.hp1 HG01074.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-985C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875217 | |||||||
chr1:15875218 | G | A | 4 | a0001c0017t0001g0049 a0001c0017t0001g0060 a0001c0029t0001g0094 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-984G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875218 | |||||||
chr1:15875264 | T | A | 1 | a0003c0003t0007g0162 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.405-938T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875264 | |||||||
chr1:15875280 | T | TTTTAA | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.405-920_405-919ins others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 15875280 | ||||||
chr1:15875399 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.405-803A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875399 | |||||||
chr1:15875440 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405-762G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875440 | |||||||
chr1:15875678 | A | T | 4 | a0001c0005t0001g0210 a0001c0005t0001g0211 a0001c0005t0001g0212 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-524A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875678 | |||||||
chr1:15875709 | C | A | 43 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(40): Show |
43 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.405-493C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875709 | |||||||
chr1:15875905 | G | A | 1 | a0002c0002t0001g0246 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.405-297G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875905 | |||||||
chr1:15875947 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-255G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 2/14 | chr1 | 15875947 | |||||||
chr1:15876852 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+174G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15876852 | |||||||
chr1:15876980 | T | C | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+302T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15876980 | |||||||
chr1:15877027 | T | C | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+349T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877027 | |||||||
chr1:15877044 | T | C | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.881+366T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877044 | |||||||
chr1:15877168 | G | T | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.881+490G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877168 | |||||||
chr1:15877198 | C | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881+520C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877198 | |||||||
chr1:15877261 | C | G | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+583C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877261 | |||||||
chr1:15877309 | C | T | 2 | a0002c0002t0001g0215 a0002c0002t0001g0216 |
2 | NA18941.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.881+631C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877309 | |||||||
chr1:15877345 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.881+667G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877345 | |||||||
chr1:15877738 | C | CT | 31 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0059 others(28): Show |
31 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.881+1083dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15877738 | ||||||
chr1:15877738 | C | CTT | 7 | a0001c0001t0001g0079 a0001c0001t0001g0098 a0001c0001t0006g0097 others(4): Show |
7 | HG01243.hp2 HG02647.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.881+1082_881+1083d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15877738 | ||||||
chr1:15877738 | CT | C | 16 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.881+1083delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15877738 | ||||||
chr1:15877795 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+1117A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15877795 | |||||||
chr1:15878006 | G | A | 22 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(19): Show |
22 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.881+1328G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878006 | |||||||
chr1:15878070 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.881+1392C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878070 | |||||||
chr1:15878170 | A | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+1492A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878170 | |||||||
chr1:15878252 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0030 |
2 | HG00280.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.881+1574A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878252 | |||||||
chr1:15878293 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.881+1615A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878293 | |||||||
chr1:15878488 | G | A | 1 | a0002c0002t0001g0263 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.881+1810G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878488 | |||||||
chr1:15878581 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.881+1903C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878581 | |||||||
chr1:15878607 | T | C | 215 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.881+1929T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878607 | |||||||
chr1:15878708 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881+2030T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878708 | |||||||
chr1:15878747 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+2069C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878747 | |||||||
chr1:15878802 | G | C | 1 | a0002c0002t0001g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.881+2124G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878802 | |||||||
chr1:15878907 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.881+2229G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15878907 | |||||||
chr1:15879004 | CA | C | 25 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.881+2346delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879004 | ||||||
chr1:15879004 | CAA | C | 206 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.881+2345_881+2346d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879004 | ||||||
chr1:15879004 | CAAA | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0205 others(4): Show |
7 | HG01175.hp2 HG01516.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+2344_881+2346d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879004 | ||||||
chr1:15879109 | T | TG | 16 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(13): Show |
16 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.881+2434dupG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879109 | ||||||
chr1:15879256 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+2578G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879256 | |||||||
chr1:15879483 | C | T | 2 | a0003c0003t0001g0109 a0003c0003t0001g0165 |
2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.881+2805C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879483 | |||||||
chr1:15879675 | A | AT | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.881+3010dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879675 | ||||||
chr1:15879675 | AT | A | 12 | a0001c0001t0001g0198 a0004c0006t0001g0002 a0004c0006t0001g0111 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.881+3010delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15879675 | ||||||
chr1:15879693 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+3015C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879693 | |||||||
chr1:15879770 | A | G | 1 | a0002c0002t0001g0263 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.881+3092A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879770 | |||||||
chr1:15879922 | G | A | 1 | a0003c0003t0001g0188 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.881+3244G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879922 | |||||||
chr1:15879961 | C | T | 1 | a0001c0004t0001g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.881+3283C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879961 | |||||||
chr1:15879962 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.881+3284G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15879962 | |||||||
chr1:15880007 | A | C | 1 | a0002c0002t0001g0213 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.881+3329A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880007 | |||||||
chr1:15880062 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01243.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.881+3384T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880062 | |||||||
chr1:15880336 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.881+3658C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880336 | |||||||
chr1:15880453 | C | CT | 42 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0031 others(39): Show |
42 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.881+3797dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15880453 | ||||||
chr1:15880453 | C | CTT | 17 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0001t0006g0097 others(14): Show |
17 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.881+3796_881+3797d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15880453 | ||||||
chr1:15880453 | CT | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0027 others(13): Show |
16 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.881+3797delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15880453 | ||||||
chr1:15880544 | C | T | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.881+3866C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880544 | |||||||
chr1:15880676 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.881+3998C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880676 | |||||||
chr1:15880811 | T | C | 1 | a0001c0004t0001g0084 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.881+4133T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880811 | |||||||
chr1:15880976 | C | T | 1 | a0003c0003t0001g0157 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.881+4298C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15880976 | |||||||
chr1:15881193 | C | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+4515C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881193 | |||||||
chr1:15881208 | G | C | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.881+4530G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881208 | |||||||
chr1:15881367 | T | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.881+4689T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881367 | |||||||
chr1:15881497 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.881+4819A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881497 | |||||||
chr1:15881768 | G | A | 1 | a0003c0003t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.881+5090G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15881768 | |||||||
chr1:15882109 | T | C | 227 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.881+5431T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882109 | |||||||
chr1:15882138 | T | A | 231 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.881+5460T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882138 | |||||||
chr1:15882384 | A | G | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+5706A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882384 | |||||||
chr1:15882385 | G | A | 1 | a0003c0003t0001g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.881+5707G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882385 | |||||||
chr1:15882422 | G | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.881+5744G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882422 | |||||||
chr1:15882433 | G | A | 21 | a0001c0001t0001g0098 a0001c0001t0006g0097 a0001c0004t0001g0064 others(18): Show |
21 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.881+5755G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882433 | |||||||
chr1:15882636 | G | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+5958G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882636 | |||||||
chr1:15882717 | G | T | 2 | a0003c0003t0001g0166 a0003c0003t0001g0174 |
2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.881+6039G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882717 | |||||||
chr1:15882915 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG01175.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.881+6237C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15882915 | |||||||
chr1:15883112 | A | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.881+6434A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883112 | |||||||
chr1:15883365 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+6687G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883365 | |||||||
