Item | Value |
---|---|
geneid | 375748 |
ensemblid | ENSG00000182150.19 |
hgncid | 26922 |
symbol | ERCC6L2 |
name | ERCC excision repair 6 like 2 |
refseq_nuc | NM_020207.7 |
refseq_prot | NP_064592.3 |
ensembl_nuc | ENST00000653738.2 |
ensembl_prot | ENSP00000499221.2 |
mane_status | MANE Select |
chr | chr9 |
start | 95875691 |
end | 96018447 |
strand | + |
ver | v1.2 |
region | chr9:95875691-96018447 |
region5000 | chr9:95870691-96023447 |
regionname0 | ERCC6L2_chr9_95875691_96018447 |
regionname5000 | ERCC6L2_chr9_95870691_96023447 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1550 | 221 | 51 | 40 | 99 | 8 | 21 | 76 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0002 | 0/0 | 1550 | 74 | 10 | 16 | 35 | 3 | 10 | 30 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0003 | 0/0 | 1550 | 31 | 0 | 5 | 25 | 1 | 0 | 19 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0004 | 0/0 | 1550 | 28 | 4 | 13 | 8 | 0 | 3 | 8 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0005 | 0/0 | 1550 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0006 | 0/0 | 1550 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0007 | 0/0 | 1550 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0008 | 0/0 | 1550 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0009 | 0/0 | 1550 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0010 | 0/0 | 1550 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0011 | 0/0 | 1550 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0012 | 0/0 | 1550 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0013 | 0/0 | 1550 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0014 | 0/0 | 1550 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0015 | 0/0 | 1550 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0016 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0017 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0018 | 0/0 | 1550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0019 | 0/0 | 13 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MASRR others(8): Show |
chr9 | 95870691 | 96023447 |
a0020 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0021 | 0/0 | 1550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0022 | 0/0 | 1550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0023 | 0/0 | 1550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0024 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
a0025 | 0/0 | 1550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | MDPSA others(1545): Show |
chr9 | 95870691 | 96023447 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4650 | 203 | 46 | 40 | 87 | 7 | 21 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0001c0005 | 0/0 | 4650 | 17 | 5 | 0 | 12 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0001c0028 | 0/0 | 4650 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0002c0002 | 0/0 | 4650 | 73 | 10 | 16 | 34 | 3 | 10 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0002c0020 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0003c0003 | 0/0 | 4650 | 30 | 0 | 5 | 24 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0003c0015 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0004c0004 | 0/0 | 4650 | 28 | 4 | 13 | 8 | 0 | 3 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0005c0006 | 0/0 | 4650 | 7 | 6 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0006c0007 | 0/0 | 4650 | 5 | 5 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0007c0008 | 0/0 | 4650 | 4 | 4 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0008c0010 | 0/0 | 4650 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0009c0011 | 0/0 | 4650 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0010c0012 | 0/0 | 4650 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0011c0009 | 0/0 | 4650 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0012c0026 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0013c0016 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0014c0022 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0015c0017 | 0/0 | 4650 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0016c0018 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0017c0024 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0018c0021 | 0/0 | 4650 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0019c0013 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AAGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0020c0014 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0021c0025 | 0/0 | 4650 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0022c0019 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0023c0023 | 0/0 | 4650 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0024c0029 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 | ||
a0025c0027 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | ATGGA others(4645): Show |
chr9 | 95870691 | 96023447 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10250 | 57 | 3 | 14 | 31 | 1 | 8 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0002 | 0/0 | 10245 | 48 | 5 | 10 | 23 | 2 | 8 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0004 | 0/0 | 10246 | 15 | 4 | 3 | 5 | 2 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0010 | 0/0 | 10248 | 8 | 7 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0011 | 1/0 | 10245 | 7 | 0 | 5 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0014 | 0/0 | 10251 | 6 | 2 | 1 | 2 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0015 | 0/0 | 10250 | 6 | 6 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0018 | 0/0 | 10245 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0019 | 0/0 | 10250 | 5 | 0 | 0 | 5 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0022 | 0/0 | 10249 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0024 | 0/0 | 10250 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0025 | 0/0 | 10249 | 3 | 2 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0026 | 0/0 | 10252 | 3 | 0 | 0 | 0 | 0 | 3 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10247): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0027 | 0/0 | 10250 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0031 | 0/0 | 10246 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0036 | 0/0 | 10251 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0039 | 0/0 | 10245 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0045 | 0/0 | 10249 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0047 | 0/0 | 10248 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0052 | 0/0 | 10245 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0053 | 0/0 | 10245 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0055 | 0/0 | 10246 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0056 | 0/0 | 10247 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0057 | 0/0 | 10247 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0060 | 0/0 | 10249 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0066 | 0/0 | 10245 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0067 | 0/0 | 10246 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0068 | 0/0 | 10251 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0070 | 0/0 | 10246 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0073 | 0/0 | 10249 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0079 | 0/0 | 10250 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0080 | 0/0 | 10246 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0081 | 0/0 | 10245 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0082 | 0/0 | 10246 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0084 | 0/0 | 10249 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0085 | 0/0 | 10250 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0086 | 0/1 | 10250 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0087 | 0/0 | 10251 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0088 | 0/0 | 10245 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0089 | 0/0 | 10249 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0090 | 0/0 | 10250 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0091 | 0/0 | 10251 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0001c0001t0092 | 0/0 | 10251 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0009 | 0/0 | 10245 | 10 | 0 | 0 | 10 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0033 | 0/0 | 10246 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0061 | 0/0 | 10246 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0062 | 0/0 | 10246 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0063 | 0/0 | 10245 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0064 | 0/0 | 10247 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0071 | 0/0 | 10245 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0001c0005t0072 | 0/0 | 10246 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0001c0028t0002 | 0/0 | 10245 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0003 | 0/0 | 10248 | 42 | 3 | 14 | 17 | 1 | 7 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0006 | 0/0 | 10249 | 11 | 2 | 1 | 6 | 0 | 2 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0007 | 0/0 | 10247 | 8 | 4 | 0 | 4 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0028 | 0/0 | 10249 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0029 | 0/0 | 10248 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0030 | 0/0 | 10249 | 2 | 1 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0035 | 0/0 | 10249 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0044 | 0/0 | 10248 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0048 | 0/0 | 10248 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0049 | 0/0 | 10243 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10238): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0051 | 0/0 | 10248 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0002c0002t0093 | 0/0 | 10248 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0002c0020t0035 | 0/0 | 10249 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0008 | 0/0 | 10240 | 11 | 0 | 0 | 11 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10235): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0012 | 0/0 | 10240 | 6 | 0 | 4 | 1 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10235): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0016 | 0/0 | 10240 | 4 | 0 | 0 | 4 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10235): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0021 | 0/0 | 10239 | 3 | 0 | 0 | 3 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10234): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0041 | 0/0 | 10238 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10233): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0042 | 0/0 | 10240 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10235): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0043 | 0/0 | 10241 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10236): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0046 | 0/0 | 10241 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10236): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0054 | 0/0 | 10238 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10233): Show |
chr9 | 95870691 | 96023447 |
a0003c0003t0059 | 0/0 | 10241 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10236): Show |
chr9 | 95870691 | 96023447 |
a0003c0015t0021 | 0/0 | 10239 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10234): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0005 | 0/0 | 10246 | 13 | 0 | 7 | 5 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0013 | 0/0 | 10247 | 6 | 0 | 4 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0037 | 0/0 | 10247 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0038 | 0/0 | 10248 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0075 | 0/0 | 10246 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0076 | 0/0 | 10246 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0077 | 0/0 | 10248 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0095 | 0/0 | 10246 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0004c0004t0096 | 0/0 | 10249 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0005c0006t0017 | 0/0 | 10250 | 5 | 5 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0005c0006t0032 | 0/0 | 10251 | 2 | 1 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10246): Show |
chr9 | 95870691 | 96023447 |
a0006c0007t0003 | 0/0 | 10248 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0006c0007t0007 | 0/0 | 10247 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10242): Show |
chr9 | 95870691 | 96023447 |
a0006c0007t0050 | 0/0 | 10248 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0007c0008t0023 | 0/0 | 10249 | 3 | 3 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0007c0008t0065 | 0/0 | 10250 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0008c0010t0001 | 0/0 | 10250 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0009c0011t0020 | 0/0 | 10245 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0010c0012t0020 | 0/0 | 10245 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10240): Show |
chr9 | 95870691 | 96023447 |
a0011c0009t0034 | 0/0 | 10246 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0012c0026t0001 | 0/0 | 10250 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0013c0016t0001 | 0/0 | 10250 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0014c0022t0006 | 0/0 | 10249 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0015c0017t0033 | 0/0 | 10246 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
a0016c0018t0058 | 0/0 | 10249 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0017c0024t0074 | 0/0 | 10252 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10247): Show |
chr9 | 95870691 | 96023447 |
a0018c0021t0003 | 0/0 | 10248 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10243): Show |
chr9 | 95870691 | 96023447 |
a0019c0013t0078 | 0/0 | 10250 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0020c0014t0040 | 0/0 | 10250 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0021c0025t0083 | 0/0 | 10240 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10235): Show |
chr9 | 95870691 | 96023447 |
a0022c0019t0016 | 0/0 | 10240 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10235): Show |
chr9 | 95870691 | 96023447 |
a0023c0023t0001 | 0/0 | 10250 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10245): Show |
chr9 | 95870691 | 96023447 |
a0024c0029t0094 | 0/0 | 10249 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10244): Show |
chr9 | 95870691 | 96023447 |
a0025c0027t0069 | 0/0 | 10246 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | AGAGC others(10241): Show |
chr9 | 95870691 | 96023447 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0011g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0014g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0015g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0015g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0018g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0018g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0018g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0018g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0018g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0019g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0019g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0019g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0019g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0022g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0022g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0024g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0024g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0024g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0025g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0025g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0025g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0026g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0027g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0027g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0027g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0031g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0031g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0036g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0036g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0039g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0045g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0047g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0052g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0053g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0055g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0056g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0057g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0060g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0066g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0067g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0068g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0070g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0073g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0079g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0080g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0081g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0082g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0084g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0085g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0086g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0087g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0088g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0089g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0090g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0091g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0001t0092g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0033g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0061g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0062g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0063g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0064g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0071g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0005t0072g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0001c0028t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0006g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0028g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0028g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0029g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0029g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0030g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0030g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0035g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0044g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0048g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0049g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0051g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0002t0093g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0002c0020t0035g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0008g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0012g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0012g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0012g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0012g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0012g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0012g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0016g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0016g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0016g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0016g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0021g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0021g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0021g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0041g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0042g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0043g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0046g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0054g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0003t0059g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0003c0015t0021g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0013g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0013g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0013g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0013g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0013g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0013g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0037g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0037g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0038g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0038g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0075g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0076g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0077g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0095g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0004c0004t0096g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0017g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0032g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0005c0006t0032g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0006c0007t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0006c0007t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0006c0007t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0006c0007t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0006c0007t0050g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0007c0008t0023g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0007c0008t0023g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0007c0008t0023g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0007c0008t0065g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0008c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0008c0010t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0009c0011t0020g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0010c0012t0020g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0010c0012t0020g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0011c0009t0034g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0011c0009t0034g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0012c0026t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0013c0016t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0014c0022t0006g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0015c0017t0033g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0016c0018t0058g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0017c0024t0074g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0018c0021t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0019c0013t0078g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0020c0014t0040g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0021c0025t0083g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0022c0019t0016g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0023c0023t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0024c0029t0094g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
a0025c0027t0069g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | GBR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00099 | hp2 | a0001 | c0001 | t0014 | g0042 | EUR | GBR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00280 | hp1 | a0001 | c0028 | t0002 | g0009 | EUR | FIN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00323 | hp1 | a0003 | c0003 | t0012 | g0290 | EUR | FIN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00323 | hp2 | a0002 | c0002 | t0003 | g0316 | EUR | FIN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00423 | hp1 | a0002 | c0002 | t0003 | g0335 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00423 | hp2 | a0001 | c0005 | t0009 | g0240 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00597 | hp1 | a0008 | c0010 | t0001 | g0049 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00597 | hp2 | a0003 | c0003 | t0042 | g0270 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00609 | hp1 | a0012 | c0026 | t0001 | g0052 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00609 | hp2 | a0003 | c0003 | t0021 | g0289 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0191 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00642 | hp2 | a0013 | c0016 | t0001 | g0086 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00673 | hp1 | a0001 | c0005 | t0009 | g0227 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00673 | hp2 | a0002 | c0020 | t0035 | g0088 | EAS | CHS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00733 | hp1 | a0001 | c0001 | t0036 | g0039 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00733 | hp2 | a0001 | c0001 | t0057 | g0187 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00735 | hp2 | a0014 | c0022 | t0006 | g0309 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00741 | hp1 | a0004 | c0004 | t0013 | g0232 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01069 | hp1 | a0004 | c0004 | t0038 | g0011 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01069 | hp2 | a0002 | c0002 | t0003 | g0349 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01070 | hp1 | a0002 | c0002 | t0003 | g0351 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01071 | hp2 | a0004 | c0004 | t0096 | g0011 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01074 | hp1 | a0001 | c0001 | t0036 | g0056 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01081 | hp1 | a0001 | c0001 | t0039 | g0164 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01081 | hp2 | a0001 | c0001 | t0089 | g0137 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01099 | hp1 | a0002 | c0002 | t0003 | g0358 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01106 | hp1 | a0002 | c0002 | t0003 | g0350 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0114 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01167 | hp1 | a0004 | c0004 | t0005 | g0234 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01169 | hp1 | a0002 | c0002 | t0003 | g0016 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01169 | hp2 | a0003 | c0003 | t0012 | g0265 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01175 | hp1 | a0001 | c0001 | t0011 | g0172 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01175 | hp2 | a0004 | c0004 | t0013 | g0236 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01192 | hp1 | a0002 | c0002 | t0003 | g0348 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01243 | hp1 | a0002 | c0002 | t0006 | g0305 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01243 | hp2 | a0005 | c0006 | t0032 | g0024 | AMR | PUR | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0343 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0257 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01261 | hp1 | a0003 | c0003 | t0012 | g0264 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0162 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01346 | hp2 | a0004 | c0004 | t0013 | g0237 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01358 | hp1 | a0004 | c0004 | t0005 | g0302 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01361 | hp1 | a0002 | c0002 | t0029 | g0362 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01361 | hp2 | a0001 | c0001 | t0011 | g0199 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0355 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01496 | hp1 | a0004 | c0004 | t0005 | g0225 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01515 | hp2 | a0002 | c0002 | t0029 | g0360 | EUR | IBS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0124 | EUR | IBS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01517 | hp2 | a0002 | c0002 | t0030 | g0359 | EUR | IBS | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0142 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0118 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0331 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0354 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0347 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01943 | hp2 | a0004 | c0004 | t0005 | g0235 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01952 | hp2 | a0015 | c0017 | t0033 | g0102 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01975 | hp1 | a0001 | c0001 | t0011 | g0166 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01975 | hp2 | a0003 | c0003 | t0012 | g0262 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01978 | hp1 | a0001 | c0001 | t0014 | g0001 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01978 | hp2 | a0004 | c0004 | t0013 | g0247 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01993 | hp2 | a0001 | c0001 | t0085 | g0074 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02015 | hp1 | a0002 | c0002 | t0093 | g0304 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02027 | hp2 | a0002 | c0002 | t0028 | g0366 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02040 | hp1 | a0001 | c0005 | t0009 | g0243 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02055 | hp1 | a0002 | c0002 | t0030 | g0361 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02056 | hp2 | a0003 | c0003 | t0008 | g0278 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02074 | hp2 | a0001 | c0001 | t0082 | g0069 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02083 | hp1 | a0003 | c0003 | t0012 | g0286 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02083 | hp2 | a0001 | c0001 | t0019 | g0217 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02135 | hp2 | a0001 | c0005 | t0009 | g0244 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02145 | hp1 | a0001 | c0001 | t0091 | g0139 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0333 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02148 | hp1 | a0004 | c0004 | t0005 | g0239 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02148 | hp2 | a0003 | c0003 | t0059 | g0263 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02155 | hp1 | a0001 | c0005 | t0009 | g0245 | EAS | CDX | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CDX | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02165 | hp1 | a0002 | c0002 | t0048 | g0325 | EAS | CDX | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02258 | hp1 | a0009 | c0011 | t0020 | g0017 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0115 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02280 | hp1 | a0005 | c0006 | t0017 | g0025 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02280 | hp2 | a0001 | c0001 | t0092 | g0371 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02293 | hp1 | a0002 | c0002 | t0003 | g0352 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02293 | hp2 | a0004 | c0004 | t0005 | g0226 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02300 | hp1 | a0004 | c0004 | t0005 | g0231 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0340 | AMR | PEL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02451 | hp2 | a0002 | c0002 | t0006 | g0341 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02523 | hp1 | a0001 | c0001 | t0019 | g0212 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02523 | hp2 | a0001 | c0005 | t0009 | g0242 | EAS | KHV | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02572 | hp1 | a0004 | c0004 | t0038 | g0258 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02602 | hp1 | a0002 | c0002 | t0003 | g0318 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0007 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02615 | hp2 | a0007 | c0008 | t0065 | g0296 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02622 | hp1 | a0001 | c0001 | t0090 | g0144 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02622 | hp2 | a0005 | c0006 | t0032 | g0019 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02630 | hp2 | a0001 | c0001 | t0027 | g0143 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02647 | hp2 | a0010 | c0012 | t0020 | g0368 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02717 | hp1 | a0007 | c0008 | t0023 | g0295 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02717 | hp2 | a0004 | c0004 | t0037 | g0259 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02723 | hp1 | a0017 | c0024 | t0074 | g0256 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02723 | hp2 | a0005 | c0006 | t0017 | g0022 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0353 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02738 | hp1 | a0002 | c0002 | t0003 | g0303 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02809 | hp1 | a0001 | c0005 | t0062 | g0105 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02809 | hp2 | a0010 | c0012 | t0020 | g0369 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02818 | hp1 | a0005 | c0006 | t0017 | g0021 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02818 | hp2 | a0006 | c0007 | t0050 | g0301 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02886 | hp1 | a0001 | c0001 | t0081 | g0100 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02886 | hp2 | a0006 | c0007 | t0007 | g0298 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02895 | hp1 | a0006 | c0007 | t0003 | g0297 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0117 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02896 | hp1 | a0001 | c0001 | t0025 | g0099 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02896 | hp2 | a0004 | c0004 | t0095 | g0261 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02897 | hp1 | a0001 | c0001 | t0025 | g0098 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02897 | hp2 | a0001 | c0001 | t0056 | g0116 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02922 | hp1 | a0002 | c0002 | t0007 | g0328 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02922 | hp2 | a0006 | c0007 | t0007 | g0299 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02965 | hp1 | a0011 | c0009 | t0034 | g0207 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02965 | hp2 | a0007 | c0008 | t0023 | g0293 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0203 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02970 | hp2 | a0001 | c0001 | t0031 | g0113 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02976 | hp1 | a0005 | c0006 | t0017 | g0020 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02976 | hp2 | a0002 | c0002 | t0007 | g0332 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03017 | hp1 | a0001 | c0001 | t0053 | g0173 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03017 | hp2 | a0018 | c0021 | t0003 | g0196 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03098 | hp1 | a0006 | c0007 | t0007 | g0300 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03098 | hp2 | a0001 | c0001 | t0045 | g0107 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0140 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03130 | hp2 | a0001 | c0001 | t0031 | g0112 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0141 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03209 | hp1 | a0001 | c0001 | t0015 | g0138 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03209 | hp2 | a0019 | c0013 | t0078 | g0101 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03225 | hp1 | a0001 | c0001 | t0047 | g0123 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0068 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03453 | hp1 | a0002 | c0002 | t0006 | g0306 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03453 | hp2 | a0001 | c0001 | t0022 | g0136 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0120 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03486 | hp2 | a0001 | c0001 | t0015 | g0145 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03491 | hp1 | a0001 | c0001 | t0026 | g0002 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0317 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0345 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03492 | hp2 | a0001 | c0001 | t0026 | g0002 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03516 | hp1 | a0001 | c0005 | t0063 | g0253 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03516 | hp2 | a0020 | c0014 | t0040 | g0189 | AFR | ESN | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03540 | hp1 | a0004 | c0004 | t0037 | g0260 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03540 | hp2 | a0001 | c0001 | t0088 | g0122 | AFR | GWD | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03579 | hp1 | a0005 | c0006 | t0017 | g0023 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03579 | hp2 | a0001 | c0001 | t0027 | g0370 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03654 | hp2 | a0002 | c0002 | t0035 | g0087 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0160 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03669 | hp2 | a0004 | c0004 | t0005 | g0228 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03688 | hp2 | a0004 | c0004 | t0075 | g0206 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | BEB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0346 | SAS | BEB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03927 | hp1 | a0002 | c0002 | t0006 | g0365 | SAS | BEB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04115 | hp2 | a0021 | c0025 | t0083 | g0037 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04199 | hp2 | a0002 | c0002 | t0006 | g0334 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04204 | hp2 | a0004 | c0004 | t0076 | g0220 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04228 | hp1 | a0001 | c0001 | t0026 | g0002 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18522 | hp1 | a0002 | c0002 | t0007 | g0307 | AFR | YRI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18522 | hp2 | a0007 | c0008 | t0023 | g0294 | AFR | YRI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18747 | hp1 | a0003 | c0003 | t0008 | g0285 | EAS | CHB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18747 | hp2 | a0003 | c0003 | t0021 | g0291 | EAS | CHB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18906 | hp1 | a0001 | c0001 | t0010 | g0108 | AFR | YRI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | YRI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18939 | hp2 | a0003 | c0003 | t0041 | g0273 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18940 | hp1 | a0004 | c0004 | t0005 | g0252 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18940 | hp2 | a0001 | c0001 | t0079 | g0081 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18943 | hp2 | a0001 | c0005 | t0071 | g0233 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18944 | hp1 | a0002 | c0002 | t0003 | g0312 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18945 | hp2 | a0003 | c0003 | t0016 | g0274 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18946 | hp2 | a0001 | c0005 | t0009 | g0223 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18947 | hp2 | a0002 | c0002 | t0006 | g0338 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18948 | hp1 | a0003 | c0003 | t0008 | g0271 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18948 | hp2 | a0001 | c0001 | t0080 | g0040 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18951 | hp2 | a0002 | c0002 | t0007 | g0015 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18954 | hp1 | a0001 | c0005 | t0009 | g0230 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0342 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18957 | hp1 | a0004 | c0004 | t0005 | g0248 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18957 | hp2 | a0008 | c0010 | t0001 | g0071 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18959 | hp2 | a0004 | c0004 | t0013 | g0246 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18962 | hp1 | a0003 | c0003 | t0016 | g0275 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18962 | hp2 | a0003 | c0015 | t0021 | g0292 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18964 | hp1 | a0003 | c0003 | t0008 | g0281 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18965 | hp1 | a0003 | c0003 | t0008 | g0283 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18965 | hp2 | a0001 | c0001 | t0018 | g0149 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18966 | hp1 | a0002 | c0002 | t0003 | g0323 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18966 | hp2 | a0001 | c0001 | t0024 | g0367 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18967 | hp1 | a0001 | c0005 | t0009 | g0224 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18967 | hp2 | a0001 | c0001 | t0014 | g0045 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18968 | hp2 | a0001 | c0001 | t0055 | g0167 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18969 | hp2 | a0002 | c0002 | t0003 | g0363 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18970 | hp2 | a0002 | c0002 | t0003 | g0320 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0013 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18973 | hp1 | a0003 | c0003 | t0008 | g0284 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18975 | hp1 | a0003 | c0003 | t0008 | g0267 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18977 | hp1 | a0002 | c0002 | t0003 | g0308 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18977 | hp2 | a0001 | c0001 | t0018 | g0147 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18978 | hp1 | a0001 | c0001 | t0019 | g0214 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18979 | hp1 | a0001 | c0005 | t0072 | g0222 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18980 | hp1 | a0001 | c0001 | t0066 | g0146 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18980 | hp2 | a0001 | c0001 | t0019 | g0211 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18981 | hp2 | a0004 | c0004 | t0013 | g0238 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18982 | hp1 | a0004 | c0004 | t0005 | g0251 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18984 | hp1 | a0001 | c0001 | t0073 | g0210 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18985 | hp1 | a0003 | c0003 | t0046 | g0276 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18985 | hp2 | a0002 | c0002 | t0003 | g0313 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18987 | hp1 | a0001 | c0001 | t0070 | g0216 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18987 | hp2 | a0022 | c0019 | t0016 | g0326 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18989 | hp2 | a0004 | c0004 | t0077 | g0249 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18990 | hp1 | a0002 | c0002 | t0007 | g0014 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18990 | hp2 | a0003 | c0003 | t0008 | g0282 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18991 | hp1 | a0003 | c0003 | t0043 | g0277 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18991 | hp2 | a0001 | c0001 | t0068 | g0218 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18993 | hp2 | a0004 | c0004 | t0005 | g0250 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0339 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18999 | hp1 | a0003 | c0003 | t0016 | g0272 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA18999 | hp2 | a0023 | c0023 | t0001 | g0072 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19000 | hp1 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19000 | hp2 | a0002 | c0002 | t0006 | g0319 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19001 | hp1 | a0002 | c0002 | t0044 | g0322 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19002 | hp1 | a0001 | c0001 | t0019 | g0215 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19002 | hp2 | a0004 | c0004 | t0005 | g0241 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19004 | hp1 | a0001 | c0005 | t0009 | g0229 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19004 | hp2 | a0002 | c0002 | t0003 | g0310 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19005 | hp1 | a0002 | c0002 | t0003 | g0311 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19009 | hp1 | a0001 | c0001 | t0067 | g0152 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19011 | hp2 | a0003 | c0003 | t0016 | g0269 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19030 | hp1 | a0001 | c0005 | t0033 | g0254 | AFR | LWK | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19030 | hp2 | a0001 | c0001 | t0060 | g0121 | AFR | LWK | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19043 | hp1 | a0001 | c0001 | t0022 | g0006 | AFR | LWK | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19043 | hp2 | a0001 | c0001 | t0010 | g0119 | AFR | LWK | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19056 | hp2 | a0002 | c0002 | t0006 | g0357 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19057 | hp1 | a0002 | c0002 | t0028 | g0329 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19058 | hp1 | a0001 | c0001 | t0084 | g0066 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0337 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19060 | hp2 | a0002 | c0002 | t0007 | g0014 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19062 | hp1 | a0003 | c0003 | t0008 | g0280 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19063 | hp1 | a0002 | c0002 | t0006 | g0324 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19064 | hp1 | a0002 | c0002 | t0006 | g0321 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19068 | hp1 | a0001 | c0001 | t0024 | g0213 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19068 | hp2 | a0003 | c0003 | t0021 | g0287 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19070 | hp1 | a0001 | c0001 | t0018 | g0205 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19070 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19074 | hp1 | a0001 | c0001 | t0018 | g0202 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19074 | hp2 | a0002 | c0002 | t0051 | g0314 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19077 | hp1 | a0003 | c0003 | t0008 | g0279 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19077 | hp2 | a0001 | c0001 | t0087 | g0070 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19078 | hp1 | a0001 | c0001 | t0024 | g0219 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19078 | hp2 | a0002 | c0002 | t0049 | g0344 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19080 | hp2 | a0001 | c0001 | t0052 | g0150 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19081 | hp2 | a0002 | c0002 | t0003 | g0315 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19084 | hp2 | a0003 | c0003 | t0008 | g0268 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19086 | hp1 | a0003 | c0003 | t0054 | g0288 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19086 | hp2 | a0001 | c0001 | t0025 | g0060 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19087 | hp1 | a0001 | c0001 | t0018 | g0153 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19089 | hp1 | a0002 | c0002 | t0003 | g0364 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19090 | hp2 | a0002 | c0002 | t0006 | g0012 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19091 | hp2 | a0002 | c0002 | t0007 | g0013 | EAS | JPT | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19240 | hp1 | a0001 | c0005 | t0064 | g0106 | AFR | YRI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | YRI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20129 | hp1 | a0024 | c0029 | t0094 | g0209 | AFR | ASW | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20129 | hp2 | a0001 | c0001 | t0015 | g0007 | AFR | ASW | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | TSI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20752 | hp2 | a0001 | c0001 | t0011 | g0163 | EUR | TSI | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20905 | hp2 | a0002 | c0002 | t0003 | g0356 | SAS | GIH | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01123 | hp1 | a0003 | c0003 | t0012 | g0266 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02109 | hp1 | a0016 | c0018 | t0058 | g0336 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02109 | hp2 | a0009 | c0011 | t0020 | g0017 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0372 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0080 | AFR | ACB | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03471 | hp1 | a0001 | c0001 | t0022 | g0006 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG06807 | hp1 | a0002 | c0002 | t0003 | g0330 | AFR | USA | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
HG06807 | hp2 | a0011 | c0009 | t0034 | g0208 | AFR | USA | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20300 | hp1 | a0001 | c0005 | t0061 | g0221 | AFR | USA | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | USA | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA21309 | hp1 | a0025 | c0027 | t0069 | g0255 | AFR | LWK | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
NA21309 | hp2 | a0002 | c0002 | t0007 | g0327 | AFR | LWK | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
homoSapiens | chm13v2 | a0001 | c0001 | t0086 | g0041 | REF | REF | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0171 | REF | REF | ERCC6L2_chr9_95870691_96023447 | ERCC6L2 | chr9 | 95870691 | 96023447 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:95876040 | T | A | 1 | a0019 | 1 | HG03209.hp2 | start_lost | HIGH | c.2T>A | p.Met1? | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 350/10245 | 2/4653 | 1/1550 | chr9 | 95876040 | |||
chr9:95876059 | G | C | 1 | a0020 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.21G>C | p.Gln7His | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 369/10245 | 21/4653 | 7/1550 | chr9 | 95876059 | |||
chr9:95881197 | C | G | 1 | a0024 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.375C>G | p.Asp125Glu | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/19 | 723/10245 | 375/4653 | 125/1550 | chr9 | 95881197 | |||
chr9:95881229 | G | A | 1 | a0006 | 5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.407G>A | p.Gly136Glu | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/19 | 755/10245 | 407/4653 | 136/1550 | chr9 | 95881229 | |||
chr9:95916375 | T | C | 1 | a0013 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1099T>C | p.Trp367Arg | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/19 | 1447/10245 | 1099/4653 | 367/1550 | chr9 | 95916375 | |||
chr9:95916416 | G | C | 1 | a0015 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.1140G>C | p.Leu380Phe | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/19 | 1488/10245 | 1140/4653 | 380/1550 | chr9 | 95916416 | |||
chr9:95921268 | C | A | 1 | a0011 | 2 | HG02965.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.1252C>A | p.Pro418Thr | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/19 | 1600/10245 | 1252/4653 | 418/1550 | chr9 | 95921268 | |||
chr9:95928855 | T | C | 7 | a0002 a0003 a0005 others(4): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
missense_variant | MODERATE | c.1742T>C | p.Val581Ala | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/19 | 2090/10245 | 1742/4653 | 581/1550 | chr9 | 95928855 | |||
chr9:95971987 | C | G | 1 | a0003 | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
missense_variant | MODERATE | c.2236C>G | p.Leu746Val | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 2584/10245 | 2236/4653 | 746/1550 | chr9 | 95971987 | |||
chr9:95972237 | C | T | 1 | a0014 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2486C>T | p.Thr829Ile | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 2834/10245 | 2486/4653 | 829/1550 | chr9 | 95972237 | |||
chr9:95972609 | A | T | 5 | a0002 a0014 a0016 others(2): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
missense_variant | MODERATE | c.2858A>T | p.Asn953Ile | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 3206/10245 | 2858/4653 | 953/1550 | chr9 | 95972609 | |||
chr9:95972611 | G | A | 1 | a0023 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.2860G>A | p.Gly954Arg | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 3208/10245 | 2860/4653 | 954/1550 | chr9 | 95972611 | |||
chr9:95972827 | G | C | 1 | a0009 | 2 | HG02109.hp2 HG02258.hp1 |
missense_variant | MODERATE | c.3076G>C | p.Val1026Leu | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 3424/10245 | 3076/4653 | 1026/1550 | chr9 | 95972827 | |||
chr9:95972944 | A | G | 4 | a0007 a0009 a0010 others(1): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
missense_variant | MODERATE | c.3193A>G | p.Ile1065Val | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 3541/10245 | 3193/4653 | 1065/1550 | chr9 | 95972944 | |||
chr9:95978139 | G | A | 1 | a0008 | 2 | HG00597.hp1 NA18957.hp2 |
missense_variant | MODERATE | c.3416G>A | p.Arg1139Gln | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/19 | 3764/10245 | 3416/4653 | 1139/1550 | chr9 | 95978139 | |||
chr9:96004620 | C | A | 2 | a0007 a0024 |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.3593C>A | p.Pro1198His | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/19 | 3941/10245 | 3593/4653 | 1198/1550 | chr9 | 96004620 | |||
chr9:96012584 | A | G | 1 | a0018 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.4034A>G | p.Tyr1345Cys | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4382/10245 | 4034/4653 | 1345/1550 | chr9 | 96012584 | |||
chr9:96012606 | T | G | 1 | a0017 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.4056T>G | p.Asn1352Lys | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4404/10245 | 4056/4653 | 1352/1550 | chr9 | 96012606 | |||
chr9:96012679 | G | A | 1 | a0016 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.4129G>A | p.Glu1377Lys | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4477/10245 | 4129/4653 | 1377/1550 | chr9 | 96012679 | |||
chr9:96012844 | A | G | 2 | a0017 a0025 |
2 | HG02723.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.4294A>G | p.Asn1432Asp | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4642/10245 | 4294/4653 | 1432/1550 | chr9 | 96012844 | |||
chr9:96012916 | C | G | 1 | a0012 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.4366C>G | p.Pro1456Ala | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4714/10245 | 4366/4653 | 1456/1550 | chr9 | 96012916 | |||
chr9:96012953 | T | C | 3 | a0003 a0021 a0022 |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
missense_variant | MODERATE | c.4403T>C | p.Met1468Thr | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4751/10245 | 4403/4653 | 1468/1550 | chr9 | 96012953 | |||
chr9:96013151 | T | G | 2 | a0017 a0025 |
2 | HG02723.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.4601T>G | p.Phe1534Cys | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4949/10245 | 4601/4653 | 1534/1550 | chr9 | 96013151 | |||
chr9:96013177 | G | A | 1 | a0004 | 28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
missense_variant | MODERATE | c.4627G>A | p.Ala1543Thr | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4975/10245 | 4627/4653 | 1543/1550 | chr9 | 96013177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:95915671 | G | A | 1 | a0003c0015 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.792G>A | p.Leu264Leu | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 5/19 | 1140/10245 | 792/4653 | 264/1550 | chr9 | 95915671 | |||
chr9:95972388 | C | T | 18 | a0001c0005 a0002c0002 a0002c0020 others(15): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
synonymous_variant | LOW | c.2637C>T | p.Asp879Asp | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 2985/10245 | 2637/4653 | 879/1550 | chr9 | 95972388 | |||
chr9:95972562 | A | G | 1 | a0001c0028 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.2811A>G | p.Val937Val | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/19 | 3159/10245 | 2811/4653 | 937/1550 | chr9 | 95972562 | |||
chr9:96004579 | G | T | 4 | a0002c0002 a0006c0007 a0014c0022 others(1): Show |
80 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(77): Show |
synonymous_variant | LOW | c.3552G>T | p.Pro1184Pro | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/19 | 3900/10245 | 3552/4653 | 1184/1550 | chr9 | 96004579 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:95875696 | C | T | 4 | a0004c0004t0037 a0004c0004t0038 a0004c0004t0095 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-343C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 343 | chr9 | 95875696 | ||||||
chr9:95875813 | C | T | 1 | a0024c0029t0094 | 1 | NA20129.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-226C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | chr9 | 95875813 | |||||||
chr9:95875851 | C | T | 1 | a0002c0002t0093 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-188C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 188 | chr9 | 95875851 | ||||||
chr9:95875960 | T | C | 4 | a0004c0004t0037 a0004c0004t0038 a0004c0004t0095 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-79T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 79 | chr9 | 95875960 | ||||||
chr9:95875960 | T | G | 2 | a0001c0001t0039 a0020c0014t0040 |
2 | HG01081.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 79 | chr9 | 95875960 | ||||||
chr9:95875974 | C | T | 6 | a0001c0001t0015 a0001c0001t0027 a0001c0001t0089 others(3): Show |
13 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-65C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 65 | chr9 | 95875974 | ||||||
chr9:95875982 | C | T | 1 | a0001c0001t0088 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 57 | chr9 | 95875982 | ||||||
chr9:95876006 | A | G | 20 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0025 others(17): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
5_prime_UTR_variant | MODIFIER | c.-33A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 33 | chr9 | 95876006 | ||||||
chr9:95876024 | C | T | 15 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0068 others(12): Show |
47 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-15C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 15 | chr9 | 95876024 | ||||||
chr9:95876026 | T | A | 3 | a0003c0003t0041 a0003c0003t0042 a0003c0003t0043 |
3 | HG00597.hp2 NA18939.hp2 NA18991.hp1 |
5_prime_UTR_variant | MODIFIER | c.-13T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 13 | chr9 | 95876026 | ||||||
chr9:95876027 | C | A | 3 | a0003c0003t0041 a0003c0003t0042 a0003c0003t0043 |
3 | HG00597.hp2 NA18939.hp2 NA18991.hp1 |
5_prime_UTR_variant | MODIFIER | c.-12C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 12 | chr9 | 95876027 | ||||||
chr9:95876031 | C | G | 3 | a0001c0001t0018 a0001c0001t0066 a0001c0001t0067 |
7 | NA18965.hp2 NA18977.hp2 NA18980.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/19 | 8 | chr9 | 95876031 | ||||||
chr9:96013325 | T | G | 1 | a0002c0002t0044 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 122 | chr9 | 96013325 | ||||||
chr9:96013527 | T | C | 1 | a0019c0013t0078 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 324 | chr9 | 96013527 | ||||||
chr9:96013829 | A | G | 9 | a0004c0004t0005 a0004c0004t0013 a0004c0004t0037 others(6): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*626A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 626 | chr9 | 96013829 | ||||||
chr9:96014127 | G | A | 2 | a0001c0001t0039 a0001c0001t0045 |
2 | HG01081.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*924G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 924 | chr9 | 96014127 | ||||||
chr9:96014174 | C | T | 2 | a0007c0008t0023 a0007c0008t0065 |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*971C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 971 | chr9 | 96014174 | ||||||
chr9:96014220 | G | A | 3 | a0003c0003t0016 a0003c0003t0046 a0022c0019t0016 |
6 | NA18945.hp2 NA18962.hp1 NA18985.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1017G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1017 | chr9 | 96014220 | ||||||
chr9:96014367 | G | A | 2 | a0001c0001t0047 a0001c0001t0079 |
2 | HG03225.hp1 NA18940.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1164G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1164 | chr9 | 96014367 | ||||||
chr9:96014443 | G | A | 2 | a0002c0002t0028 a0002c0002t0048 |
3 | HG02027.hp2 HG02165.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1240G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1240 | chr9 | 96014443 | ||||||
chr9:96014476 | G | T | 7 | a0001c0005t0033 a0001c0005t0061 a0001c0005t0062 others(4): Show |
8 | HG01952.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1273G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1273 | chr9 | 96014476 | ||||||
chr9:96014552 | T | C | 1 | a0001c0001t0066 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1349 | chr9 | 96014552 | ||||||
chr9:96014746 | C | T | 2 | a0005c0006t0017 a0005c0006t0032 |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1543C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1543 | chr9 | 96014746 | ||||||
chr9:96014784 | T | C | 2 | a0001c0001t0024 a0001c0001t0068 |
4 | NA18966.hp2 NA18991.hp2 NA19068.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1581T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1581 | chr9 | 96014784 | ||||||
chr9:96014848 | T | C | 18 | a0002c0002t0003 a0002c0002t0006 a0002c0002t0007 others(15): Show |
81 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1645T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1645 | chr9 | 96014848 | ||||||
chr9:96015015 | G | GT | 10 | a0001c0001t0004 a0001c0001t0056 a0001c0001t0067 others(7): Show |
32 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1837dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1838 | INFO_REALIGN_3_PRIME | chr9 | 96015015 | |||||
chr9:96015015 | G | GTT | 11 | a0001c0001t0010 a0001c0001t0047 a0001c0001t0057 others(8): Show |
37 | HG00323.hp1 HG00597.hp2 HG00733.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1836_*1837dupTT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1838 | INFO_REALIGN_3_PRIME | chr9 | 96015015 | |||||
chr9:96015015 | G | GTTT | 13 | a0001c0001t0022 a0001c0001t0045 a0001c0001t0060 others(10): Show |
17 | HG01071.hp2 HG01081.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1835_*1837dupTTT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1838 | INFO_REALIGN_3_PRIME | chr9 | 96015015 | |||||
chr9:96015015 | G | GTTTT | 20 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0019 others(17): Show |
105 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1834_*1837dupTTTT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1838 | INFO_REALIGN_3_PRIME | chr9 | 96015015 | |||||
chr9:96015015 | G | GTTTTT | 15 | a0001c0001t0014 a0001c0001t0036 a0001c0001t0068 others(12): Show |
64 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1833_*1837dupTTTT others(1): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1838 | INFO_REALIGN_3_PRIME | chr9 | 96015015 | |||||
chr9:96015015 | G | GTTTTTT | 8 | a0001c0001t0026 a0002c0002t0006 a0002c0002t0028 others(5): Show |
22 | HG00673.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1832_*1837dupTTTT others(2): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 1838 | INFO_REALIGN_3_PRIME | chr9 | 96015015 | |||||
chr9:96015190 | A | AT | 6 | a0001c0001t0010 a0001c0001t0047 a0001c0001t0055 others(3): Show |
13 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2002dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2003 | INFO_REALIGN_3_PRIME | chr9 | 96015190 | |||||
chr9:96015210 | C | T | 1 | a0001c0001t0090 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2007C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2007 | chr9 | 96015210 | ||||||
chr9:96015250 | G | A | 1 | a0001c0005t0061 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2047 | chr9 | 96015250 | ||||||
chr9:96015333 | G | A | 2 | a0017c0024t0074 a0025c0027t0069 |
2 | HG02723.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2130G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2130 | chr9 | 96015333 | ||||||
chr9:96015360 | G | T | 13 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(10): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2157G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2157 | chr9 | 96015360 | ||||||
chr9:96015380 | G | T | 1 | a0003c0003t0054 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2177 | chr9 | 96015380 | ||||||
chr9:96015399 | G | A | 6 | a0001c0005t0033 a0001c0005t0061 a0001c0005t0062 others(3): Show |
6 | HG01952.hp2 HG02809.hp1 HG03516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2196G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2196 | chr9 | 96015399 | ||||||
chr9:96015538 | G | A | 20 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0019 others(17): Show |
93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2335G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2335 | chr9 | 96015538 | ||||||
chr9:96015611 | C | T | 1 | a0001c0001t0053 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2408C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2408 | chr9 | 96015611 | ||||||
chr9:96015623 | G | A | 1 | a0001c0001t0085 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2420G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2420 | chr9 | 96015623 | ||||||
chr9:96015631 | T | TA | 65 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0015 others(62): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2442dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2443 | INFO_REALIGN_3_PRIME | chr9 | 96015631 | |||||
chr9:96015647 | A | G | 45 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0015 others(42): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2444A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2444 | chr9 | 96015647 | ||||||
chr9:96015880 | C | T | 2 | a0001c0005t0062 a0001c0005t0064 |
2 | HG02809.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2677C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2677 | chr9 | 96015880 | ||||||
chr9:96015973 | A | G | 13 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(10): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2770A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2770 | chr9 | 96015973 | ||||||
chr9:96016038 | A | C | 13 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(10): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2835A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2835 | chr9 | 96016038 | ||||||
chr9:96016128 | G | A | 16 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(13): Show |
38 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2925G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2925 | chr9 | 96016128 | ||||||
chr9:96016193 | A | G | 1 | a0001c0001t0052 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 2990 | chr9 | 96016193 | ||||||
chr9:96016494 | C | T | 7 | a0003c0003t0008 a0003c0003t0016 a0003c0003t0041 others(4): Show |
20 | HG00597.hp2 HG02056.hp2 NA18747.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3291C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 3291 | chr9 | 96016494 | ||||||
chr9:96016542 | G | A | 4 | a0001c0001t0015 a0001c0001t0089 a0001c0001t0091 others(1): Show |
9 | HG01081.hp2 HG02145.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3339G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 3339 | chr9 | 96016542 | ||||||
chr9:96016700 | C | T | 1 | a0004c0004t0076 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3497C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 3497 | chr9 | 96016700 | ||||||
chr9:96016713 | T | C | 4 | a0001c0001t0010 a0001c0001t0047 a0001c0001t0056 others(1): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3510T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 3510 | chr9 | 96016713 | ||||||
chr9:96016904 | TTTTGTGT others(1): Show |
T | 13 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(10): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3707_*3714delGTGT others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 3707 | INFO_REALIGN_3_PRIME | chr9 | 96016904 | |||||
chr9:96016926 | T | C | 4 | a0001c0001t0010 a0001c0001t0047 a0001c0001t0056 others(1): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3723T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 3723 | chr9 | 96016926 | ||||||
chr9:96017700 | A | G | 1 | a0001c0001t0036 | 2 | HG00733.hp1 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4497A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4497 | chr9 | 96017700 | ||||||
chr9:96017811 | A | G | 13 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(10): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4608A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4608 | chr9 | 96017811 | ||||||
chr9:96017885 | TAC | T | 18 | a0002c0002t0003 a0002c0002t0006 a0002c0002t0007 others(15): Show |
81 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4690_*4691delCA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4690 | INFO_REALIGN_3_PRIME | chr9 | 96017885 | |||||
chr9:96017945 | A | G | 13 | a0003c0003t0008 a0003c0003t0012 a0003c0003t0016 others(10): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4742A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4742 | chr9 | 96017945 | ||||||
chr9:96018026 | A | G | 2 | a0002c0002t0029 a0002c0002t0030 |
4 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4823A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4823 | chr9 | 96018026 | ||||||
chr9:96018056 | G | A | 1 | a0001c0001t0087 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4853G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4853 | chr9 | 96018056 | ||||||
chr9:96018100 | A | C | 1 | a0016c0018t0058 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4897A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4897 | chr9 | 96018100 | ||||||
chr9:96018161 | T | C | 1 | a0004c0004t0075 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4958T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4958 | chr9 | 96018161 | ||||||
chr9:96018185 | A | C | 1 | a0002c0002t0051 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4982A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 4982 | chr9 | 96018185 | ||||||
chr9:96018218 | C | T | 1 | a0001c0005t0071 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5015C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 5015 | chr9 | 96018218 | ||||||
chr9:96018324 | T | C | 108 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(105): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
3_prime_UTR_variant | MODIFIER | c.*5121T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 19/19 | 5121 | chr9 | 96018324 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:95876104 | C | T | 1 | a0001c0001t0002g0372 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.46+20C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876104 | |||||||
chr9:95876155 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.46+71T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876155 | |||||||
chr9:95876280 | C | G | 2 | a0001c0001t0027g0370 a0001c0001t0092g0371 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.46+196C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876280 | |||||||
chr9:95876390 | G | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.46+306G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876390 | |||||||
chr9:95876560 | T | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(80): Show |
88 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.46+476T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876560 | |||||||
chr9:95876650 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.46+566A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876650 | |||||||
chr9:95876830 | G | C | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.46+746G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95876830 | |||||||
chr9:95877165 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(264): Show |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.46+1081C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877165 | |||||||
chr9:95877228 | A | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+1144A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877228 | |||||||
chr9:95877339 | C | CT | 82 | a0001c0001t0001g0103 a0001c0001t0018g0205 a0001c0001t0024g0367 others(79): Show |
84 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.46+1267dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr9 | 95877339 | ||||||
chr9:95877391 | C | T | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+1307C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877391 | |||||||
chr9:95877622 | A | G | 1 | a0001c0001t0024g0367 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.46+1538A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877622 | |||||||
chr9:95877758 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.46+1674A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877758 | |||||||
chr9:95877804 | AAAAAAAA others(4): Show |
A | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+1734_46+1744del others(11): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr9 | 95877804 | ||||||
chr9:95877817 | A | G | 1 | a0001c0001t0010g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46+1733A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877817 | |||||||
chr9:95877902 | A | C | 117 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(114): Show |
119 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.46+1818A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877902 | |||||||
chr9:95877962 | C | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(311): Show |
326 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.46+1878C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95877962 | |||||||
chr9:95878042 | C | T | 1 | a0001c0001t0018g0202 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.46+1958C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878042 | |||||||
chr9:95878148 | T | G | 1 | a0004c0004t0075g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.46+2064T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878148 | |||||||
chr9:95878300 | C | T | 2 | a0010c0012t0020g0368 a0010c0012t0020g0369 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.46+2216C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878300 | |||||||
chr9:95878333 | G | C | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+2249G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878333 | |||||||
chr9:95878336 | A | T | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+2252A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878336 | |||||||
chr9:95878389 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(153): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.46+2305T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878389 | |||||||
chr9:95878507 | C | CT | 71 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(68): Show |
71 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2352dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr9 | 95878507 | ||||||
chr9:95878589 | T | G | 1 | a0001c0001t0045g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.47-2280T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878589 | |||||||
chr9:95878612 | G | A | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.47-2257G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878612 | |||||||
chr9:95878654 | C | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.47-2215C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878654 | |||||||
chr9:95878748 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.47-2121T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878748 | |||||||
chr9:95878776 | G | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.47-2093G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878776 | |||||||
chr9:95878871 | G | A | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-1998G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878871 | |||||||
chr9:95878884 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(153): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.47-1985A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878884 | |||||||
chr9:95878954 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-1915G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95878954 | |||||||
chr9:95879063 | C | T | 1 | a0002c0002t0028g0366 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.47-1806C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879063 | |||||||
chr9:95879148 | A | G | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.47-1721A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879148 | |||||||
chr9:95879190 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(73): Show |
81 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.47-1679T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879190 | |||||||
chr9:95879206 | G | A | 16 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0154 others(13): Show |
16 | HG00621.hp1 HG02155.hp2 NA18959.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-1663G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879206 | |||||||
chr9:95879305 | T | C | 1 | a0001c0001t0073g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.47-1564T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879305 | |||||||
chr9:95879361 | C | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.47-1508C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879361 | |||||||
chr9:95879446 | T | C | 11 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(8): Show |
11 | HG02083.hp2 HG02523.hp1 NA18966.hp2 others(8): Show |
intron_variant | MODIFIER | c.47-1423T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879446 | |||||||
chr9:95879563 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.47-1306T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879563 | |||||||
chr9:95879742 | G | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.47-1127G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879742 | |||||||
chr9:95879898 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.47-971G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879898 | |||||||
chr9:95879978 | C | T | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.47-891C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95879978 | |||||||
chr9:95880057 | G | C | 4 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0258 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-812G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880057 | |||||||
chr9:95880174 | G | A | 1 | a0004c0004t0076g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.47-695G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880174 | |||||||
chr9:95880191 | G | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.47-678G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880191 | |||||||
chr9:95880248 | A | G | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.47-621A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880248 | |||||||
chr9:95880397 | C | T | 1 | a0007c0008t0065g0296 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.47-472C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880397 | |||||||
chr9:95880415 | A | G | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.47-454A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880415 | |||||||
chr9:95880422 | A | G | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.47-447A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880422 | |||||||
chr9:95880441 | C | T | 16 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0154 others(13): Show |
16 | HG00621.hp1 HG02155.hp2 NA18959.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-428C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880441 | |||||||
chr9:95880570 | A | C | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.47-299A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880570 | |||||||
chr9:95880672 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.47-197C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880672 | |||||||
chr9:95880765 | A | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.47-104A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 1/18 | chr9 | 95880765 | |||||||
chr9:95881309 | A | T | 1 | a0001c0001t0002g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.471+16A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95881309 | |||||||
chr9:95881460 | A | G | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.471+167A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95881460 | |||||||
chr9:95881670 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+377G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95881670 | |||||||
chr9:95881954 | G | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(264): Show |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.471+661G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95881954 | |||||||
chr9:95882009 | C | T | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.471+716C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882009 | |||||||
chr9:95882266 | C | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+973C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882266 | |||||||
chr9:95882343 | G | C | 47 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(44): Show |
47 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.471+1050G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882343 | |||||||
chr9:95882464 | G | C | 5 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(2): Show |
5 | HG01123.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+1171G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882464 | |||||||
chr9:95882556 | C | T | 1 | a0001c0001t0011g0199 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.471+1263C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882556 | |||||||
chr9:95882667 | GA | G | 88 | a0001c0001t0001g0091 a0001c0001t0002g0197 a0001c0001t0002g0198 others(85): Show |
91 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.471+1384delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95882667 | ||||||
chr9:95882763 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0004g0134 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.471+1470C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882763 | |||||||
chr9:95882806 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.471+1513A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882806 | |||||||
chr9:95882896 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.471+1603C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882896 | |||||||
chr9:95882896 | C | T | 1 | a0002c0002t0006g0365 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.471+1603C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95882896 | |||||||
chr9:95883033 | C | T | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.471+1740C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883033 | |||||||
chr9:95883034 | T | A | 1 | a0002c0002t0003g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.471+1741T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883034 | |||||||
chr9:95883059 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.471+1766T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883059 | |||||||
chr9:95883088 | G | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.471+1795G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883088 | |||||||
chr9:95883120 | A | G | 2 | a0010c0012t0020g0368 a0010c0012t0020g0369 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.471+1827A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883120 | |||||||
