Item | Value |
---|---|
geneid | 23137 |
ensemblid | ENSG00000198887.9 |
hgncid | 20465 |
symbol | SMC5 |
name | structural maintenance of chromosomes 5 |
refseq_nuc | NM_015110.4 |
refseq_prot | NP_055925.2 |
ensembl_nuc | ENST00000361138.7 |
ensembl_prot | ENSP00000354957.5 |
mane_status | MANE Select |
chr | chr9 |
start | 70258978 |
end | 70354873 |
strand | + |
ver | v1.2 |
region | chr9:70258978-70354873 |
region5000 | chr9:70253978-70359873 |
regionname0 | SMC5_chr9_70258978_70354873 |
regionname5000 | SMC5_chr9_70253978_70359873 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1101 | 158 | 38 | 40 | 64 | 4 | 12 | 45 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0002 | 0/0 | 1101 | 90 | 6 | 11 | 56 | 1 | 16 | 47 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0003 | 1/1 | 1101 | 68 | 20 | 8 | 29 | 3 | 6 | 21 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0004 | 0/0 | 1101 | 31 | 15 | 10 | 2 | 2 | 2 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0005 | 0/0 | 1101 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0006 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0007 | 0/0 | 1101 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0008 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0009 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0010 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0011 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0012 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0013 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0014 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0015 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
a0016 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | MATPS others(1096): Show |
chr9 | 70253978 | 70359873 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3303 | 148 | 32 | 39 | 61 | 4 | 12 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0001c0005 | 0/0 | 3303 | 7 | 6 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0001c0010 | 0/0 | 3303 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0002c0002 | 0/0 | 3303 | 86 | 2 | 11 | 56 | 1 | 16 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0002c0009 | 0/0 | 3303 | 3 | 3 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0002c0013 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0003c0003 | 1/1 | 3303 | 68 | 20 | 8 | 29 | 3 | 6 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0004c0004 | 0/0 | 3303 | 20 | 7 | 8 | 2 | 1 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0004c0006 | 0/0 | 3303 | 6 | 6 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0004c0008 | 0/0 | 3303 | 5 | 2 | 2 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0005c0007 | 0/0 | 3303 | 6 | 5 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0006c0011 | 0/0 | 3303 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0007c0012 | 0/0 | 3303 | 2 | 0 | 0 | 0 | 0 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0008c0014 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0009c0015 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0010c0022 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0011c0021 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0012c0020 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0013c0019 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0014c0018 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0015c0017 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 | ||
a0016c0016 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | ATGGC others(3298): Show |
chr9 | 70253978 | 70359873 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5949 | 140 | 30 | 36 | 59 | 4 | 11 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0001t0007 | 0/0 | 5949 | 3 | 1 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0001t0015 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0001t0016 | 0/0 | 5949 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0001t0017 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0001t0021 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0001t0023 | 0/0 | 5949 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0001c0005t0003 | 0/0 | 5948 | 7 | 6 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5943): Show |
chr9 | 70253978 | 70359873 |
a0001c0010t0002 | 0/0 | 5949 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0002t0001 | 0/0 | 5949 | 75 | 1 | 6 | 51 | 1 | 16 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0002t0004 | 0/0 | 5949 | 7 | 0 | 5 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0002t0010 | 0/0 | 5973 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5968): Show |
chr9 | 70253978 | 70359873 |
a0002c0002t0013 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0002t0019 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0002t0022 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0009t0006 | 0/0 | 5949 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0009t0014 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0002c0013t0006 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0003c0003t0001 | 1/1 | 5949 | 64 | 19 | 7 | 28 | 2 | 6 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0003c0003t0008 | 0/0 | 5949 | 3 | 1 | 1 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0003c0003t0020 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0004c0004t0001 | 0/0 | 5949 | 19 | 6 | 8 | 2 | 1 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0004c0004t0018 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0004c0006t0001 | 0/0 | 5949 | 6 | 6 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0004c0008t0005 | 0/0 | 5949 | 5 | 2 | 2 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0005c0007t0002 | 0/0 | 5949 | 6 | 5 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0006c0011t0009 | 0/0 | 5949 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0007c0012t0001 | 0/0 | 5949 | 2 | 0 | 0 | 0 | 0 | 2 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0008c0014t0001 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0009c0015t0011 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0010c0022t0012 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0011c0021t0001 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0012c0020t0006 | 0/0 | 5949 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0013c0019t0003 | 0/0 | 5948 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5943): Show |
chr9 | 70253978 | 70359873 |
a0014c0018t0001 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0015c0017t0002 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
a0016c0016t0002 | 0/0 | 5949 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | AGTTC others(5944): Show |
chr9 | 70253978 | 70359873 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0007g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0007g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0016g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0021g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0001t0023g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0005t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0010t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0010t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0001c0010t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0004g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0019g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0002t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0009t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0009t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0009t0014g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0002c0013t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0008g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0003c0003t0020g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0004t0018g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0006t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0006t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0006t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0006t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0006t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0006t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0008t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0008t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0008t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0008t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0004c0008t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0005c0007t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0005c0007t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0005c0007t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0005c0007t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0005c0007t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0006c0011t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0006c0011t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0007c0012t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0007c0012t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0008c0014t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0009c0015t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0010c0022t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0011c0021t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0012c0020t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0013c0019t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0014c0018t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0015c0017t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
a0016c0016t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0001 | g0170 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0291 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00140 | hp2 | a0004 | c0004 | t0001 | g0334 | EUR | GBR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0173 | EUR | FIN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0134 | EUR | FIN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00597 | hp2 | a0008 | c0014 | t0001 | g0069 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | CHS | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00738 | hp1 | a0001 | c0001 | t0007 | g0284 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00738 | hp2 | a0004 | c0008 | t0005 | g0101 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0286 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0322 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01071 | hp2 | a0004 | c0004 | t0001 | g0323 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0172 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01099 | hp1 | a0004 | c0004 | t0001 | g0314 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01106 | hp1 | a0003 | c0003 | t0008 | g0196 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01106 | hp2 | a0004 | c0004 | t0001 | g0332 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01243 | hp1 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0168 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01255 | hp2 | a0004 | c0004 | t0001 | g0319 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01256 | hp2 | a0004 | c0004 | t0001 | g0316 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01258 | hp2 | a0004 | c0004 | t0001 | g0315 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01346 | hp1 | a0004 | c0004 | t0001 | g0318 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01358 | hp2 | a0005 | c0007 | t0002 | g0267 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0158 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01433 | hp1 | a0004 | c0008 | t0005 | g0102 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01496 | hp1 | a0001 | c0005 | t0003 | g0029 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0197 | AMR | CLM | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01884 | hp2 | a0009 | c0015 | t0011 | g0108 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01891 | hp2 | a0002 | c0009 | t0006 | g0097 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01943 | hp1 | a0002 | c0002 | t0004 | g0087 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01975 | hp2 | a0002 | c0002 | t0004 | g0088 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01978 | hp2 | a0003 | c0003 | t0001 | g0163 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG01993 | hp2 | a0002 | c0002 | t0004 | g0008 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02040 | hp2 | a0001 | c0010 | t0002 | g0021 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02055 | hp2 | a0004 | c0006 | t0001 | g0325 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02071 | hp1 | a0001 | c0001 | t0017 | g0214 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0188 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0193 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02135 | hp1 | a0001 | c0010 | t0002 | g0275 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02145 | hp1 | a0003 | c0003 | t0008 | g0194 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0187 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02165 | hp1 | a0003 | c0003 | t0020 | g0190 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | CDX | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02257 | hp1 | a0001 | c0001 | t0021 | g0310 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02257 | hp2 | a0004 | c0006 | t0001 | g0333 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0302 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0086 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0146 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0337 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02293 | hp1 | a0001 | c0001 | t0023 | g0247 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02293 | hp2 | a0002 | c0002 | t0004 | g0089 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02300 | hp1 | a0003 | c0003 | t0001 | g0153 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02451 | hp1 | a0001 | c0005 | t0003 | g0028 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02451 | hp2 | a0010 | c0022 | t0012 | g0149 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02523 | hp1 | a0011 | c0021 | t0001 | g0068 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02572 | hp1 | a0001 | c0005 | t0003 | g0024 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02572 | hp2 | a0001 | c0005 | t0003 | g0027 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0305 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02615 | hp2 | a0002 | c0009 | t0014 | g0099 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02622 | hp1 | a0003 | c0003 | t0001 | g0307 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02630 | hp2 | a0005 | c0007 | t0002 | g0016 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0339 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02717 | hp2 | a0004 | c0006 | t0001 | g0324 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0166 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0145 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0290 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02809 | hp1 | a0004 | c0008 | t0005 | g0103 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02809 | hp2 | a0004 | c0006 | t0001 | g0335 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02818 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02818 | hp2 | a0004 | c0006 | t0001 | g0326 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0169 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02895 | hp1 | a0006 | c0011 | t0009 | g0303 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02895 | hp2 | a0004 | c0004 | t0001 | g0327 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02897 | hp1 | a0006 | c0011 | t0009 | g0304 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02965 | hp1 | a0001 | c0005 | t0003 | g0026 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02970 | hp1 | a0012 | c0020 | t0006 | g0098 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02976 | hp1 | a0004 | c0004 | t0001 | g0331 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03041 | hp1 | a0001 | c0005 | t0003 | g0025 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03130 | hp1 | a0005 | c0007 | t0002 | g0016 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03209 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03209 | hp2 | a0002 | c0013 | t0006 | g0009 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03225 | hp1 | a0002 | c0009 | t0006 | g0009 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03453 | hp1 | a0004 | c0008 | t0005 | g0100 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0082 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0283 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03486 | hp2 | a0004 | c0004 | t0001 | g0330 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0313 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03516 | hp2 | a0013 | c0019 | t0003 | g0022 | AFR | ESN | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03540 | hp2 | a0005 | c0007 | t0002 | g0265 | AFR | GWD | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0106 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0198 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03654 | hp2 | a0004 | c0004 | t0001 | g0321 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0152 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03669 | hp2 | a0007 | c0012 | t0001 | g0175 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03831 | hp1 | a0007 | c0012 | t0001 | g0107 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0154 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0119 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04115 | hp2 | a0004 | c0004 | t0001 | g0320 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0155 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0039 | SAS | BEB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04204 | hp2 | a0003 | c0003 | t0001 | g0176 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0004 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18522 | hp2 | a0005 | c0007 | t0002 | g0266 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | CHB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18906 | hp1 | a0003 | c0003 | t0001 | g0148 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18940 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18947 | hp2 | a0002 | c0002 | t0004 | g0096 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18949 | hp2 | a0002 | c0002 | t0010 | g0059 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18953 | hp2 | a0001 | c0010 | t0002 | g0258 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18961 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18969 | hp1 | a0014 | c0018 | t0001 | g0192 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18986 | hp1 | a0002 | c0002 | t0019 | g0048 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18986 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18987 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18989 | hp1 | a0003 | c0003 | t0001 | g0177 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18994 | hp1 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18995 | hp2 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18999 | hp2 | a0004 | c0004 | t0001 | g0317 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19005 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19010 | hp1 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19011 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19012 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0150 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0167 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19043 | hp2 | a0004 | c0004 | t0018 | g0338 | AFR | LWK | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19055 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19057 | hp1 | a0015 | c0017 | t0002 | g0210 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19058 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19078 | hp2 | a0002 | c0002 | t0022 | g0076 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19080 | hp2 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19081 | hp1 | a0016 | c0016 | t0002 | g0294 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19084 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19240 | hp1 | a0001 | c0005 | t0003 | g0023 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA19240 | hp2 | a0004 | c0004 | t0001 | g0328 | AFR | YRI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ASW | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20129 | hp2 | a0002 | c0002 | t0013 | g0312 | AFR | ASW | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20752 | hp2 | a0004 | c0008 | t0005 | g0104 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20805 | hp1 | a0003 | c0003 | t0008 | g0171 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | TSI | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02109 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02109 | hp2 | a0004 | c0006 | t0001 | g0329 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03471 | hp1 | a0005 | c0007 | t0002 | g0268 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA18955 | hp2 | a0004 | c0004 | t0001 | g0336 | EAS | JPT | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | USA | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0195 | REF | REF | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0165 | REF | REF | SMC5_chr9_70253978_70359873 | SMC5 | chr9 | 70253978 | 70359873 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:70264314 | A | G | 1 | a0010 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.196A>G | p.Ile66Val | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/25 | 297/5949 | 196/3306 | 66/1101 | chr9 | 70264314 | |||