chr1:15883516 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+6838G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883516 | |||||||
chr1:15883546 | G | A | 1 | a0002c0002t0001g0213 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.881+6868G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883546 | |||||||
chr1:15883572 | C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+6894C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883572 | |||||||
chr1:15883617 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.881+6939G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883617 | |||||||
chr1:15883675 | T | C | 1 | a0001c0004t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.881+6997T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883675 | |||||||
chr1:15883715 | AT | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+7046delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15883715 | ||||||
chr1:15883807 | CT | C | 220 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.881+7149delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15883807 | ||||||
chr1:15883807 | CTT | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0036 others(4): Show |
7 | HG01109.hp1 HG01168.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+7148_881+7149d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15883807 | ||||||
chr1:15883848 | C | T | 1 | a0017c0030t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.881+7170C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883848 | |||||||
chr1:15883862 | T | G | 1 | a0001c0015t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.881+7184T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883862 | |||||||
chr1:15883878 | C | T | 215 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.881+7200C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883878 | |||||||
chr1:15883937 | G | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+7259G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883937 | |||||||
chr1:15883941 | C | G | 1 | a0003c0003t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.881+7263C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15883941 | |||||||
chr1:15884056 | C | T | 2 | a0009c0013t0002g0054 a0009c0013t0002g0055 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.881+7378C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884056 | |||||||
chr1:15884505 | T | C | 2 | a0002c0002t0001g0280 a0002c0002t0001g0283 |
2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.881+7827T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884505 | |||||||
chr1:15884520 | A | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+7842A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884520 | |||||||
chr1:15884701 | C | CTTTCCT | 3 | a0001c0001t0001g0075 a0001c0001t0001g0102 a0001c0027t0001g0076 |
3 | HG01891.hp1 HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.881+8039_881+8044d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15884701 | ||||||
chr1:15884739 | CT | C | 232 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(229): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.881+8073delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15884739 | ||||||
chr1:15884743 | T | C | 9 | a0003c0003t0001g0125 a0003c0003t0001g0126 a0003c0003t0001g0127 others(6): Show |
9 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+8065T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884743 | |||||||
chr1:15884770 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.881+8092C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884770 | |||||||
chr1:15884778 | G | T | 1 | a0003c0003t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.881+8100G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884778 | |||||||
chr1:15884782 | A | G | 227 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.881+8104A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884782 | |||||||
chr1:15884816 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.881+8138C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884816 | |||||||
chr1:15884889 | C | G | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881+8211C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884889 | |||||||
chr1:15884984 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+8306G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15884984 | |||||||
chr1:15885232 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+8554C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885232 | |||||||
chr1:15885323 | C | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+8645C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885323 | |||||||
chr1:15885396 | C | G | 1 | a0003c0003t0001g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.881+8718C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885396 | |||||||
chr1:15885447 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+8769C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885447 | |||||||
chr1:15885696 | C | G | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+9018C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885696 | |||||||
chr1:15885724 | G | T | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.881+9046G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885724 | |||||||
chr1:15885810 | C | CT | 4 | a0001c0005t0001g0210 a0001c0005t0001g0211 a0001c0005t0001g0212 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+9139dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15885810 | ||||||
chr1:15885810 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+9132C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885810 | |||||||
chr1:15885999 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+9321G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15885999 | |||||||
chr1:15886011 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.881+9333C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886011 | |||||||
chr1:15886140 | T | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+9462T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886140 | |||||||
chr1:15886244 | G | A | 223 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.881+9566G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886244 | |||||||
chr1:15886415 | C | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.881+9737C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886415 | |||||||
chr1:15886494 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG01106.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+9816G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886494 | |||||||
chr1:15886792 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+10114G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15886792 | |||||||
chr1:15887018 | G | A | 75 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(72): Show |
75 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.881+10340G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887018 | |||||||
chr1:15887108 | T | G | 1 | a0002c0002t0001g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.881+10430T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887108 | |||||||
chr1:15887276 | A | AT | 120 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(117): Show |
120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.881+10620dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887276 | ||||||
chr1:15887276 | A | ATT | 86 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.881+10619_881+1062 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887276 | ||||||
chr1:15887276 | A | ATTT | 17 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0050 others(14): Show |
17 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+10618_881+1062 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887276 | ||||||
chr1:15887373 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.881+10695C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887373 | |||||||
chr1:15887575 | G | T | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+10897G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887575 | |||||||
chr1:15887590 | T | A | 2 | a0003c0003t0001g0144 a0003c0003t0001g0145 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.881+10912T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887590 | |||||||
chr1:15887653 | T | C | 2 | a0002c0002t0001g0280 a0002c0002t0001g0283 |
2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.881+10975T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15887653 | |||||||
chr1:15887720 | T | TA | 7 | a0001c0004t0001g0081 a0001c0004t0001g0083 a0001c0004t0001g0084 others(4): Show |
7 | HG00741.hp2 HG01074.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+11055dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15887720 | ||||||
chr1:15888322 | T | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+11644T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888322 | |||||||
chr1:15888326 | TTTA | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+11654_881+1165 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15888326 | ||||||
chr1:15888481 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881+11803G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888481 | |||||||
chr1:15888711 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.881+12033C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888711 | |||||||
chr1:15888757 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881+12079G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888757 | |||||||
chr1:15888841 | G | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881+12163G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888841 | |||||||
chr1:15888958 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.881+12280C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15888958 | |||||||
chr1:15889113 | G | C | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.881+12435G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889113 | |||||||
chr1:15889164 | C | CT | 172 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.881+12502dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15889164 | ||||||
chr1:15889164 | C | CTT | 35 | a0001c0001t0001g0077 a0001c0001t0001g0098 a0001c0001t0001g0191 others(32): Show |
35 | HG00642.hp2 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.881+12501_881+1250 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15889164 | ||||||
chr1:15889170 | T | C | 1 | a0002c0002t0001g0282 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.881+12492T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889170 | |||||||
chr1:15889424 | C | T | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.881+12746C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889424 | |||||||
chr1:15889457 | T | C | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.881+12779T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889457 | |||||||
chr1:15889608 | A | G | 1 | a0002c0002t0001g0260 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.881+12930A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889608 | |||||||
chr1:15889928 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.881+13250T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889928 | |||||||
chr1:15889983 | G | A | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.881+13305G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15889983 | |||||||
chr1:15890008 | C | T | 1 | a0003c0003t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.881+13330C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890008 | |||||||
chr1:15890123 | T | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+13445T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890123 | |||||||
chr1:15890148 | A | G | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.881+13470A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890148 | |||||||
chr1:15890207 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881+13529A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890207 | |||||||
chr1:15890389 | A | C | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.881+13711A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890389 | |||||||
chr1:15890556 | AG | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0014t0001g0018 |
3 | HG00323.hp2 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.881+13880delG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890556 | ||||||
chr1:15890558 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(20): Show |
23 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.881+13880G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890558 | |||||||
chr1:15890558 | G | GT | 11 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0079 others(8): Show |
11 | HG02486.hp1 HG02572.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+13902dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890558 | ||||||
chr1:15890558 | G | GTTT | 8 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.881+13900_881+1390 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890558 | ||||||