chr9:95883144 | A | G | 117 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(114): Show |
119 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.471+1851A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883144 | |||||||
chr9:95883258 | A | G | 1 | a0003c0015t0021g0292 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.471+1965A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883258 | |||||||
chr9:95883365 | G | A | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471+2072G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883365 | |||||||
chr9:95883392 | G | A | 73 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(70): Show |
75 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.471+2099G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883392 | |||||||
chr9:95883429 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.471+2136A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883429 | |||||||
chr9:95883537 | C | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.471+2244C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883537 | |||||||
chr9:95883889 | A | G | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+2596A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95883889 | |||||||
chr9:95884489 | C | CT | 67 | a0001c0001t0001g0034 a0001c0001t0002g0159 a0001c0001t0019g0211 others(64): Show |
67 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.471+3208dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95884489 | ||||||
chr9:95884489 | C | CTT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(75): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.471+3207_471+3208d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95884489 | ||||||
chr9:95884559 | G | A | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.471+3266G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95884559 | |||||||
chr9:95884673 | G | A | 2 | a0003c0003t0008g0267 a0003c0003t0008g0268 |
2 | NA18975.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.471+3380G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95884673 | |||||||
chr9:95884799 | C | T | 2 | a0002c0002t0003g0363 a0002c0002t0003g0364 |
2 | NA18969.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.471+3506C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95884799 | |||||||
chr9:95884912 | T | C | 4 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0258 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+3619T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95884912 | |||||||
chr9:95884971 | G | T | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.471+3678G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95884971 | |||||||
chr9:95885101 | G | T | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 |
3 | HG02572.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.471+3808G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885101 | |||||||
chr9:95885117 | T | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+3824T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885117 | |||||||
chr9:95885284 | A | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.471+3991A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885284 | |||||||
chr9:95885333 | A | G | 1 | a0001c0001t0015g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.471+4040A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885333 | |||||||
chr9:95885350 | G | T | 3 | a0001c0001t0027g0142 a0001c0001t0027g0143 a0001c0001t0090g0144 |
3 | HG01884.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.471+4057G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885350 | |||||||
chr9:95885594 | A | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(4): Show |
8 | HG00639.hp1 HG01109.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.471+4301A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885594 | |||||||
chr9:95885625 | C | CA | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(264): Show |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.471+4333dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95885625 | ||||||
chr9:95885660 | G | C | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+4367G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885660 | |||||||
chr9:95885803 | G | A | 86 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(83): Show |
88 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.471+4510G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885803 | |||||||
chr9:95885915 | G | A | 2 | a0001c0005t0009g0223 a0001c0005t0072g0222 |
2 | NA18946.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.471+4622G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885915 | |||||||
chr9:95885993 | A | G | 12 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0007c0008t0023g0293 others(9): Show |
13 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.471+4700A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95885993 | |||||||
chr9:95886358 | T | TA | 47 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(44): Show |
47 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.471+5075dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95886358 | ||||||
chr9:95886372 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.471+5079A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95886372 | |||||||
chr9:95886529 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.471+5236C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95886529 | |||||||
chr9:95886610 | A | G | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471+5317A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95886610 | |||||||
chr9:95886868 | A | G | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.471+5575A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95886868 | |||||||
chr9:95886950 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(140): Show |
149 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.471+5657G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95886950 | |||||||
chr9:95887014 | G | C | 1 | a0002c0002t0093g0304 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.471+5721G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887014 | |||||||
chr9:95887134 | A | G | 2 | a0001c0001t0004g0004 a0001c0001t0004g0124 |
3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.471+5841A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887134 | |||||||
chr9:95887196 | T | C | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+5903T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887196 | |||||||
chr9:95887200 | G | C | 5 | a0001c0001t0019g0211 a0001c0005t0062g0105 a0001c0005t0064g0106 others(2): Show |
5 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+5907G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887200 | |||||||
chr9:95887245 | G | A | 1 | a0006c0007t0007g0298 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.471+5952G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887245 | |||||||
chr9:95887532 | G | A | 9 | a0003c0003t0008g0271 a0003c0003t0016g0269 a0003c0003t0016g0272 others(6): Show |
9 | HG00597.hp2 NA18939.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.471+6239G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887532 | |||||||
chr9:95887603 | C | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+6310C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887603 | |||||||
chr9:95887680 | ACT | A | 5 | a0004c0004t0005g0248 a0004c0004t0005g0250 a0004c0004t0005g0251 others(2): Show |
5 | NA18940.hp1 NA18957.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+6390_471+6391d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95887680 | ||||||
chr9:95887710 | T | G | 42 | a0001c0001t0001g0035 a0001c0005t0009g0223 a0001c0005t0009g0224 others(39): Show |
42 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.471+6417T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887710 | |||||||
chr9:95887764 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(202): Show |
212 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.471+6471A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887764 | |||||||
chr9:95887885 | A | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.471+6592A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887885 | |||||||
chr9:95887952 | G | A | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.471+6659G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95887952 | |||||||
chr9:95888068 | G | GT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(192): Show |
202 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.471+6790dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95888068 | ||||||
chr9:95888068 | G | GTT | 10 | a0001c0001t0001g0089 a0002c0002t0003g0340 a0002c0002t0006g0365 others(7): Show |
10 | HG01243.hp2 HG02280.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.471+6789_471+6790d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95888068 | ||||||
chr9:95888442 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.471+7149T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95888442 | |||||||
chr9:95888593 | C | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.471+7300C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95888593 | |||||||
chr9:95888658 | C | G | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.471+7365C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95888658 | |||||||
chr9:95888739 | C | T | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.471+7446C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95888739 | |||||||
chr9:95888927 | G | A | 3 | a0001c0001t0015g0138 a0001c0001t0089g0137 a0001c0001t0091g0139 |
3 | HG01081.hp2 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.471+7634G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95888927 | |||||||
chr9:95889032 | A | G | 1 | a0013c0016t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.471+7739A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889032 | |||||||
chr9:95889102 | C | G | 1 | a0004c0004t0013g0246 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.471+7809C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889102 | |||||||
chr9:95889139 | A | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(312): Show |
327 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.471+7846A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889139 | |||||||
chr9:95889154 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.471+7861C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889154 | |||||||
chr9:95889360 | A | G | 1 | a0005c0006t0032g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.471+8067A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889360 | |||||||
chr9:95889383 | G | A | 1 | a0021c0025t0083g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.471+8090G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889383 | |||||||
chr9:95889459 | G | A | 12 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(9): Show |
13 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+8166G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889459 | |||||||
chr9:95889467 | A | ATG | 6 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+8189_471+8190d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95889467 | ||||||
chr9:95889585 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.472-8264G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889585 | |||||||
chr9:95889621 | C | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-8228C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889621 | |||||||
chr9:95889678 | AC | A | 4 | a0001c0005t0009g0242 a0001c0005t0009g0243 a0001c0005t0009g0244 others(1): Show |
4 | HG02040.hp1 HG02135.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-8170delC | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889678 | |||||||
chr9:95889796 | G | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.472-8053G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889796 | |||||||
chr9:95889818 | A | G | 1 | a0001c0001t0004g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.472-8031A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889818 | |||||||
chr9:95889841 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.472-8008A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889841 | |||||||
chr9:95889966 | C | T | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.472-7883C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95889966 | |||||||
chr9:95890181 | T | G | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.472-7668T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95890181 | |||||||
chr9:95890541 | C | G | 4 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0258 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-7308C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95890541 | |||||||
chr9:95890629 | A | G | 1 | a0003c0003t0012g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.472-7220A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95890629 | |||||||
chr9:95890638 | A | G | 7 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(4): Show |
7 | HG02809.hp1 HG02965.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.472-7211A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95890638 | |||||||
chr9:95890775 | C | T | 7 | a0002c0002t0003g0015 a0002c0002t0003g0337 a0002c0002t0003g0339 others(4): Show |
7 | NA18947.hp2 NA18951.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-7074C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95890775 | |||||||
chr9:95890877 | C | T | 4 | a0002c0002t0029g0360 a0002c0002t0029g0362 a0002c0002t0030g0359 others(1): Show |
4 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-6972C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95890877 | |||||||
chr9:95891060 | A | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-6789A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95891060 | |||||||
chr9:95891301 | A | G | 1 | a0004c0004t0005g0241 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.472-6548A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95891301 | |||||||
chr9:95891314 | A | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-6535A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95891314 | |||||||
chr9:95891593 | C | CT | 9 | a0001c0001t0092g0371 a0007c0008t0023g0293 a0007c0008t0023g0294 others(6): Show |
10 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-6243dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95891593 | ||||||
chr9:95891689 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.472-6160A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95891689 | |||||||
chr9:95891879 | T | C | 1 | a0001c0001t0036g0039 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.472-5970T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95891879 | |||||||
chr9:95891946 | C | T | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.472-5903C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95891946 | |||||||
chr9:95892110 | A | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0130 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.472-5739A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892110 | |||||||
chr9:95892136 | G | A | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.472-5713G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892136 | |||||||
chr9:95892147 | C | A | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.472-5702C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892147 | |||||||
chr9:95892323 | A | G | 1 | a0002c0002t0003g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.472-5526A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892323 | |||||||
chr9:95892372 | T | C | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-5477T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892372 | |||||||
chr9:95892424 | C | CT | 168 | a0001c0001t0001g0085 a0001c0001t0002g0154 a0001c0001t0002g0155 others(165): Show |
171 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.472-5406dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95892424 | ||||||
chr9:95892478 | C | T | 1 | a0003c0003t0008g0285 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.472-5371C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892478 | |||||||
chr9:95892504 | A | G | 1 | a0001c0005t0009g0240 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.472-5345A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892504 | |||||||
chr9:95892512 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.472-5337C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892512 | |||||||
chr9:95892597 | A | T | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.472-5252A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892597 | |||||||
chr9:95892890 | T | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.472-4959T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95892890 | |||||||
chr9:95893031 | T | G | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.472-4818T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893031 | |||||||
chr9:95893416 | T | C | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-4433T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893416 | |||||||
chr9:95893511 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.472-4338G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893511 | |||||||
chr9:95893608 | T | C | 1 | a0004c0004t0005g0241 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.472-4241T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893608 | |||||||
chr9:95893781 | A | G | 1 | a0001c0005t0009g0245 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.472-4068A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893781 | |||||||
chr9:95893855 | G | A | 2 | a0001c0001t0004g0004 a0001c0001t0004g0124 |
3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.472-3994G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893855 | |||||||
chr9:95893916 | A | C | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.472-3933A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893916 | |||||||
chr9:95893925 | G | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.472-3924G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893925 | |||||||
chr9:95893935 | T | G | 1 | a0001c0001t0002g0372 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.472-3914T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95893935 | |||||||
chr9:95894062 | C | T | 9 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-3787C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894062 | |||||||
chr9:95894078 | A | G | 1 | a0021c0025t0083g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.472-3771A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894078 | |||||||
chr9:95894090 | A | G | 1 | a0001c0001t0031g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.472-3759A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894090 | |||||||
chr9:95894091 | C | A | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.472-3758C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894091 | |||||||
chr9:95894106 | T | TA | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-3742dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95894106 | ||||||
chr9:95894210 | CAAT | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(91): Show |
99 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.472-3638_472-3636d others(5): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894210 | |||||||
chr9:95894238 | G | A | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-3611G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894238 | |||||||
chr9:95894377 | G | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.472-3472G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894377 | |||||||
chr9:95894443 | C | T | 5 | a0001c0001t0015g0138 a0001c0001t0015g0140 a0001c0001t0015g0141 others(2): Show |
5 | HG01081.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-3406C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894443 | |||||||
chr9:95894584 | C | CT | 53 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0075 others(50): Show |
53 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.472-3238dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95894584 | ||||||
chr9:95894584 | CT | C | 117 | a0001c0001t0001g0018 a0001c0001t0001g0092 a0001c0001t0002g0161 others(114): Show |
120 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.472-3238delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95894584 | ||||||
chr9:95894616 | C | T | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-3233C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894616 | |||||||
chr9:95894672 | G | A | 2 | a0002c0002t0006g0305 a0002c0002t0006g0306 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.472-3177G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894672 | |||||||
chr9:95894681 | A | G | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-3168A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894681 | |||||||
chr9:95894715 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.472-3134C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894715 | |||||||
chr9:95894876 | G | A | 2 | a0002c0002t0003g0333 a0002c0002t0007g0307 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.472-2973G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894876 | |||||||
chr9:95894880 | G | A | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.472-2969G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95894880 | |||||||
chr9:95895169 | C | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.472-2680C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895169 | |||||||
chr9:95895728 | C | CT | 12 | a0001c0001t0001g0073 a0001c0001t0002g0154 a0001c0001t0002g0190 others(9): Show |
12 | HG00099.hp1 HG01361.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.472-2104dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95895728 | ||||||
chr9:95895728 | C | CTT | 40 | a0001c0005t0009g0223 a0001c0005t0009g0227 a0001c0005t0009g0229 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.472-2105_472-2104d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95895728 | ||||||
chr9:95895728 | CT | C | 12 | a0001c0001t0025g0098 a0001c0001t0080g0040 a0001c0005t0033g0254 others(9): Show |
13 | HG00673.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.472-2104delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95895728 | ||||||
chr9:95895751 | A | AGC | 12 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(9): Show |
14 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-2097_472-2096i others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95895751 | ||||||
chr9:95895790 | G | A | 34 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(31): Show |
34 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.472-2059G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895790 | |||||||
chr9:95895792 | T | G | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.472-2057T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895792 | |||||||
chr9:95895887 | C | T | 7 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.472-1962C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895887 | |||||||
chr9:95895888 | G | A | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.472-1961G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895888 | |||||||
chr9:95895896 | T | C | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.472-1953T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895896 | |||||||
chr9:95895928 | G | A | 2 | a0001c0001t0010g0114 a0001c0001t0010g0115 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.472-1921G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95895928 | |||||||
chr9:95896004 | G | A | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-1845G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896004 | |||||||
chr9:95896400 | GTTTTTTG others(3): Show |
G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-1442_472-1433d others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95896400 | ||||||
chr9:95896400 | GTTTTTTG others(7): Show |
G | 6 | a0001c0001t0011g0162 a0007c0008t0023g0293 a0007c0008t0023g0294 others(3): Show |
6 | HG01261.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-1428_472-1415d others(16): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95896400 | ||||||
chr9:95896401 | T | G | 1 | a0001c0001t0055g0167 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.472-1448T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896401 | |||||||
chr9:95896408 | A | AT | 39 | a0002c0002t0007g0015 a0003c0003t0008g0267 a0003c0003t0008g0268 others(36): Show |
39 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.472-1429dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95896408 | ||||||
chr9:95896408 | AT | A | 43 | a0001c0001t0004g0004 a0001c0005t0009g0223 a0001c0005t0009g0224 others(40): Show |
43 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.472-1429delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95896408 | ||||||
chr9:95896408 | ATTTTTTT others(8): Show |
A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.472-1429_472-1415d others(17): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95896408 | ||||||
chr9:95896414 | T | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-1435T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896414 | |||||||
chr9:95896421 | G | T | 2 | a0001c0001t0060g0121 a0003c0003t0016g0275 |
2 | NA18962.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.472-1428G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896421 | |||||||
chr9:95896422 | A | AT | 13 | a0001c0001t0002g0200 a0001c0001t0018g0153 a0001c0001t0027g0370 others(10): Show |
13 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.472-1415dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95896422 | ||||||
chr9:95896434 | T | G | 1 | a0004c0004t0005g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.472-1415T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896434 | |||||||
chr9:95896624 | A | G | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.472-1225A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896624 | |||||||
chr9:95896799 | C | T | 1 | a0023c0023t0001g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.472-1050C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95896799 | |||||||
chr9:95897001 | G | T | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.472-848G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897001 | |||||||
chr9:95897030 | C | T | 1 | a0002c0002t0028g0366 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.472-819C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897030 | |||||||
chr9:95897058 | TTTC | T | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.472-785_472-783del others(3): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr9 | 95897058 | ||||||
chr9:95897088 | A | T | 1 | a0002c0020t0035g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.472-761A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897088 | |||||||
chr9:95897211 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.472-638T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897211 | |||||||
chr9:95897378 | G | A | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.472-471G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897378 | |||||||
chr9:95897533 | C | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.472-316C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897533 | |||||||
chr9:95897573 | A | G | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.472-276A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897573 | |||||||
chr9:95897769 | T | A | 1 | a0003c0003t0021g0287 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.472-80T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 2/18 | chr9 | 95897769 | |||||||
chr9:95898044 | TCA | T | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+78_594+79delCA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95898044 | ||||||
chr9:95898094 | A | G | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.594+123A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95898094 | |||||||
chr9:95898311 | A | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.594+340A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95898311 | |||||||
chr9:95898770 | G | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.594+799G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95898770 | |||||||
chr9:95898874 | A | G | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.594+903A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95898874 | |||||||
chr9:95899066 | G | A | 1 | a0001c0001t0011g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.594+1095G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899066 | |||||||
chr9:95899067 | C | G | 1 | a0001c0001t0011g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.594+1096C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899067 | |||||||
chr9:95899111 | A | G | 1 | a0002c0002t0003g0356 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.594+1140A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899111 | |||||||
chr9:95899176 | G | A | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.594+1205G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899176 | |||||||
chr9:95899176 | G | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.594+1205G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899176 | |||||||
chr9:95899214 | C | T | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1243C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899214 | |||||||
chr9:95899345 | G | A | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.594+1374G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899345 | |||||||
chr9:95899590 | T | TTA | 10 | a0001c0001t0001g0036 a0001c0001t0001g0082 a0001c0001t0001g0083 others(7): Show |
11 | HG01346.hp1 HG02615.hp2 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.594+1629_594+1630d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899590 | ||||||
chr9:95899590 | T | TTATA | 10 | a0001c0001t0001g0084 a0001c0005t0063g0253 a0005c0006t0017g0020 others(7): Show |
10 | HG01243.hp2 HG02132.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.594+1627_594+1630d others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899590 | ||||||
chr9:95899590 | T | TTATATAT others(3): Show |
1 | a0006c0007t0003g0297 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.594+1621_594+1630d others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899590 | ||||||
chr9:95899590 | T | TTATATAT others(5): Show |
1 | a0006c0007t0007g0298 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.594+1630_594+1631i others(14): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899590 | ||||||
chr9:95899590 | T | TTATATAT others(7): Show |
3 | a0006c0007t0007g0299 a0006c0007t0007g0300 a0006c0007t0050g0301 |
3 | HG02818.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.594+1630_594+1631i others(16): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899590 | ||||||
chr9:95899598 | A | ATGTGTG | 3 | a0002c0002t0003g0333 a0002c0002t0007g0307 a0016c0018t0058g0336 |
3 | HG02109.hp1 HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.594+1628_594+1629i others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899598 | ||||||
chr9:95899598 | A | ATGTGTGT others(3): Show |
1 | a0002c0002t0007g0332 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.594+1628_594+1629i others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899598 | ||||||
chr9:95899600 | A | ATATATAT others(3): Show |
1 | a0001c0005t0062g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.594+1630_594+1631i others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATATATAT others(5): Show |
1 | a0001c0005t0064g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.594+1630_594+1631i others(14): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATATATGT others(7): Show |
1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.594+1630_594+1631i others(16): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATATGTG | 15 | a0002c0002t0003g0015 a0002c0002t0003g0308 a0002c0002t0003g0310 others(12): Show |
15 | HG00735.hp2 HG03927.hp1 HG04199.hp2 others(12): Show |
intron_variant | MODIFIER | c.594+1630_594+1631i others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATATGTGT others(1): Show |
16 | a0002c0002t0003g0016 a0002c0002t0003g0257 a0002c0002t0003g0303 others(13): Show |
17 | HG00323.hp2 HG00423.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.594+1630_594+1631i others(10): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATATGTGT others(3): Show |
14 | a0001c0005t0033g0254 a0002c0002t0003g0012 a0002c0002t0003g0013 others(11): Show |
14 | HG00673.hp2 HG01517.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.594+1630_594+1631i others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATATGTGT others(5): Show |
1 | a0002c0002t0029g0360 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.594+1630_594+1631i others(14): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATG | 24 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(21): Show |
26 | HG00733.hp2 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.594+1660_594+1661d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATGTG | 22 | a0001c0001t0002g0109 a0001c0001t0002g0135 a0001c0001t0002g0148 others(19): Show |
22 | HG00621.hp1 HG01255.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.594+1658_594+1661d others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATGTGTG | 7 | a0001c0001t0004g0111 a0001c0001t0067g0152 a0002c0002t0003g0348 others(4): Show |
7 | HG01099.hp1 HG01192.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+1656_594+1661d others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATGTGTGT others(1): Show |
15 | a0001c0001t0031g0112 a0001c0001t0031g0113 a0002c0002t0003g0342 others(12): Show |
16 | HG01069.hp2 HG01070.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.594+1654_594+1661d others(10): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATGTGTGT others(3): Show |
4 | a0002c0002t0003g0330 a0002c0002t0003g0340 a0002c0002t0003g0355 others(1): Show |
4 | HG01361.hp1 HG01433.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1652_594+1661d others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | ATGTGTGT others(5): Show |
1 | a0002c0002t0003g0331 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.594+1650_594+1661d others(14): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899600 | A | G | 6 | a0001c0001t0047g0123 a0002c0002t0003g0333 a0002c0002t0007g0307 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+1629A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899600 | |||||||
chr9:95899600 | ATG | A | 12 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(9): Show |
13 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.594+1660_594+1661d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899600 | ||||||
chr9:95899602 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(180): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.594+1631G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899602 | |||||||
chr9:95899604 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(180): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.594+1633G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899604 | |||||||
chr9:95899606 | G | A | 85 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(82): Show |
86 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.594+1635G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899606 | |||||||
chr9:95899608 | G | A | 10 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(7): Show |
11 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.594+1637G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899608 | |||||||
chr9:95899610 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1639G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899610 | |||||||
chr9:95899612 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1641G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899612 | |||||||
chr9:95899627 | TGTGTGC | T | 38 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(35): Show |
38 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.594+1659_594+1664d others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899627 | ||||||
chr9:95899631 | TGC | T | 28 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(25): Show |
28 | HG00597.hp2 HG01952.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.594+1662_594+1663d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95899631 | ||||||
chr9:95899632 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.594+1661G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899632 | |||||||
chr9:95899633 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(197): Show |
208 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.594+1662C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899633 | |||||||
chr9:95899636 | A | G | 1 | a0002c0002t0003g0347 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.594+1665A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899636 | |||||||
chr9:95899864 | G | T | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.594+1893G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899864 | |||||||
chr9:95899891 | C | T | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.594+1920C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899891 | |||||||
chr9:95899894 | C | T | 9 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.594+1923C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95899894 | |||||||
chr9:95900004 | G | A | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.594+2033G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95900004 | |||||||
chr9:95900036 | CTTAA | C | 3 | a0002c0002t0003g0330 a0002c0002t0003g0340 a0002c0002t0007g0332 |
3 | HG02300.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.594+2068_594+2071d others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95900036 | ||||||
chr9:95900099 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.594+2128C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95900099 | |||||||
chr9:95900198 | A | G | 1 | a0003c0003t0008g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.594+2227A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95900198 | |||||||
chr9:95900207 | C | G | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.594+2236C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95900207 | |||||||
chr9:95900386 | C | CA | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.594+2428dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95900386 | ||||||
chr9:95900619 | A | G | 1 | a0003c0003t0008g0282 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.594+2648A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95900619 | |||||||
chr9:95900857 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.594+2886C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95900857 | |||||||
chr9:95901075 | GA | G | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.594+3119delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95901075 | ||||||
chr9:95901076 | A | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+3105A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95901076 | |||||||
chr9:95901235 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(330): Show |
345 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.594+3264G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95901235 | |||||||
chr9:95901318 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(264): Show |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.594+3347T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95901318 | |||||||
chr9:95901318 | T | G | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594+3347T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95901318 | |||||||
chr9:95901499 | A | G | 2 | a0004c0004t0005g0234 a0004c0004t0013g0247 |
2 | HG01167.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.594+3528A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95901499 | |||||||
chr9:95901630 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.594+3659C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95901630 | |||||||
chr9:95902082 | G | T | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.594+4111G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902082 | |||||||
chr9:95902154 | CTGAA | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.594+4185_594+4188d others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95902154 | ||||||
chr9:95902211 | C | G | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.594+4240C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902211 | |||||||
chr9:95902308 | T | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.594+4337T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902308 | |||||||
chr9:95902361 | T | C | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 |
3 | HG02572.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.594+4390T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902361 | |||||||
chr9:95902364 | T | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.594+4393T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902364 | |||||||
chr9:95902404 | C | T | 175 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(172): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.594+4433C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902404 | |||||||
chr9:95902439 | C | A | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.594+4468C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902439 | |||||||
chr9:95902449 | T | G | 3 | a0004c0004t0005g0226 a0004c0004t0005g0234 a0004c0004t0013g0247 |
3 | HG01167.hp1 HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.594+4478T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902449 | |||||||