chr9:70264329 | C | G | 1 | a0011 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.211C>G | p.Pro71Ala | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/25 | 312/5949 | 211/3306 | 71/1101 | chr9 | 70264329 | |||
chr9:70277425 | G | T | 1 | a0012 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.496G>T | p.Ala166Ser | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/25 | 597/5949 | 496/3306 | 166/1101 | chr9 | 70277425 | |||
chr9:70277458 | C | G | 1 | a0013 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.529C>G | p.Gln177Glu | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/25 | 630/5949 | 529/3306 | 177/1101 | chr9 | 70277458 | |||
chr9:70282518 | G | A | 12 | a0001 a0002 a0004 others(9): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
missense_variant | MODERATE | c.916G>A | p.Val306Ile | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/25 | 1017/5949 | 916/3306 | 306/1101 | chr9 | 70282518 | |||
chr9:70282524 | T | C | 7 | a0002 a0004 a0006 others(4): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
missense_variant | MODERATE | c.922T>C | p.Cys308Arg | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/25 | 1023/5949 | 922/3306 | 308/1101 | chr9 | 70282524 | |||
chr9:70298125 | A | G | 1 | a0006 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1213A>G | p.Asn405Asp | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/25 | 1314/5949 | 1213/3306 | 405/1101 | chr9 | 70298125 | |||
chr9:70298137 | C | T | 1 | a0015 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1225C>T | p.Arg409Trp | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/25 | 1326/5949 | 1225/3306 | 409/1101 | chr9 | 70298137 | |||
chr9:70318858 | A | G | 2 | a0004 a0009 |
32 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
missense_variant | MODERATE | c.2045A>G | p.His682Arg | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/25 | 2146/5949 | 2045/3306 | 682/1101 | chr9 | 70318858 | |||
chr9:70323530 | G | A | 1 | a0005 | 6 | HG01358.hp2 HG02630.hp2 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.2198G>A | p.Arg733Gln | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/25 | 2299/5949 | 2198/3306 | 733/1101 | chr9 | 70323530 | |||
chr9:70324117 | G | A | 1 | a0009 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.2371G>A | p.Ala791Thr | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/25 | 2472/5949 | 2371/3306 | 791/1101 | chr9 | 70324117 | |||
chr9:70347640 | G | A | 1 | a0014 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.2692G>A | p.Glu898Lys | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 21/25 | 2793/5949 | 2692/3306 | 898/1101 | chr9 | 70347640 | |||
chr9:70347983 | A | G | 1 | a0016 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.2834A>G | p.Asn945Ser | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/25 | 2935/5949 | 2834/3306 | 945/1101 | chr9 | 70347983 | |||
chr9:70350160 | G | A | 1 | a0007 | 2 | HG03669.hp2 HG03831.hp1 |
missense_variant | MODERATE | c.2936G>A | p.Ser979Asn | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 23/25 | 3037/5949 | 2936/3306 | 979/1101 | chr9 | 70350160 | |||
chr9:70352303 | G | A | 1 | a0008 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.3278G>A | p.Arg1093His | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 3379/5949 | 3278/3306 | 1093/1101 | chr9 | 70352303 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:70264388 | G | A | 1 | a0004c0006 | 6 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
synonymous_variant | LOW | c.270G>A | p.Val90Val | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/25 | 371/5949 | 270/3306 | 90/1101 | chr9 | 70264388 | |||
chr9:70282547 | C | T | 1 | a0001c0010 | 3 | HG02040.hp2 HG02135.hp1 NA18953.hp2 |
synonymous_variant | LOW | c.945C>T | p.Asn315Asn | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/25 | 1046/5949 | 945/3306 | 315/1101 | chr9 | 70282547 | |||
chr9:70297998 | G | A | 1 | a0004c0008 | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1086G>A | p.Lys362Lys | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/25 | 1187/5949 | 1086/3306 | 362/1101 | chr9 | 70297998 | |||
chr9:70300125 | G | A | 1 | a0002c0013 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1389G>A | p.Thr463Thr | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/25 | 1490/5949 | 1389/3306 | 463/1101 | chr9 | 70300125 | |||
chr9:70318682 | C | T | 2 | a0001c0005 a0013c0019 |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.1975C>T | p.Leu659Leu | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 14/25 | 2076/5949 | 1975/3306 | 659/1101 | chr9 | 70318682 | |||
chr9:70318889 | A | G | 3 | a0002c0009 a0002c0013 a0012c0020 |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.2076A>G | p.Gln692Gln | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/25 | 2177/5949 | 2076/3306 | 692/1101 | chr9 | 70318889 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:70258992 | C | CGGGGCGC others(17): Show |
1 | a0002c0002t0010 | 1 | NA18949.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86_-63dupGGGGCGCC others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/25 | 62 | INFO_REALIGN_3_PRIME | chr9 | 70258992 | |||||
chr9:70259022 | G | C | 1 | a0009c0015t0011 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/25 | 57 | chr9 | 70259022 | ||||||
chr9:70352358 | A | T | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*27A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 27 | chr9 | 70352358 | ||||||
chr9:70352514 | A | G | 1 | a0001c0001t0023 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 183 | chr9 | 70352514 | ||||||
chr9:70352541 | G | A | 1 | a0010c0022t0012 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 210 | chr9 | 70352541 | ||||||
chr9:70352656 | T | C | 1 | a0002c0002t0013 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 325 | chr9 | 70352656 | ||||||
chr9:70352808 | C | T | 1 | a0002c0002t0022 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 477 | chr9 | 70352808 | ||||||
chr9:70352978 | AT | A | 2 | a0001c0005t0003 a0013c0019t0003 |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*648delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 648 | chr9 | 70352978 | ||||||
chr9:70353052 | G | A | 4 | a0002c0009t0006 a0002c0009t0014 a0002c0013t0006 others(1): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*721G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 721 | chr9 | 70353052 | ||||||
chr9:70353122 | A | G | 1 | a0004c0008t0005 | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*791A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 791 | chr9 | 70353122 | ||||||
chr9:70353240 | G | A | 1 | a0009c0015t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 909 | chr9 | 70353240 | ||||||
chr9:70353271 | C | A | 1 | a0001c0001t0023 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 940 | chr9 | 70353271 | ||||||
chr9:70353297 | A | G | 1 | a0001c0001t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 966 | chr9 | 70353297 | ||||||
chr9:70353646 | G | A | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1315G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1315 | chr9 | 70353646 | ||||||
chr9:70353714 | T | G | 2 | a0001c0005t0003 a0013c0019t0003 |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1383T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1383 | chr9 | 70353714 | ||||||
chr9:70353824 | G | A | 1 | a0001c0001t0015 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1493 | chr9 | 70353824 | ||||||
chr9:70353878 | G | A | 1 | a0001c0001t0016 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1547 | chr9 | 70353878 | ||||||
chr9:70353988 | G | C | 1 | a0001c0001t0017 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1657G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1657 | chr9 | 70353988 | ||||||
chr9:70354240 | T | G | 1 | a0001c0001t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1909T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 1909 | chr9 | 70354240 | ||||||
chr9:70354386 | C | G | 1 | a0003c0003t0020 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2055C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2055 | chr9 | 70354386 | ||||||
chr9:70354472 | G | A | 2 | a0001c0001t0007 a0002c0009t0014 |
4 | HG00738.hp1 HG01070.hp1 HG02615.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2141G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2141 | chr9 | 70354472 | ||||||
chr9:70354477 | G | A | 1 | a0004c0004t0018 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2146 | chr9 | 70354477 | ||||||
chr9:70354505 | G | A | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2174G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2174 | chr9 | 70354505 | ||||||
chr9:70354517 | A | G | 1 | a0006c0011t0009 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2186A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2186 | chr9 | 70354517 | ||||||
chr9:70354553 | C | T | 1 | a0002c0002t0004 | 7 | HG01943.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2222C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2222 | chr9 | 70354553 | ||||||
chr9:70354601 | A | T | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 others(8): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2270A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2270 | chr9 | 70354601 | ||||||
chr9:70354629 | A | C | 1 | a0004c0008t0005 | 5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2298A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2298 | chr9 | 70354629 | ||||||
chr9:70354738 | C | T | 1 | a0003c0003t0008 | 3 | HG01106.hp1 HG02145.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2407C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2407 | chr9 | 70354738 | ||||||
chr9:70354761 | C | G | 1 | a0002c0002t0019 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 25/25 | 2430 | chr9 | 70354761 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:70259267 | A | C | 1 | a0001c0001t0002g0340 | 1 | NA18945.hp1 | splice_region_variant&intron_variant | LOW | c.185+4A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259267 | |||||||
chr9:70259338 | G | A | 1 | a0001c0010t0002g0021 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.185+75G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259338 | |||||||
chr9:70259373 | G | A | 5 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+110G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259373 | |||||||
chr9:70259393 | C | G | 1 | a0003c0003t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.185+130C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259393 | |||||||
chr9:70259430 | A | G | 26 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(23): Show |
26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.185+167A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259430 | |||||||
chr9:70259434 | T | A | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+171T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259434 | |||||||
chr9:70259434 | T | G | 3 | a0002c0002t0001g0030 a0002c0002t0001g0031 a0002c0002t0001g0032 |
3 | NA18947.hp1 NA18969.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.185+171T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259434 | |||||||
chr9:70259437 | C | T | 7 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(4): Show |
7 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+174C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259437 | |||||||
chr9:70259556 | G | T | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+293G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259556 | |||||||
chr9:70259688 | C | T | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+425C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259688 | |||||||
chr9:70259715 | G | T | 1 | a0002c0002t0001g0311 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.185+452G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259715 | |||||||
chr9:70259777 | C | T | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.185+514C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259777 | |||||||
chr9:70259832 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.185+569C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259832 | |||||||
chr9:70259927 | C | CT | 9 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(6): Show |
9 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.185+681dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70259927 | ||||||
chr9:70259927 | CT | C | 115 | a0001c0001t0002g0105 a0002c0002t0001g0002 a0002c0002t0001g0003 others(112): Show |
123 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.185+681delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70259927 | ||||||
chr9:70259953 | T | A | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.185+690T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70259953 | |||||||
chr9:70260158 | G | T | 1 | a0002c0002t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.185+895G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260158 | |||||||
chr9:70260174 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.185+911G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260174 | |||||||
chr9:70260244 | A | G | 1 | a0001c0005t0003g0026 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.185+981A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260244 | |||||||
chr9:70260282 | A | G | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185+1019A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260282 | |||||||
chr9:70260294 | T | A | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.185+1031T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260294 | |||||||
chr9:70260469 | A | G | 1 | a0007c0012t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.185+1206A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260469 | |||||||
chr9:70260817 | C | T | 1 | a0003c0003t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.185+1554C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260817 | |||||||
chr9:70260895 | A | C | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+1632A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70260895 | |||||||
chr9:70261288 | A | T | 1 | a0001c0001t0002g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.185+2025A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70261288 | |||||||
chr9:70261559 | T | G | 1 | a0001c0001t0002g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.185+2296T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70261559 | |||||||
chr9:70261728 | T | C | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185+2465T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70261728 | |||||||
chr9:70262254 | T | C | 7 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(4): Show |
7 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-2050T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262254 | |||||||
chr9:70262533 | G | A | 1 | a0004c0004t0001g0313 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.186-1771G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262533 | |||||||
chr9:70262621 | A | G | 2 | a0003c0003t0001g0305 a0004c0004t0001g0336 |
2 | HG02615.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.186-1683A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262621 | |||||||
chr9:70262642 | A | C | 64 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(61): Show |
66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.186-1662A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262642 | |||||||
chr9:70262935 | G | A | 5 | a0001c0001t0002g0105 a0001c0001t0002g0115 a0001c0001t0002g0116 others(2): Show |
5 | HG01978.hp1 NA19004.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-1369G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262935 | |||||||
chr9:70262959 | C | CA | 57 | a0001c0001t0002g0306 a0001c0005t0003g0027 a0002c0002t0001g0002 others(54): Show |
63 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.186-1332dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70262959 | ||||||
chr9:70262967 | A | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.186-1337A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70262967 | |||||||
chr9:70263022 | G | A | 26 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(23): Show |
26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.186-1282G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263022 | |||||||
chr9:70263114 | T | C | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.186-1190T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263114 | |||||||
chr9:70263143 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-1161A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263143 | |||||||
chr9:70263206 | G | C | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.186-1098G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263206 | |||||||
chr9:70263244 | C | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.186-1060C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263244 | |||||||
chr9:70263431 | G | GA | 26 | a0001c0001t0002g0010 a0001c0001t0002g0120 a0001c0001t0002g0121 others(23): Show |
27 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.186-871dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70263431 | ||||||
chr9:70263689 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-615T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263689 | |||||||
chr9:70263778 | C | T | 1 | a0003c0003t0001g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-526C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263778 | |||||||
chr9:70263813 | A | G | 12 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0063 others(9): Show |
14 | HG00597.hp2 HG02523.hp1 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-491A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263813 | |||||||
chr9:70263908 | A | C | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.186-396A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263908 | |||||||
chr9:70263957 | G | A | 1 | a0001c0005t0003g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-347G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263957 | |||||||
chr9:70263962 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.186-342G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70263962 | |||||||
chr9:70264106 | TTTAG | T | 5 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0299 others(2): Show |
5 | HG00544.hp2 HG00609.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-194_186-191del others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr9 | 70264106 | ||||||
chr9:70264140 | A | G | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.186-164A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 1/24 | chr9 | 70264140 | |||||||
chr9:70264559 | C | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.327+114C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264559 | |||||||
chr9:70264623 | T | C | 127 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(124): Show |
135 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.327+178T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264623 | |||||||
chr9:70264684 | G | A | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+239G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264684 | |||||||
chr9:70264706 | C | G | 1 | a0002c0002t0004g0096 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.327+261C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264706 | |||||||
chr9:70264748 | AC | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+304delC | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264748 | |||||||
chr9:70264859 | G | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.327+414G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264859 | |||||||
chr9:70264898 | T | C | 6 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(3): Show |