chr1:15890558 | GT | G | 10 | a0001c0001t0001g0042 a0001c0037t0001g0197 a0002c0002t0001g0240 others(7): Show |
10 | HG00099.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.881+13902delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15890558 | ||||||
chr1:15890559 | T | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0014t0001g0018 |
3 | HG00323.hp2 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.881+13881T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890559 | |||||||
chr1:15890712 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+14034C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890712 | |||||||
chr1:15890870 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.881+14192C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890870 | |||||||
chr1:15890916 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.881+14238C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890916 | |||||||
chr1:15890999 | G | A | 2 | a0002c0002t0001g0230 a0002c0002t0001g0241 |
2 | HG03490.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.881+14321G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15890999 | |||||||
chr1:15891216 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.881+14538T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891216 | |||||||
chr1:15891270 | T | C | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881+14592T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891270 | |||||||
chr1:15891352 | A | AT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(21): Show |
24 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.881+14691dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15891352 | ||||||
chr1:15891403 | G | T | 1 | a0001c0029t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.881+14725G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891403 | |||||||
chr1:15891435 | T | G | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+14757T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891435 | |||||||
chr1:15891476 | C | T | 1 | a0001c0017t0001g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881+14798C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891476 | |||||||
chr1:15891601 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.881+14923C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891601 | |||||||
chr1:15891694 | T | C | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.881+15016T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891694 | |||||||
chr1:15891777 | G | T | 2 | a0001c0014t0001g0018 a0001c0014t0001g0033 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.881+15099G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891777 | |||||||
chr1:15891786 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.881+15108G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891786 | |||||||
chr1:15891794 | A | G | 2 | a0001c0015t0001g0046 a0001c0015t0001g0062 |
2 | HG02132.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.881+15116A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891794 | |||||||
chr1:15891899 | G | GT | 4 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0005g0001 others(1): Show |
4 | HG01168.hp2 HG03041.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+15228dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15891899 | ||||||
chr1:15891906 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.881+15228T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891906 | |||||||
chr1:15891906 | T | TA | 81 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0298 others(78): Show |
81 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.881+15240dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15891906 | ||||||
chr1:15891907 | A | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0203 a0001c0014t0001g0033 others(1): Show |
4 | HG01069.hp1 HG01106.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+15229A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15891907 | |||||||
chr1:15892012 | C | CT | 9 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0108 others(6): Show |
9 | HG00639.hp2 HG00741.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+15359dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | ||||||
chr1:15892012 | C | CTT | 10 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.881+15358_881+1535 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | ||||||
chr1:15892012 | CT | C | 137 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.881+15359delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | ||||||
chr1:15892012 | CTTTTTTT | C | 71 | a0001c0001t0001g0106 a0001c0029t0001g0094 a0003c0003t0001g0109 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.881+15353_881+1535 others(11): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | ||||||
chr1:15892012 | CTTTTTTT others(3): Show |
C | 1 | a0022c0032t0001g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.881+15350_881+1535 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | ||||||
chr1:15892012 | CTTTTTTT others(5): Show |
C | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.881+15348_881+1535 others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15892012 | ||||||
chr1:15892071 | A | C | 3 | a0001c0004t0001g0083 a0001c0004t0001g0084 a0001c0038t0001g0093 |
3 | HG00741.hp2 HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.881+15393A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892071 | |||||||
chr1:15892240 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881+15562G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892240 | |||||||
chr1:15892328 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881+15650G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892328 | |||||||
chr1:15892361 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.881+15683T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892361 | |||||||
chr1:15892991 | A | G | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+16313A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15892991 | |||||||
chr1:15893025 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.882-16296G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893025 | |||||||
chr1:15893055 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-16266G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893055 | |||||||
chr1:15893114 | C | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-16207C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893114 | |||||||
chr1:15893342 | G | A | 1 | a0002c0002t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882-15979G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893342 | |||||||
chr1:15893623 | G | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.882-15698G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893623 | |||||||
chr1:15893825 | G | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.882-15496G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893825 | |||||||
chr1:15893979 | A | G | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.882-15342A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15893979 | |||||||
chr1:15894024 | A | G | 1 | a0002c0002t0001g0282 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.882-15297A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894024 | |||||||
chr1:15894121 | G | C | 1 | a0004c0009t0001g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.882-15200G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894121 | |||||||
chr1:15894533 | G | GTTTTTTT others(3): Show |
3 | a0004c0006t0001g0111 a0004c0006t0001g0113 a0004c0009t0001g0118 |
3 | HG01071.hp2 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.882-14786_882-1478 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894533 | ||||||
chr1:15894535 | T | G | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-14786T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894535 | |||||||
chr1:15894535 | T | TG | 3 | a0001c0005t0001g0208 a0001c0005t0001g0209 a0001c0005t0001g0288 |
3 | HG01069.hp2 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.882-14785dupG | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894535 | ||||||
chr1:15894536 | G | GT | 80 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(77): Show |
80 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.882-14762dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894536 | ||||||
chr1:15894536 | G | GTT | 6 | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0196 others(3): Show |
6 | HG03453.hp1 HG04115.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-14763_882-1476 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15894536 | ||||||
chr1:15894536 | G | T | 10 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-14785G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894536 | |||||||
chr1:15894545 | T | G | 1 | a0001c0029t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.882-14776T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894545 | |||||||
chr1:15894690 | G | A | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.882-14631G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894690 | |||||||
chr1:15894860 | A | C | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-14461A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15894860 | |||||||
chr1:15895123 | T | G | 2 | a0001c0014t0001g0018 a0001c0014t0001g0033 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.882-14198T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895123 | |||||||
chr1:15895238 | T | G | 4 | a0002c0002t0001g0226 a0002c0002t0001g0232 a0002c0002t0001g0250 others(1): Show |
4 | HG00323.hp1 HG01074.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-14083T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895238 | |||||||
chr1:15895288 | A | C | 1 | a0007c0012t0001g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.882-14033A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895288 | |||||||
chr1:15895319 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.882-14002C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895319 | |||||||
chr1:15895414 | A | C | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882-13907A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895414 | |||||||
chr1:15895678 | C | CT | 46 | a0001c0001t0001g0106 a0001c0001t0001g0299 a0001c0001t0001g0300 others(43): Show |
46 | HG00558.hp2 HG00741.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.882-13624dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15895678 | ||||||
chr1:15895678 | CT | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0298 others(5): Show |
8 | HG00642.hp2 HG00673.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.882-13624delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15895678 | ||||||
chr1:15895708 | T | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-13613T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895708 | |||||||
chr1:15895734 | G | T | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-13587G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895734 | |||||||
chr1:15895772 | C | T | 6 | a0002c0002t0001g0234 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | NA18971.hp2 NA19005.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-13549C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895772 | |||||||
chr1:15895847 | T | A | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-13474T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15895847 | |||||||
chr1:15896099 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-13222T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896099 | |||||||
chr1:15896187 | C | CT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0044 others(19): Show |
22 | HG00099.hp2 HG00621.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.882-13106dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | ||||||
chr1:15896187 | CT | C | 38 | a0001c0001t0001g0024 a0001c0001t0001g0191 a0001c0001t0001g0192 others(35): Show |
38 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.882-13106delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | ||||||
chr1:15896187 | CTT | C | 42 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(39): Show |
42 | HG00642.hp2 HG01071.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.882-13107_882-1310 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | ||||||
chr1:15896187 | CTTT | C | 89 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(86): Show |
89 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.882-13108_882-1310 others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15896187 | ||||||
chr1:15896318 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.882-13003C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896318 | |||||||
chr1:15896332 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01243.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.882-12989A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896332 | |||||||