chr9:95902526 | T | C | 1 | a0003c0003t0012g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.595-4552T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902526 | |||||||
chr9:95902529 | C | G | 1 | a0001c0001t0004g0186 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.595-4549C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902529 | |||||||
chr9:95902529 | C | T | 1 | a0001c0001t0082g0069 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.595-4549C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902529 | |||||||
chr9:95902530 | G | A | 4 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0014g0042 others(1): Show |
6 | HG00099.hp2 HG02738.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-4548G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902530 | |||||||
chr9:95902601 | A | T | 1 | a0017c0024t0074g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.595-4477A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902601 | |||||||
chr9:95902602 | G | C | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.595-4476G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902602 | |||||||
chr9:95902622 | A | T | 1 | a0001c0001t0002g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.595-4456A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902622 | |||||||
chr9:95902665 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.595-4413G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902665 | |||||||
chr9:95902783 | A | G | 4 | a0002c0002t0003g0303 a0002c0002t0003g0316 a0002c0002t0003g0317 others(1): Show |
4 | HG00323.hp2 HG02602.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-4295A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95902783 | |||||||
chr9:95903479 | A | C | 1 | a0006c0007t0003g0297 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.595-3599A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95903479 | |||||||
chr9:95903523 | CTT | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.595-3550_595-3549d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95903523 | ||||||
chr9:95903584 | A | C | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.595-3494A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95903584 | |||||||
chr9:95903631 | TTAGAAAA | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.595-3441_595-3435d others(9): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95903631 | ||||||
chr9:95903798 | C | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.595-3280C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95903798 | |||||||
chr9:95903803 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.595-3275A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95903803 | |||||||
chr9:95903873 | G | A | 1 | a0003c0003t0016g0269 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.595-3205G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95903873 | |||||||
chr9:95903987 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.595-3091T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95903987 | |||||||
chr9:95904100 | ATTATG | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.595-2974_595-2970d others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr9 | 95904100 | ||||||
chr9:95904138 | G | A | 1 | a0002c0002t0003g0349 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.595-2940G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904138 | |||||||
chr9:95904182 | G | A | 39 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(36): Show |
39 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.595-2896G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904182 | |||||||
chr9:95904189 | A | T | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.595-2889A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904189 | |||||||
chr9:95904280 | T | C | 1 | a0002c0002t0030g0361 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.595-2798T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904280 | |||||||
chr9:95904337 | T | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-2741T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904337 | |||||||
chr9:95904350 | G | T | 1 | a0004c0004t0005g0302 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.595-2728G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904350 | |||||||
chr9:95904433 | C | G | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.595-2645C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904433 | |||||||
chr9:95904461 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-2617G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904461 | |||||||
chr9:95904496 | G | C | 1 | a0003c0003t0042g0270 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.595-2582G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904496 | |||||||
chr9:95904699 | A | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.595-2379A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904699 | |||||||
chr9:95904760 | C | T | 2 | a0004c0004t0005g0235 a0004c0004t0005g0239 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.595-2318C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904760 | |||||||
chr9:95904996 | T | C | 1 | a0002c0002t0003g0335 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.595-2082T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95904996 | |||||||
chr9:95905147 | T | C | 1 | a0001c0001t0002g0372 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.595-1931T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905147 | |||||||
chr9:95905568 | A | G | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.595-1510A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905568 | |||||||
chr9:95905641 | A | G | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.595-1437A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905641 | |||||||
chr9:95905696 | G | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-1382G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905696 | |||||||
chr9:95905792 | C | A | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.595-1286C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905792 | |||||||
chr9:95905928 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(82): Show |
90 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.595-1150T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905928 | |||||||
chr9:95905939 | C | T | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-1139C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95905939 | |||||||
chr9:95906070 | G | A | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.595-1008G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906070 | |||||||
chr9:95906088 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.595-990C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906088 | |||||||
chr9:95906158 | A | G | 1 | a0001c0001t0002g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.595-920A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906158 | |||||||
chr9:95906180 | A | T | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.595-898A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906180 | |||||||
chr9:95906517 | G | T | 1 | a0001c0001t0014g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.595-561G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906517 | |||||||
chr9:95906564 | C | T | 3 | a0002c0002t0003g0016 a0002c0002t0003g0257 a0002c0002t0003g0343 |
4 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-514C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906564 | |||||||
chr9:95906575 | T | C | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-503T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906575 | |||||||
chr9:95906898 | C | T | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-180C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95906898 | |||||||
chr9:95907046 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.595-32A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95907046 | |||||||
chr9:95907053 | C | G | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.595-25C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 3/18 | chr9 | 95907053 | |||||||
chr9:95907338 | G | GT | 131 | a0001c0001t0001g0032 a0001c0001t0001g0067 a0001c0001t0001g0084 others(128): Show |
133 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.788+86dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907338 | ||||||
chr9:95907338 | G | GTT | 7 | a0001c0005t0009g0224 a0001c0005t0071g0233 a0002c0002t0003g0313 others(4): Show |
7 | HG01928.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+85_788+86dupTT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907338 | ||||||
chr9:95907417 | C | G | 2 | a0003c0003t0021g0287 a0003c0003t0021g0291 |
2 | NA18747.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.788+146C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907417 | |||||||
chr9:95907463 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.788+192C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907463 | |||||||
chr9:95907537 | G | T | 175 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(172): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.788+266G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907537 | |||||||
chr9:95907757 | A | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+486A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907757 | |||||||
chr9:95907788 | A | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+517A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907788 | |||||||
chr9:95907826 | T | TAC | 6 | a0001c0001t0002g0005 a0001c0001t0002g0128 a0001c0001t0002g0131 others(3): Show |
7 | HG01257.hp1 HG01258.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+584_788+585dup others(2): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907826 | T | TACAC | 28 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0004g0133 others(25): Show |
30 | HG01081.hp2 HG01109.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.788+582_788+585dup others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907826 | T | TACACACA others(11): Show |
1 | a0002c0002t0003g0345 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.788+568_788+585dup others(18): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907826 | T | TACACACA others(13): Show |
1 | a0001c0001t0070g0216 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.788+566_788+585dup others(20): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907826 | T | TACACACA others(15): Show |
1 | a0001c0001t0019g0217 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.788+564_788+585dup others(22): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907826 | T | TACACACA others(17): Show |
1 | a0001c0001t0019g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.788+562_788+585dup others(24): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907826 | T | TACACACA others(21): Show |
1 | a0001c0001t0019g0214 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.788+558_788+585dup others(28): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907826 | ||||||
chr9:95907830 | C | CACACACA others(27): Show |
1 | a0004c0004t0038g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(34): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907830 | ||||||
chr9:95907832 | C | CACACACA others(23): Show |
2 | a0004c0004t0038g0011 a0004c0004t0096g0011 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.788+585_788+586ins others(30): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907832 | ||||||
chr9:95907832 | C | CACACACA others(25): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(32): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907832 | ||||||
chr9:95907832 | C | CACACACA others(27): Show |
1 | a0017c0024t0074g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(34): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907832 | ||||||
chr9:95907834 | C | CACACACA others(3): Show |
3 | a0002c0002t0003g0316 a0002c0002t0003g0317 a0002c0002t0003g0318 |
3 | HG00323.hp2 HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.788+572_788+573ins others(10): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(21): Show |
2 | a0002c0002t0003g0350 a0002c0002t0093g0304 |
2 | HG01106.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.788+585_788+586ins others(28): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(23): Show |
21 | a0001c0001t0001g0033 a0002c0002t0003g0257 a0002c0002t0003g0340 others(18): Show |
21 | HG01070.hp1 HG01099.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(30): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(25): Show |
54 | a0001c0001t0001g0073 a0001c0001t0019g0211 a0001c0001t0019g0212 others(51): Show |
56 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(32): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(26): Show |
1 | a0002c0002t0006g0334 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.788+585_788+586ins others(33): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(27): Show |
23 | a0001c0001t0024g0213 a0001c0001t0024g0219 a0001c0001t0068g0218 others(20): Show |
23 | HG00597.hp2 HG02056.hp2 NA18747.hp1 others(20): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(34): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(29): Show |
1 | a0003c0003t0012g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(36): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907834 | C | CACACACA others(30): Show |
1 | a0003c0003t0008g0281 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(37): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907834 | ||||||
chr9:95907836 | C | CACACACA others(11): Show |
1 | a0001c0001t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.788+582_788+583ins others(18): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(13): Show |
4 | a0001c0001t0001g0097 a0001c0001t0025g0098 a0001c0001t0025g0099 others(1): Show |
4 | HG02451.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+584_788+585ins others(20): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(17): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0014g0045 others(6): Show |
9 | HG02165.hp2 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(24): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(19): Show |
15 | a0001c0001t0080g0040 a0003c0003t0012g0262 a0003c0003t0012g0264 others(12): Show |
15 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(26): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(20): Show |
1 | a0003c0003t0021g0287 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.788+585_788+586ins others(27): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(21): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0034 others(23): Show |
28 | HG00597.hp1 HG01255.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(28): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(23): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0027 others(36): Show |
42 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(30): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907836 | C | CACACACA others(25): Show |
1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.788+585_788+586ins others(32): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907836 | ||||||
chr9:95907838 | C | CACACACA others(15): Show |
5 | a0001c0005t0009g0227 a0001c0005t0033g0254 a0004c0004t0013g0236 others(2): Show |
5 | HG00673.hp1 HG01175.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(22): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907838 | C | CACACACA others(17): Show |
29 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0229 others(26): Show |
30 | HG00423.hp2 HG00741.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(24): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907838 | C | CACACACA others(19): Show |
6 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0004c0004t0005g0250 others(3): Show |
6 | NA18940.hp1 NA18982.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(26): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907838 | C | CACACACA others(21): Show |
4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+585_788+586ins others(28): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907838 | C | CACACACA others(22): Show |
1 | a0004c0004t0005g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(29): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907838 | C | CACACACA others(23): Show |
1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(30): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907838 | C | CACACACA others(25): Show |
1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(32): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907838 | ||||||
chr9:95907840 | C | CACACACA others(19): Show |
1 | a0002c0002t0003g0339 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.788+585_788+586ins others(26): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907840 | ||||||
chr9:95907855 | A | C | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.788+584A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907855 | |||||||
chr9:95907857 | C | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(270): Show |
280 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.788+586C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907857 | |||||||
chr9:95907859 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(131): Show |
139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.788+588C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907859 | |||||||
chr9:95907863 | A | ACACAAAC others(25): Show |
1 | a0001c0001t0014g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.788+593_788+594ins others(32): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95907863 | ||||||
chr9:95907863 | A | C | 3 | a0001c0001t0025g0098 a0001c0001t0025g0099 a0001c0001t0081g0100 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.788+592A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907863 | |||||||
chr9:95907905 | C | T | 1 | a0002c0002t0003g0345 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.788+634C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907905 | |||||||
chr9:95907933 | G | C | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.788+662G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907933 | |||||||
chr9:95907978 | A | G | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.788+707A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907978 | |||||||
chr9:95907986 | C | G | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+715C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95907986 | |||||||
chr9:95908011 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+740C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908011 | |||||||
chr9:95908174 | A | C | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.788+903A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908174 | |||||||
chr9:95908339 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(82): Show |
90 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.788+1068C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908339 | |||||||
chr9:95908362 | A | G | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+1091A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908362 | |||||||
chr9:95908376 | G | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+1105G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908376 | |||||||
chr9:95908558 | A | T | 7 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(4): Show |
7 | HG02809.hp1 HG02965.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.788+1287A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908558 | |||||||
chr9:95908595 | G | A | 1 | a0021c0025t0083g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.788+1324G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908595 | |||||||
chr9:95908706 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.788+1435C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908706 | |||||||
chr9:95908761 | A | AT | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+1490_788+1491i others(3): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908761 | |||||||
chr9:95908762 | A | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+1491A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95908762 | |||||||
chr9:95909122 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.788+1851G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909122 | |||||||
chr9:95909136 | C | G | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.788+1865C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909136 | |||||||
chr9:95909481 | A | C | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.788+2210A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909481 | |||||||
chr9:95909485 | A | G | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.788+2214A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909485 | |||||||
chr9:95909568 | G | T | 2 | a0001c0001t0018g0202 a0001c0001t0066g0146 |
2 | NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.788+2297G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909568 | |||||||
chr9:95909749 | A | G | 1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.788+2478A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909749 | |||||||
chr9:95909809 | T | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.788+2538T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909809 | |||||||
chr9:95909914 | G | A | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.788+2643G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909914 | |||||||
chr9:95909941 | G | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.788+2670G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909941 | |||||||
chr9:95909977 | A | T | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.788+2706A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909977 | |||||||
chr9:95909982 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.788+2711T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95909982 | |||||||
chr9:95910078 | A | G | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.788+2807A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910078 | |||||||
chr9:95910360 | T | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+3089T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910360 | |||||||
chr9:95910601 | G | A | 1 | a0005c0006t0032g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.788+3330G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910601 | |||||||
chr9:95910759 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.788+3488C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910759 | |||||||
chr9:95910789 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.788+3518A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910789 | |||||||
chr9:95910804 | A | G | 2 | a0001c0001t0015g0007 a0001c0001t0015g0145 |
3 | HG02615.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.788+3533A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910804 | |||||||
chr9:95910840 | TC | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+3570delC | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95910840 | |||||||
chr9:95911024 | A | G | 1 | a0001c0001t0027g0143 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.788+3753A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95911024 | |||||||
chr9:95911307 | C | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.788+4036C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95911307 | |||||||
chr9:95911484 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.789-4184T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95911484 | |||||||
chr9:95911657 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.789-4011C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95911657 | |||||||
chr9:95911990 | T | C | 2 | a0010c0012t0020g0368 a0010c0012t0020g0369 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.789-3678T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95911990 | |||||||
chr9:95912033 | C | T | 1 | a0002c0002t0006g0338 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.789-3635C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912033 | |||||||
chr9:95912258 | A | G | 34 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(31): Show |
34 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.789-3410A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912258 | |||||||
chr9:95912311 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.789-3357A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912311 | |||||||
chr9:95912377 | T | TTG | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789-3277_789-3276d others(4): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95912377 | ||||||
chr9:95912456 | A | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-3212A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912456 | |||||||
chr9:95912785 | C | G | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-2883C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912785 | |||||||
chr9:95912786 | C | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.789-2882C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912786 | |||||||
chr9:95912891 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.789-2777G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95912891 | |||||||
chr9:95913035 | G | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.789-2633G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913035 | |||||||
chr9:95913313 | C | T | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789-2355C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913313 | |||||||
chr9:95913350 | G | A | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.789-2318G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913350 | |||||||
chr9:95913394 | A | C | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.789-2274A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913394 | |||||||
chr9:95913435 | TCGCTTGC others(5): Show |
T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(97): Show |
106 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.789-2209_789-2198d others(14): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95913435 | ||||||
chr9:95913482 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.789-2186C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913482 | |||||||
chr9:95913486 | C | T | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.789-2182C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913486 | |||||||
chr9:95913562 | T | G | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.789-2106T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913562 | |||||||
chr9:95913600 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.789-2068T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913600 | |||||||
chr9:95913697 | C | T | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.789-1971C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913697 | |||||||
chr9:95913710 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.789-1958C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95913710 | |||||||
chr9:95914137 | C | G | 1 | a0001c0001t0001g0003 | 2 | NA18939.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.789-1531C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914137 | |||||||
chr9:95914275 | A | G | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.789-1393A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914275 | |||||||
chr9:95914356 | T | C | 2 | a0001c0001t0010g0117 a0001c0001t0056g0116 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.789-1312T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914356 | |||||||
chr9:95914487 | G | A | 1 | a0006c0007t0007g0298 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.789-1181G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914487 | |||||||
chr9:95914508 | C | T | 2 | a0001c0001t0002g0165 a0002c0002t0006g0321 |
2 | HG00408.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.789-1160C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914508 | |||||||
chr9:95914510 | C | T | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789-1158C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914510 | |||||||
chr9:95914621 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.789-1047G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914621 | |||||||
chr9:95914709 | G | A | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.789-959G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914709 | |||||||
chr9:95914800 | A | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.789-868A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914800 | |||||||
chr9:95914885 | TA | T | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.789-779delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 95914885 | ||||||
chr9:95914938 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.789-730G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95914938 | |||||||
chr9:95915003 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.789-665A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915003 | |||||||
chr9:95915024 | A | G | 1 | a0018c0021t0003g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.789-644A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915024 | |||||||
chr9:95915061 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.789-607G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915061 | |||||||
chr9:95915170 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.789-498C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915170 | |||||||
chr9:95915172 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.789-496G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915172 | |||||||
chr9:95915202 | C | A | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.789-466C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915202 | |||||||
chr9:95915217 | A | C | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.789-451A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915217 | |||||||
chr9:95915267 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.789-401A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915267 | |||||||
chr9:95915459 | A | C | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.789-209A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915459 | |||||||
chr9:95915521 | A | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.789-147A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915521 | |||||||
chr9:95915528 | T | C | 1 | a0012c0026t0001g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.789-140T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915528 | |||||||
chr9:95915567 | A | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.789-101A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 4/18 | chr9 | 95915567 | |||||||
chr9:95915882 | G | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(312): Show |
327 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.950+53G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 5/18 | chr9 | 95915882 | |||||||
chr9:95915979 | G | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.950+150G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 5/18 | chr9 | 95915979 | |||||||
chr9:95916173 | G | A | 1 | a0003c0003t0008g0271 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.951-54G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 5/18 | chr9 | 95916173 | |||||||
chr9:95916555 | G | GA | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1158+127dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr9 | 95916555 | ||||||
chr9:95916568 | C | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1158+134C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95916568 | |||||||
chr9:95916684 | C | CT | 18 | a0001c0001t0001g0027 a0001c0001t0001g0096 a0001c0001t0015g0138 others(15): Show |
18 | HG00741.hp1 HG01346.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1158+266dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr9 | 95916684 | ||||||
chr9:95916684 | CT | C | 7 | a0001c0001t0002g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 others(4): Show |
7 | HG01069.hp2 HG01255.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1158+266delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr9 | 95916684 | ||||||
chr9:95916982 | G | C | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1158+548G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95916982 | |||||||
chr9:95917013 | C | G | 1 | a0002c0002t0003g0343 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1158+579C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917013 | |||||||
chr9:95917086 | A | C | 3 | a0001c0001t0002g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 |
3 | HG01255.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1158+652A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917086 | |||||||
chr9:95917093 | A | G | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+659A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917093 | |||||||
chr9:95917201 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+767A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917201 | |||||||
chr9:95917231 | A | G | 2 | a0004c0004t0038g0011 a0004c0004t0096g0011 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1158+797A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917231 | |||||||
chr9:95917252 | T | C | 4 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0240 others(1): Show |
4 | HG00423.hp2 NA18946.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158+818T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917252 | |||||||
chr9:95917270 | T | G | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1158+836T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917270 | |||||||
chr9:95917359 | G | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1158+925G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917359 | |||||||
chr9:95917536 | A | G | 75 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(72): Show |
77 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.1158+1102A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917536 | |||||||
chr9:95917587 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1158+1153T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917587 | |||||||
chr9:95917850 | G | A | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1158+1416G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917850 | |||||||
chr9:95917941 | A | G | 1 | a0001c0001t0002g0372 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1158+1507A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917941 | |||||||
chr9:95917963 | A | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0194 |
2 | NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1158+1529A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95917963 | |||||||
chr9:95918152 | T | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1158+1718T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918152 | |||||||
chr9:95918303 | C | A | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1158+1869C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918303 | |||||||
chr9:95918374 | G | A | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158+1940G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918374 | |||||||
chr9:95918389 | C | A | 1 | a0007c0008t0065g0296 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1158+1955C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918389 | |||||||
chr9:95918870 | G | A | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1159-2305G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918870 | |||||||
chr9:95918922 | C | T | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1159-2253C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918922 | |||||||
chr9:95918972 | G | A | 1 | a0002c0002t0003g0308 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1159-2203G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918972 | |||||||
chr9:95918988 | T | C | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1159-2187T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95918988 | |||||||
chr9:95919013 | C | T | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1159-2162C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919013 | |||||||
chr9:95919157 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159-2018G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919157 | |||||||
chr9:95919166 | C | T | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1159-2009C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919166 | |||||||
chr9:95919213 | A | G | 4 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0014g0042 others(1): Show |
6 | HG00099.hp2 HG02738.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159-1962A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919213 | |||||||
chr9:95919231 | T | C | 1 | a0003c0003t0008g0278 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1159-1944T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919231 | |||||||
chr9:95919480 | C | T | 7 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(4): Show |
7 | HG02809.hp1 HG02965.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159-1695C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919480 | |||||||
chr9:95919836 | T | A | 1 | a0002c0002t0051g0314 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1159-1339T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919836 | |||||||
chr9:95919839 | A | C | 1 | a0001c0005t0009g0244 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1159-1336A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919839 | |||||||
chr9:95919947 | G | A | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1159-1228G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95919947 | |||||||
chr9:95920214 | C | G | 5 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1159-961C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95920214 | |||||||
chr9:95920335 | T | C | 2 | a0003c0003t0008g0267 a0003c0003t0008g0268 |
2 | NA18975.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1159-840T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95920335 | |||||||
chr9:95920439 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1159-736G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95920439 | |||||||
chr9:95920856 | A | G | 1 | a0020c0014t0040g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1159-319A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95920856 | |||||||
chr9:95920864 | A | T | 1 | a0001c0001t0014g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1159-311A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95920864 | |||||||
chr9:95920934 | G | A | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1159-241G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95920934 | |||||||
chr9:95921018 | G | A | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1159-157G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95921018 | |||||||
chr9:95921028 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1159-147G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95921028 | |||||||
chr9:95921070 | C | T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(15): Show |
20 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1159-105C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95921070 | |||||||
chr9:95921089 | T | C | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1159-86T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 6/18 | chr9 | 95921089 | |||||||
chr9:95921464 | A | C | 1 | a0001c0001t0084g0066 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1299+149A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95921464 | |||||||
chr9:95921689 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1299+374G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95921689 | |||||||
chr9:95921725 | G | C | 10 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1299+410G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95921725 | |||||||
chr9:95921845 | G | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-460G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95921845 | |||||||
chr9:95921967 | A | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-338A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95921967 | |||||||
chr9:95922066 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1300-239T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95922066 | |||||||
chr9:95922125 | G | A | 1 | a0004c0004t0005g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1300-180G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95922125 | |||||||
chr9:95922135 | A | G | 2 | a0001c0001t0027g0370 a0001c0001t0092g0371 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1300-170A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 7/18 | chr9 | 95922135 | |||||||
chr9:95922436 | C | T | 1 | a0018c0021t0003g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1413+18C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 8/18 | chr9 | 95922436 | |||||||
chr9:95922438 | T | C | 4 | a0001c0005t0009g0242 a0001c0005t0009g0243 a0001c0005t0009g0244 others(1): Show |
4 | HG02040.hp1 HG02135.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1413+20T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 8/18 | chr9 | 95922438 | |||||||
chr9:95922634 | C | T | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1413+216C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 8/18 | chr9 | 95922634 | |||||||
chr9:95922693 | A | G | 1 | a0002c0002t0003g0315 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1413+275A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 8/18 | chr9 | 95922693 | |||||||
chr9:95922890 | T | C | 1 | a0003c0003t0012g0262 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1414-370T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 8/18 | chr9 | 95922890 | |||||||