6 | HG00738.hp2 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+453T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70264898 | |||||||
chr9:70265079 | A | T | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+634A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265079 | |||||||
chr9:70265156 | A | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.327+711A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265156 | |||||||
chr9:70265201 | G | A | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.327+756G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265201 | |||||||
chr9:70265204 | C | T | 1 | a0003c0003t0001g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.327+759C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265204 | |||||||
chr9:70265328 | G | A | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.327+883G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265328 | |||||||
chr9:70265338 | A | T | 1 | a0004c0004t0001g0336 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.327+893A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265338 | |||||||
chr9:70265635 | A | T | 1 | a0001c0001t0002g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.327+1190A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265635 | |||||||
chr9:70265758 | A | G | 1 | a0001c0001t0002g0295 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.327+1313A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70265758 | |||||||
chr9:70266285 | T | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328-1638T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266285 | |||||||
chr9:70266307 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328-1616T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266307 | |||||||
chr9:70266320 | C | G | 1 | a0002c0002t0001g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.328-1603C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266320 | |||||||
chr9:70266335 | T | G | 1 | a0002c0002t0001g0063 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.328-1588T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266335 | |||||||
chr9:70266393 | A | G | 1 | a0003c0003t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328-1530A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266393 | |||||||
chr9:70266831 | C | A | 129 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(126): Show |
138 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.328-1092C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266831 | |||||||
chr9:70266850 | A | G | 1 | a0002c0002t0001g0063 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.328-1073A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70266850 | |||||||
chr9:70267032 | CT | C | 118 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(115): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.328-875delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr9 | 70267032 | ||||||
chr9:70267082 | A | G | 1 | a0003c0003t0001g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.328-841A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267082 | |||||||
chr9:70267095 | A | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.328-828A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267095 | |||||||
chr9:70267329 | A | G | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.328-594A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267329 | |||||||
chr9:70267472 | T | C | 1 | a0002c0002t0001g0074 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.328-451T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267472 | |||||||
chr9:70267539 | T | C | 1 | a0003c0003t0001g0151 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.328-384T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267539 | |||||||
chr9:70267581 | G | A | 4 | a0002c0002t0001g0064 a0002c0002t0001g0065 a0002c0002t0001g0066 others(1): Show |
4 | NA18950.hp2 NA18995.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-342G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267581 | |||||||
chr9:70267726 | A | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.328-197A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267726 | |||||||
chr9:70267859 | A | G | 3 | a0001c0001t0002g0299 a0001c0001t0002g0300 a0001c0001t0002g0301 |
3 | NA18965.hp1 NA18966.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.328-64A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267859 | |||||||
chr9:70267876 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.328-47C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267876 | |||||||
chr9:70267920 | T | C | 3 | a0004c0004t0001g0314 a0004c0004t0001g0315 a0004c0004t0001g0316 |
3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.328-3T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 2/24 | chr9 | 70267920 | |||||||
chr9:70268119 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+144T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268119 | |||||||
chr9:70268462 | C | A | 63 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(60): Show |
65 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.380+487C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268462 | |||||||
chr9:70268462 | C | CA | 51 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(48): Show |
57 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.380+497dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70268462 | ||||||
chr9:70268524 | C | T | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.380+549C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268524 | |||||||
chr9:70268697 | T | G | 1 | a0003c0003t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.380+722T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268697 | |||||||
chr9:70268698 | T | C | 1 | a0003c0003t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.380+723T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268698 | |||||||
chr9:70268780 | G | C | 6 | a0003c0003t0001g0145 a0003c0003t0001g0152 a0003c0003t0001g0153 others(3): Show |
6 | HG01496.hp2 HG02300.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.380+805G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70268780 | |||||||
chr9:70269206 | A | G | 1 | a0004c0004t0001g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.380+1231A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70269206 | |||||||
chr9:70269439 | A | C | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+1464A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70269439 | |||||||
chr9:70270095 | A | T | 1 | a0002c0002t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.380+2120A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270095 | |||||||
chr9:70270115 | C | T | 3 | a0004c0004t0001g0314 a0004c0004t0001g0315 a0004c0004t0001g0316 |
3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.380+2140C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270115 | |||||||
chr9:70270117 | A | C | 1 | a0016c0016t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.380+2142A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270117 | |||||||
chr9:70270161 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2186T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270161 | |||||||
chr9:70270189 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2214C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270189 | |||||||
chr9:70270351 | T | C | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.380+2376T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270351 | |||||||
chr9:70270376 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2401C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270376 | |||||||
chr9:70270458 | A | T | 1 | a0004c0004t0001g0313 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.380+2483A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270458 | |||||||
chr9:70270459 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.380+2484T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270459 | |||||||
chr9:70270549 | G | C | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.380+2574G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270549 | |||||||
chr9:70270642 | A | AT | 27 | a0001c0001t0002g0144 a0001c0001t0002g0199 a0001c0001t0002g0202 others(24): Show |
27 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.380+2691dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | ||||||
chr9:70270642 | A | ATT | 86 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(83): Show |
94 | HG00099.hp2 HG00597.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.380+2690_380+2691d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | ||||||
chr9:70270642 | A | ATTT | 16 | a0002c0002t0001g0032 a0002c0002t0001g0060 a0002c0002t0001g0061 others(13): Show |
16 | HG01099.hp1 HG01106.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.380+2689_380+2691d others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | ||||||
chr9:70270642 | AT | A | 63 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0115 others(60): Show |
68 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.380+2691delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70270642 | ||||||
chr9:70270710 | A | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+2735A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270710 | |||||||
chr9:70270725 | C | G | 1 | a0004c0008t0005g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.380+2750C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270725 | |||||||
chr9:70270844 | G | A | 11 | a0003c0003t0001g0012 a0003c0003t0001g0156 a0003c0003t0001g0157 others(8): Show |
12 | HG01361.hp1 HG01978.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.380+2869G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270844 | |||||||
chr9:70270893 | C | T | 109 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(106): Show |
119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.380+2918C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270893 | |||||||
chr9:70270902 | C | G | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.380+2927C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70270902 | |||||||
chr9:70271005 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.380+3030G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271005 | |||||||
chr9:70271105 | A | T | 1 | a0001c0001t0002g0248 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.380+3130A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271105 | |||||||
chr9:70271141 | GTTTTGGA others(10): Show |
G | 220 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(217): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.380+3182_380+3198d others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70271141 | ||||||
chr9:70271212 | A | T | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.380+3237A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271212 | |||||||
chr9:70271340 | G | A | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+3365G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271340 | |||||||
chr9:70271437 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.380+3462A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271437 | |||||||
chr9:70271610 | A | G | 1 | a0014c0018t0001g0192 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.380+3635A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271610 | |||||||
chr9:70271624 | G | A | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+3649G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271624 | |||||||
chr9:70271733 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0254 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.380+3758G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271733 | |||||||
chr9:70271786 | G | A | 1 | a0002c0002t0001g0035 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.380+3811G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70271786 | |||||||
chr9:70272113 | C | G | 1 | a0001c0001t0023g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.380+4138C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272113 | |||||||
chr9:70272127 | A | C | 1 | a0001c0001t0023g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.380+4152A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272127 | |||||||
chr9:70272217 | C | G | 1 | a0003c0003t0001g0191 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.380+4242C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272217 | |||||||
chr9:70272494 | T | A | 109 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(106): Show |
119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.380+4519T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272494 | |||||||
chr9:70272540 | C | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.380+4565C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272540 | |||||||
chr9:70272750 | T | C | 1 | a0001c0001t0002g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.381-4560T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272750 | |||||||
chr9:70272769 | A | C | 1 | a0004c0006t0001g0333 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.381-4541A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70272769 | |||||||
chr9:70273049 | G | C | 1 | a0002c0002t0022g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.381-4261G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273049 | |||||||
chr9:70273064 | A | G | 1 | a0002c0002t0010g0059 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.381-4246A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273064 | |||||||
chr9:70273189 | C | CT | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.381-4110dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70273189 | ||||||
chr9:70273212 | G | A | 1 | a0003c0003t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.381-4098G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273212 | |||||||
chr9:70273326 | A | AT | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.381-3979dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70273326 | ||||||
chr9:70273361 | C | T | 32 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(29): Show |
32 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.381-3949C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273361 | |||||||
chr9:70273470 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381-3840A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273470 | |||||||
chr9:70273596 | C | T | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.381-3714C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273596 | |||||||
chr9:70273740 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0118 |
2 | HG01978.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.381-3570A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273740 | |||||||
chr9:70273974 | A | G | 33 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(30): Show |
34 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.381-3336A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70273974 | |||||||
chr9:70274142 | C | T | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381-3168C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274142 | |||||||
chr9:70274171 | T | C | 1 | a0003c0003t0001g0146 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381-3139T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274171 | |||||||
chr9:70274183 | G | A | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.381-3127G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274183 | |||||||
chr9:70274207 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-3103G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274207 | |||||||
chr9:70274275 | G | T | 5 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(2): Show |
5 | HG00544.hp1 HG00642.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-3035G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274275 | |||||||
chr9:70274324 | A | G | 1 | a0004c0004t0001g0336 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.381-2986A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274324 | |||||||
chr9:70274377 | G | A | 5 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-2933G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274377 | |||||||
chr9:70274469 | C | CT | 6 | a0001c0001t0002g0288 a0004c0008t0005g0100 a0004c0008t0005g0101 others(3): Show |
6 | HG00738.hp2 HG01433.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.381-2829dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70274469 | ||||||
chr9:70274470 | T | C | 1 | a0002c0002t0001g0112 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.381-2840T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274470 | |||||||
chr9:70274496 | A | C | 46 | a0003c0003t0001g0012 a0003c0003t0001g0014 a0003c0003t0001g0119 others(43): Show |
48 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.381-2814A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274496 | |||||||
chr9:70274548 | T | C | 6 | a0003c0003t0001g0170 a0003c0003t0001g0172 a0003c0003t0001g0173 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-2762T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274548 | |||||||
chr9:70274565 | A | T | 1 | a0001c0005t0003g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.381-2745A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274565 | |||||||
chr9:70274880 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-2430G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274880 | |||||||
chr9:70274908 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381-2402A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274908 | |||||||
chr9:70274933 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-2377A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274933 | |||||||
chr9:70274996 | C | A | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381-2314C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70274996 | |||||||
chr9:70275347 | C | T | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.381-1963C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275347 | |||||||
chr9:70275415 | G | A | 2 | a0003c0003t0001g0147 a0003c0003t0001g0305 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.381-1895G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275415 | |||||||
chr9:70275446 | C | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381-1864C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275446 | |||||||
chr9:70275493 | A | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381-1817A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275493 | |||||||
chr9:70275505 | T | G | 5 | a0002c0002t0001g0002 a0002c0002t0001g0036 a0002c0002t0001g0037 others(2): Show |
7 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.381-1805T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275505 | |||||||
chr9:70275516 | AATGTGAA others(53): Show |
A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-1685_381-1626d others(62): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr9 | 70275516 | ||||||
chr9:70275615 | C | A | 32 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(29): Show |
32 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.381-1695C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275615 | |||||||
chr9:70275710 | T | C | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-1600T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275710 | |||||||
chr9:70275798 | G | A | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.381-1512G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275798 | |||||||
chr9:70275938 | G | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381-1372G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275938 | |||||||
chr9:70275998 | TG | T | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-1311delG | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70275998 | |||||||
chr9:70276070 | G | A | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-1240G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276070 | |||||||
chr9:70276232 | C | A | 1 | a0001c0001t0002g0209 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.381-1078C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276232 | |||||||
chr9:70276659 | T | C | 1 | a0003c0003t0001g0174 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.381-651T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276659 | |||||||
chr9:70276722 | C | T | 1 | a0002c0002t0004g0096 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.381-588C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276722 | |||||||
chr9:70276911 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.381-399G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276911 | |||||||
chr9:70276912 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.381-398G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70276912 | |||||||