chr1:15896424 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-12897G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896424 | |||||||
chr1:15896509 | T | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-12812T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896509 | |||||||
chr1:15896582 | A | G | 1 | a0005c0011t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.882-12739A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896582 | |||||||
chr1:15896728 | A | G | 2 | a0003c0003t0001g0109 a0003c0003t0001g0165 |
2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.882-12593A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896728 | |||||||
chr1:15896826 | G | C | 1 | a0002c0002t0001g0268 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.882-12495G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896826 | |||||||
chr1:15896836 | C | T | 87 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(84): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-12485C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896836 | |||||||
chr1:15896879 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.882-12442G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896879 | |||||||
chr1:15896893 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.882-12428A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15896893 | |||||||
chr1:15897181 | G | T | 1 | a0002c0002t0001g0260 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.882-12140G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897181 | |||||||
chr1:15897200 | G | T | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.882-12121G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897200 | |||||||
chr1:15897314 | G | A | 1 | a0003c0003t0001g0132 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.882-12007G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897314 | |||||||
chr1:15897345 | T | C | 223 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.882-11976T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897345 | |||||||
chr1:15897365 | CT | C | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-11942delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15897365 | ||||||
chr1:15897642 | G | A | 1 | a0003c0003t0001g0147 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.882-11679G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897642 | |||||||
chr1:15897673 | T | A | 3 | a0001c0004t0001g0089 a0001c0004t0001g0090 a0001c0004t0001g0091 |
3 | HG02486.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882-11648T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897673 | |||||||
chr1:15897845 | T | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.882-11476T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15897845 | |||||||
chr1:15898002 | T | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.882-11319T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898002 | |||||||
chr1:15898167 | T | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-11154T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898167 | |||||||
chr1:15898173 | T | TTG | 19 | a0001c0001t0001g0079 a0001c0001t0001g0106 a0001c0001t0001g0196 others(16): Show |
19 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.882-11112_882-1111 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | T | TTGTG | 20 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0068 others(17): Show |
20 | HG00639.hp2 HG01175.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.882-11114_882-1111 others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | T | TTGTGTG | 16 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0108 others(13): Show |
16 | HG01106.hp1 HG01106.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.882-11116_882-1111 others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | T | TTGTGTGT others(1): Show |
7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | HG01256.hp1 HG01261.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.882-11118_882-1111 others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | TTG | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
61 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.882-11112_882-1111 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | TTGTG | T | 9 | a0001c0001t0001g0098 a0001c0001t0001g0289 a0001c0001t0001g0290 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.882-11114_882-1111 others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | TTGTGTG | T | 13 | a0001c0001t0001g0025 a0002c0002t0001g0004 a0002c0002t0001g0213 others(10): Show |
13 | HG00280.hp1 HG00621.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.882-11116_882-1111 others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | TTGTGTGT others(1): Show |
T | 3 | a0002c0002t0001g0190 a0002c0002t0001g0278 a0004c0009t0001g0114 |
3 | HG02970.hp1 NA18966.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.882-11118_882-1111 others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | TTGTGTGT others(3): Show |
T | 10 | a0001c0027t0001g0076 a0003c0003t0001g0125 a0003c0003t0001g0126 others(7): Show |
10 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-11120_882-1111 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898173 | TTGTGTGT others(5): Show |
T | 62 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(59): Show |
62 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.882-11122_882-1111 others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898173 | ||||||
chr1:15898233 | C | T | 1 | a0002c0002t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.882-11088C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898233 | |||||||
chr1:15898382 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.882-10939G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898382 | |||||||
chr1:15898503 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.882-10818T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898503 | |||||||
chr1:15898558 | C | CT | 51 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(48): Show |
51 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.882-10748dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15898558 | ||||||
chr1:15898681 | T | G | 1 | a0003c0003t0001g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.882-10640T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898681 | |||||||
chr1:15898682 | C | G | 1 | a0003c0003t0001g0156 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.882-10639C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15898682 | |||||||
chr1:15899003 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.882-10318A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899003 | |||||||
chr1:15899022 | G | A | 2 | a0002c0002t0001g0240 a0002c0002t0001g0245 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.882-10299G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899022 | |||||||
chr1:15899069 | G | T | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-10252G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899069 | |||||||
chr1:15899174 | T | G | 4 | a0008c0010t0001g0218 a0008c0010t0001g0219 a0008c0010t0001g0220 others(1): Show |
4 | NA18954.hp1 NA19064.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-10147T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899174 | |||||||
chr1:15899233 | C | T | 25 | a0003c0003t0001g0122 a0003c0003t0001g0134 a0003c0003t0001g0135 others(22): Show |
25 | HG00438.hp1 HG00544.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.882-10088C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899233 | |||||||
chr1:15899342 | T | A | 3 | a0007c0012t0001g0103 a0007c0012t0001g0104 a0007c0012t0001g0105 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.882-9979T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899342 | |||||||
chr1:15899394 | G | C | 1 | a0003c0003t0007g0162 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.882-9927G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899394 | |||||||
chr1:15899458 | G | A | 1 | a0002c0002t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.882-9863G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899458 | |||||||
chr1:15899477 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.882-9844G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899477 | |||||||
chr1:15899537 | G | GT | 105 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0037 others(102): Show |
105 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.882-9758dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15899537 | ||||||
chr1:15899537 | G | GTT | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(26): Show |
29 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.882-9759_882-9758d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15899537 | ||||||
chr1:15899537 | GT | G | 21 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0001t0006g0097 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.882-9758delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15899537 | ||||||
chr1:15899668 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.882-9653A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15899668 | |||||||
chr1:15900139 | A | C | 196 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.882-9182A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900139 | |||||||
chr1:15900378 | G | A | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-8943G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900378 | |||||||
chr1:15900405 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-8916G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900405 | |||||||
chr1:15900713 | GAA | G | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-8606_882-8605d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15900713 | ||||||
chr1:15900855 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-8466G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900855 | |||||||
chr1:15900949 | T | C | 1 | a0003c0003t0001g0150 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.882-8372T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15900949 | |||||||
chr1:15901024 | T | C | 1 | a0011c0034t0001g0264 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.882-8297T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901024 | |||||||
chr1:15901028 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.882-8293T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901028 | |||||||
chr1:15901125 | G | A | 2 | a0002c0002t0001g0240 a0002c0002t0001g0245 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.882-8196G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901125 | |||||||
chr1:15901294 | G | A | 1 | a0003c0003t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882-8027G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901294 | |||||||
chr1:15901327 | T | A | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-7994T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901327 | |||||||
chr1:15901348 | T | TA | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-7963dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901348 | ||||||
chr1:15901415 | T | C | 1 | a0003c0003t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.882-7906T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901415 | |||||||
chr1:15901512 | T | C | 87 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(84): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-7809T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901512 | |||||||
chr1:15901591 | A | G | 1 | a0021c0035t0001g0176 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.882-7730A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901591 | |||||||
chr1:15901649 | C | CA | 28 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0047 others(25): Show |
28 | HG00673.hp1 HG01123.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.882-7652dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901649 | ||||||
chr1:15901649 | CA | C | 13 | a0001c0001t0001g0027 a0001c0001t0001g0205 a0001c0001t0001g0206 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.882-7652delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901649 | ||||||
chr1:15901665 | A | AC | 4 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0001g0153 others(1): Show |
4 | HG01934.hp2 HG02015.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-7656_882-7655i others(3): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901665 | |||||||
chr1:15901665 | A | C | 82 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(79): Show |
82 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.882-7656A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901665 | |||||||
chr1:15901703 | C | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-7618C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901703 | |||||||
chr1:15901839 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-7482C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901839 | |||||||
chr1:15901861 | A | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0297 |