chr9:95923193 | A | T | 1 | a0001c0001t0002g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1414-67A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 8/18 | chr9 | 95923193 | |||||||
chr9:95923515 | A | G | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1533+136A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95923515 | |||||||
chr9:95923583 | G | C | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1533+204G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95923583 | |||||||
chr9:95923828 | T | C | 10 | a0002c0002t0003g0342 a0002c0002t0003g0347 a0002c0002t0003g0348 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1533+449T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95923828 | |||||||
chr9:95923942 | GGGTGGGA | G | 33 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0034 others(30): Show |
33 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1533+564_1533+570d others(9): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95923942 | |||||||
chr9:95924808 | C | T | 4 | a0002c0002t0029g0360 a0002c0002t0029g0362 a0002c0002t0030g0359 others(1): Show |
4 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+1429C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95924808 | |||||||
chr9:95925277 | C | A | 1 | a0003c0003t0054g0288 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1533+1898C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95925277 | |||||||
chr9:95925507 | G | A | 1 | a0003c0003t0016g0275 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1533+2128G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95925507 | |||||||
chr9:95925544 | C | G | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1533+2165C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95925544 | |||||||
chr9:95925743 | T | G | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-2336T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95925743 | |||||||
chr9:95925831 | T | TATA | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1534-2247_1534-224 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 95925831 | ||||||
chr9:95925833 | G | A | 54 | a0001c0001t0047g0123 a0001c0005t0009g0223 a0001c0005t0009g0224 others(51): Show |
54 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1534-2246G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95925833 | |||||||
chr9:95926146 | A | G | 1 | a0005c0006t0017g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1534-1933A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95926146 | |||||||
chr9:95926335 | C | G | 1 | a0002c0002t0003g0318 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1534-1744C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95926335 | |||||||
chr9:95926516 | G | A | 1 | a0004c0004t0005g0302 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1534-1563G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95926516 | |||||||
chr9:95926677 | A | G | 1 | a0001c0001t0022g0006 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1534-1402A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95926677 | |||||||
chr9:95926729 | C | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534-1350C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95926729 | |||||||
chr9:95927102 | A | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534-977A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927102 | |||||||
chr9:95927300 | A | G | 2 | a0002c0002t0006g0357 a0002c0002t0049g0344 |
2 | NA19056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1534-779A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927300 | |||||||
chr9:95927318 | G | C | 1 | a0002c0002t0003g0343 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1534-761G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927318 | |||||||
chr9:95927531 | A | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1534-548A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927531 | |||||||
chr9:95927648 | A | G | 1 | a0002c0002t0007g0328 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1534-431A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927648 | |||||||
chr9:95927864 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1534-215T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927864 | |||||||
chr9:95927932 | T | C | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-147T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927932 | |||||||
chr9:95927963 | A | G | 1 | a0002c0002t0003g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1534-116A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 9/18 | chr9 | 95927963 | |||||||
chr9:95928318 | A | C | 1 | a0001c0001t0002g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1605+168A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 10/18 | chr9 | 95928318 | |||||||
chr9:95928318 | A | G | 1 | a0001c0001t0015g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1605+168A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 10/18 | chr9 | 95928318 | |||||||
chr9:95928511 | C | T | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1606-208C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 10/18 | chr9 | 95928511 | |||||||
chr9:95928902 | A | G | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1751+38A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95928902 | |||||||
chr9:95928975 | G | A | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1751+111G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95928975 | |||||||
chr9:95928998 | G | A | 1 | a0001c0001t0004g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1751+134G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95928998 | |||||||
chr9:95929064 | C | T | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1751+200C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95929064 | |||||||
chr9:95929529 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1751+665A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95929529 | |||||||
chr9:95929744 | G | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+880G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95929744 | |||||||
chr9:95929902 | C | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751+1038C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95929902 | |||||||
chr9:95929909 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1751+1045C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95929909 | |||||||
chr9:95930002 | A | G | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1751+1138A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930002 | |||||||
chr9:95930030 | G | A | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1751+1166G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930030 | |||||||
chr9:95930163 | T | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1751+1299T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930163 | |||||||
chr9:95930201 | A | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0194 |
2 | NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1751+1337A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930201 | |||||||
chr9:95930617 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1751+1753G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930617 | |||||||
chr9:95930733 | T | G | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+1869T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930733 | |||||||
chr9:95930753 | G | A | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1751+1889G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930753 | |||||||
chr9:95930787 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1751+1923T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930787 | |||||||
chr9:95930849 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1751+1985G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930849 | |||||||
chr9:95930962 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1751+2098G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95930962 | |||||||
chr9:95931002 | A | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1751+2138A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931002 | |||||||
chr9:95931019 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1751+2155A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931019 | |||||||
chr9:95931130 | A | G | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751+2266A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931130 | |||||||
chr9:95931131 | T | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+2267T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931131 | |||||||
chr9:95931245 | C | T | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+2381C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931245 | |||||||
chr9:95931466 | C | T | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1751+2602C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931466 | |||||||
chr9:95931492 | T | C | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1751+2628T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931492 | |||||||
chr9:95931507 | C | T | 1 | a0022c0019t0016g0326 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1751+2643C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931507 | |||||||
chr9:95931534 | G | A | 1 | a0001c0001t0027g0142 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1751+2670G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931534 | |||||||
chr9:95931728 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1751+2864A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931728 | |||||||
chr9:95931794 | C | T | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1751+2930C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931794 | |||||||
chr9:95931799 | A | AT | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1751+2942dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95931799 | ||||||
chr9:95931839 | C | T | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+2975C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931839 | |||||||
chr9:95931875 | A | G | 1 | a0016c0018t0058g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1751+3011A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95931875 | |||||||
chr9:95931895 | C | CT | 32 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(29): Show |
32 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1751+3041dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95931895 | ||||||
chr9:95932008 | T | G | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1751+3144T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932008 | |||||||
chr9:95932074 | C | CT | 18 | a0001c0001t0011g0199 a0001c0001t0014g0045 a0001c0005t0033g0254 others(15): Show |
18 | HG01175.hp2 HG01361.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.1751+3224dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95932074 | ||||||
chr9:95932121 | A | G | 1 | a0004c0004t0005g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1751+3257A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932121 | |||||||
chr9:95932157 | C | T | 2 | a0001c0001t0001g0090 a0001c0005t0063g0253 |
2 | HG03516.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1751+3293C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932157 | |||||||
chr9:95932172 | TCTC | T | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751+3311_1751+331 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95932172 | ||||||
chr9:95932191 | G | A | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1751+3327G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932191 | |||||||
chr9:95932302 | G | A | 1 | a0002c0002t0003g0311 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1751+3438G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932302 | |||||||
chr9:95932311 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1751+3447G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932311 | |||||||
chr9:95932339 | T | C | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1751+3475T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932339 | |||||||
chr9:95932341 | G | A | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751+3477G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932341 | |||||||
chr9:95932359 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1751+3495T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932359 | |||||||
chr9:95932553 | T | G | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1751+3689T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932553 | |||||||
chr9:95932555 | A | G | 1 | a0003c0003t0012g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1751+3691A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932555 | |||||||
chr9:95932775 | T | C | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1751+3911T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932775 | |||||||
chr9:95932901 | C | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751+4037C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95932901 | |||||||
chr9:95933017 | C | T | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1751+4153C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933017 | |||||||
chr9:95933169 | T | C | 5 | a0001c0005t0061g0221 a0001c0005t0062g0105 a0001c0005t0064g0106 others(2): Show |
5 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1751+4305T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933169 | |||||||
chr9:95933238 | G | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1751+4374G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933238 | |||||||
chr9:95933417 | A | G | 1 | a0001c0001t0039g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1751+4553A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933417 | |||||||
chr9:95933436 | A | G | 1 | a0001c0001t0004g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1751+4572A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933436 | |||||||
chr9:95933676 | C | T | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1751+4812C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933676 | |||||||
chr9:95933800 | C | T | 3 | a0001c0001t0025g0098 a0001c0001t0025g0099 a0001c0001t0081g0100 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1751+4936C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95933800 | |||||||
chr9:95933845 | CA | C | 69 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0009 others(66): Show |
72 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1751+5000delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95933845 | ||||||
chr9:95933845 | CAA | C | 175 | a0001c0001t0001g0095 a0001c0001t0002g0169 a0001c0001t0002g0177 others(172): Show |
177 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.1751+4999_1751+500 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95933845 | ||||||
chr9:95933845 | CAAA | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(120): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1751+4998_1751+500 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95933845 | ||||||
chr9:95933992 | A | AT | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1751+5133dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95933992 | ||||||
chr9:95934004 | C | T | 1 | a0002c0002t0007g0328 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1751+5140C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934004 | |||||||
chr9:95934074 | G | C | 2 | a0002c0002t0006g0357 a0002c0002t0049g0344 |
2 | NA19056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1751+5210G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934074 | |||||||
chr9:95934267 | T | C | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 |
3 | HG02572.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1751+5403T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934267 | |||||||
chr9:95934423 | G | T | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1751+5559G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934423 | |||||||
chr9:95934454 | A | ATGTGATT others(306): Show |
66 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0016 others(63): Show |
68 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1751+5600_1751+560 others(317): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95934454 | ||||||
chr9:95934454 | A | ATGTGATT others(307): Show |
1 | a0002c0002t0003g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1751+5600_1751+560 others(318): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95934454 | ||||||
chr9:95934454 | A | ATGTGATT others(307): Show |
9 | a0002c0002t0003g0015 a0002c0002t0003g0337 a0002c0002t0003g0339 others(6): Show |
9 | HG01243.hp1 HG01928.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1751+5600_1751+560 others(318): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95934454 | ||||||
chr9:95934625 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1751+5761T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934625 | |||||||
chr9:95934827 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1751+5963G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934827 | |||||||
chr9:95934889 | C | T | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1751+6025C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95934889 | |||||||
chr9:95935008 | C | G | 1 | a0002c0002t0035g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1751+6144C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935008 | |||||||
chr9:95935041 | G | C | 1 | a0002c0002t0035g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1751+6177G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935041 | |||||||
chr9:95935054 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1751+6190T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935054 | |||||||
chr9:95935116 | G | A | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1751+6252G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935116 | |||||||
chr9:95935361 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1752-6093A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935361 | |||||||
chr9:95935408 | C | T | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1752-6046C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935408 | |||||||
chr9:95935504 | C | T | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1752-5950C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935504 | |||||||
chr9:95935681 | T | A | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1752-5773T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935681 | |||||||
chr9:95935701 | G | A | 1 | a0001c0001t0018g0147 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1752-5753G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935701 | |||||||
chr9:95935714 | A | G | 3 | a0001c0001t0002g0151 a0001c0001t0002g0154 a0001c0001t0002g0155 |
3 | NA18969.hp1 NA18975.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1752-5740A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935714 | |||||||
chr9:95935894 | G | T | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1752-5560G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935894 | |||||||
chr9:95935899 | T | C | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-5555T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935899 | |||||||
chr9:95935973 | A | G | 5 | a0001c0005t0061g0221 a0001c0005t0062g0105 a0001c0005t0064g0106 others(2): Show |
5 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1752-5481A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95935973 | |||||||
chr9:95936087 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1752-5367G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936087 | |||||||
chr9:95936189 | GAGA | G | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-5256_1752-525 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95936189 | ||||||
chr9:95936197 | G | C | 3 | a0002c0002t0003g0330 a0002c0002t0003g0340 a0002c0002t0007g0332 |
3 | HG02300.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1752-5257G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936197 | |||||||
chr9:95936230 | C | A | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1752-5224C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936230 | |||||||
chr9:95936276 | G | A | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1752-5178G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936276 | |||||||
chr9:95936445 | G | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1752-5009G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936445 | |||||||
chr9:95936528 | C | T | 371 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(368): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1752-4926C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936528 | |||||||
chr9:95936548 | T | C | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1752-4906T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936548 | |||||||
chr9:95936571 | G | A | 1 | a0003c0015t0021g0292 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1752-4883G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936571 | |||||||
chr9:95936630 | C | T | 2 | a0002c0002t0006g0305 a0002c0002t0006g0306 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1752-4824C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936630 | |||||||
chr9:95936718 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1752-4736A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936718 | |||||||
chr9:95936746 | C | T | 1 | a0002c0002t0028g0329 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1752-4708C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936746 | |||||||
chr9:95936797 | C | A | 2 | a0001c0005t0009g0229 a0001c0005t0009g0230 |
2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1752-4657C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936797 | |||||||
chr9:95936914 | G | A | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1752-4540G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936914 | |||||||
chr9:95936976 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1752-4478C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95936976 | |||||||
chr9:95937016 | C | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1752-4438C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937016 | |||||||
chr9:95937172 | G | A | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1752-4282G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937172 | |||||||
chr9:95937213 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1752-4241G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937213 | |||||||
chr9:95937381 | T | C | 3 | a0002c0002t0006g0305 a0002c0002t0006g0306 a0002c0002t0006g0341 |
3 | HG01243.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1752-4073T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937381 | |||||||
chr9:95937419 | G | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1752-4035G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937419 | |||||||
chr9:95937539 | A | C | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1752-3915A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937539 | |||||||
chr9:95937550 | C | T | 1 | a0001c0001t0010g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1752-3904C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937550 | |||||||
chr9:95937568 | T | G | 1 | a0016c0018t0058g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1752-3886T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937568 | |||||||
chr9:95937691 | GTTTCA | G | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1752-3758_1752-375 others(9): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95937691 | ||||||
chr9:95937789 | A | G | 1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1752-3665A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937789 | |||||||
chr9:95937795 | C | A | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1752-3659C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937795 | |||||||
chr9:95937946 | A | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-3508A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95937946 | |||||||
chr9:95938038 | A | G | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1752-3416A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938038 | |||||||
chr9:95938114 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(82): Show |
90 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1752-3340C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938114 | |||||||
chr9:95938189 | C | T | 2 | a0001c0001t0031g0112 a0001c0001t0031g0113 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1752-3265C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938189 | |||||||
chr9:95938604 | C | G | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1752-2850C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938604 | |||||||
chr9:95938677 | T | C | 1 | a0001c0001t0025g0098 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1752-2777T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938677 | |||||||
chr9:95938704 | G | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1752-2750G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938704 | |||||||
chr9:95938721 | GTGTTT | G | 6 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(3): Show |
6 | HG02723.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1752-2721_1752-271 others(9): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95938721 | ||||||
chr9:95938729 | T | C | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1752-2725T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938729 | |||||||
chr9:95938750 | T | A | 1 | a0001c0001t0025g0098 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1752-2704T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938750 | |||||||
chr9:95938773 | C | A | 1 | a0001c0001t0015g0140 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1752-2681C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95938773 | |||||||
chr9:95938979 | AT | A | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1752-2472delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95938979 | ||||||
chr9:95939066 | A | G | 11 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(8): Show |
11 | HG02083.hp2 HG02523.hp1 NA18966.hp2 others(8): Show |
intron_variant | MODIFIER | c.1752-2388A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939066 | |||||||
chr9:95939072 | C | CT | 4 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0240 others(1): Show |
4 | HG00423.hp2 NA18946.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1752-2378dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95939072 | ||||||
chr9:95939247 | T | C | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1752-2207T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939247 | |||||||
chr9:95939283 | C | CT | 9 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1752-2158dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95939283 | ||||||
chr9:95939285 | T | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1752-2169T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939285 | |||||||
chr9:95939414 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1752-2040C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939414 | |||||||
chr9:95939507 | C | T | 2 | a0002c0002t0006g0357 a0002c0002t0049g0344 |
2 | NA19056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1752-1947C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939507 | |||||||
chr9:95939514 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1752-1940G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939514 | |||||||
chr9:95939519 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1752-1935T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939519 | |||||||
chr9:95939692 | A | G | 1 | a0001c0001t0004g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1752-1762A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939692 | |||||||
chr9:95939738 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1752-1716T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939738 | |||||||
chr9:95939749 | G | A | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-1705G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939749 | |||||||
chr9:95939754 | G | A | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-1700G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939754 | |||||||
chr9:95939773 | A | G | 1 | a0002c0002t0003g0313 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1752-1681A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939773 | |||||||
chr9:95939780 | A | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0176 a0001c0001t0002g0183 others(3): Show |
7 | HG02004.hp2 NA18956.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1752-1674A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939780 | |||||||
chr9:95939785 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1752-1669T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939785 | |||||||
chr9:95939796 | A | G | 1 | a0001c0001t0052g0150 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1752-1658A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939796 | |||||||
chr9:95939819 | A | G | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1752-1635A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939819 | |||||||
chr9:95939945 | C | A | 1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1752-1509C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939945 | |||||||
chr9:95939958 | G | A | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1752-1496G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939958 | |||||||
chr9:95939980 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1752-1474C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95939980 | |||||||
chr9:95940088 | G | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1752-1366G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95940088 | |||||||
chr9:95940340 | G | GAT | 8 | a0001c0001t0002g0125 a0001c0005t0033g0254 a0001c0005t0061g0221 others(5): Show |
8 | HG02735.hp1 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1752-1101_1752-110 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95940340 | ||||||
chr9:95940340 | G | GATAT | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-1103_1752-110 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95940340 | ||||||
chr9:95940375 | G | A | 1 | a0004c0004t0005g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1752-1079G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95940375 | |||||||
chr9:95940459 | T | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1752-995T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95940459 | |||||||
chr9:95940586 | A | G | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1752-868A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95940586 | |||||||
chr9:95941116 | C | T | 1 | a0002c0002t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1752-338C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95941116 | |||||||
chr9:95941355 | C | T | 1 | a0002c0002t0035g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1752-99C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | chr9 | 95941355 | |||||||
chr9:95941429 | CT | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1752-14delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 95941429 | ||||||
chr9:95941587 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1847+38C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95941587 | |||||||
chr9:95941868 | A | C | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1847+319A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95941868 | |||||||
chr9:95941893 | G | A | 1 | a0001c0001t0055g0167 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1847+344G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95941893 | |||||||
chr9:95941940 | T | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1847+391T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95941940 | |||||||
chr9:95941964 | G | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1847+415G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95941964 | |||||||
chr9:95941990 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1847+441A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95941990 | |||||||
chr9:95942064 | C | T | 1 | a0001c0001t0045g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1847+515C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95942064 | |||||||
chr9:95942430 | A | T | 1 | a0016c0018t0058g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1847+881A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95942430 | |||||||
chr9:95942549 | G | A | 1 | a0001c0001t0036g0056 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1847+1000G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95942549 | |||||||
chr9:95942855 | G | A | 4 | a0001c0005t0062g0105 a0001c0005t0064g0106 a0011c0009t0034g0207 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1847+1306G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95942855 | |||||||
chr9:95943093 | T | C | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1847+1544T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943093 | |||||||
chr9:95943237 | T | C | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1847+1688T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943237 | |||||||
chr9:95943247 | G | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(82): Show |
90 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1847+1698G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943247 | |||||||
chr9:95943350 | G | A | 1 | a0020c0014t0040g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1847+1801G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943350 | |||||||
chr9:95943566 | G | A | 10 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1847+2017G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943566 | |||||||
chr9:95943734 | C | G | 107 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(104): Show |
109 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1847+2185C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943734 | |||||||
chr9:95943735 | A | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1847+2186A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943735 | |||||||
chr9:95943798 | G | A | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1847+2249G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943798 | |||||||
chr9:95943818 | C | T | 5 | a0001c0005t0061g0221 a0001c0005t0062g0105 a0001c0005t0064g0106 others(2): Show |
5 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1847+2269C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943818 | |||||||
chr9:95943877 | A | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1847+2328A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943877 | |||||||
chr9:95943946 | A | G | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1847+2397A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943946 | |||||||
chr9:95943960 | G | A | 1 | a0003c0015t0021g0292 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1847+2411G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943960 | |||||||
chr9:95943961 | T | C | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1847+2412T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943961 | |||||||
chr9:95943992 | G | A | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1847+2443G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95943992 | |||||||
chr9:95944085 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1847+2536A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944085 | |||||||
chr9:95944132 | C | T | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1847+2583C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944132 | |||||||
chr9:95944273 | G | C | 1 | a0002c0002t0003g0303 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1847+2724G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944273 | |||||||
chr9:95944480 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1847+2931G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944480 | |||||||
chr9:95944588 | C | G | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1847+3039C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944588 | |||||||
chr9:95944644 | G | A | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1847+3095G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944644 | |||||||
chr9:95944647 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1847+3098C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944647 | |||||||
chr9:95944675 | GT | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(264): Show |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.1847+3134delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95944675 | ||||||
chr9:95944705 | C | T | 116 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0002c0002t0003g0012 others(113): Show |
118 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1847+3156C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944705 | |||||||
chr9:95944779 | C | CG | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | NA18979.hp2 NA18988.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1847+3232dupG | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95944779 | ||||||
chr9:95944829 | A | T | 1 | a0004c0004t0076g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1847+3280A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944829 | |||||||
chr9:95944850 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1847+3301G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944850 | |||||||
chr9:95944944 | C | T | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1847+3395C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944944 | |||||||
chr9:95944975 | T | A | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1847+3426T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95944975 | |||||||
chr9:95945200 | CT | C | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1847+3652delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95945200 | |||||||
chr9:95945220 | T | C | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1847+3671T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95945220 | |||||||
chr9:95945470 | A | T | 2 | a0001c0001t0015g0007 a0001c0001t0015g0145 |
3 | HG02615.hp1 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1847+3921A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95945470 | |||||||
chr9:95945575 | T | C | 1 | a0022c0019t0016g0326 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1847+4026T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95945575 | |||||||
chr9:95945797 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1847+4248T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95945797 | |||||||
chr9:95945889 | CT | C | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1847+4347delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95945889 | ||||||
chr9:95945956 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1847+4407A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95945956 | |||||||
chr9:95946007 | TAAAA | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1847+4462_1847+446 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95946007 | ||||||
chr9:95946028 | A | T | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1847+4479A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946028 | |||||||
chr9:95946159 | A | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1847+4610A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946159 | |||||||
chr9:95946227 | C | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1847+4678C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946227 | |||||||
chr9:95946258 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1847+4709G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946258 | |||||||
chr9:95946304 | G | A | 2 | a0001c0001t0027g0370 a0001c0001t0092g0371 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1847+4755G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946304 | |||||||
chr9:95946348 | G | A | 1 | a0001c0005t0009g0227 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1847+4799G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946348 | |||||||
chr9:95946426 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0046 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1847+4877G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946426 | |||||||
chr9:95946709 | A | T | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1847+5160A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946709 | |||||||
chr9:95946747 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1847+5198C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95946747 | |||||||
chr9:95947459 | C | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1847+5910C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95947459 | |||||||
chr9:95947500 | A | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1847+5951A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95947500 | |||||||
chr9:95947534 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1847+5985A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95947534 | |||||||
chr9:95947880 | G | GA | 9 | a0001c0001t0002g0131 a0005c0006t0017g0020 a0005c0006t0017g0021 others(6): Show |
9 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1847+6340dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95947880 | ||||||
chr9:95947958 | T | C | 1 | a0025c0027t0069g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1847+6409T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95947958 | |||||||
chr9:95948046 | T | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1847+6497T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948046 | |||||||