chr9:70277022 | C | T | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.381-288C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 3/24 | chr9 | 70277022 | |||||||
chr9:70277534 | G | A | 2 | a0003c0003t0001g0145 a0003c0003t0001g0152 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.543+62G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277534 | |||||||
chr9:70277718 | A | G | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.543+246A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277718 | |||||||
chr9:70277756 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.543+284C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277756 | |||||||
chr9:70277759 | T | C | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+287T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277759 | |||||||
chr9:70277803 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+331A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277803 | |||||||
chr9:70277854 | CTATATT | C | 9 | a0004c0004t0001g0317 a0004c0004t0001g0318 a0004c0004t0001g0319 others(6): Show |
9 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+387_543+392del others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 70277854 | ||||||
chr9:70277993 | T | C | 1 | a0003c0003t0008g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-498T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70277993 | |||||||
chr9:70278020 | CAAT | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.544-470_544-468del others(3): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278020 | |||||||
chr9:70278077 | T | C | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-414T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278077 | |||||||
chr9:70278126 | G | A | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-365G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278126 | |||||||
chr9:70278382 | GT | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.544-101delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr9 | 70278382 | ||||||
chr9:70278433 | A | T | 1 | a0001c0001t0002g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.544-58A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 4/24 | chr9 | 70278433 | |||||||
chr9:70278663 | T | C | 1 | a0001c0001t0002g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.678+38T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278663 | |||||||
chr9:70278701 | A | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.678+76A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278701 | |||||||
chr9:70278775 | G | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.678+150G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278775 | |||||||
chr9:70278838 | C | T | 2 | a0003c0003t0001g0189 a0003c0003t0020g0190 |
2 | HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.678+213C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278838 | |||||||
chr9:70278928 | A | G | 1 | a0001c0005t0003g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.678+303A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70278928 | |||||||
chr9:70279181 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.678+556C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279181 | |||||||
chr9:70279266 | A | C | 2 | a0002c0002t0001g0090 a0002c0002t0001g0091 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.678+641A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279266 | |||||||
chr9:70279407 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.678+782C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279407 | |||||||
chr9:70279415 | A | T | 1 | a0001c0005t0003g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.678+790A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279415 | |||||||
chr9:70279513 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.678+888T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279513 | |||||||
chr9:70279661 | A | G | 6 | a0002c0002t0004g0008 a0002c0002t0004g0086 a0002c0002t0004g0087 others(3): Show |
7 | HG01943.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.678+1036A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279661 | |||||||
chr9:70279674 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.678+1049G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279674 | |||||||
chr9:70279678 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.678+1053G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279678 | |||||||
chr9:70279689 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.678+1064C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279689 | |||||||
chr9:70279732 | G | A | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.679-1027G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279732 | |||||||
chr9:70279813 | G | A | 2 | a0001c0010t0002g0021 a0001c0010t0002g0258 |
2 | HG02040.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.679-946G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279813 | |||||||
chr9:70279817 | C | CA | 14 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0259 others(11): Show |
14 | HG00544.hp1 HG00733.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.679-921dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr9 | 70279817 | ||||||
chr9:70279817 | CA | C | 33 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0256 others(30): Show |
35 | HG00323.hp1 HG00609.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.679-921delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr9 | 70279817 | ||||||
chr9:70279817 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0001g0057 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.679-931_679-921del others(11): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr9 | 70279817 | ||||||
chr9:70279911 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.679-848G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70279911 | |||||||
chr9:70280080 | G | A | 1 | a0001c0005t0003g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.679-679G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280080 | |||||||
chr9:70280131 | G | A | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.679-628G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280131 | |||||||
chr9:70280208 | C | T | 1 | a0003c0003t0001g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.679-551C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280208 | |||||||
chr9:70280426 | A | G | 1 | a0003c0003t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.679-333A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280426 | |||||||
chr9:70280449 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.679-310A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280449 | |||||||
chr9:70280466 | T | G | 5 | a0004c0006t0001g0324 a0004c0006t0001g0325 a0004c0006t0001g0326 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.679-293T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 5/24 | chr9 | 70280466 | |||||||
chr9:70280928 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.819+29C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70280928 | |||||||
chr9:70281107 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.819+208G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281107 | |||||||
chr9:70281112 | A | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.819+213A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281112 | |||||||
chr9:70281133 | G | A | 1 | a0004c0004t0001g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.819+234G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281133 | |||||||
chr9:70281193 | C | T | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.819+294C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281193 | |||||||
chr9:70281204 | C | T | 2 | a0003c0003t0001g0155 a0003c0003t0001g0197 |
2 | HG01496.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.819+305C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281204 | |||||||
chr9:70281262 | G | A | 4 | a0001c0001t0002g0140 a0001c0001t0002g0142 a0001c0001t0002g0143 others(1): Show |
4 | HG00544.hp1 HG00642.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+363G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281262 | |||||||
chr9:70281267 | C | A | 118 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(115): Show |
126 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.819+368C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281267 | |||||||
chr9:70281319 | T | C | 120 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(117): Show |
128 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.819+420T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281319 | |||||||
chr9:70281332 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0255 a0001c0001t0002g0256 |
3 | HG01175.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.819+433G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281332 | |||||||
chr9:70281512 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.819+613G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281512 | |||||||
chr9:70281543 | G | A | 2 | a0004c0004t0001g0330 a0004c0004t0001g0331 |
2 | HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.819+644G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281543 | |||||||
chr9:70281571 | T | C | 2 | a0003c0003t0001g0012 a0003c0003t0001g0164 |
3 | NA18987.hp2 NA19055.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.819+672T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281571 | |||||||
chr9:70281683 | G | C | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820-739G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281683 | |||||||
chr9:70281749 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.820-673G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281749 | |||||||
chr9:70281780 | A | G | 1 | a0004c0004t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.820-642A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281780 | |||||||
chr9:70281842 | CT | C | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.820-573delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr9 | 70281842 | ||||||
chr9:70281850 | C | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.820-572C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281850 | |||||||
chr9:70281898 | T | A | 1 | a0001c0010t0002g0258 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.820-524T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281898 | |||||||
chr9:70281959 | G | A | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.820-463G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70281959 | |||||||
chr9:70282039 | G | GT | 6 | a0001c0001t0002g0285 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG00738.hp1 HG01070.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-371dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr9 | 70282039 | ||||||
chr9:70282041 | T | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-381T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282041 | |||||||
chr9:70282051 | T | TTC | 115 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(112): Show |
123 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.820-371_820-370ins others(2): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282051 | |||||||
chr9:70282172 | G | T | 1 | a0001c0001t0002g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.820-250G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282172 | |||||||
chr9:70282213 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.820-209G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282213 | |||||||
chr9:70282384 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.820-38G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 6/24 | chr9 | 70282384 | |||||||
chr9:70282600 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.981+17A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282600 | |||||||
chr9:70282625 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.981+42T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282625 | |||||||
chr9:70282857 | C | T | 5 | a0003c0003t0001g0004 a0003c0003t0001g0013 a0003c0003t0001g0166 others(2): Show |
8 | HG02109.hp1 HG02723.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.981+274C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282857 | |||||||
chr9:70282997 | A | G | 1 | a0003c0003t0008g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.981+414A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70282997 | |||||||
chr9:70283054 | A | G | 57 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(54): Show |
59 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.981+471A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283054 | |||||||
chr9:70283109 | G | A | 7 | a0004c0004t0001g0337 a0004c0008t0005g0100 a0004c0008t0005g0101 others(4): Show |
7 | HG00738.hp2 HG01433.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+526G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283109 | |||||||
chr9:70283192 | A | C | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.981+609A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283192 | |||||||
chr9:70283235 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.981+652G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283235 | |||||||
chr9:70283238 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.981+655C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283238 | |||||||
chr9:70283625 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.981+1042C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283625 | |||||||
chr9:70283717 | T | C | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.981+1134T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283717 | |||||||
chr9:70283795 | A | AT | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+1221dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 70283795 | ||||||
chr9:70283977 | T | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.981+1394T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70283977 | |||||||
chr9:70284173 | C | T | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.981+1590C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284173 | |||||||
chr9:70284225 | A | C | 1 | a0004c0004t0001g0332 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.981+1642A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284225 | |||||||
chr9:70284358 | A | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.981+1775A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284358 | |||||||
chr9:70284556 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.982-1644A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284556 | |||||||
chr9:70284567 | G | C | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-1633G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284567 | |||||||
chr9:70284610 | C | G | 2 | a0003c0003t0001g0189 a0003c0003t0020g0190 |
2 | HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.982-1590C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284610 | |||||||
chr9:70284641 | A | T | 1 | a0001c0005t0003g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.982-1559A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284641 | |||||||
chr9:70284649 | C | T | 1 | a0002c0002t0001g0056 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.982-1551C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284649 | |||||||
chr9:70284740 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-1460G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284740 | |||||||
chr9:70284890 | AT | A | 28 | a0001c0001t0002g0298 a0002c0002t0001g0007 a0002c0002t0001g0073 others(25): Show |
30 | HG00609.hp2 HG00673.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.982-1298delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 70284890 | ||||||
chr9:70284904 | A | G | 1 | a0003c0003t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.982-1296A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284904 | |||||||
chr9:70284920 | G | A | 334 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.982-1280G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284920 | |||||||
chr9:70284951 | A | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-1249A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70284951 | |||||||
chr9:70285024 | T | TA | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-1175dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr9 | 70285024 | ||||||
chr9:70285238 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-962A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285238 | |||||||
chr9:70285294 | A | C | 6 | a0001c0001t0002g0120 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
6 | HG00438.hp1 HG00597.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.982-906A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285294 | |||||||
chr9:70285373 | A | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.982-827A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285373 | |||||||
chr9:70285432 | G | A | 8 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0250 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-768G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285432 | |||||||
chr9:70285443 | A | G | 25 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0122 others(22): Show |
26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.982-757A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285443 | |||||||
chr9:70285583 | A | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.982-617A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285583 | |||||||
chr9:70285638 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-562G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285638 | |||||||
chr9:70285802 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.982-398A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285802 | |||||||
chr9:70285868 | A | G | 2 | a0004c0004t0001g0322 a0004c0004t0001g0323 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.982-332A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70285868 | |||||||
chr9:70286176 | C | T | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.982-24C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70286176 | |||||||
chr9:70286180 | T | C | 332 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(329): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.982-20T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 7/24 | chr9 | 70286180 | |||||||
chr9:70286343 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+72A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286343 | |||||||
chr9:70286404 | G | T | 5 | a0001c0001t0002g0208 a0001c0001t0002g0237 a0001c0001t0002g0254 others(2): Show |
5 | HG02647.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+133G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286404 | |||||||
chr9:70286490 | T | C | 1 | a0004c0004t0001g0330 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1053+219T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286490 | |||||||
chr9:70286562 | G | C | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1053+291G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286562 | |||||||
chr9:70286639 | T | C | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+368T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286639 | |||||||
chr9:70286650 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1053+379C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286650 | |||||||
chr9:70286651 | G | T | 5 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+380G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286651 | |||||||
chr9:70286717 | C | CT | 10 | a0001c0001t0002g0136 a0001c0001t0002g0138 a0001c0001t0002g0139 others(7): Show |
10 | HG02145.hp2 HG02300.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+467dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70286717 | ||||||
chr9:70286717 | CT | C | 118 | a0001c0001t0002g0123 a0001c0005t0003g0023 a0001c0005t0003g0024 others(115): Show |
125 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.1053+467delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70286717 | ||||||
chr9:70286717 | CTT | C | 6 | a0002c0002t0001g0090 a0002c0002t0001g0092 a0003c0003t0001g0145 others(3): Show |
6 | HG00323.hp1 HG01099.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+466_1053+467d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70286717 | ||||||
chr9:70286991 | G | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1053+720G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70286991 | |||||||
chr9:70287109 | C | A | 2 | a0001c0001t0002g0211 a0001c0001t0015g0261 |
2 | NA18944.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1053+838C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287109 | |||||||
chr9:70287149 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+878A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287149 | |||||||