2 | HG00639.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.882-7460A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901861 | |||||||
chr1:15901867 | T | C | 3 | a0001c0004t0001g0089 a0001c0004t0001g0090 a0001c0004t0001g0091 |
3 | HG02486.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882-7454T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901867 | |||||||
chr1:15901914 | T | C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.882-7407T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901914 | |||||||
chr1:15901928 | G | GT | 10 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(7): Show |
10 | HG02258.hp2 HG02273.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-7373dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | ||||||
chr1:15901928 | GT | G | 125 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.882-7373delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | ||||||
chr1:15901928 | GTT | G | 68 | a0001c0023t0003g0006 a0003c0003t0001g0109 a0003c0003t0001g0121 others(65): Show |
68 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.882-7374_882-7373d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | ||||||
chr1:15901928 | GTTT | G | 10 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.882-7375_882-7373d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15901928 | ||||||
chr1:15901948 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.882-7373T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15901948 | |||||||
chr1:15902031 | C | T | 1 | a0001c0026t0001g0096 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.882-7290C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902031 | |||||||
chr1:15902055 | A | G | 19 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(16): Show |
19 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.882-7266A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902055 | |||||||
chr1:15902244 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882-7077C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902244 | |||||||
chr1:15902285 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.882-7036T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902285 | |||||||
chr1:15902356 | C | T | 1 | a0002c0002t0001g0269 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.882-6965C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902356 | |||||||
chr1:15902357 | A | C | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-6964A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902357 | |||||||
chr1:15902418 | T | C | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-6903T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902418 | |||||||
chr1:15902464 | T | TA | 87 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(84): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-6849dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15902464 | ||||||
chr1:15902476 | G | C | 1 | a0002c0002t0001g0258 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.882-6845G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902476 | |||||||
chr1:15902589 | C | T | 56 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(53): Show |
56 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.882-6732C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902589 | |||||||
chr1:15902639 | G | A | 1 | a0002c0002t0004g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.882-6682G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902639 | |||||||
chr1:15902734 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.882-6587T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902734 | |||||||
chr1:15902879 | C | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0278 |
2 | NA18966.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.882-6442C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15902879 | |||||||
chr1:15903102 | A | T | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.882-6219A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903102 | |||||||
chr1:15903239 | G | A | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-6082G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903239 | |||||||
chr1:15903567 | G | A | 86 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(83): Show |
86 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.882-5754G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903567 | |||||||
chr1:15903597 | A | T | 1 | a0001c0004t0001g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.882-5724A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903597 | |||||||
chr1:15903897 | A | G | 2 | a0001c0029t0001g0094 a0017c0030t0001g0080 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.882-5424A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15903897 | |||||||
chr1:15904162 | T | C | 87 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(84): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.882-5159T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904162 | |||||||
chr1:15904215 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882-5106T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904215 | |||||||
chr1:15904245 | A | G | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-5076A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904245 | |||||||
chr1:15904452 | C | CA | 16 | a0001c0001t0001g0203 a0002c0002t0001g0004 a0002c0002t0001g0005 others(13): Show |
16 | HG00621.hp1 HG01123.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.882-4844dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAA | 41 | a0001c0001t0001g0078 a0002c0002t0001g0230 a0002c0002t0001g0241 others(38): Show |
41 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.882-4845_882-4844d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAA | 22 | a0001c0001t0001g0079 a0003c0003t0001g0109 a0003c0003t0001g0121 others(19): Show |
22 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.882-4846_882-4844d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAA | 14 | a0001c0001t0001g0045 a0003c0003t0001g0125 a0003c0003t0001g0126 others(11): Show |
14 | HG00673.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.882-4847_882-4844d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAA | 6 | a0003c0003t0001g0130 a0003c0003t0001g0132 a0003c0003t0001g0165 others(3): Show |
6 | HG01123.hp2 HG01192.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.882-4848_882-4844d others(7): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAA | 10 | a0001c0001t0001g0202 a0001c0005t0001g0204 a0001c0005t0001g0208 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-4849_882-4844d others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA | 10 | a0001c0001t0001g0192 a0001c0001t0001g0196 a0001c0001t0001g0198 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-4850_882-4844d others(9): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0194 others(5): Show |
8 | HG01106.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-4851_882-4844d others(10): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882-4853_882-4844d others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0051 |
2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.882-4855_882-4844d others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0290 others(5): Show |
8 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-4856_882-4844d others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(7): Show |
11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(8): Show |
11 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-4857_882-4844d others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0027 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-4858_882-4844d others(17): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG01175.hp1 HG01243.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-4859_882-4844d others(18): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0009 a0015c0031t0001g0007 |
2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.882-4860_882-4844d others(19): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0058 |
3 | HG00280.hp1 HG01168.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.882-4863_882-4844d others(22): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0056 others(1): Show |
4 | HG00544.hp1 HG00621.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-4865_882-4844d others(24): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0061 a0001c0015t0001g0046 a0001c0015t0001g0062 |
3 | HG02132.hp1 HG03654.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.882-4866_882-4844d others(25): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.882-4868_882-4844d others(27): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.882-4844_882-4843i others(31): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882-4844_882-4843i others(32): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.882-4844_882-4843i others(38): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | CAA | C | 8 | a0001c0001t0001g0289 a0001c0004t0001g0086 a0001c0007t0001g0293 others(5): Show |
8 | HG02622.hp2 HG03130.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-4845_882-4844d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | CAAAA | C | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.882-4847_882-4844d others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904452 | CAAAAAAA | C | 33 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(30): Show |
33 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.882-4850_882-4844d others(9): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904452 | ||||||
chr1:15904478 | G | A | 69 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(66): Show |
69 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.882-4843G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904478 | |||||||
chr1:15904479 | T | A | 69 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(66): Show |
69 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.882-4842T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904479 | |||||||
chr1:15904535 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.882-4786C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904535 | |||||||
chr1:15904648 | A | AT | 23 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(20): Show |
23 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.882-4657dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904648 | ||||||
chr1:15904648 | AT | A | 90 | a0001c0001t0001g0024 a0001c0001t0001g0074 a0001c0005t0001g0208 others(87): Show |
90 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.882-4657delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15904648 | ||||||
chr1:15904712 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-4609C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904712 | |||||||
chr1:15904717 | T | C | 24 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(21): Show |
24 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.882-4604T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15904717 | |||||||
chr1:15905012 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.882-4309C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905012 | |||||||
chr1:15905076 | T | C | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882-4245T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905076 | |||||||
chr1:15905251 | T | C | 220 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.882-4070T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905251 | |||||||
chr1:15905314 | C | G | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.882-4007C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905314 | |||||||
chr1:15905324 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-3997C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905324 | |||||||
chr1:15905338 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.882-3983C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905338 | |||||||
chr1:15905527 | T | A | 1 | a0002c0002t0001g0216 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.882-3794T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905527 | |||||||
chr1:15905913 | C | T | 2 | a0003c0003t0001g0166 a0003c0003t0001g0174 |
2 | HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.882-3408C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905913 | |||||||
chr1:15905956 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-3365G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15905956 | |||||||
chr1:15906139 | C | T | 5 | a0003c0003t0001g0168 a0003c0003t0001g0169 a0003c0003t0001g0170 others(2): Show |
5 | HG01168.hp2 HG01255.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-3182C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906139 | |||||||
chr1:15906196 | C | T | 1 | a0002c0002t0001g0238 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.882-3125C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906196 | |||||||
chr1:15906345 | T | G | 2 | a0002c0002t0001g0237 a0002c0002t0001g0249 |