chr9:95948179 | T | C | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1847+6630T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948179 | |||||||
chr9:95948371 | G | A | 1 | a0001c0001t0027g0370 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1847+6822G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948371 | |||||||
chr9:95948386 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0176 a0001c0001t0002g0183 others(3): Show |
7 | HG02004.hp2 NA18956.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1847+6837C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948386 | |||||||
chr9:95948543 | CTCAG | C | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1847+6995_1847+699 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948543 | |||||||
chr9:95948553 | T | G | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1847+7004T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948553 | |||||||
chr9:95948576 | G | A | 1 | a0001c0005t0009g0224 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1847+7027G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948576 | |||||||
chr9:95948610 | C | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1847+7061C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948610 | |||||||
chr9:95948637 | C | G | 9 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1847+7088C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948637 | |||||||
chr9:95948665 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1847+7116T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948665 | |||||||
chr9:95948678 | G | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1847+7129G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948678 | |||||||
chr9:95948778 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0014g0045 others(1): Show |
4 | HG02165.hp2 NA18967.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848-7136C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948778 | |||||||
chr9:95948791 | GA | G | 121 | a0001c0001t0010g0117 a0001c0001t0018g0149 a0001c0001t0053g0173 others(118): Show |
123 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1848-7106delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95948791 | ||||||
chr9:95948792 | A | G | 4 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(1): Show |
4 | HG02809.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1848-7122A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948792 | |||||||
chr9:95948793 | A | G | 1 | a0002c0020t0035g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1848-7121A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948793 | |||||||
chr9:95948804 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1848-7110A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948804 | |||||||
chr9:95948805 | A | G | 1 | a0006c0007t0003g0297 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1848-7109A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948805 | |||||||
chr9:95948936 | T | G | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1848-6978T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95948936 | |||||||
chr9:95949083 | A | G | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1848-6831A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949083 | |||||||
chr9:95949204 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1848-6710G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949204 | |||||||
chr9:95949248 | G | A | 34 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(31): Show |
34 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1848-6666G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949248 | |||||||
chr9:95949432 | A | G | 1 | a0003c0003t0012g0265 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1848-6482A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949432 | |||||||
chr9:95949437 | G | T | 5 | a0002c0002t0003g0331 a0002c0002t0003g0333 a0002c0002t0007g0307 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1848-6477G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949437 | |||||||
chr9:95949563 | A | G | 12 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0315 others(9): Show |
13 | HG00423.hp1 NA18970.hp2 NA18971.hp2 others(10): Show |
intron_variant | MODIFIER | c.1848-6351A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949563 | |||||||
chr9:95949568 | A | C | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1848-6346A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949568 | |||||||
chr9:95949571 | AC | A | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848-6342delC | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949571 | |||||||
chr9:95949572 | C | A | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1848-6342C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949572 | |||||||
chr9:95949581 | T | A | 2 | a0001c0001t0002g0178 a0004c0004t0005g0302 |
2 | HG01358.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1848-6333T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949581 | |||||||
chr9:95949836 | C | T | 1 | a0002c0002t0093g0304 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1848-6078C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949836 | |||||||
chr9:95949900 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1848-6014T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949900 | |||||||
chr9:95949981 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1848-5933C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95949981 | |||||||
chr9:95950010 | G | T | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1848-5904G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950010 | |||||||
chr9:95950014 | C | CA | 7 | a0001c0001t0010g0114 a0001c0001t0019g0214 a0001c0001t0091g0139 others(4): Show |
7 | HG01109.hp2 HG01978.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848-5883dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95950014 | ||||||
chr9:95950039 | G | A | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1848-5875G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950039 | |||||||
chr9:95950071 | A | G | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1848-5843A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950071 | |||||||
chr9:95950117 | G | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848-5797G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950117 | |||||||
chr9:95950229 | A | G | 1 | a0001c0001t0018g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1848-5685A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950229 | |||||||
chr9:95950263 | A | T | 4 | a0004c0004t0005g0250 a0004c0004t0005g0251 a0004c0004t0005g0252 others(1): Show |
4 | NA18940.hp1 NA18982.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848-5651A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950263 | |||||||
chr9:95950453 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1848-5461G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950453 | |||||||
chr9:95950515 | G | A | 10 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1848-5399G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950515 | |||||||
chr9:95950542 | G | A | 12 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(9): Show |
14 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1848-5372G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950542 | |||||||
chr9:95950579 | T | C | 1 | a0007c0008t0023g0294 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1848-5335T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950579 | |||||||
chr9:95950872 | T | C | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1848-5042T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950872 | |||||||
chr9:95950912 | A | C | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1848-5002A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95950912 | |||||||
chr9:95951008 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1848-4906G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951008 | |||||||
chr9:95951161 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1848-4753C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951161 | |||||||
chr9:95951314 | C | T | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1848-4600C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951314 | |||||||
chr9:95951350 | A | T | 1 | a0006c0007t0003g0297 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1848-4564A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951350 | |||||||
chr9:95951368 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1848-4546A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951368 | |||||||
chr9:95951398 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1848-4516A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951398 | |||||||
chr9:95951511 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1848-4403A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951511 | |||||||
chr9:95951633 | A | G | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848-4281A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951633 | |||||||
chr9:95951694 | C | G | 1 | a0001c0001t0087g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1848-4220C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951694 | |||||||
chr9:95951755 | G | GA | 175 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(172): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1848-4156dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95951755 | ||||||
chr9:95951785 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1848-4129G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951785 | |||||||
chr9:95951838 | AG | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1848-4074delG | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95951838 | ||||||
chr9:95951840 | G | C | 4 | a0001c0001t0001g0096 a0001c0001t0025g0098 a0001c0001t0025g0099 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1848-4074G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951840 | |||||||
chr9:95951864 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0053g0173 a0001c0028t0002g0009 |
3 | HG00280.hp1 HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1848-4050C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95951864 | |||||||
chr9:95952029 | G | A | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1848-3885G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952029 | |||||||
chr9:95952166 | T | TAAAAAAA others(3): Show |
76 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0097 others(73): Show |
76 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1848-3738_1848-372 others(14): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952166 | ||||||
chr9:95952166 | T | TAAAAAAA others(4): Show |
159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(156): Show |
169 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1848-3739_1848-372 others(15): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952166 | ||||||
chr9:95952166 | T | TAAAAAAA others(5): Show |
58 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0057 others(55): Show |
58 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1848-3740_1848-372 others(16): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952166 | ||||||
chr9:95952166 | T | TAAAAAAA others(6): Show |
10 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0022g0006 others(7): Show |
12 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1848-3741_1848-372 others(17): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952166 | ||||||
chr9:95952166 | T | TAAAAAAA others(7): Show |
1 | a0010c0012t0020g0369 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1848-3742_1848-372 others(18): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952166 | ||||||
chr9:95952166 | T | TAAAAAAA others(8): Show |
1 | a0010c0012t0020g0368 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1848-3743_1848-372 others(19): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952166 | ||||||
chr9:95952271 | C | A | 1 | a0002c0002t0007g0328 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1848-3643C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952271 | |||||||
chr9:95952277 | T | C | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1848-3637T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952277 | |||||||
chr9:95952279 | C | T | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1848-3635C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952279 | |||||||
chr9:95952296 | A | G | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1848-3618A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952296 | |||||||
chr9:95952609 | G | A | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1848-3305G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952609 | |||||||
chr9:95952678 | A | T | 3 | a0001c0001t0001g0035 a0005c0006t0017g0025 a0005c0006t0032g0019 |
3 | HG02027.hp1 HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1848-3236A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952678 | |||||||
chr9:95952703 | G | A | 1 | a0001c0001t0025g0060 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1848-3211G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952703 | |||||||
chr9:95952773 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1848-3141A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952773 | |||||||
chr9:95952797 | A | C | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1848-3117A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952797 | |||||||
chr9:95952840 | T | TA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1848-3062dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952840 | ||||||
chr9:95952840 | TA | T | 10 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(7): Show |
11 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1848-3062delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95952840 | ||||||
chr9:95952843 | A | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1848-3071A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95952843 | |||||||
chr9:95953158 | A | G | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1848-2756A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953158 | |||||||
chr9:95953265 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1848-2649G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953265 | |||||||
chr9:95953298 | C | T | 1 | a0021c0025t0083g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1848-2616C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953298 | |||||||
chr9:95953343 | G | A | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1848-2571G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953343 | |||||||
chr9:95953347 | C | T | 3 | a0002c0002t0003g0316 a0002c0002t0003g0317 a0002c0002t0003g0318 |
3 | HG00323.hp2 HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1848-2567C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953347 | |||||||
chr9:95953348 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1848-2566A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953348 | |||||||
chr9:95953427 | A | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1848-2487A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953427 | |||||||
chr9:95953506 | C | T | 1 | a0001c0001t0018g0149 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1848-2408C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953506 | |||||||
chr9:95953574 | C | CA | 111 | a0001c0001t0001g0032 a0001c0001t0079g0081 a0001c0005t0063g0253 others(108): Show |
113 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1848-2325dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95953574 | ||||||
chr9:95953574 | C | CAA | 7 | a0002c0002t0003g0335 a0002c0002t0006g0319 a0002c0002t0028g0366 others(4): Show |
7 | HG00423.hp1 HG01169.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848-2326_1848-232 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95953574 | ||||||
chr9:95953611 | A | G | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1848-2303A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953611 | |||||||
chr9:95953704 | G | C | 1 | a0002c0002t0003g0312 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1848-2210G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953704 | |||||||
chr9:95953754 | A | C | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1848-2160A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953754 | |||||||
chr9:95953761 | G | A | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1848-2153G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953761 | |||||||
chr9:95953769 | T | C | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1848-2145T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953769 | |||||||
chr9:95953843 | C | A | 1 | a0004c0004t0013g0236 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1848-2071C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953843 | |||||||
chr9:95953882 | C | A | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1848-2032C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95953882 | |||||||
chr9:95954063 | G | A | 1 | a0001c0001t0053g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1848-1851G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954063 | |||||||
chr9:95954082 | A | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0130 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1848-1832A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954082 | |||||||
chr9:95954123 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1848-1791G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954123 | |||||||
chr9:95954151 | G | A | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1848-1763G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954151 | |||||||
chr9:95954166 | G | A | 4 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 others(1): Show |
5 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1848-1748G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954166 | |||||||
chr9:95954227 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1848-1687G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954227 | |||||||
chr9:95954462 | G | A | 5 | a0001c0005t0061g0221 a0001c0005t0062g0105 a0001c0005t0064g0106 others(2): Show |
5 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1848-1452G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954462 | |||||||
chr9:95954565 | A | G | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1848-1349A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954565 | |||||||
chr9:95954839 | A | G | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1848-1075A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954839 | |||||||
chr9:95954966 | C | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848-948C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95954966 | |||||||
chr9:95955086 | C | T | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1848-828C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955086 | |||||||
chr9:95955102 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1848-812A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955102 | |||||||
chr9:95955129 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1848-785A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955129 | |||||||
chr9:95955293 | C | T | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1848-621C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955293 | |||||||
chr9:95955310 | G | T | 2 | a0001c0001t0001g0064 a0001c0005t0063g0253 |
2 | HG03516.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1848-604G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955310 | |||||||
chr9:95955311 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1848-603T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955311 | |||||||
chr9:95955317 | T | A | 1 | a0003c0003t0008g0279 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1848-597T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955317 | |||||||
chr9:95955394 | TTTGACTT others(326): Show |
T | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848-517_1848-185d others(2): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 95955394 | ||||||
chr9:95955806 | T | A | 1 | a0001c0001t0036g0039 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1848-108T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955806 | |||||||
chr9:95955896 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1848-18T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 12/18 | chr9 | 95955896 | |||||||
chr9:95956119 | G | A | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1947+106G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956119 | |||||||
chr9:95956197 | C | T | 1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1947+184C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956197 | |||||||
chr9:95956213 | G | A | 1 | a0004c0004t0005g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1947+200G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956213 | |||||||
chr9:95956251 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1947+238A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956251 | |||||||
chr9:95956381 | G | C | 1 | a0001c0001t0002g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1947+368G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956381 | |||||||
chr9:95956391 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(265): Show |
276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1947+378T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956391 | |||||||
chr9:95956569 | C | T | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1947+556C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956569 | |||||||
chr9:95956574 | T | G | 1 | a0002c0002t0003g0350 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1947+561T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956574 | |||||||
chr9:95956823 | T | C | 11 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(8): Show |
11 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1947+810T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956823 | |||||||
chr9:95956831 | G | A | 12 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(9): Show |
12 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1947+818G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956831 | |||||||
chr9:95956836 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1947+823G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95956836 | |||||||
chr9:95956880 | AC | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+869delC | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95956880 | ||||||
chr9:95957077 | G | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+1064G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957077 | |||||||
chr9:95957081 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1947+1068G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957081 | |||||||
chr9:95957140 | TA | T | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1947+1130delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95957140 | ||||||
chr9:95957197 | G | A | 1 | a0005c0006t0017g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1947+1184G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957197 | |||||||
chr9:95957197 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1947+1184G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957197 | |||||||
chr9:95957238 | A | G | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1947+1225A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957238 | |||||||
chr9:95957279 | C | T | 1 | a0002c0002t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1947+1266C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957279 | |||||||
chr9:95957408 | A | AT | 14 | a0001c0001t0001g0090 a0001c0001t0010g0114 a0001c0001t0010g0115 others(11): Show |
14 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1947+1412dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95957408 | ||||||
chr9:95957408 | AT | A | 79 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0154 others(76): Show |
79 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1947+1412delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95957408 | ||||||
chr9:95957408 | ATT | A | 103 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1947+1411_1947+141 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95957408 | ||||||
chr9:95957491 | G | A | 1 | a0004c0004t0013g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1947+1478G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957491 | |||||||
chr9:95957517 | C | A | 114 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(111): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1947+1504C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957517 | |||||||
chr9:95957688 | C | G | 3 | a0001c0001t0010g0120 a0001c0001t0010g0203 a0001c0001t0060g0121 |
3 | HG02970.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1947+1675C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957688 | |||||||
chr9:95957721 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1947+1708T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957721 | |||||||
chr9:95957808 | C | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1947+1795C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957808 | |||||||
chr9:95957876 | G | GT | 53 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(50): Show |
53 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1947+1874dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95957876 | ||||||
chr9:95957882 | T | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0061 others(4): Show |
8 | HG02015.hp2 NA18939.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1947+1869T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957882 | |||||||
chr9:95957888 | A | T | 1 | a0002c0002t0003g0311 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1947+1875A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957888 | |||||||
chr9:95957915 | T | C | 1 | a0010c0012t0020g0369 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1947+1902T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95957915 | |||||||
chr9:95958020 | C | T | 1 | a0003c0003t0008g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1947+2007C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958020 | |||||||
chr9:95958021 | T | C | 1 | a0003c0003t0008g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1947+2008T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958021 | |||||||
chr9:95958023 | C | T | 1 | a0003c0003t0008g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1947+2010C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958023 | |||||||
chr9:95958036 | C | A | 1 | a0003c0003t0008g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1947+2023C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958036 | |||||||
chr9:95958199 | G | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+2186G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958199 | |||||||
chr9:95958238 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1947+2225G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958238 | |||||||
chr9:95958326 | G | T | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.1947+2313G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958326 | |||||||
chr9:95958426 | G | C | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1947+2413G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958426 | |||||||
chr9:95958529 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
5 | HG01257.hp1 HG01258.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1947+2516C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958529 | |||||||
chr9:95958637 | G | A | 83 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1947+2624G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958637 | |||||||
chr9:95958736 | G | A | 1 | a0020c0014t0040g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1947+2723G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958736 | |||||||
chr9:95958849 | T | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+2836T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958849 | |||||||
chr9:95958912 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1947+2899C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958912 | |||||||
chr9:95958915 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(291): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.1947+2902A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958915 | |||||||
chr9:95958932 | C | T | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1947+2919C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95958932 | |||||||
chr9:95959013 | A | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1947+3000A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959013 | |||||||
chr9:95959020 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0192 |
2 | HG02004.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1947+3007A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959020 | |||||||
chr9:95959029 | T | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1947+3016T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959029 | |||||||
chr9:95959066 | C | T | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1947+3053C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959066 | |||||||
chr9:95959184 | G | A | 175 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(172): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1947+3171G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959184 | |||||||
chr9:95959224 | C | A | 1 | a0003c0003t0008g0283 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1947+3211C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959224 | |||||||
chr9:95959257 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1947+3244C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959257 | |||||||
chr9:95959359 | C | A | 41 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1947+3346C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959359 | |||||||
chr9:95959527 | G | A | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1947+3514G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959527 | |||||||
chr9:95959682 | A | G | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1947+3669A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959682 | |||||||
chr9:95959755 | TA | T | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1947+3752delA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95959755 | ||||||
chr9:95959848 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1947+3835G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95959848 | |||||||
chr9:95960174 | G | T | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1947+4161G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960174 | |||||||
chr9:95960303 | G | A | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1947+4290G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960303 | |||||||
chr9:95960325 | G | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1947+4312G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960325 | |||||||
chr9:95960364 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1947+4351A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960364 | |||||||
chr9:95960409 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1947+4396G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960409 | |||||||
chr9:95960547 | G | T | 1 | a0002c0002t0003g0339 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1947+4534G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960547 | |||||||
chr9:95960780 | G | A | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1947+4767G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960780 | |||||||
chr9:95960881 | T | TCC | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1947+4870_1947+487 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95960881 | ||||||
chr9:95960904 | C | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1947+4891C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95960904 | |||||||
chr9:95961189 | G | C | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1947+5176G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95961189 | |||||||
chr9:95961214 | C | T | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1947+5201C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95961214 | |||||||
chr9:95961468 | G | C | 2 | a0003c0003t0008g0267 a0003c0003t0008g0268 |
2 | NA18975.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1948-5094G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95961468 | |||||||
chr9:95961887 | C | T | 77 | a0001c0005t0063g0253 a0002c0002t0003g0012 a0002c0002t0003g0013 others(74): Show |
79 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.1948-4675C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95961887 | |||||||
chr9:95961952 | T | C | 1 | a0001c0001t0052g0150 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1948-4610T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95961952 | |||||||
chr9:95961972 | T | C | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1948-4590T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95961972 | |||||||
chr9:95962000 | C | CCCA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(103): Show |
112 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1948-4560_1948-455 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95962000 | ||||||
chr9:95962146 | A | G | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1948-4416A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95962146 | |||||||
chr9:95962180 | A | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1948-4382A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95962180 | |||||||
chr9:95962207 | A | G | 1 | a0001c0001t0004g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1948-4355A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95962207 | |||||||
chr9:95962227 | T | TA | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1948-4329dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95962227 | ||||||
chr9:95962389 | C | T | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1948-4173C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95962389 | |||||||
chr9:95962762 | C | T | 3 | a0002c0002t0006g0305 a0002c0002t0006g0306 a0002c0002t0006g0341 |
3 | HG01243.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1948-3800C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95962762 | |||||||
chr9:95962830 | A | G | 1 | a0003c0003t0008g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1948-3732A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95962830 | |||||||
chr9:95963027 | G | C | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1948-3535G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963027 | |||||||
chr9:95963147 | C | CTG | 21 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0089 others(18): Show |
21 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1948-3383_1948-338 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95963147 | ||||||
chr9:95963147 | CTG | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(94): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1948-3383_1948-338 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95963147 | ||||||
chr9:95963147 | CTGTG | C | 84 | a0001c0001t0001g0078 a0001c0001t0002g0183 a0001c0001t0010g0108 others(81): Show |
84 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1948-3385_1948-338 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95963147 | ||||||
chr9:95963147 | CTGTGTG | C | 114 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(111): Show |
119 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(116): Show |
intron_variant | MODIFIER | c.1948-3387_1948-338 others(10): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95963147 | ||||||
chr9:95963187 | T | A | 1 | a0001c0001t0018g0149 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1948-3375T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963187 | |||||||
chr9:95963197 | T | C | 1 | a0003c0015t0021g0292 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1948-3365T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963197 | |||||||
chr9:95963283 | T | G | 83 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1948-3279T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963283 | |||||||
chr9:95963455 | T | C | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1948-3107T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963455 | |||||||
chr9:95963467 | C | A | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1948-3095C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963467 | |||||||
chr9:95963530 | T | C | 167 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(164): Show |
169 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1948-3032T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963530 | |||||||
chr9:95963532 | C | G | 83 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1948-3030C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963532 | |||||||
chr9:95963566 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1948-2996A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963566 | |||||||
chr9:95963630 | C | T | 4 | a0002c0002t0003g0308 a0002c0002t0003g0310 a0002c0002t0003g0312 others(1): Show |
4 | NA18944.hp1 NA18977.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1948-2932C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963630 | |||||||
chr9:95963739 | C | T | 1 | a0002c0002t0035g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1948-2823C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963739 | |||||||
chr9:95963832 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0195 a0001c0001t0004g0008 others(1): Show |
4 | HG00733.hp2 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1948-2730G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963832 | |||||||
chr9:95963906 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1948-2656C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963906 | |||||||
chr9:95963937 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0004g0130 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1948-2625C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963937 | |||||||
chr9:95963999 | A | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1948-2563A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95963999 | |||||||
chr9:95964058 | C | T | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-2504C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964058 | |||||||
chr9:95964059 | G | T | 1 | a0001c0001t0055g0167 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1948-2503G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964059 | |||||||
chr9:95964061 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1948-2501A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964061 | |||||||
chr9:95964114 | G | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1948-2448G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964114 | |||||||
chr9:95964426 | C | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1948-2136C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964426 | |||||||
chr9:95964455 | A | G | 12 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(9): Show |
12 | HG00423.hp2 HG00673.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1948-2107A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964455 | |||||||
chr9:95964488 | A | G | 1 | a0004c0004t0013g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1948-2074A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964488 | |||||||
chr9:95964538 | G | A | 1 | a0001c0001t0004g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1948-2024G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964538 | |||||||
chr9:95964713 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(208): Show |
219 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1948-1849G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964713 | |||||||
chr9:95964753 | C | A | 79 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(76): Show |
79 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1948-1809C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964753 | |||||||
chr9:95964954 | C | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1948-1608C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95964954 | |||||||
chr9:95965008 | A | G | 1 | a0006c0007t0007g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1948-1554A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965008 | |||||||
chr9:95965058 | C | T | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1948-1504C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965058 | |||||||
chr9:95965175 | A | C | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 |
3 | HG02572.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1948-1387A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965175 | |||||||
chr9:95965282 | T | C | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1948-1280T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965282 | |||||||
chr9:95965358 | G | A | 1 | a0002c0002t0028g0366 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1948-1204G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965358 | |||||||
chr9:95965404 | T | C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0190 |
2 | HG00099.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1948-1158T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965404 | |||||||
chr9:95965501 | T | C | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1948-1061T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965501 | |||||||
chr9:95965535 | C | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1948-1027C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965535 | |||||||
chr9:95965706 | C | T | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1948-856C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965706 | |||||||