chr9:70287156 | A | T | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+885A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287156 | |||||||
chr9:70287159 | T | G | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+888T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287159 | |||||||
chr9:70287470 | A | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1053+1199A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287470 | |||||||
chr9:70287485 | T | G | 1 | a0001c0001t0002g0262 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1053+1214T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287485 | |||||||
chr9:70287501 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+1230A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287501 | |||||||
chr9:70287583 | T | C | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+1312T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287583 | |||||||
chr9:70287587 | G | A | 52 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(49): Show |
57 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1053+1316G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287587 | |||||||
chr9:70287591 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+1320A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287591 | |||||||
chr9:70287755 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+1484G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287755 | |||||||
chr9:70287820 | AAGAATTT others(18): Show |
A | 1 | a0002c0002t0001g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1550_1053+157 others(29): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287820 | |||||||
chr9:70287829 | TG | T | 25 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(22): Show |
27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1053+1562delG | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70287829 | ||||||
chr9:70287846 | T | G | 1 | a0002c0002t0001g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1575T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287846 | |||||||
chr9:70287848 | T | C | 1 | a0002c0002t0001g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1577T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287848 | |||||||
chr9:70287849 | A | C | 1 | a0002c0002t0001g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1578A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287849 | |||||||
chr9:70287851 | T | A | 1 | a0002c0002t0001g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1053+1580T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70287851 | |||||||
chr9:70288041 | C | T | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1053+1770C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288041 | |||||||
chr9:70288088 | T | C | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1053+1817T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288088 | |||||||
chr9:70288116 | G | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+1845G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288116 | |||||||
chr9:70288238 | G | A | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+1967G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288238 | |||||||
chr9:70288238 | G | T | 64 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(61): Show |
66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1053+1967G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288238 | |||||||
chr9:70288445 | A | T | 5 | a0004c0004t0001g0314 a0004c0004t0001g0315 a0004c0004t0001g0316 others(2): Show |
5 | HG01099.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+2174A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288445 | |||||||
chr9:70288455 | TTTA | T | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1053+2187_1053+218 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70288455 | ||||||
chr9:70288499 | A | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1053+2228A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288499 | |||||||
chr9:70288528 | T | C | 1 | a0007c0012t0001g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1053+2257T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288528 | |||||||
chr9:70288851 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1053+2580G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288851 | |||||||
chr9:70288983 | T | C | 4 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053+2712T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288983 | |||||||
chr9:70288991 | C | T | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+2720C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70288991 | |||||||
chr9:70289026 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1053+2755A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289026 | |||||||
chr9:70289060 | C | T | 2 | a0004c0004t0001g0322 a0004c0004t0001g0323 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1053+2789C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289060 | |||||||
chr9:70289064 | G | T | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+2793G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289064 | |||||||
chr9:70289074 | G | A | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+2803G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289074 | |||||||
chr9:70289132 | G | A | 2 | a0001c0001t0002g0140 a0001c0001t0002g0143 |
2 | HG00544.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1053+2861G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289132 | |||||||
chr9:70289239 | C | T | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1053+2968C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289239 | |||||||
chr9:70289303 | G | A | 332 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(329): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1053+3032G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289303 | |||||||
chr9:70289532 | G | A | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+3261G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289532 | |||||||
chr9:70289875 | A | ATAT | 40 | a0001c0001t0021g0310 a0001c0005t0003g0027 a0002c0002t0001g0063 others(37): Show |
40 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1053+3627_1053+362 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70289875 | ||||||
chr9:70289875 | A | ATATTAT | 29 | a0002c0002t0001g0007 a0002c0002t0001g0035 a0002c0002t0001g0042 others(26): Show |
31 | HG00673.hp1 HG00673.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1053+3624_1053+362 others(10): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70289875 | ||||||
chr9:70289961 | C | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+3690C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289961 | |||||||
chr9:70289969 | G | A | 2 | a0004c0004t0001g0328 a0004c0004t0001g0332 |
2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1053+3698G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70289969 | |||||||
chr9:70290052 | A | T | 60 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0105 others(57): Show |
65 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1053+3781A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290052 | |||||||
chr9:70290446 | G | A | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1053+4175G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290446 | |||||||
chr9:70290488 | G | A | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1053+4217G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290488 | |||||||
chr9:70290558 | T | C | 1 | a0001c0001t0017g0214 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1053+4287T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290558 | |||||||
chr9:70290825 | A | T | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+4554A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290825 | |||||||
chr9:70290839 | A | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+4568A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70290839 | |||||||
chr9:70291006 | T | G | 7 | a0001c0001t0002g0209 a0001c0001t0002g0215 a0001c0001t0002g0216 others(4): Show |
7 | HG00735.hp1 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1053+4735T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291006 | |||||||
chr9:70291128 | CTAGT | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+4859_1053+486 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70291128 | ||||||
chr9:70291168 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+4897T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291168 | |||||||
chr9:70291196 | G | A | 5 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+4925G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291196 | |||||||
chr9:70291235 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+4964T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291235 | |||||||
chr9:70291553 | A | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1053+5282A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291553 | |||||||
chr9:70291610 | A | G | 1 | a0002c0002t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1053+5339A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291610 | |||||||
chr9:70291755 | A | G | 4 | a0002c0002t0001g0053 a0002c0002t0001g0054 a0002c0002t0001g0055 others(1): Show |
4 | NA18953.hp1 NA18963.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+5484A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291755 | |||||||
chr9:70291778 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1053+5507C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291778 | |||||||
chr9:70291845 | AT | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1053+5586delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70291845 | ||||||
chr9:70291925 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+5654A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291925 | |||||||
chr9:70291972 | T | G | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1053+5701T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291972 | |||||||
chr9:70291985 | G | A | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053+5714G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70291985 | |||||||
chr9:70292052 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1053+5781A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292052 | |||||||
chr9:70292176 | AC | A | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1054-5788delC | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70292176 | ||||||
chr9:70292228 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1054-5738G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292228 | |||||||
chr9:70292293 | C | T | 1 | a0003c0003t0001g0172 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1054-5673C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292293 | |||||||
chr9:70292341 | T | C | 1 | a0003c0003t0001g0157 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1054-5625T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292341 | |||||||
chr9:70292345 | A | G | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-5621A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292345 | |||||||
chr9:70292349 | G | A | 1 | a0003c0003t0001g0176 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1054-5617G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292349 | |||||||
chr9:70292451 | A | C | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054-5515A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292451 | |||||||
chr9:70292691 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1054-5275A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292691 | |||||||
chr9:70292791 | T | C | 5 | a0004c0004t0001g0318 a0004c0004t0001g0319 a0004c0004t0001g0322 others(2): Show |
5 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-5175T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292791 | |||||||
chr9:70292897 | C | T | 1 | a0003c0003t0001g0163 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1054-5069C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70292897 | |||||||
chr9:70293156 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-4810G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293156 | |||||||
chr9:70293265 | A | G | 1 | a0003c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1054-4701A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293265 | |||||||
chr9:70293380 | C | G | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-4586C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293380 | |||||||
chr9:70293458 | C | G | 64 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(61): Show |
66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1054-4508C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293458 | |||||||
chr9:70293535 | T | G | 1 | a0004c0006t0001g0335 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1054-4431T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293535 | |||||||
chr9:70293580 | A | G | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1054-4386A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293580 | |||||||
chr9:70293588 | C | T | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1054-4378C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293588 | |||||||
chr9:70293839 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-4127T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293839 | |||||||
chr9:70293963 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1054-4003G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70293963 | |||||||
chr9:70294079 | G | C | 2 | a0001c0001t0002g0211 a0001c0001t0015g0261 |
2 | NA18944.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1054-3887G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294079 | |||||||
chr9:70294196 | G | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-3770G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294196 | |||||||
chr9:70294331 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1054-3635G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294331 | |||||||
chr9:70294422 | A | G | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1054-3544A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294422 | |||||||
chr9:70294489 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-3477G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294489 | |||||||
chr9:70294706 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1054-3260A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294706 | |||||||
chr9:70294817 | G | C | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1054-3149G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70294817 | |||||||
chr9:70295046 | A | T | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1054-2920A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295046 | |||||||
chr9:70295066 | C | T | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1054-2900C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295066 | |||||||
chr9:70295069 | C | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-2897C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295069 | |||||||
chr9:70295203 | C | A | 2 | a0003c0003t0001g0170 a0003c0003t0001g0173 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1054-2763C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295203 | |||||||
chr9:70295232 | A | G | 1 | a0001c0001t0002g0298 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1054-2734A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295232 | |||||||
chr9:70295250 | G | T | 2 | a0004c0004t0001g0317 a0004c0004t0001g0336 |
2 | NA18955.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1054-2716G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295250 | |||||||
chr9:70295301 | TA | T | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1054-2654delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70295301 | ||||||
chr9:70295329 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1054-2637G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295329 | |||||||
chr9:70295361 | C | T | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-2605C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295361 | |||||||
chr9:70295363 | C | T | 116 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(113): Show |
124 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1054-2603C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295363 | |||||||
chr9:70295425 | T | G | 1 | a0004c0004t0001g0332 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1054-2541T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295425 | |||||||
chr9:70295470 | C | CA | 60 | a0001c0001t0016g0290 a0002c0002t0001g0007 a0002c0002t0001g0041 others(57): Show |
62 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1054-2479dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70295470 | ||||||
chr9:70295470 | C | CAA | 48 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(45): Show |
54 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1054-2480_1054-247 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70295470 | ||||||
chr9:70295485 | A | G | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-2481A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295485 | |||||||
chr9:70295515 | A | G | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-2451A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295515 | |||||||
chr9:70295577 | C | T | 1 | a0003c0003t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1054-2389C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295577 | |||||||
chr9:70295649 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1054-2317G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295649 | |||||||
chr9:70295681 | A | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-2285A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295681 | |||||||
chr9:70295705 | G | A | 3 | a0004c0004t0001g0314 a0004c0004t0001g0315 a0004c0004t0001g0316 |
3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1054-2261G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295705 | |||||||
chr9:70295748 | C | T | 3 | a0001c0001t0002g0199 a0001c0001t0002g0213 a0001c0001t0002g0276 |
3 | HG01168.hp2 HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1054-2218C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295748 | |||||||
chr9:70295764 | C | A | 4 | a0003c0003t0001g0014 a0003c0003t0001g0178 a0003c0003t0001g0179 others(1): Show |
5 | NA18940.hp2 NA18954.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-2202C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295764 | |||||||
chr9:70295817 | G | A | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1054-2149G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295817 | |||||||
chr9:70295833 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-2133G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295833 | |||||||
chr9:70295885 | A | G | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1054-2081A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295885 | |||||||
chr9:70295909 | G | A | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1054-2057G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295909 | |||||||
chr9:70295968 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1054-1998C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295968 | |||||||
chr9:70295971 | T | C | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-1995T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70295971 | |||||||
chr9:70296036 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-1930G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296036 | |||||||
chr9:70296269 | A | G | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1054-1697A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296269 | |||||||
chr9:70296318 | A | G | 109 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(106): Show |
119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1054-1648A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296318 | |||||||
chr9:70296425 | G | A | 8 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0250 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1054-1541G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296425 | |||||||
chr9:70296466 | A | G | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1054-1500A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296466 | |||||||
chr9:70296524 | G | T | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1054-1442G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296524 | |||||||
chr9:70296532 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1054-1434A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296532 | |||||||
chr9:70296534 | C | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-1432C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296534 | |||||||
chr9:70296539 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-1427T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296539 | |||||||