2 | NA18944.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.882-2976T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906345 | |||||||
chr1:15906453 | C | CT | 24 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(21): Show |
24 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.882-2843dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | ||||||
chr1:15906453 | CT | C | 54 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0021 others(51): Show |
54 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.882-2843delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | ||||||
chr1:15906453 | CTT | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0025 others(6): Show |
9 | HG00280.hp1 HG01069.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-2844_882-2843d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | ||||||
chr1:15906453 | CTTT | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
41 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.882-2845_882-2843d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | ||||||
chr1:15906453 | CTTTTTTT others(7): Show |
C | 74 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0002c0002t0001g0216 others(71): Show |
74 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.882-2856_882-2843d others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906453 | ||||||
chr1:15906485 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.882-2836G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906485 | |||||||
chr1:15906557 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-2764C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906557 | |||||||
chr1:15906605 | C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-2716C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906605 | |||||||
chr1:15906631 | T | C | 1 | a0002c0002t0004g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.882-2690T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906631 | |||||||
chr1:15906773 | C | CT | 29 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0037 others(26): Show |
29 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.882-2527dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906773 | ||||||
chr1:15906773 | C | CTT | 16 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.882-2528_882-2527d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906773 | ||||||
chr1:15906773 | CT | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0061 others(112): Show |
115 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.882-2527delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15906773 | ||||||
chr1:15906876 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-2445G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15906876 | |||||||
chr1:15907384 | G | A | 1 | a0002c0002t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.882-1937G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15907384 | |||||||
chr1:15907645 | C | G | 1 | a0010c0016t0001g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.882-1676C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15907645 | |||||||
chr1:15908111 | C | T | 1 | a0004c0009t0001g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.882-1210C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908111 | |||||||
chr1:15908170 | G | GCTA | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-1135_882-1133d others(5): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15908170 | ||||||
chr1:15908297 | C | T | 6 | a0002c0002t0001g0234 a0002c0002t0001g0256 a0002c0002t0001g0257 others(3): Show |
6 | NA18971.hp2 NA19005.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-1024C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908297 | |||||||
chr1:15908427 | C | CT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(22): Show |
25 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.882-883dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 15908427 | ||||||
chr1:15908523 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.882-798C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908523 | |||||||
chr1:15908595 | A | G | 2 | a0001c0014t0001g0018 a0001c0014t0001g0033 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.882-726A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908595 | |||||||
chr1:15908623 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.882-698A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908623 | |||||||
chr1:15908660 | C | T | 2 | a0009c0013t0002g0054 a0009c0013t0002g0055 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.882-661C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908660 | |||||||
chr1:15908885 | A | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.882-436A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908885 | |||||||
chr1:15908908 | C | T | 2 | a0002c0002t0001g0221 a0002c0002t0001g0292 |
2 | HG02071.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.882-413C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908908 | |||||||
chr1:15908996 | C | T | 2 | a0003c0003t0001g0160 a0003c0003t0001g0161 |
2 | NA18968.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.882-325C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15908996 | |||||||
chr1:15909229 | T | G | 1 | a0022c0032t0001g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.882-92T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 3/14 | chr1 | 15909229 | |||||||
chr1:15909500 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02155.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1042+19G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909500 | |||||||
chr1:15909532 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+51G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909532 | |||||||
chr1:15909605 | C | T | 1 | a0002c0002t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1042+124C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909605 | |||||||
chr1:15909985 | G | A | 1 | a0003c0003t0001g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1042+504G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15909985 | |||||||
chr1:15910055 | C | T | 1 | a0003c0003t0001g0160 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1042+574C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910055 | |||||||
chr1:15910124 | T | TA | 40 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0019 others(37): Show |
40 | HG00438.hp2 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1042+670dupA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | ||||||
chr1:15910124 | TA | T | 91 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0191 others(88): Show |
91 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1042+670delA | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | ||||||
chr1:15910124 | TAA | T | 9 | a0001c0004t0001g0091 a0004c0006t0001g0111 a0004c0006t0001g0112 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1042+669_1042+670d others(4): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | ||||||
chr1:15910124 | TAAAAAAA others(6): Show |
T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1042+658_1042+670d others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910124 | ||||||
chr1:15910125 | A | T | 2 | a0001c0014t0001g0018 a0001c0014t0001g0033 |
2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1042+644A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910125 | |||||||
chr1:15910199 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1042+718G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910199 | |||||||
chr1:15910438 | C | T | 1 | a0001c0004t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1043-663C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910438 | |||||||
chr1:15910519 | A | G | 1 | a0024c0021t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1043-582A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910519 | |||||||
chr1:15910627 | G | GT | 27 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(24): Show |
27 | HG00639.hp2 HG01106.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1043-463dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 15910627 | ||||||
chr1:15910816 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1043-285C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910816 | |||||||
chr1:15910817 | G | A | 1 | a0003c0003t0001g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1043-284G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15910817 | |||||||
chr1:15911082 | G | T | 24 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(21): Show |
24 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1043-19G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 4/14 | chr1 | 15911082 | |||||||
chr1:15911312 | A | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+11A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15911312 | |||||||
chr1:15911521 | A | G | 1 | a0002c0002t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1243+220A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15911521 | |||||||
chr1:15911522 | A | T | 1 | a0002c0002t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1243+221A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15911522 | |||||||
chr1:15912048 | A | G | 2 | a0001c0029t0001g0094 a0017c0030t0001g0080 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1243+747A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912048 | |||||||
chr1:15912204 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1243+903G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912204 | |||||||
chr1:15912516 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1243+1215A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912516 | |||||||
chr1:15912717 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1243+1416G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912717 | |||||||
chr1:15912790 | C | T | 1 | a0003c0003t0001g0135 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1243+1489C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912790 | |||||||
chr1:15912820 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0005g0001 |
3 | HG03041.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1243+1519T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912820 | |||||||
chr1:15912879 | A | G | 2 | a0002c0002t0001g0280 a0002c0002t0001g0283 |
2 | NA18953.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1243+1578A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912879 | |||||||
chr1:15912907 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1243+1606C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912907 | |||||||
chr1:15912945 | G | C | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243+1644G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15912945 | |||||||
chr1:15913153 | A | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1243+1852A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913153 | |||||||
chr1:15913281 | A | G | 2 | a0003c0003t0001g0144 a0003c0003t0001g0145 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1243+1980A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913281 | |||||||
chr1:15913377 | C | T | 2 | a0004c0006t0001g0112 a0004c0006t0001g0113 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1243+2076C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913377 | |||||||
chr1:15913435 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1243+2134C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913435 | |||||||
chr1:15913715 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1244-2413C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15913715 | |||||||
chr1:15914171 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1244-1957G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914171 | |||||||
chr1:15914420 | A | G | 1 | a0018c0020t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1244-1708A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914420 | |||||||
chr1:15914454 | C | T | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.1244-1674C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914454 | |||||||
chr1:15914548 | C | T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0192 others(2): Show |
5 | HG01106.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1244-1580C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914548 | |||||||
chr1:15914622 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1244-1506A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914622 | |||||||
chr1:15914639 | A | G | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1244-1489A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914639 | |||||||
chr1:15914775 | G | A | 1 | a0004c0009t0001g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1244-1353G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914775 | |||||||
chr1:15914959 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1244-1169G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15914959 | |||||||