chr9:95965873 | A | G | 2 | a0001c0001t0018g0202 a0001c0001t0066g0146 |
2 | NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1948-689A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95965873 | |||||||
chr9:95966136 | C | G | 4 | a0002c0002t0003g0303 a0002c0002t0003g0316 a0002c0002t0003g0317 others(1): Show |
4 | HG00323.hp2 HG02602.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1948-426C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95966136 | |||||||
chr9:95966154 | ATTAC | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1948-405_1948-402d others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr9 | 95966154 | ||||||
chr9:95966282 | T | C | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1948-280T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95966282 | |||||||
chr9:95966384 | G | T | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1948-178G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95966384 | |||||||
chr9:95966402 | A | G | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1948-160A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95966402 | |||||||
chr9:95966405 | A | G | 1 | a0001c0001t0002g0372 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1948-157A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 13/18 | chr9 | 95966405 | |||||||
chr9:95966906 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.2100+192C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95966906 | |||||||
chr9:95966943 | C | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2100+229C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95966943 | |||||||
chr9:95967046 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2100+332A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967046 | |||||||
chr9:95967100 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2100+386A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967100 | |||||||
chr9:95967243 | T | A | 3 | a0001c0001t0010g0120 a0001c0001t0010g0203 a0001c0001t0060g0121 |
3 | HG02970.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2100+529T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967243 | |||||||
chr9:95967607 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2100+893A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967607 | |||||||
chr9:95967619 | G | C | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2100+905G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967619 | |||||||
chr9:95967679 | T | C | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2100+965T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967679 | |||||||
chr9:95967727 | C | G | 1 | a0001c0001t0004g0186 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2100+1013C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967727 | |||||||
chr9:95967871 | A | C | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2100+1157A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95967871 | |||||||
chr9:95968217 | A | G | 2 | a0001c0001t0031g0112 a0001c0001t0031g0113 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2100+1503A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968217 | |||||||
chr9:95968235 | C | T | 1 | a0020c0014t0040g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2100+1521C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968235 | |||||||
chr9:95968351 | G | T | 2 | a0001c0001t0025g0098 a0001c0001t0025g0099 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2100+1637G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968351 | |||||||
chr9:95968472 | G | A | 1 | a0001c0005t0072g0222 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2100+1758G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968472 | |||||||
chr9:95968473 | C | T | 1 | a0001c0001t0015g0140 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2100+1759C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968473 | |||||||
chr9:95968551 | G | A | 1 | a0003c0003t0008g0279 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2100+1837G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968551 | |||||||
chr9:95968978 | A | G | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2101-1598A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95968978 | |||||||
chr9:95969068 | G | A | 1 | a0002c0002t0003g0345 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2101-1508G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969068 | |||||||
chr9:95969236 | A | C | 2 | a0001c0001t0002g0180 a0001c0001t0002g0194 |
2 | NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.2101-1340A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969236 | |||||||
chr9:95969298 | T | G | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2101-1278T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969298 | |||||||
chr9:95969323 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(88): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.2101-1253G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969323 | |||||||
chr9:95969446 | A | G | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2101-1130A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969446 | |||||||
chr9:95969621 | C | G | 15 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(12): Show |
17 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2101-955C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969621 | |||||||
chr9:95969703 | C | T | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2101-873C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969703 | |||||||
chr9:95969884 | G | T | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2101-692G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969884 | |||||||
chr9:95969963 | T | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0154 |
2 | NA18969.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2101-613T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95969963 | |||||||
chr9:95970374 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2101-202G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 14/18 | chr9 | 95970374 | |||||||
chr9:95970750 | G | A | 1 | a0001c0001t0019g0217 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2181+94G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95970750 | |||||||
chr9:95970751 | T | TA | 40 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2181+106dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr9 | 95970751 | ||||||
chr9:95970902 | T | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(90): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.2181+246T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95970902 | |||||||
chr9:95971029 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2181+373C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95971029 | |||||||
chr9:95971259 | A | C | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2181+603A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95971259 | |||||||
chr9:95971500 | A | C | 84 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(81): Show |
84 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2182-433A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95971500 | |||||||
chr9:95971525 | A | G | 1 | a0009c0011t0020g0017 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2182-408A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95971525 | |||||||
chr9:95971790 | T | A | 1 | a0001c0001t0002g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2182-143T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95971790 | |||||||
chr9:95971890 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0047 others(17): Show |
22 | HG00408.hp1 HG00597.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.2182-43A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 15/18 | chr9 | 95971890 | |||||||
chr9:95973122 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3337+34G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973122 | |||||||
chr9:95973154 | C | T | 1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3337+66C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973154 | |||||||
chr9:95973186 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3337+98A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973186 | |||||||
chr9:95973521 | C | T | 2 | a0001c0001t0010g0117 a0001c0001t0056g0116 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3337+433C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973521 | |||||||
chr9:95973528 | C | T | 1 | a0001c0001t0004g0175 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3337+440C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973528 | |||||||
chr9:95973556 | G | A | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3337+468G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973556 | |||||||
chr9:95973604 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(98): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.3337+516A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973604 | |||||||
chr9:95973672 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3337+584T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973672 | |||||||
chr9:95973777 | G | A | 1 | a0004c0004t0005g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3337+689G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95973777 | |||||||
chr9:95974256 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0025g0098 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3337+1168G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974256 | |||||||
chr9:95974355 | C | G | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3337+1267C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974355 | |||||||
chr9:95974480 | G | T | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3337+1392G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974480 | |||||||
chr9:95974722 | T | TTG | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(118): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.3337+1658_3337+165 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974722 | T | TTGTG | 14 | a0001c0001t0010g0108 a0001c0001t0010g0115 a0001c0001t0010g0117 others(11): Show |
14 | HG01167.hp1 HG01175.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.3337+1656_3337+165 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974722 | T | TTGTGTG | 27 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(24): Show |
27 | HG00323.hp1 HG00597.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.3337+1654_3337+165 others(10): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974722 | T | TTGTGTGT others(1): Show |
12 | a0003c0003t0021g0287 a0003c0003t0021g0289 a0003c0003t0021g0291 others(9): Show |
13 | HG00609.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3337+1652_3337+165 others(12): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974722 | T | TTGTGTGT others(5): Show |
1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3337+1648_3337+165 others(16): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974722 | T | TTTTG | 28 | a0004c0004t0005g0225 a0004c0004t0005g0231 a0004c0004t0005g0235 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3337+1635_3337+163 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974722 | TTGTG | T | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.3337+1656_3337+165 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95974722 | ||||||
chr9:95974783 | G | A | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3337+1695G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974783 | |||||||
chr9:95974807 | A | G | 1 | a0003c0015t0021g0292 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3337+1719A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974807 | |||||||
chr9:95974882 | G | A | 72 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3337+1794G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974882 | |||||||
chr9:95974936 | T | C | 10 | a0002c0002t0003g0342 a0002c0002t0003g0347 a0002c0002t0003g0348 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.3337+1848T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95974936 | |||||||
chr9:95975047 | T | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(268): Show |
281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.3337+1959T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975047 | |||||||
chr9:95975130 | T | C | 1 | a0002c0002t0003g0356 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3337+2042T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975130 | |||||||
chr9:95975204 | A | G | 3 | a0001c0001t0002g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 |
3 | HG01255.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3337+2116A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975204 | |||||||
chr9:95975246 | A | G | 1 | a0007c0008t0023g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3337+2158A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975246 | |||||||
chr9:95975255 | C | T | 83 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(80): Show |
85 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.3337+2167C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975255 | |||||||
chr9:95975368 | A | AAGTC | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(268): Show |
281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.3337+2283_3337+228 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95975368 | ||||||
chr9:95975378 | G | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.3337+2290G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975378 | |||||||
chr9:95975471 | C | CT | 107 | a0001c0001t0001g0097 a0001c0001t0002g0197 a0001c0001t0002g0198 others(104): Show |
110 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.3337+2400dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95975471 | ||||||
chr9:95975471 | C | CTT | 11 | a0001c0001t0010g0108 a0001c0001t0027g0142 a0001c0001t0027g0143 others(8): Show |
11 | HG01884.hp1 HG01952.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.3337+2399_3337+240 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95975471 | ||||||
chr9:95975471 | C | CTTT | 61 | a0001c0005t0061g0221 a0002c0002t0003g0012 a0002c0002t0003g0013 others(58): Show |
63 | HG00423.hp1 HG00673.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.3337+2398_3337+240 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95975471 | ||||||
chr9:95975471 | C | CTTTT | 14 | a0001c0005t0033g0254 a0002c0002t0003g0303 a0002c0002t0003g0316 others(11): Show |
14 | HG00323.hp2 HG01070.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.3337+2397_3337+240 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95975471 | ||||||
chr9:95975496 | C | A | 1 | a0001c0001t0011g0166 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3337+2408C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975496 | |||||||
chr9:95975539 | A | G | 1 | a0002c0002t0006g0319 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3337+2451A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975539 | |||||||
chr9:95975654 | A | G | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3338-2407A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975654 | |||||||
chr9:95975719 | T | C | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3338-2342T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975719 | |||||||
chr9:95975842 | T | C | 1 | a0004c0004t0005g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3338-2219T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95975842 | |||||||
chr9:95976003 | G | A | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.3338-2058G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976003 | |||||||
chr9:95976080 | T | A | 1 | a0004c0004t0005g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3338-1981T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976080 | |||||||
chr9:95976211 | T | G | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-1850T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976211 | |||||||
chr9:95976231 | A | G | 4 | a0001c0001t0024g0213 a0001c0001t0024g0219 a0001c0001t0024g0367 others(1): Show |
4 | NA18966.hp2 NA18991.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.3338-1830A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976231 | |||||||
chr9:95976367 | C | A | 1 | a0002c0002t0003g0354 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3338-1694C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976367 | |||||||
chr9:95976431 | A | G | 155 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(152): Show |
157 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.3338-1630A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976431 | |||||||
chr9:95976432 | C | G | 155 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(152): Show |
157 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.3338-1629C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976432 | |||||||
chr9:95976485 | G | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3338-1576G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976485 | |||||||
chr9:95976517 | G | C | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3338-1544G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976517 | |||||||
chr9:95976793 | T | C | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3338-1268T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976793 | |||||||
chr9:95976921 | G | T | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3338-1140G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95976921 | |||||||
chr9:95977026 | G | C | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3338-1035G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977026 | |||||||
chr9:95977072 | TTTTG | T | 72 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3338-977_3338-974d others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr9 | 95977072 | ||||||
chr9:95977131 | A | G | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.3338-930A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977131 | |||||||
chr9:95977205 | CT | C | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.3338-855delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977205 | |||||||
chr9:95977216 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(301): Show |
316 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.3338-845G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977216 | |||||||
chr9:95977290 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(268): Show |
281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.3338-771T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977290 | |||||||
chr9:95977331 | A | G | 72 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3338-730A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977331 | |||||||
chr9:95977412 | G | C | 2 | a0008c0010t0001g0049 a0008c0010t0001g0071 |
2 | HG00597.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.3338-649G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977412 | |||||||
chr9:95977713 | A | T | 1 | a0001c0001t0087g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3338-348A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977713 | |||||||
chr9:95977747 | T | A | 5 | a0001c0005t0061g0221 a0001c0005t0062g0105 a0001c0005t0064g0106 others(2): Show |
5 | HG02809.hp1 HG02965.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.3338-314T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977747 | |||||||
chr9:95977823 | C | G | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3338-238C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977823 | |||||||
chr9:95977899 | C | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3338-162C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977899 | |||||||
chr9:95977970 | C | G | 1 | a0004c0004t0005g0248 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3338-91C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 16/18 | chr9 | 95977970 | |||||||
chr9:95978841 | G | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3492+626G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95978841 | |||||||
chr9:95978984 | A | G | 35 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(32): Show |
35 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.3492+769A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95978984 | |||||||
chr9:95979018 | G | T | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3492+803G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979018 | |||||||
chr9:95979100 | T | C | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3492+885T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979100 | |||||||
chr9:95979124 | A | G | 1 | a0001c0005t0009g0240 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3492+909A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979124 | |||||||
chr9:95979384 | A | G | 1 | a0017c0024t0074g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3492+1169A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979384 | |||||||
chr9:95979426 | A | G | 1 | a0001c0001t0019g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3492+1211A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979426 | |||||||
chr9:95979723 | C | T | 12 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(9): Show |
12 | HG00609.hp1 HG02083.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.3492+1508C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979723 | |||||||
chr9:95979774 | A | G | 2 | a0004c0004t0005g0235 a0004c0004t0005g0239 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3492+1559A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979774 | |||||||
chr9:95979893 | T | A | 35 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(32): Show |
35 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.3492+1678T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95979893 | |||||||
chr9:95980042 | G | T | 1 | a0001c0001t0011g0172 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3492+1827G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980042 | |||||||
chr9:95980188 | A | G | 1 | a0002c0002t0007g0332 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3492+1973A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980188 | |||||||
chr9:95980400 | T | G | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3492+2185T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980400 | |||||||
chr9:95980437 | A | T | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3492+2222A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980437 | |||||||
chr9:95980464 | A | G | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3492+2249A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980464 | |||||||
chr9:95980507 | C | G | 1 | a0004c0004t0075g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3492+2292C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980507 | |||||||
chr9:95980664 | T | A | 3 | a0002c0002t0003g0330 a0002c0002t0003g0340 a0002c0002t0007g0332 |
3 | HG02300.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3492+2449T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980664 | |||||||
chr9:95980805 | C | G | 1 | a0001c0001t0018g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3492+2590C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980805 | |||||||
chr9:95980917 | T | C | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3492+2702T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95980917 | |||||||
chr9:95981576 | C | A | 1 | a0002c0002t0003g0320 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3492+3361C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95981576 | |||||||
chr9:95981622 | C | T | 2 | a0004c0004t0038g0011 a0004c0004t0096g0011 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3492+3407C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95981622 | |||||||
chr9:95981935 | A | G | 2 | a0002c0002t0006g0305 a0002c0002t0006g0306 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3492+3720A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95981935 | |||||||
chr9:95982140 | T | A | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.3492+3925T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982140 | |||||||
chr9:95982238 | A | G | 4 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3492+4023A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982238 | |||||||
chr9:95982545 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3492+4330G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982545 | |||||||
chr9:95982553 | A | T | 1 | a0001c0001t0001g0018 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3492+4338A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982553 | |||||||
chr9:95982659 | G | T | 1 | a0004c0004t0005g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3492+4444G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982659 | |||||||
chr9:95982711 | G | A | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3492+4496G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982711 | |||||||
chr9:95982711 | G | GTA | 8 | a0002c0002t0003g0363 a0005c0006t0017g0020 a0005c0006t0017g0021 others(5): Show |
8 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3492+4508_3492+450 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95982711 | ||||||
chr9:95982711 | G | GTATA | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3492+4506_3492+450 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95982711 | ||||||
chr9:95982767 | T | A | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3492+4552T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982767 | |||||||
chr9:95982820 | A | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | NA18979.hp2 NA18988.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.3492+4605A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982820 | |||||||
chr9:95982970 | C | T | 5 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3492+4755C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95982970 | |||||||
chr9:95983030 | T | G | 1 | a0003c0003t0008g0280 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3492+4815T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983030 | |||||||
chr9:95983127 | A | G | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3492+4912A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983127 | |||||||
chr9:95983188 | C | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3492+4973C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983188 | |||||||
chr9:95983203 | A | G | 77 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(74): Show |
77 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.3492+4988A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983203 | |||||||
chr9:95983286 | T | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3492+5071T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983286 | |||||||
chr9:95983353 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3492+5138T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983353 | |||||||
chr9:95983359 | C | T | 31 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.3492+5144C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983359 | |||||||
chr9:95983448 | T | C | 16 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0154 others(13): Show |
16 | HG00621.hp2 HG02155.hp2 NA18959.hp1 others(13): Show |
intron_variant | MODIFIER | c.3492+5233T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983448 | |||||||
chr9:95983613 | T | C | 1 | a0002c0002t0003g0308 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3492+5398T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983613 | |||||||
chr9:95983723 | T | G | 4 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3492+5508T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983723 | |||||||
chr9:95983729 | T | G | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3492+5514T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983729 | |||||||
chr9:95983744 | T | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0025g0098 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3492+5529T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983744 | |||||||
chr9:95983799 | C | T | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3492+5584C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983799 | |||||||
chr9:95983820 | A | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(108): Show |
119 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3492+5605A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983820 | |||||||
chr9:95983860 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+5645G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95983860 | |||||||
chr9:95984071 | CCTTT | C | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3492+5857_3492+586 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984071 | |||||||
chr9:95984132 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(108): Show |
119 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.3492+5917T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984132 | |||||||
chr9:95984168 | A | G | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.3492+5953A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984168 | |||||||
chr9:95984249 | T | C | 1 | a0001c0001t0079g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3492+6034T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984249 | |||||||
chr9:95984262 | A | G | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3492+6047A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984262 | |||||||
chr9:95984327 | A | G | 87 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(84): Show |
89 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.3492+6112A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984327 | |||||||
chr9:95984470 | G | C | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.3492+6255G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984470 | |||||||
chr9:95984479 | C | T | 1 | a0001c0005t0009g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3492+6264C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984479 | |||||||
chr9:95984481 | A | G | 1 | a0002c0002t0028g0329 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3492+6266A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984481 | |||||||
chr9:95984531 | C | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(266): Show |
279 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.3492+6316C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984531 | |||||||
chr9:95984695 | A | G | 1 | a0002c0002t0003g0363 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3492+6480A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984695 | |||||||
chr9:95984840 | G | A | 5 | a0002c0002t0003g0331 a0002c0002t0003g0333 a0002c0002t0007g0307 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+6625G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984840 | |||||||
chr9:95984949 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3492+6734C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95984949 | |||||||
chr9:95984953 | CAGTG | C | 9 | a0002c0002t0003g0331 a0002c0002t0003g0333 a0002c0002t0006g0305 others(6): Show |
9 | HG00735.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.3492+6741_3492+674 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95984953 | ||||||
chr9:95985259 | C | T | 72 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3492+7044C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985259 | |||||||
chr9:95985313 | A | C | 32 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(29): Show |
32 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.3492+7098A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985313 | |||||||
chr9:95985377 | A | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3492+7162A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985377 | |||||||
chr9:95985525 | G | C | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3492+7310G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985525 | |||||||
chr9:95985528 | A | G | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3492+7313A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985528 | |||||||
chr9:95985537 | G | A | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3492+7322G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985537 | |||||||
chr9:95985554 | A | T | 1 | a0001c0001t0014g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3492+7339A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985554 | |||||||
chr9:95985667 | A | T | 5 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3492+7452A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985667 | |||||||
chr9:95985706 | G | A | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3492+7491G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985706 | |||||||
chr9:95985738 | A | G | 76 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(73): Show |
78 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.3492+7523A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985738 | |||||||
chr9:95985752 | G | A | 72 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3492+7537G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985752 | |||||||
chr9:95985957 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0082 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3492+7742A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95985957 | |||||||
chr9:95986059 | G | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3492+7844G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986059 | |||||||
chr9:95986194 | A | G | 32 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(29): Show |
32 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.3492+7979A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986194 | |||||||
chr9:95986259 | A | T | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3492+8044A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986259 | |||||||
chr9:95986324 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3492+8109A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986324 | |||||||
chr9:95986401 | A | G | 1 | a0011c0009t0034g0207 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3492+8186A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986401 | |||||||
chr9:95986492 | C | A | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3492+8277C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986492 | |||||||
chr9:95986497 | C | CT | 23 | a0001c0001t0004g0004 a0001c0001t0004g0124 a0001c0001t0085g0074 others(20): Show |
24 | HG00597.hp2 HG01099.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.3492+8301dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95986497 | ||||||
chr9:95986497 | C | CTT | 11 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(8): Show |
11 | HG00323.hp1 HG00609.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.3492+8300_3492+830 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95986497 | ||||||
chr9:95986497 | CT | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(224): Show |
237 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.3492+8301delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95986497 | ||||||
chr9:95986560 | A | C | 1 | a0004c0004t0005g0231 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3492+8345A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986560 | |||||||
chr9:95986799 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3492+8584A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95986799 | |||||||
chr9:95987099 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+8884G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987099 | |||||||
chr9:95987132 | G | A | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3492+8917G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987132 | |||||||
chr9:95987189 | C | T | 8 | a0002c0002t0003g0347 a0002c0002t0003g0348 a0002c0002t0003g0350 others(5): Show |
8 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3492+8974C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987189 | |||||||
chr9:95987327 | C | G | 72 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.3492+9112C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987327 | |||||||
chr9:95987339 | G | C | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+9124G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987339 | |||||||
chr9:95987382 | A | G | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3492+9167A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987382 | |||||||
chr9:95987388 | G | A | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+9173G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987388 | |||||||
chr9:95987526 | T | C | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3492+9311T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987526 | |||||||
chr9:95987551 | T | C | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3492+9336T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987551 | |||||||
chr9:95987647 | G | A | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3492+9432G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987647 | |||||||
chr9:95987701 | T | C | 4 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0004g0133 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3492+9486T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987701 | |||||||
chr9:95987743 | G | C | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3492+9528G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987743 | |||||||
chr9:95987814 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3492+9599G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95987814 | |||||||
chr9:95988212 | G | A | 5 | a0003c0003t0012g0262 a0003c0003t0012g0264 a0003c0003t0012g0265 others(2): Show |
5 | HG01123.hp1 HG01169.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+9997G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988212 | |||||||
chr9:95988224 | A | G | 8 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3492+10009A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988224 | |||||||
chr9:95988324 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(268): Show |
281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.3492+10109G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988324 | |||||||
chr9:95988340 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(268): Show |
281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.3492+10125T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988340 | |||||||
chr9:95988348 | G | A | 3 | a0002c0002t0006g0305 a0002c0002t0006g0306 a0002c0002t0006g0341 |
3 | HG01243.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3492+10133G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988348 | |||||||
chr9:95988391 | G | A | 1 | a0008c0010t0001g0049 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3492+10176G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988391 | |||||||
chr9:95988425 | G | A | 35 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(32): Show |
35 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.3492+10210G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988425 | |||||||
chr9:95988546 | A | T | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3492+10331A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988546 | |||||||
chr9:95988574 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3492+10359C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988574 | |||||||
chr9:95988642 | G | C | 20 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(17): Show |
20 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3492+10427G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95988642 | |||||||
chr9:95989199 | A | G | 2 | a0004c0004t0005g0235 a0004c0004t0005g0239 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3492+10984A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989199 | |||||||
chr9:95989357 | G | T | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3492+11142G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989357 | |||||||
chr9:95989458 | T | C | 1 | a0001c0001t0011g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3492+11243T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989458 | |||||||
chr9:95989528 | A | G | 1 | a0004c0004t0013g0246 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3492+11313A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989528 | |||||||
chr9:95989628 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3492+11413A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989628 | |||||||
chr9:95989644 | G | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3492+11429G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989644 | |||||||
chr9:95989775 | A | G | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3492+11560A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989775 | |||||||
chr9:95989791 | G | T | 1 | a0004c0004t0005g0248 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3492+11576G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989791 | |||||||
chr9:95989814 | C | T | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3492+11599C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95989814 | |||||||
chr9:95990027 | C | T | 5 | a0006c0007t0003g0297 a0006c0007t0007g0298 a0006c0007t0007g0299 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+11812C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990027 | |||||||
chr9:95990125 | A | G | 21 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(18): Show |
21 | HG00597.hp2 HG02056.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.3492+11910A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990125 | |||||||
chr9:95990209 | T | G | 5 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3492+11994T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990209 | |||||||