chr9:70296552 | C | CA | 31 | a0002c0002t0001g0041 a0002c0002t0001g0065 a0002c0002t0013g0312 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-1400dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70296552 | ||||||
chr9:70296552 | C | CAA | 6 | a0004c0004t0001g0334 a0004c0008t0005g0100 a0004c0008t0005g0101 others(3): Show |
6 | HG00140.hp2 HG00738.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054-1401_1054-140 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70296552 | ||||||
chr9:70296571 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-1395A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296571 | |||||||
chr9:70296725 | A | G | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-1241A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296725 | |||||||
chr9:70296775 | A | G | 1 | a0003c0003t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1054-1191A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296775 | |||||||
chr9:70296962 | C | G | 109 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(106): Show |
119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1054-1004C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296962 | |||||||
chr9:70296999 | T | C | 1 | a0002c0002t0004g0096 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1054-967T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70296999 | |||||||
chr9:70297014 | TTATTTC | T | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-950_1054-945d others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70297014 | ||||||
chr9:70297047 | C | CT | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-918dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr9 | 70297047 | ||||||
chr9:70297059 | C | G | 57 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(54): Show |
59 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1054-907C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297059 | |||||||
chr9:70297133 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1054-833T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297133 | |||||||
chr9:70297202 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1054-764G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297202 | |||||||
chr9:70297534 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-432A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297534 | |||||||
chr9:70297540 | A | G | 5 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-426A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 8/24 | chr9 | 70297540 | |||||||
chr9:70298800 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1309+579G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298800 | |||||||
chr9:70298844 | C | G | 1 | a0003c0003t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1309+623C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298844 | |||||||
chr9:70298903 | T | C | 1 | a0002c0002t0004g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1309+682T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298903 | |||||||
chr9:70298993 | T | C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0125 a0001c0001t0002g0126 |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309+772T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70298993 | |||||||
chr9:70299128 | A | G | 26 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(23): Show |
26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1309+907A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299128 | |||||||
chr9:70299307 | A | G | 1 | a0004c0004t0001g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1310-739A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299307 | |||||||
chr9:70299336 | T | A | 64 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(61): Show |
66 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1310-710T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299336 | |||||||
chr9:70299436 | C | T | 1 | a0003c0003t0001g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1310-610C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299436 | |||||||
chr9:70299586 | A | C | 334 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1310-460A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299586 | |||||||
chr9:70299627 | T | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1310-419T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299627 | |||||||
chr9:70299631 | C | T | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1310-415C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299631 | |||||||
chr9:70299657 | TC | T | 54 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(51): Show |
60 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1310-380delC | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 70299657 | ||||||
chr9:70299732 | A | G | 332 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(329): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1310-314A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299732 | |||||||
chr9:70299733 | G | T | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1310-313G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | chr9 | 70299733 | |||||||
chr9:70299787 | T | TTTTG | 9 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(6): Show |
9 | HG01496.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1310-235_1310-232d others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 70299787 | ||||||
chr9:70299787 | TTTTG | T | 55 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(52): Show |
60 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1310-235_1310-232d others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr9 | 70299787 | ||||||
chr9:70300363 | G | C | 1 | a0001c0001t0017g0214 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1464+163G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300363 | |||||||
chr9:70300374 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+174G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300374 | |||||||
chr9:70300376 | A | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+176A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300376 | |||||||
chr9:70300434 | T | C | 4 | a0002c0002t0001g0077 a0002c0002t0001g0078 a0002c0002t0001g0083 others(1): Show |
4 | HG00673.hp2 NA18967.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464+234T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300434 | |||||||
chr9:70300568 | A | G | 6 | a0003c0003t0001g0145 a0003c0003t0001g0152 a0003c0003t0001g0153 others(3): Show |
6 | HG01496.hp2 HG02300.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1464+368A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300568 | |||||||
chr9:70300719 | T | G | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1464+519T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70300719 | |||||||
chr9:70301027 | C | T | 109 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(106): Show |
119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1464+827C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301027 | |||||||
chr9:70301623 | C | T | 1 | a0004c0004t0001g0313 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1464+1423C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301623 | |||||||
chr9:70301689 | A | G | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1464+1489A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301689 | |||||||
chr9:70301790 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1464+1590T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301790 | |||||||
chr9:70301810 | A | G | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1464+1610A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301810 | |||||||
chr9:70301878 | A | G | 2 | a0001c0001t0002g0252 a0001c0001t0002g0309 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1464+1678A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70301878 | |||||||
chr9:70302028 | A | T | 1 | a0001c0001t0002g0309 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1464+1828A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302028 | |||||||
chr9:70302040 | C | A | 1 | a0001c0001t0002g0264 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1464+1840C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302040 | |||||||
chr9:70302188 | A | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1464+1988A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302188 | |||||||
chr9:70302220 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1464+2020G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302220 | |||||||
chr9:70302233 | G | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(101): Show |
114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1464+2033G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302233 | |||||||
chr9:70302278 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1464+2078G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302278 | |||||||
chr9:70302458 | A | G | 2 | a0003c0003t0001g0147 a0003c0003t0001g0305 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1464+2258A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302458 | |||||||
chr9:70302466 | C | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1464+2266C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302466 | |||||||
chr9:70302494 | G | GA | 12 | a0001c0001t0002g0010 a0001c0001t0002g0125 a0001c0001t0002g0126 others(9): Show |
13 | HG00544.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1464+2303dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302494 | ||||||
chr9:70302494 | G | GAA | 19 | a0002c0002t0001g0002 a0002c0002t0001g0038 a0002c0002t0001g0043 others(16): Show |
21 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1464+2302_1464+230 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302494 | ||||||
chr9:70302494 | G | GAAA | 35 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(32): Show |
37 | HG00140.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1464+2301_1464+230 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302494 | ||||||
chr9:70302502 | A | AAAT | 13 | a0004c0004t0001g0313 a0004c0004t0001g0328 a0004c0004t0001g0330 others(10): Show |
13 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1464+2303_1464+230 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302502 | ||||||
chr9:70302502 | A | AAT | 46 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0006 others(43): Show |
50 | HG00438.hp2 HG00597.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1464+2318_1464+231 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70302502 | ||||||
chr9:70302504 | T | A | 201 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(198): Show |
216 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1464+2304T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302504 | |||||||
chr9:70302506 | T | A | 50 | a0001c0001t0002g0010 a0001c0001t0002g0015 a0001c0001t0002g0110 others(47): Show |
52 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1464+2306T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302506 | |||||||
chr9:70302732 | C | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1465-2515C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302732 | |||||||
chr9:70302813 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-2434A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302813 | |||||||
chr9:70302894 | T | G | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1465-2353T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70302894 | |||||||
chr9:70303237 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1465-2010A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303237 | |||||||
chr9:70303247 | A | C | 9 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(6): Show |
9 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-2000A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303247 | |||||||
chr9:70303249 | AAT | A | 6 | a0001c0001t0002g0288 a0005c0007t0002g0016 a0005c0007t0002g0265 others(3): Show |
7 | HG01358.hp2 HG01891.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-1996_1465-199 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70303249 | ||||||
chr9:70303251 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(100): Show |
112 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1465-1996T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303251 | |||||||
chr9:70303301 | CTATAAT | C | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1465-1941_1465-193 others(10): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70303301 | ||||||
chr9:70303307 | T | C | 281 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(278): Show |
299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1465-1940T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303307 | |||||||
chr9:70303310 | T | C | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1465-1937T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303310 | |||||||
chr9:70303319 | T | A | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-1928T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303319 | |||||||
chr9:70303341 | C | A | 1 | a0001c0001t0002g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1465-1906C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303341 | |||||||
chr9:70303447 | C | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1465-1800C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303447 | |||||||
chr9:70303457 | G | A | 1 | a0004c0004t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1465-1790G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303457 | |||||||
chr9:70303671 | C | T | 2 | a0001c0001t0002g0241 a0001c0001t0002g0242 |
2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1465-1576C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303671 | |||||||
chr9:70303692 | A | G | 1 | a0002c0002t0001g0308 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1465-1555A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303692 | |||||||
chr9:70303918 | A | C | 1 | a0002c0002t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1465-1329A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303918 | |||||||
chr9:70303975 | T | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1465-1272T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70303975 | |||||||
chr9:70304115 | G | T | 1 | a0003c0003t0001g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1465-1132G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304115 | |||||||
chr9:70304178 | T | A | 1 | a0003c0003t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1465-1069T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304178 | |||||||
chr9:70304300 | A | G | 4 | a0002c0002t0001g0030 a0002c0002t0001g0031 a0006c0011t0009g0303 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-947A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304300 | |||||||
chr9:70304413 | A | G | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1465-834A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304413 | |||||||
chr9:70304558 | A | T | 1 | a0001c0010t0002g0275 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1465-689A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304558 | |||||||
chr9:70304611 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1465-636C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304611 | |||||||
chr9:70304718 | C | A | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1465-529C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304718 | |||||||
chr9:70304752 | G | T | 1 | a0001c0001t0002g0292 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1465-495G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70304752 | |||||||
chr9:70304796 | G | GT | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1465-440dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr9 | 70304796 | ||||||
chr9:70305134 | A | G | 1 | a0004c0004t0001g0332 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1465-113A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70305134 | |||||||
chr9:70305159 | A | G | 3 | a0001c0001t0002g0233 a0001c0001t0002g0246 a0001c0001t0002g0281 |
3 | NA18961.hp1 NA18994.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1465-88A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 10/24 | chr9 | 70305159 | |||||||
chr9:70305707 | C | T | 1 | a0002c0002t0001g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1578+347C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70305707 | |||||||
chr9:70305764 | T | C | 2 | a0003c0003t0001g0147 a0003c0003t0001g0305 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1578+404T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70305764 | |||||||
chr9:70305808 | A | G | 57 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(54): Show |
59 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1578+448A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70305808 | |||||||
chr9:70306102 | T | G | 1 | a0004c0006t0001g0324 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1578+742T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306102 | |||||||
chr9:70306121 | A | G | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1578+761A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306121 | |||||||
chr9:70306129 | A | G | 2 | a0003c0003t0001g0152 a0004c0004t0001g0332 |
2 | HG01106.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1578+769A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306129 | |||||||
chr9:70306458 | A | G | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1578+1098A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306458 | |||||||
chr9:70306564 | G | T | 1 | a0003c0003t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1578+1204G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70306564 | |||||||
chr9:70307117 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+1757G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307117 | |||||||
chr9:70307147 | C | T | 1 | a0002c0002t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1578+1787C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307147 | |||||||
chr9:70307221 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+1861T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307221 | |||||||
chr9:70307251 | G | A | 5 | a0005c0007t0002g0016 a0005c0007t0002g0265 a0005c0007t0002g0266 others(2): Show |
6 | HG01358.hp2 HG02630.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578+1891G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307251 | |||||||
chr9:70307361 | A | G | 1 | a0003c0003t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1578+2001A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307361 | |||||||
chr9:70307382 | A | C | 2 | a0002c0002t0001g0081 a0002c0002t0001g0085 |
2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1578+2022A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307382 | |||||||
chr9:70307399 | T | C | 1 | a0002c0002t0001g0055 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1578+2039T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307399 | |||||||
chr9:70307433 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+2073C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307433 | |||||||
chr9:70307550 | T | C | 1 | a0002c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1578+2190T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307550 | |||||||
chr9:70307585 | C | T | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1578+2225C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307585 | |||||||
chr9:70307603 | A | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1578+2243A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307603 | |||||||
chr9:70307628 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1578+2268G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307628 | |||||||
chr9:70307799 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1578+2439C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307799 | |||||||
chr9:70307803 | C | T | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+2443C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307803 | |||||||
chr9:70307809 | A | G | 10 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0128 others(7): Show |
10 | HG00323.hp2 HG00408.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1578+2449A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70307809 | |||||||
chr9:70308006 | T | A | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1578+2646T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308006 | |||||||
chr9:70308095 | G | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1578+2735G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308095 | |||||||
chr9:70308250 | C | G | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+2890C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308250 | |||||||