chr1:15915013 | T | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1244-1115T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915013 | |||||||
chr1:15915067 | C | T | 1 | a0002c0002t0001g0004 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1244-1061C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915067 | |||||||
chr1:15915086 | A | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1244-1042A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915086 | |||||||
chr1:15915105 | T | C | 1 | a0002c0002t0001g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1244-1023T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915105 | |||||||
chr1:15915325 | G | A | 1 | a0003c0003t0001g0146 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1244-803G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915325 | |||||||
chr1:15915327 | G | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(21): Show |
24 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1244-801G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915327 | |||||||
chr1:15915335 | A | G | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1244-793A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915335 | |||||||
chr1:15915419 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1244-709G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915419 | |||||||
chr1:15915420 | T | G | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1244-708T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915420 | |||||||
chr1:15915489 | A | C | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1244-639A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915489 | |||||||
chr1:15915532 | T | G | 1 | a0005c0011t0001g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1244-596T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915532 | |||||||
chr1:15915680 | G | A | 1 | a0003c0003t0001g0168 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1244-448G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915680 | |||||||
chr1:15915683 | C | T | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1244-445C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15915683 | |||||||
chr1:15915906 | AT | A | 72 | a0002c0002t0001g0270 a0003c0003t0001g0109 a0003c0003t0001g0121 others(69): Show |
72 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1244-213delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr1 | 15915906 | ||||||
chr1:15916125 | C | A | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
splice_region_variant&intron_variant | LOW | c.1244-3C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 5/14 | chr1 | 15916125 | |||||||
chr1:15916510 | CT | C | 105 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1395+249delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 15916510 | ||||||
chr1:15916599 | C | T | 1 | a0001c0004t0001g0275 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1395+320C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916599 | |||||||
chr1:15916755 | T | C | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1395+476T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916755 | |||||||
chr1:15916841 | A | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+562A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916841 | |||||||
chr1:15916929 | C | A | 87 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(84): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1395+650C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916929 | |||||||
chr1:15916987 | C | T | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1395+708C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15916987 | |||||||
chr1:15917068 | C | T | 72 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(69): Show |
72 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1395+789C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917068 | |||||||
chr1:15917076 | C | T | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1395+797C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917076 | |||||||
chr1:15917103 | G | A | 86 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(83): Show |
86 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1395+824G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917103 | |||||||
chr1:15917452 | C | T | 1 | a0002c0002t0001g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1395+1173C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917452 | |||||||
chr1:15917530 | C | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395+1251C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917530 | |||||||
chr1:15917612 | A | G | 3 | a0001c0005t0001g0208 a0001c0005t0001g0209 a0001c0005t0001g0288 |
3 | HG01069.hp2 HG01071.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1396-1314A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917612 | |||||||
chr1:15917840 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1396-1086A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15917840 | |||||||
chr1:15918049 | C | CT | 8 | a0002c0002t0001g0223 a0002c0002t0001g0234 a0002c0002t0001g0256 others(5): Show |
8 | NA18971.hp2 NA18980.hp2 NA19005.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-876dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 15918049 | ||||||
chr1:15918101 | T | A | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-825T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918101 | |||||||
chr1:15918319 | A | G | 1 | a0001c0004t0001g0084 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1396-607A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918319 | |||||||
chr1:15918438 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-488C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918438 | |||||||
chr1:15918461 | C | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1396-465C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918461 | |||||||
chr1:15918465 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1396-461C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918465 | |||||||
chr1:15918476 | C | T | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1396-450C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918476 | |||||||
chr1:15918513 | G | A | 1 | a0003c0003t0001g0160 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1396-413G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918513 | |||||||
chr1:15918578 | A | T | 1 | a0001c0005t0001g0204 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1396-348A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918578 | |||||||
chr1:15918745 | G | A | 2 | a0003c0003t0001g0183 a0003c0003t0001g0184 |
2 | HG00423.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1396-181G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918745 | |||||||
chr1:15918867 | G | A | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1396-59G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 6/14 | chr1 | 15918867 | |||||||
chr1:15919115 | GT | G | 27 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(24): Show |
27 | HG00639.hp2 HG00735.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1521+74delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 15919115 | ||||||
chr1:15919523 | C | T | 2 | a0002c0002t0001g0271 a0002c0002t0001g0279 |
2 | HG01255.hp1 HG01261.hp1 |
splice_region_variant&intron_variant | LOW | c.1635+6C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15919523 | |||||||
chr1:15919649 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0005g0001 |
3 | HG03041.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1635+132A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15919649 | |||||||
chr1:15920051 | CT | C | 76 | a0001c0001t0001g0301 a0001c0007t0001g0293 a0001c0007t0001g0294 others(73): Show |
76 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1635+546delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 15920051 | ||||||
chr1:15920063 | T | A | 1 | a0019c0024t0001g0304 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1635+546T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920063 | |||||||
chr1:15920064 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1635+547A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920064 | |||||||
chr1:15920173 | G | A | 2 | a0001c0029t0001g0094 a0017c0030t0001g0080 |
2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1635+656G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920173 | |||||||
chr1:15920179 | C | T | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1635+662C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920179 | |||||||
chr1:15920347 | G | C | 15 | a0001c0004t0001g0064 a0001c0004t0001g0081 a0001c0004t0001g0083 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1636-523G>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920347 | |||||||
chr1:15920708 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0006g0097 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1636-162G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920708 | |||||||
chr1:15920825 | C | G | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1636-45C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 8/14 | chr1 | 15920825 | |||||||
chr1:15921029 | A | G | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1749+46A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921029 | |||||||
chr1:15921099 | G | T | 1 | a0002c0002t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1749+116G>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921099 | |||||||
chr1:15921186 | G | A | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1749+203G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921186 | |||||||
chr1:15921421 | T | C | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1749+438T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921421 | |||||||
chr1:15921568 | C | G | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1749+585C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921568 | |||||||
chr1:15921737 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02258.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1750-512C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921737 | |||||||
chr1:15921973 | T | G | 7 | a0001c0005t0001g0208 a0001c0005t0001g0209 a0001c0005t0001g0210 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1750-276T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 9/14 | chr1 | 15921973 | |||||||
chr1:15922453 | A | G | 1 | a0001c0004t0001g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1850+104A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15922453 | |||||||
chr1:15922621 | C | G | 2 | a0002c0002t0001g0257 a0002c0018t0001g0276 |
2 | NA19011.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1850+272C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15922621 | |||||||
chr1:15922630 | C | CT | 34 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(31): Show |
34 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1850+291dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15922630 | ||||||
chr1:15923435 | A | G | 31 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1850+1086A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923435 | |||||||
chr1:15923479 | CTTGAGTT others(3): Show |
C | 1 | a0004c0009t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1850+1131_1850+114 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923479 | |||||||
chr1:15923673 | C | CT | 15 | a0001c0004t0001g0092 a0002c0002t0001g0005 a0002c0002t0001g0260 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1850+1338dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15923673 | ||||||
chr1:15923784 | C | T | 3 | a0002c0002t0001g0248 a0002c0002t0001g0254 a0002c0002t0004g0243 |
3 | NA18978.hp1 NA18995.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1850+1435C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923784 | |||||||
chr1:15923893 | C | T | 1 | a0018c0020t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1850+1544C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923893 | |||||||
chr1:15923963 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1850+1614C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923963 | |||||||
chr1:15923971 | C | G | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1850+1622C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15923971 | |||||||
chr1:15924011 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1850+1662C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924011 | |||||||
chr1:15924066 | A | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1850+1717A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924066 | |||||||
chr1:15924171 | A | G | 87 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(84): Show |
87 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1850+1822A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924171 | |||||||
chr1:15924286 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1850+1937G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924286 | |||||||