chr9:95990214 | G | A | 68 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.3492+11999G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990214 | |||||||
chr9:95990562 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3492+12347G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990562 | |||||||
chr9:95990733 | AGT | A | 5 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(2): Show |
5 | HG01952.hp2 HG02809.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.3492+12523_3492+12 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95990733 | ||||||
chr9:95990756 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(270): Show |
283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.3492+12541C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990756 | |||||||
chr9:95990857 | A | G | 1 | a0001c0001t0014g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3492+12642A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990857 | |||||||
chr9:95990924 | C | T | 2 | a0002c0002t0006g0357 a0002c0002t0049g0344 |
2 | NA19056.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.3492+12709C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95990924 | |||||||
chr9:95991199 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(270): Show |
283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.3492+12984A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991199 | |||||||
chr9:95991323 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(270): Show |
283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.3492+13108C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991323 | |||||||
chr9:95991333 | T | C | 1 | a0002c0002t0003g0312 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3492+13118T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991333 | |||||||
chr9:95991358 | G | A | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3492+13143G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991358 | |||||||
chr9:95991633 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3493-12887G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991633 | |||||||
chr9:95991674 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3493-12846G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991674 | |||||||
chr9:95991785 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3493-12735A>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991785 | |||||||
chr9:95991880 | T | C | 2 | a0001c0001t0031g0112 a0001c0001t0031g0113 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3493-12640T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95991880 | |||||||
chr9:95992038 | A | G | 5 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3493-12482A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95992038 | |||||||
chr9:95992126 | A | T | 7 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(4): Show |
7 | HG01952.hp2 HG02809.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3493-12394A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95992126 | |||||||
chr9:95992196 | G | A | 6 | a0003c0003t0016g0269 a0003c0003t0016g0272 a0003c0003t0016g0274 others(3): Show |
6 | NA18945.hp2 NA18962.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.3493-12324G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95992196 | |||||||
chr9:95992353 | G | A | 79 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(76): Show |
81 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.3493-12167G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95992353 | |||||||
chr9:95992475 | C | G | 3 | a0001c0001t0015g0007 a0001c0001t0015g0145 a0020c0014t0040g0189 |
4 | HG02615.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-12045C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95992475 | |||||||
chr9:95992869 | T | A | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3493-11651T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95992869 | |||||||
chr9:95993100 | C | T | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-11420C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993100 | |||||||
chr9:95993139 | T | C | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-11381T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993139 | |||||||
chr9:95993294 | G | A | 1 | a0001c0001t0087g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3493-11226G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993294 | |||||||
chr9:95993462 | G | A | 1 | a0009c0011t0020g0017 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.3493-11058G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993462 | |||||||
chr9:95993535 | A | G | 12 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0315 others(9): Show |
13 | HG00423.hp1 NA18970.hp2 NA18971.hp2 others(10): Show |
intron_variant | MODIFIER | c.3493-10985A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993535 | |||||||
chr9:95993548 | G | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3493-10972G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993548 | |||||||
chr9:95993605 | G | A | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-10915G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993605 | |||||||
chr9:95993860 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3493-10660G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993860 | |||||||
chr9:95993871 | C | T | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-10649C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95993871 | |||||||
chr9:95994121 | G | A | 12 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0315 others(9): Show |
13 | HG00423.hp1 NA18970.hp2 NA18971.hp2 others(10): Show |
intron_variant | MODIFIER | c.3493-10399G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994121 | |||||||
chr9:95994366 | C | T | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3493-10154C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994366 | |||||||
chr9:95994381 | CCTT | C | 33 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3493-10138_3493-10 others(9): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994381 | |||||||
chr9:95994405 | C | T | 2 | a0001c0001t0027g0370 a0001c0001t0092g0371 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3493-10115C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994405 | |||||||
chr9:95994527 | T | C | 5 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(2): Show |
5 | HG01952.hp2 HG02809.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.3493-9993T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994527 | |||||||
chr9:95994537 | C | T | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3493-9983C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994537 | |||||||
chr9:95994788 | TC | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(276): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3493-9730delC | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95994788 | ||||||
chr9:95994994 | A | G | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3493-9526A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95994994 | |||||||
chr9:95995175 | T | A | 1 | a0001c0001t0002g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3493-9345T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95995175 | |||||||
chr9:95995459 | T | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3493-9061T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95995459 | |||||||
chr9:95995512 | A | G | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-9008A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95995512 | |||||||
chr9:95995561 | A | G | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3493-8959A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95995561 | |||||||
chr9:95995568 | T | C | 2 | a0001c0001t0014g0045 a0001c0001t0014g0076 |
2 | NA18967.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.3493-8952T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95995568 | |||||||
chr9:95995793 | G | A | 2 | a0017c0024t0074g0256 a0025c0027t0069g0255 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3493-8727G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95995793 | |||||||
chr9:95996095 | G | A | 1 | a0002c0002t0003g0337 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3493-8425G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95996095 | |||||||
chr9:95996340 | A | G | 1 | a0001c0001t0087g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3493-8180A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95996340 | |||||||
chr9:95996501 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(276): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3493-8019T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95996501 | |||||||
chr9:95997045 | C | T | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-7475C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997045 | |||||||
chr9:95997058 | C | T | 74 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(71): Show |
76 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.3493-7462C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997058 | |||||||
chr9:95997067 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(142): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.3493-7453T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997067 | |||||||
chr9:95997145 | G | A | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-7375G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997145 | |||||||
chr9:95997146 | CAAAGTCA others(7): Show |
C | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-7372_3493-735 others(18): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95997146 | ||||||
chr9:95997161 | A | T | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-7359A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997161 | |||||||
chr9:95997273 | T | C | 1 | a0016c0018t0058g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3493-7247T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997273 | |||||||
chr9:95997306 | T | C | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3493-7214T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997306 | |||||||
chr9:95997321 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(276): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3493-7199T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997321 | |||||||
chr9:95997330 | T | G | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3493-7190T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997330 | |||||||
chr9:95997405 | C | CT | 9 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3493-7112dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95997405 | ||||||
chr9:95997431 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3493-7089A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997431 | |||||||
chr9:95997462 | G | C | 1 | a0006c0007t0007g0298 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3493-7058G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997462 | |||||||
chr9:95997674 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(276): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3493-6846T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997674 | |||||||
chr9:95997675 | T | G | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-6845T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997675 | |||||||
chr9:95997815 | GAGTTA | G | 79 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(76): Show |
81 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.3493-6700_3493-669 others(9): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95997815 | ||||||
chr9:95997940 | A | G | 1 | a0001c0001t0019g0217 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3493-6580A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997940 | |||||||
chr9:95997976 | C | T | 13 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(10): Show |
14 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3493-6544C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997976 | |||||||
chr9:95997995 | A | G | 1 | a0003c0003t0012g0264 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3493-6525A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95997995 | |||||||
chr9:95998003 | T | C | 6 | a0004c0004t0037g0259 a0004c0004t0037g0260 a0004c0004t0038g0011 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3493-6517T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998003 | |||||||
chr9:95998005 | T | C | 1 | a0019c0013t0078g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3493-6515T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998005 | |||||||
chr9:95998079 | CTTTCTGG others(12): Show |
C | 1 | a0017c0024t0074g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3493-6419_3493-640 others(23): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95998079 | ||||||
chr9:95998145 | CT | C | 10 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3493-6366delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95998145 | ||||||
chr9:95998161 | C | T | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3493-6359C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998161 | |||||||
chr9:95998350 | A | G | 3 | a0001c0001t0002g0008 a0001c0001t0004g0008 a0001c0001t0057g0187 |
3 | HG00733.hp2 HG00741.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3493-6170A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998350 | |||||||
chr9:95998441 | T | C | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3493-6079T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998441 | |||||||
chr9:95998529 | A | G | 7 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(4): Show |
7 | HG01952.hp2 HG02809.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3493-5991A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998529 | |||||||
chr9:95998640 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3493-5880G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998640 | |||||||
chr9:95998798 | C | T | 2 | a0011c0009t0034g0207 a0011c0009t0034g0208 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3493-5722C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95998798 | |||||||
chr9:95999121 | G | A | 1 | a0001c0005t0063g0253 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3493-5399G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999121 | |||||||
chr9:95999203 | A | T | 2 | a0002c0002t0028g0366 a0002c0002t0048g0325 |
2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.3493-5317A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999203 | |||||||
chr9:95999293 | G | A | 2 | a0004c0004t0005g0235 a0004c0004t0005g0239 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3493-5227G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999293 | |||||||
chr9:95999307 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3493-5213G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999307 | |||||||
chr9:95999360 | C | CA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(140): Show |
151 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.3493-5147dupA | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95999360 | ||||||
chr9:95999442 | C | T | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3493-5078C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999442 | |||||||
chr9:95999447 | GT | G | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-5072delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999447 | |||||||
chr9:95999451 | A | ATGG | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-5069_3493-506 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999451 | |||||||
chr9:95999452 | A | T | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-5068A>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999452 | |||||||
chr9:95999799 | G | T | 1 | a0001c0001t0002g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3493-4721G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999799 | |||||||
chr9:95999866 | TTTTC | T | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG01952.hp2 HG02809.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3493-4648_3493-464 others(8): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95999866 | ||||||
chr9:95999895 | AT | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(274): Show |
287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.3493-4611delT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 95999895 | ||||||
chr9:95999918 | C | G | 3 | a0001c0001t0027g0142 a0001c0001t0027g0143 a0001c0001t0090g0144 |
3 | HG01884.hp1 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3493-4602C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999918 | |||||||
chr9:95999949 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3493-4571C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 95999949 | |||||||
chr9:96000073 | G | A | 2 | a0010c0012t0020g0368 a0010c0012t0020g0369 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3493-4447G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000073 | |||||||
chr9:96000178 | C | T | 33 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3493-4342C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000178 | |||||||
chr9:96000295 | C | G | 1 | a0011c0009t0034g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3493-4225C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000295 | |||||||
chr9:96000370 | G | A | 33 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3493-4150G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000370 | |||||||
chr9:96000393 | A | G | 1 | a0002c0002t0003g0352 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3493-4127A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000393 | |||||||
chr9:96000488 | G | A | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3493-4032G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000488 | |||||||
chr9:96000533 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(317): Show |
332 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.3493-3987A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000533 | |||||||
chr9:96000614 | A | G | 1 | a0001c0001t0010g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3493-3906A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000614 | |||||||
chr9:96000619 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(130): Show |
140 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.3493-3901C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000619 | |||||||
chr9:96000778 | G | A | 74 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0015 others(71): Show |
76 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.3493-3742G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96000778 | |||||||
chr9:96001016 | G | A | 1 | a0001c0005t0061g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3493-3504G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001016 | |||||||
chr9:96001046 | G | A | 8 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(5): Show |
8 | HG00423.hp2 HG00673.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.3493-3474G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001046 | |||||||
chr9:96001056 | T | C | 5 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3493-3464T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001056 | |||||||
chr9:96001099 | C | T | 1 | a0008c0010t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3493-3421C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001099 | |||||||
chr9:96001186 | A | G | 1 | a0001c0005t0033g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3493-3334A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001186 | |||||||
chr9:96001263 | G | T | 2 | a0004c0004t0005g0235 a0004c0004t0005g0239 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3493-3257G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001263 | |||||||
chr9:96001270 | A | G | 1 | a0002c0002t0003g0317 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3493-3250A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001270 | |||||||
chr9:96001311 | C | T | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-3209C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001311 | |||||||
chr9:96001341 | G | A | 1 | a0002c0002t0003g0257 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3493-3179G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001341 | |||||||
chr9:96001412 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(142): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.3493-3108G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001412 | |||||||
chr9:96001547 | T | C | 4 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-2973T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001547 | |||||||
chr9:96001674 | G | A | 1 | a0001c0001t0036g0039 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3493-2846G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001674 | |||||||
chr9:96001707 | G | A | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3493-2813G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001707 | |||||||
chr9:96001709 | C | T | 5 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3493-2811C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001709 | |||||||
chr9:96001710 | G | A | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG01952.hp2 HG02809.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3493-2810G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001710 | |||||||
chr9:96001754 | C | T | 33 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3493-2766C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001754 | |||||||
chr9:96001763 | G | T | 1 | a0001c0005t0009g0240 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3493-2757G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001763 | |||||||
chr9:96001765 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3493-2755A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001765 | |||||||
chr9:96001774 | C | T | 33 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3493-2746C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001774 | |||||||
chr9:96001776 | C | T | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3493-2744C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001776 | |||||||
chr9:96001884 | C | T | 13 | a0001c0001t0019g0211 a0001c0001t0019g0212 a0001c0001t0019g0214 others(10): Show |
13 | HG02523.hp1 HG02809.hp1 NA18966.hp2 others(10): Show |
intron_variant | MODIFIER | c.3493-2636C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001884 | |||||||
chr9:96001908 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(276): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3493-2612A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001908 | |||||||
chr9:96001918 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(84): Show |
92 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.3493-2602C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001918 | |||||||
chr9:96001977 | T | C | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3493-2543T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001977 | |||||||
chr9:96001986 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(271): Show |
284 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.3493-2534A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96001986 | |||||||
chr9:96002011 | G | A | 1 | a0004c0004t0005g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3493-2509G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002011 | |||||||
chr9:96002016 | C | T | 2 | a0003c0003t0008g0267 a0003c0003t0008g0268 |
2 | NA18975.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3493-2504C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002016 | |||||||
chr9:96002029 | G | A | 1 | a0001c0001t0002g0198 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3493-2491G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002029 | |||||||
chr9:96002066 | G | A | 1 | a0001c0001t0039g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3493-2454G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002066 | |||||||
chr9:96002088 | G | A | 1 | a0005c0006t0017g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3493-2432G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002088 | |||||||
chr9:96002092 | G | A | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3493-2428G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002092 | |||||||
chr9:96002380 | G | A | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3493-2140G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002380 | |||||||
chr9:96002382 | A | G | 10 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3493-2138A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002382 | |||||||
chr9:96002423 | C | CT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(259): Show |
272 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.3493-2084dupT | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 96002423 | ||||||
chr9:96002423 | C | CTT | 14 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(11): Show |
14 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3493-2085_3493-208 others(6): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 96002423 | ||||||
chr9:96002456 | C | T | 1 | a0002c0002t0003g0342 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3493-2064C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002456 | |||||||
chr9:96002571 | G | A | 4 | a0006c0007t0007g0298 a0006c0007t0007g0299 a0006c0007t0007g0300 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3493-1949G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002571 | |||||||
chr9:96002811 | A | G | 5 | a0003c0003t0021g0287 a0003c0003t0021g0289 a0003c0003t0021g0291 others(2): Show |
5 | HG00609.hp2 NA18747.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.3493-1709A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002811 | |||||||
chr9:96002847 | G | A | 1 | a0001c0001t0053g0173 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3493-1673G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002847 | |||||||
chr9:96002860 | TTTTTCAG | T | 5 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3493-1656_3493-165 others(11): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 96002860 | ||||||
chr9:96002867 | G | T | 1 | a0001c0001t0018g0147 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3493-1653G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96002867 | |||||||
chr9:96003113 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3493-1407A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003113 | |||||||
chr9:96003496 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(102): Show |
112 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.3493-1024C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003496 | |||||||
chr9:96003536 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0089 |
2 | NA18993.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3493-984T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003536 | |||||||
chr9:96003587 | T | A | 1 | a0001c0001t0052g0150 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3493-933T>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003587 | |||||||
chr9:96003616 | G | GGGTGCTA others(19): Show |
1 | a0002c0002t0007g0328 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3493-894_3493-869d others(28): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | 96003616 | ||||||
chr9:96003699 | G | A | 2 | a0001c0005t0033g0254 a0015c0017t0033g0102 |
2 | HG01952.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3493-821G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003699 | |||||||
chr9:96003800 | T | C | 1 | a0001c0001t0047g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3493-720T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003800 | |||||||
chr9:96003853 | C | T | 1 | a0008c0010t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3493-667C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96003853 | |||||||
chr9:96004009 | T | C | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3493-511T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96004009 | |||||||
chr9:96004198 | G | A | 19 | a0001c0001t0002g0005 a0001c0001t0002g0125 a0001c0001t0002g0126 others(16): Show |
21 | HG00639.hp1 HG01099.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3493-322G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96004198 | |||||||
chr9:96004448 | A | G | 17 | a0001c0001t0015g0007 a0001c0001t0015g0138 a0001c0001t0015g0140 others(14): Show |
19 | HG01081.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3493-72A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 17/18 | chr9 | 96004448 | |||||||
chr9:96004824 | C | A | 16 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0154 others(13): Show |
16 | HG00621.hp2 HG02155.hp2 NA18959.hp1 others(13): Show |
intron_variant | MODIFIER | c.3674+123C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96004824 | |||||||
chr9:96004827 | A | G | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3674+126A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96004827 | |||||||
chr9:96005042 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3674+341G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005042 | |||||||
chr9:96005358 | T | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(276): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.3674+657T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005358 | |||||||
chr9:96005448 | G | A | 4 | a0002c0002t0029g0360 a0002c0002t0029g0362 a0002c0002t0030g0359 others(1): Show |
4 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.3674+747G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005448 | |||||||
chr9:96005486 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0025g0098 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3674+785G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005486 | |||||||
chr9:96005552 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3674+851C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005552 | |||||||
chr9:96005553 | G | A | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG01952.hp2 HG02809.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3674+852G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005553 | |||||||
chr9:96005553 | G | T | 3 | a0001c0001t0002g0135 a0001c0001t0004g0134 a0001c0001t0088g0122 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3674+852G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005553 | |||||||
chr9:96005625 | G | C | 1 | a0016c0018t0058g0336 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3674+924G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005625 | |||||||
chr9:96005849 | G | A | 5 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3674+1148G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005849 | |||||||
chr9:96005900 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3674+1199A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96005900 | |||||||
chr9:96006297 | G | A | 33 | a0003c0003t0008g0267 a0003c0003t0008g0268 a0003c0003t0008g0271 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3674+1596G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006297 | |||||||
chr9:96006307 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3674+1606C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006307 | |||||||
chr9:96006312 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3674+1611G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006312 | |||||||
chr9:96006479 | C | T | 1 | a0002c0002t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3674+1778C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006479 | |||||||
chr9:96006480 | G | T | 1 | a0002c0002t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3674+1779G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006480 | |||||||
chr9:96006498 | C | T | 7 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3674+1797C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006498 | |||||||
chr9:96006558 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3674+1857G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006558 | |||||||
chr9:96006774 | CAAT | C | 3 | a0001c0001t0018g0149 a0001c0001t0018g0202 a0001c0001t0066g0146 |
3 | NA18965.hp2 NA18980.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3674+2074_3674+207 others(7): Show |
ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006774 | |||||||
chr9:96006776 | A | G | 8 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0227 others(5): Show |
8 | HG00423.hp2 HG00673.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.3674+2075A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006776 | |||||||
chr9:96006926 | G | T | 1 | a0001c0001t0004g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3674+2225G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96006926 | |||||||
chr9:96007114 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3674+2413G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007114 | |||||||
chr9:96007170 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3674+2469C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007170 | |||||||
chr9:96007321 | T | C | 1 | a0004c0004t0013g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3674+2620T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007321 | |||||||
chr9:96007466 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(102): Show |
112 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.3674+2765A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007466 | |||||||
chr9:96007473 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3674+2772G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007473 | |||||||
chr9:96007476 | C | T | 1 | a0004c0004t0013g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3674+2775C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007476 | |||||||
chr9:96007721 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0104 |
2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3674+3020C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007721 | |||||||
chr9:96007957 | C | T | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3674+3256C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96007957 | |||||||
chr9:96008159 | C | G | 1 | a0001c0001t0004g0124 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3674+3458C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008159 | |||||||
chr9:96008208 | G | A | 1 | a0010c0012t0020g0368 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3674+3507G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008208 | |||||||
chr9:96008237 | C | A | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3674+3536C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008237 | |||||||
chr9:96008378 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3674+3677G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008378 | |||||||
chr9:96008476 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(278): Show |
291 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.3675-3749T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008476 | |||||||
chr9:96008621 | C | T | 1 | a0002c0002t0003g0345 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3675-3604C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008621 | |||||||
chr9:96008646 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(142): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.3675-3579T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008646 | |||||||
chr9:96008690 | T | G | 3 | a0009c0011t0020g0017 a0010c0012t0020g0368 a0010c0012t0020g0369 |
4 | HG02109.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3675-3535T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008690 | |||||||
chr9:96008752 | A | G | 1 | a0024c0029t0094g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3675-3473A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008752 | |||||||
chr9:96008767 | C | T | 11 | a0001c0001t0010g0108 a0001c0001t0010g0114 a0001c0001t0010g0115 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3675-3458C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008767 | |||||||
chr9:96008886 | C | G | 6 | a0007c0008t0023g0293 a0007c0008t0023g0294 a0007c0008t0023g0295 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3675-3339C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008886 | |||||||
chr9:96008979 | C | T | 2 | a0001c0001t0004g0004 a0001c0001t0004g0124 |
3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3675-3246C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96008979 | |||||||
chr9:96009147 | C | T | 1 | a0003c0003t0016g0275 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3675-3078C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009147 | |||||||
chr9:96009187 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0018 others(142): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.3675-3038G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009187 | |||||||
chr9:96009230 | C | T | 1 | a0013c0016t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3675-2995C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009230 | |||||||
chr9:96009326 | A | G | 28 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(25): Show |
28 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3675-2899A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009326 | |||||||
chr9:96009408 | T | G | 2 | a0001c0001t0002g0129 a0001c0001t0004g0130 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.3675-2817T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009408 | |||||||
chr9:96009436 | C | T | 5 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(2): Show |
5 | HG01952.hp2 HG02809.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.3675-2789C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009436 | |||||||
chr9:96009538 | T | G | 9 | a0001c0001t0010g0114 a0001c0001t0010g0115 a0001c0001t0010g0117 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3675-2687T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009538 | |||||||
chr9:96009637 | C | T | 4 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3675-2588C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009637 | |||||||
chr9:96009664 | G | T | 3 | a0001c0001t0022g0006 a0001c0001t0022g0136 a0001c0001t0045g0107 |
4 | HG03098.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3675-2561G>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009664 | |||||||
chr9:96009945 | G | C | 2 | a0002c0002t0006g0305 a0002c0002t0006g0306 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3675-2280G>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96009945 | |||||||
chr9:96010169 | T | C | 2 | a0001c0001t0002g0180 a0001c0001t0002g0194 |
2 | NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.3675-2056T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010169 | |||||||
chr9:96010375 | C | T | 1 | a0005c0006t0032g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3675-1850C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010375 | |||||||
chr9:96010653 | A | G | 1 | a0015c0017t0033g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3675-1572A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010653 | |||||||
chr9:96010656 | C | T | 35 | a0004c0004t0005g0225 a0004c0004t0005g0226 a0004c0004t0005g0228 others(32): Show |
35 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.3675-1569C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010656 | |||||||
chr9:96010747 | G | A | 4 | a0001c0005t0009g0223 a0001c0005t0009g0224 a0001c0005t0009g0240 others(1): Show |
4 | HG00423.hp2 NA18946.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.3675-1478G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010747 | |||||||
chr9:96010758 | C | G | 7 | a0005c0006t0017g0020 a0005c0006t0017g0021 a0005c0006t0017g0022 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3675-1467C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010758 | |||||||
chr9:96010798 | A | G | 1 | a0025c0027t0069g0255 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3675-1427A>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010798 | |||||||
chr9:96010846 | T | C | 3 | a0001c0001t0002g0180 a0001c0001t0002g0194 a0001c0005t0063g0253 |
3 | HG03516.hp1 NA18944.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.3675-1379T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96010846 | |||||||
chr9:96011147 | C | T | 2 | a0001c0005t0062g0105 a0001c0005t0064g0106 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3675-1078C>T | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96011147 | |||||||
chr9:96011538 | C | G | 1 | a0002c0002t0003g0342 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3675-687C>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96011538 | |||||||
chr9:96011678 | T | G | 1 | a0002c0002t0007g0328 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3675-547T>G | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96011678 | |||||||
chr9:96011736 | C | A | 8 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0320 others(5): Show |
8 | NA18970.hp2 NA18971.hp2 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.3675-489C>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96011736 | |||||||
chr9:96011786 | T | C | 6 | a0001c0005t0033g0254 a0001c0005t0061g0221 a0001c0005t0062g0105 others(3): Show |
6 | HG01952.hp2 HG02809.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3675-439T>C | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96011786 | |||||||
chr9:96011931 | G | A | 1 | a0001c0001t0082g0069 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3675-294G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96011931 | |||||||
chr9:96012081 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3675-144G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96012081 | |||||||
chr9:96012106 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3675-119G>A | ERCC6L2 | ENSG00000182150.19 | transcript | ENST00000653738.2 | protein_coding | 18/18 | chr9 | 96012106 |