chr9:70308274 | T | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1578+2914T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308274 | |||||||
chr9:70308332 | G | A | 1 | a0013c0019t0003g0022 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1578+2972G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308332 | |||||||
chr9:70308334 | G | A | 4 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+2974G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308334 | |||||||
chr9:70308399 | T | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1578+3039T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308399 | |||||||
chr9:70308409 | C | T | 7 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(4): Show |
7 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+3049C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308409 | |||||||
chr9:70308590 | C | CA | 12 | a0001c0001t0002g0128 a0001c0001t0002g0135 a0001c0001t0002g0136 others(9): Show |
12 | HG01358.hp2 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1578+3259dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | ||||||
chr9:70308590 | CA | C | 130 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(127): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1578+3259delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | ||||||
chr9:70308590 | CAAAAAAA others(3): Show |
C | 1 | a0002c0009t0014g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1578+3250_1578+325 others(14): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | ||||||
chr9:70308590 | CAAAAAAA others(4): Show |
C | 6 | a0002c0002t0001g0052 a0002c0009t0006g0009 a0002c0009t0006g0097 others(3): Show |
6 | HG01891.hp2 HG02056.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+3249_1578+325 others(15): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | ||||||
chr9:70308590 | CAAAAAAA others(5): Show |
C | 110 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(107): Show |
118 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1578+3248_1578+325 others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70308590 | ||||||
chr9:70308619 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1578+3259A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308619 | |||||||
chr9:70308662 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1578+3302G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308662 | |||||||
chr9:70308687 | T | G | 1 | a0002c0002t0001g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1578+3327T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308687 | |||||||
chr9:70308702 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+3342T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70308702 | |||||||
chr9:70309016 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1578+3656G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309016 | |||||||
chr9:70309219 | A | C | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1578+3859A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309219 | |||||||
chr9:70309248 | C | A | 1 | a0001c0001t0002g0117 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1578+3888C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309248 | |||||||
chr9:70309250 | T | C | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+3890T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309250 | |||||||
chr9:70309318 | C | CTT | 7 | a0001c0001t0002g0208 a0001c0001t0002g0237 a0001c0001t0002g0250 others(4): Show |
7 | HG01070.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+3988_1578+398 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | C | CTTTT | 7 | a0001c0001t0002g0211 a0001c0001t0002g0243 a0001c0001t0002g0244 others(4): Show |
7 | HG00544.hp2 HG00609.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+3986_1578+398 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | C | CTTTTT | 39 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(36): Show |
43 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1578+3985_1578+398 others(9): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | C | CTTTTTT | 31 | a0001c0001t0002g0001 a0001c0001t0002g0120 a0001c0001t0002g0200 others(28): Show |
35 | HG00408.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1578+3984_1578+398 others(10): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | C | CTTTTTTT | 7 | a0001c0001t0002g0201 a0001c0001t0002g0240 a0001c0001t0002g0241 others(4): Show |
7 | HG00438.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+3983_1578+398 others(11): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1578+3980_1578+398 others(14): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | C | CTTTTTTT others(5): Show |
1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1578+3978_1578+398 others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CT | C | 9 | a0001c0001t0002g0204 a0001c0001t0002g0207 a0001c0005t0003g0024 others(6): Show |
10 | HG01884.hp1 HG02080.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1578+3989delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTT | C | 24 | a0001c0001t0002g0270 a0001c0005t0003g0023 a0001c0005t0003g0025 others(21): Show |
25 | HG00673.hp2 HG00738.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1578+3988_1578+398 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTT | C | 34 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(31): Show |
37 | HG00741.hp1 HG01256.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.1578+3987_1578+398 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTT | C | 20 | a0002c0002t0001g0079 a0003c0003t0001g0004 a0003c0003t0001g0014 others(17): Show |
23 | HG00609.hp1 HG01255.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578+3986_1578+398 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTT | C | 16 | a0003c0003t0001g0106 a0003c0003t0001g0151 a0003c0003t0001g0170 others(13): Show |
16 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1578+3985_1578+398 others(9): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTTTT others(3): Show |
C | 1 | a0004c0004t0001g0330 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1578+3980_1578+398 others(14): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTTTT others(4): Show |
C | 23 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(20): Show |
23 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578+3979_1578+398 others(15): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0002g0015 a0001c0001t0002g0221 a0001c0001t0002g0295 others(2): Show |
6 | NA18747.hp1 NA18949.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+3978_1578+398 others(16): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTTTT others(6): Show |
C | 54 | a0001c0001t0002g0220 a0001c0001t0002g0222 a0001c0001t0002g0278 others(51): Show |
60 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1578+3977_1578+398 others(17): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0002g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1578+3976_1578+398 others(18): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309318 | CTTTTTTT others(8): Show |
C | 24 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0122 others(21): Show |
25 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1578+3975_1578+398 others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70309318 | ||||||
chr9:70309330 | TTTTTTTT others(13): Show |
T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+3971_1578+399 others(24): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309330 | |||||||
chr9:70309349 | T | G | 4 | a0002c0002t0001g0030 a0002c0002t0001g0031 a0002c0002t0001g0032 others(1): Show |
4 | HG00597.hp2 NA18947.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578+3989T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309349 | |||||||
chr9:70309349 | T | TTTTTTTT others(13): Show |
1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1578+3989_1578+399 others(24): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309349 | |||||||
chr9:70309373 | C | T | 2 | a0001c0005t0003g0028 a0001c0005t0003g0029 |
2 | HG01496.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1578+4013C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309373 | |||||||
chr9:70309589 | T | G | 55 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(52): Show |
60 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1578+4229T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309589 | |||||||
chr9:70309872 | C | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1578+4512C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70309872 | |||||||
chr9:70310192 | C | T | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1579-4550C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310192 | |||||||
chr9:70310200 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579-4542G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310200 | |||||||
chr9:70310381 | CAGTG | C | 25 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(22): Show |
27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1579-4358_1579-435 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70310381 | ||||||
chr9:70310475 | G | C | 1 | a0001c0001t0002g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1579-4267G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310475 | |||||||
chr9:70310602 | A | G | 1 | a0002c0002t0001g0308 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1579-4140A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310602 | |||||||
chr9:70310666 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-4076T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310666 | |||||||
chr9:70310731 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-4011G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310731 | |||||||
chr9:70310761 | T | C | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-3981T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310761 | |||||||
chr9:70310763 | CATCAG | C | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-3978_1579-397 others(9): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310763 | |||||||
chr9:70310782 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-3960A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310782 | |||||||
chr9:70310985 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-3757T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70310985 | |||||||
chr9:70311470 | A | C | 1 | a0002c0002t0001g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1579-3272A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70311470 | |||||||
chr9:70311701 | CA | C | 14 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(11): Show |
14 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1579-3026delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70311701 | ||||||
chr9:70311959 | A | T | 1 | a0001c0001t0002g0243 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1579-2783A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70311959 | |||||||
chr9:70311992 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-2750G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70311992 | |||||||
chr9:70312075 | C | T | 1 | a0003c0003t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1579-2667C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312075 | |||||||
chr9:70312120 | C | CA | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-2594dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | ||||||
chr9:70312120 | CA | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0126 others(31): Show |
34 | HG00609.hp2 HG00735.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1579-2594delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | ||||||
chr9:70312120 | CAA | C | 196 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(193): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1579-2595_1579-259 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | ||||||
chr9:70312120 | CAAA | C | 71 | a0001c0001t0002g0295 a0001c0001t0002g0300 a0001c0001t0007g0286 others(68): Show |
76 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1579-2596_1579-259 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | ||||||
chr9:70312120 | CAAAA | C | 25 | a0002c0002t0001g0007 a0002c0002t0001g0074 a0002c0002t0001g0075 others(22): Show |
27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1579-2597_1579-259 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70312120 | ||||||
chr9:70312299 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1579-2443G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312299 | |||||||
chr9:70312315 | C | T | 1 | a0001c0005t0003g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1579-2427C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312315 | |||||||
chr9:70312560 | C | T | 2 | a0002c0002t0001g0036 a0002c0002t0001g0037 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1579-2182C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312560 | |||||||
chr9:70312631 | T | A | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-2111T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312631 | |||||||
chr9:70312677 | A | T | 11 | a0001c0001t0002g0015 a0001c0001t0002g0221 a0001c0001t0002g0223 others(8): Show |
12 | HG01099.hp2 HG01261.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579-2065A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312677 | |||||||
chr9:70312781 | C | T | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1579-1961C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70312781 | |||||||
chr9:70313078 | G | T | 1 | a0008c0014t0001g0069 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1579-1664G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313078 | |||||||
chr9:70313250 | A | T | 25 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0122 others(22): Show |
26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1579-1492A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313250 | |||||||
chr9:70313352 | C | T | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1579-1390C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313352 | |||||||
chr9:70313466 | T | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-1276T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313466 | |||||||
chr9:70313470 | G | A | 1 | a0003c0003t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1579-1272G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313470 | |||||||
chr9:70313569 | C | G | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-1173C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313569 | |||||||
chr9:70313603 | T | C | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-1139T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313603 | |||||||
chr9:70313796 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-946A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313796 | |||||||
chr9:70313887 | T | C | 6 | a0003c0003t0001g0170 a0003c0003t0001g0172 a0003c0003t0001g0173 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-855T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313887 | |||||||
chr9:70313937 | G | T | 1 | a0001c0001t0002g0273 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1579-805G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70313937 | |||||||
chr9:70314118 | CCTT | C | 3 | a0004c0004t0001g0318 a0004c0004t0001g0322 a0004c0004t0001g0323 |
3 | HG01070.hp2 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1579-619_1579-617d others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr9 | 70314118 | ||||||
chr9:70314183 | A | G | 24 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(21): Show |
24 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1579-559A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314183 | |||||||
chr9:70314207 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1579-535A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314207 | |||||||
chr9:70314310 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-432A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314310 | |||||||
chr9:70314364 | C | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1579-378C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314364 | |||||||
chr9:70314377 | G | T | 2 | a0004c0004t0001g0337 a0009c0015t0011g0108 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1579-365G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314377 | |||||||
chr9:70314467 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-275A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314467 | |||||||
chr9:70314493 | A | C | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1579-249A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314493 | |||||||
chr9:70314495 | T | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1579-247T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314495 | |||||||
chr9:70314587 | T | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(101): Show |
114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1579-155T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 11/24 | chr9 | 70314587 | |||||||
chr9:70314849 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1673+13A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70314849 | |||||||
chr9:70314852 | A | G | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673+16A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70314852 | |||||||
chr9:70314853 | C | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1673+17C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70314853 | |||||||
chr9:70315308 | T | TAAAA | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1674-137_1674-134d others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr9 | 70315308 | ||||||
chr9:70315428 | C | T | 1 | a0001c0005t0003g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1674-18C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 12/24 | chr9 | 70315428 | |||||||
chr9:70315931 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1806+353T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70315931 | |||||||
chr9:70316082 | G | T | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1806+504G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316082 | |||||||
chr9:70316275 | G | A | 24 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(21): Show |
24 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1806+697G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316275 | |||||||
chr9:70316317 | A | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1806+739A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316317 | |||||||
chr9:70316385 | A | G | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1806+807A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316385 | |||||||
chr9:70316451 | CTTAACAG others(6): Show |
C | 6 | a0003c0003t0001g0170 a0003c0003t0001g0172 a0003c0003t0001g0173 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+874_1806+886d others(15): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316451 | |||||||
chr9:70316453 | TA | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1806+877delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 70316453 | ||||||
chr9:70316582 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1806+1004A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70316582 | |||||||
chr9:70317165 | T | A | 1 | a0003c0003t0001g0119 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1807-1349T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317165 | |||||||
chr9:70317233 | A | G | 20 | a0001c0001t0002g0001 a0001c0001t0002g0211 a0001c0001t0002g0220 others(17): Show |
24 | HG00408.hp2 HG00735.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1807-1281A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317233 | |||||||
chr9:70317245 | C | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1807-1269C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317245 | |||||||
chr9:70317260 | T | G | 8 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0250 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1807-1254T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317260 | |||||||
chr9:70317295 | C | T | 1 | a0002c0002t0001g0056 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1807-1219C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317295 | |||||||
chr9:70317528 | T | C | 1 | a0003c0003t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1807-986T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317528 | |||||||
chr9:70317838 | T | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1807-676T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317838 | |||||||
chr9:70317952 | A | ACTCTTCT others(10): Show |
55 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(52): Show |
57 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.1807-549_1807-548i others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr9 | 70317952 | ||||||