chr1:15924714 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1850+2365C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924714 | |||||||
chr1:15924860 | C | T | 3 | a0006c0008t0001g0099 a0006c0008t0001g0100 a0006c0008t0001g0101 |
3 | HG01167.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1850+2511C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924860 | |||||||
chr1:15924868 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1850+2519C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15924868 | |||||||
chr1:15925076 | A | G | 59 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(56): Show |
59 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1850+2727A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925076 | |||||||
chr1:15925168 | T | G | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1850+2819T>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925168 | |||||||
chr1:15925197 | G | A | 1 | a0003c0003t0001g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1850+2848G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925197 | |||||||
chr1:15925252 | C | T | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1851-2839C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925252 | |||||||
chr1:15925264 | C | T | 1 | a0003c0003t0001g0151 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1851-2827C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925264 | |||||||
chr1:15925312 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1851-2779T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925312 | |||||||
chr1:15925405 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(19): Show |
22 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.1851-2686C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925405 | |||||||
chr1:15925557 | CT | C | 25 | a0003c0003t0001g0122 a0003c0003t0001g0134 a0003c0003t0001g0135 others(22): Show |
25 | HG00438.hp1 HG00544.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1851-2527delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15925557 | ||||||
chr1:15925594 | A | ATT | 18 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(15): Show |
18 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1851-2483_1851-248 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15925594 | ||||||
chr1:15925608 | T | C | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-2483T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15925608 | |||||||
chr1:15926038 | A | G | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1851-2053A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926038 | |||||||
chr1:15926175 | C | A | 86 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(83): Show |
86 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1851-1916C>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926175 | |||||||
chr1:15926372 | C | T | 1 | a0003c0003t0001g0184 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1851-1719C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926372 | |||||||
chr1:15926384 | T | C | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1851-1707T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926384 | |||||||
chr1:15926384 | T | TAC | 41 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
41 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1851-1679_1851-167 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | ||||||
chr1:15926384 | T | TACAC | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 |
3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1851-1681_1851-167 others(8): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | ||||||
chr1:15926384 | TAC | T | 17 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0074 others(14): Show |
17 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1851-1679_1851-167 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | ||||||
chr1:15926384 | TACACACA others(5): Show |
T | 1 | a0001c0015t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1851-1689_1851-167 others(16): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926384 | ||||||
chr1:15926412 | C | T | 2 | a0001c0004t0001g0083 a0001c0038t0001g0093 |
2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1851-1679C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926412 | |||||||
chr1:15926501 | T | C | 71 | a0003c0003t0001g0109 a0003c0003t0001g0121 a0003c0003t0001g0122 others(68): Show |
71 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1851-1590T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926501 | |||||||
chr1:15926606 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1851-1485C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926606 | |||||||
chr1:15926617 | G | A | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1851-1474G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926617 | |||||||
chr1:15926694 | C | CT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(22): Show |
25 | HG00099.hp1 HG00544.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1851-1381dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926694 | ||||||
chr1:15926694 | CT | C | 69 | a0001c0023t0003g0006 a0003c0003t0001g0109 a0003c0003t0001g0122 others(66): Show |
69 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1851-1381delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 15926694 | ||||||
chr1:15926837 | C | T | 26 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1851-1254C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926837 | |||||||
chr1:15926922 | A | G | 199 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1851-1169A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926922 | |||||||
chr1:15926969 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-1122G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15926969 | |||||||
chr1:15927010 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG00099.hp2 HG01175.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-1081A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927010 | |||||||
chr1:15927087 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1851-1004A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927087 | |||||||
chr1:15927212 | G | A | 2 | a0002c0002t0001g0248 a0002c0002t0001g0254 |
2 | NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1851-879G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927212 | |||||||
chr1:15927224 | A | G | 1 | a0002c0002t0001g0238 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1851-867A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927224 | |||||||
chr1:15927391 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1851-700T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927391 | |||||||
chr1:15927411 | G | A | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-680G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927411 | |||||||
chr1:15927504 | G | A | 8 | a0001c0005t0001g0204 a0001c0005t0001g0208 a0001c0005t0001g0209 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851-587G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927504 | |||||||
chr1:15927523 | T | A | 1 | a0002c0002t0001g0223 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1851-568T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927523 | |||||||
chr1:15927529 | T | A | 1 | a0002c0002t0001g0223 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1851-562T>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927529 | |||||||
chr1:15927532 | G | A | 1 | a0002c0002t0001g0223 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1851-559G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927532 | |||||||
chr1:15927663 | G | A | 4 | a0006c0008t0001g0099 a0006c0008t0001g0100 a0006c0008t0001g0101 others(1): Show |
4 | HG01167.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1851-428G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15927663 | |||||||
chr1:15928003 | A | T | 2 | a0003c0003t0001g0109 a0003c0003t0001g0165 |
2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1851-88A>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15928003 | |||||||
chr1:15928076 | G | A | 24 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(21): Show |
24 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1851-15G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 10/14 | chr1 | 15928076 | |||||||
chr1:15936389 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.10026+123C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936389 | |||||||
chr1:15936438 | C | T | 11 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.10026+172C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936438 | |||||||
chr1:15936642 | C | CAAAAAAA others(1): Show |
89 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.10026+382_10026+38 others(12): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | ||||||
chr1:15936642 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0003c0003t0001g0122 others(3): Show |
6 | HG01175.hp1 HG01975.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.10026+381_10026+38 others(13): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | ||||||
chr1:15936642 | C | CAAAAAAA others(3): Show |
9 | a0004c0006t0001g0002 a0004c0006t0001g0111 a0004c0006t0001g0112 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.10026+380_10026+38 others(14): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | ||||||
chr1:15936642 | C | CAAAAAAA others(4): Show |
1 | a0004c0006t0001g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.10026+379_10026+38 others(15): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 15936642 | ||||||
chr1:15936703 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.10026+437A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936703 | |||||||
chr1:15936832 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.10027-331T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936832 | |||||||
chr1:15936957 | A | G | 199 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.10027-206A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15936957 | |||||||
chr1:15937107 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10027-56A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 11/14 | chr1 | 15937107 | |||||||
chr1:15937652 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.10509+7A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/14 | chr1 | 15937652 | |||||||
chr1:15937728 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10509+83C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/14 | chr1 | 15937728 | |||||||
chr1:15937769 | G | A | 74 | a0001c0004t0001g0089 a0001c0004t0001g0090 a0001c0004t0001g0091 others(71): Show |
74 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.10510-43G>A | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 12/14 | chr1 | 15937769 | |||||||
chr1:15938217 | C | G | 1 | a0017c0030t0001g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.10704+211C>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | chr1 | 15938217 | |||||||
chr1:15938565 | C | CT | 19 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0031 others(16): Show |
19 | HG00741.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.10705-134dupT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 15938565 | ||||||
chr1:15938565 | CT | C | 55 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0044 others(52): Show |
55 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.10705-134delT | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 15938565 | ||||||
chr1:15938565 | CTT | C | 58 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0029t0001g0094 others(55): Show |
58 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.10705-135_10705-13 others(6): Show |
SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 15938565 | ||||||
chr1:15938584 | T | C | 16 | a0003c0003t0001g0123 a0003c0003t0001g0139 a0003c0003t0001g0140 others(13): Show |
16 | HG00423.hp1 HG00423.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.10705-134T>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | chr1 | 15938584 | |||||||
chr1:15938589 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10705-129C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 13/14 | chr1 | 15938589 | |||||||
chr1:15938927 | A | G | 199 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.10863+51A>G | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15938927 | |||||||
chr1:15938965 | A | C | 1 | a0001c0023t0003g0006 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.10863+89A>C | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15938965 | |||||||
chr1:15939030 | C | T | 1 | a0003c0003t0001g0179 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.10863+154C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15939030 | |||||||
chr1:15939264 | C | T | 4 | a0001c0007t0001g0293 a0001c0007t0001g0294 a0001c0007t0001g0295 others(1): Show |
4 | HG03130.hp1 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.10864-32C>T | SPEN | ENSG00000065526.13 | transcript | ENST00000375759.8 | protein_coding | 14/14 | chr1 | 15939264 |