chr9:70317966 | C | G | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1807-548C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70317966 | |||||||
chr9:70318023 | G | A | 1 | a0002c0002t0001g0311 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1807-491G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318023 | |||||||
chr9:70318149 | C | G | 1 | a0001c0005t0003g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1807-365C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318149 | |||||||
chr9:70318292 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1807-222G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318292 | |||||||
chr9:70318305 | T | C | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1807-209T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318305 | |||||||
chr9:70318343 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1807-171G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318343 | |||||||
chr9:70318357 | C | G | 1 | a0001c0001t0002g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1807-157C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318357 | |||||||
chr9:70318361 | C | G | 2 | a0003c0003t0001g0147 a0003c0003t0001g0305 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1807-153C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 13/24 | chr9 | 70318361 | |||||||
chr9:70318983 | G | C | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2150+20G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70318983 | |||||||
chr9:70319042 | G | C | 332 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(329): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2150+79G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319042 | |||||||
chr9:70319082 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2150+119C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319082 | |||||||
chr9:70319114 | T | C | 1 | a0003c0003t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2150+151T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319114 | |||||||
chr9:70319174 | T | C | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2150+211T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319174 | |||||||
chr9:70319278 | T | C | 1 | a0003c0003t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2150+315T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319278 | |||||||
chr9:70319448 | A | T | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2150+485A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319448 | |||||||
chr9:70319713 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2150+750C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319713 | |||||||
chr9:70319795 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2150+832A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70319795 | |||||||
chr9:70320287 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2150+1324A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320287 | |||||||
chr9:70320403 | G | A | 4 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150+1440G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320403 | |||||||
chr9:70320514 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2150+1551A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320514 | |||||||
chr9:70320561 | A | G | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150+1598A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70320561 | |||||||
chr9:70321082 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2150+2119G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321082 | |||||||
chr9:70321153 | G | A | 1 | a0002c0002t0001g0311 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2150+2190G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321153 | |||||||
chr9:70321236 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2151-2247T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321236 | |||||||
chr9:70321248 | C | T | 2 | a0001c0001t0002g0232 a0001c0001t0002g0243 |
2 | NA18972.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2151-2235C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321248 | |||||||
chr9:70321252 | A | G | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-2231A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321252 | |||||||
chr9:70321392 | G | A | 3 | a0001c0001t0002g0228 a0001c0001t0002g0234 a0004c0006t0001g0335 |
3 | HG02129.hp1 HG02809.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2151-2091G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321392 | |||||||
chr9:70321394 | C | CT | 65 | a0001c0001t0002g0208 a0001c0001t0002g0243 a0001c0001t0002g0249 others(62): Show |
67 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2151-2073dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321394 | ||||||
chr9:70321394 | C | CTT | 52 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(49): Show |
58 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2151-2074_2151-207 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321394 | ||||||
chr9:70321414 | A | G | 1 | a0004c0004t0001g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2151-2069A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321414 | |||||||
chr9:70321429 | GT | G | 110 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(107): Show |
120 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2151-2052delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321429 | ||||||
chr9:70321647 | G | A | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2151-1836G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321647 | |||||||
chr9:70321826 | A | C | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2151-1657A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321826 | |||||||
chr9:70321901 | TTTG | T | 64 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(61): Show |
66 | HG00140.hp2 HG00544.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2151-1567_2151-156 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70321901 | ||||||
chr9:70321933 | A | G | 5 | a0002c0002t0001g0002 a0002c0002t0001g0036 a0002c0002t0001g0037 others(2): Show |
7 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2151-1550A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321933 | |||||||
chr9:70321969 | A | T | 1 | a0001c0001t0002g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2151-1514A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70321969 | |||||||
chr9:70322103 | T | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2151-1380T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322103 | |||||||
chr9:70322183 | CTATT | C | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2151-1297_2151-129 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70322183 | ||||||
chr9:70322345 | G | C | 1 | a0002c0002t0001g0080 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2151-1138G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322345 | |||||||
chr9:70322426 | A | C | 4 | a0002c0002t0001g0064 a0002c0002t0001g0065 a0002c0002t0001g0066 others(1): Show |
4 | NA18950.hp2 NA18995.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.2151-1057A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322426 | |||||||
chr9:70322522 | G | A | 1 | a0004c0004t0001g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2151-961G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322522 | |||||||
chr9:70322573 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2151-910C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322573 | |||||||
chr9:70322641 | GCCTGGCC others(13): Show |
G | 4 | a0001c0001t0002g0285 a0001c0001t0007g0283 a0001c0001t0007g0284 others(1): Show |
4 | HG00738.hp1 HG01070.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151-837_2151-818d others(22): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr9 | 70322641 | ||||||
chr9:70322665 | G | C | 1 | a0001c0001t0002g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2151-818G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322665 | |||||||
chr9:70322837 | A | G | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151-646A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322837 | |||||||
chr9:70322909 | C | T | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2151-574C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322909 | |||||||
chr9:70322915 | T | C | 4 | a0001c0001t0002g0122 a0001c0001t0002g0129 a0001c0001t0002g0130 others(1): Show |
4 | HG00408.hp1 NA18612.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151-568T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322915 | |||||||
chr9:70322985 | C | G | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2151-498C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322985 | |||||||
chr9:70322986 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2151-497G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70322986 | |||||||
chr9:70323022 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2151-461G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70323022 | |||||||
chr9:70323337 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2151-146T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 15/24 | chr9 | 70323337 | |||||||
chr9:70323612 | G | A | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2274+6G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/24 | chr9 | 70323612 | |||||||
chr9:70323782 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2274+176G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/24 | chr9 | 70323782 | |||||||
chr9:70323962 | T | G | 1 | a0003c0003t0001g0187 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2275-59T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 16/24 | chr9 | 70323962 | |||||||
chr9:70324157 | C | G | 2 | a0003c0003t0001g0170 a0003c0003t0001g0173 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2397+14C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324157 | |||||||
chr9:70324209 | C | T | 4 | a0004c0008t0005g0101 a0004c0008t0005g0102 a0004c0008t0005g0103 others(1): Show |
4 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2397+66C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324209 | |||||||
chr9:70324279 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2397+136G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324279 | |||||||
chr9:70324394 | A | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+251A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324394 | |||||||
chr9:70324487 | T | C | 332 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(329): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2397+344T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324487 | |||||||
chr9:70324519 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+376A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324519 | |||||||
chr9:70324767 | C | T | 1 | a0004c0004t0018g0338 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2397+624C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324767 | |||||||
chr9:70324786 | C | T | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2397+643C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324786 | |||||||
chr9:70324884 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+741T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324884 | |||||||
chr9:70324990 | G | A | 123 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0142 others(120): Show |
131 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.2397+847G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70324990 | |||||||
chr9:70325169 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+1026G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325169 | |||||||
chr9:70325236 | G | A | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2397+1093G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325236 | |||||||
chr9:70325249 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+1106T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325249 | |||||||
chr9:70325253 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2397+1110C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325253 | |||||||
chr9:70325348 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+1205G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325348 | |||||||
chr9:70325381 | A | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397+1238A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325381 | |||||||
chr9:70325381 | A | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0127 |
2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2397+1238A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325381 | |||||||
chr9:70325579 | T | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2397+1436T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325579 | |||||||
chr9:70325670 | T | C | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2397+1527T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325670 | |||||||
chr9:70325818 | A | G | 2 | a0004c0004t0001g0317 a0004c0004t0001g0336 |
2 | NA18955.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2397+1675A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70325818 | |||||||
chr9:70326054 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0271 a0001c0001t0002g0282 |
4 | HG01257.hp2 HG01975.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397+1911A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326054 | |||||||
chr9:70326384 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2397+2241G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326384 | |||||||
chr9:70326596 | CT | C | 44 | a0001c0001t0002g0122 a0001c0001t0002g0125 a0001c0001t0002g0131 others(41): Show |
46 | HG00609.hp1 HG00673.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2397+2469delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70326596 | ||||||
chr9:70326650 | G | A | 2 | a0001c0001t0002g0211 a0001c0001t0015g0261 |
2 | NA18944.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2397+2507G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326650 | |||||||
chr9:70326818 | T | G | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2397+2675T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326818 | |||||||
chr9:70326851 | C | T | 6 | a0001c0001t0002g0288 a0005c0007t0002g0016 a0005c0007t0002g0265 others(3): Show |
7 | HG01358.hp2 HG01891.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2397+2708C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326851 | |||||||
chr9:70326889 | G | A | 2 | a0003c0003t0001g0147 a0003c0003t0001g0305 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2397+2746G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70326889 | |||||||
chr9:70327037 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2397+2894T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327037 | |||||||
chr9:70327080 | A | G | 60 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0105 others(57): Show |
65 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2397+2937A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327080 | |||||||
chr9:70327090 | T | G | 3 | a0002c0002t0001g0112 a0002c0002t0001g0114 a0002c0002t0001g0308 |
3 | NA18940.hp1 NA19006.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2397+2947T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327090 | |||||||
chr9:70327231 | C | T | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2397+3088C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327231 | |||||||
chr9:70327320 | A | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2397+3177A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327320 | |||||||
chr9:70327582 | A | G | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+3439A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327582 | |||||||
chr9:70327628 | A | G | 1 | a0002c0002t0001g0050 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2397+3485A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327628 | |||||||
chr9:70327828 | G | T | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2397+3685G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327828 | |||||||
chr9:70327897 | G | A | 3 | a0004c0004t0001g0314 a0004c0004t0001g0315 a0004c0004t0001g0316 |
3 | HG01099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2397+3754G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327897 | |||||||
chr9:70327944 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2397+3801G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70327944 | |||||||
chr9:70328019 | C | T | 26 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(23): Show |
26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2397+3876C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328019 | |||||||
chr9:70328140 | C | T | 1 | a0001c0001t0002g0132 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2397+3997C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328140 | |||||||
chr9:70328183 | C | T | 1 | a0004c0004t0018g0338 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2397+4040C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328183 | |||||||
chr9:70328185 | A | T | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+4042A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328185 | |||||||
chr9:70328373 | C | T | 2 | a0002c0002t0001g0090 a0002c0002t0001g0091 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2397+4230C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328373 | |||||||
chr9:70328434 | A | G | 3 | a0003c0003t0001g0153 a0003c0003t0001g0155 a0003c0003t0001g0197 |
3 | HG01496.hp2 HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2397+4291A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328434 | |||||||
chr9:70328543 | T | C | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2397+4400T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328543 | |||||||
chr9:70328596 | C | T | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+4453C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328596 | |||||||
chr9:70328655 | G | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2397+4512G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328655 | |||||||
chr9:70328808 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2397+4665G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328808 | |||||||
chr9:70328861 | C | T | 15 | a0003c0003t0001g0014 a0003c0003t0001g0145 a0003c0003t0001g0152 others(12): Show |
16 | HG01496.hp2 HG02083.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.2397+4718C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328861 | |||||||
chr9:70328998 | C | T | 6 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(3): Show |
6 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2397+4855C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70328998 | |||||||
chr9:70329000 | T | G | 5 | a0003c0003t0001g0174 a0003c0003t0001g0182 a0003c0003t0001g0183 others(2): Show |
5 | NA18945.hp2 NA18961.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+4857T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329000 | |||||||
chr9:70329012 | C | T | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2397+4869C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329012 | |||||||
chr9:70329044 | A | C | 1 | a0004c0008t0005g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2397+4901A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329044 | |||||||
chr9:70329082 | A | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2397+4939A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329082 | |||||||
chr9:70329115 | T | A | 1 | a0001c0001t0002g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2397+4972T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329115 | |||||||
chr9:70329412 | G | A | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2397+5269G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329412 | |||||||
chr9:70329486 | C | T | 55 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(52): Show |
60 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2397+5343C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329486 | |||||||
chr9:70329499 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+5356G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329499 | |||||||
chr9:70329510 | G | A | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2397+5367G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329510 | |||||||
chr9:70329526 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2397+5383A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329526 | |||||||
chr9:70329628 | C | G | 1 | a0001c0001t0002g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2397+5485C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329628 | |||||||
chr9:70329882 | G | T | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2397+5739G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329882 | |||||||
chr9:70329944 | G | T | 1 | a0003c0003t0001g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2397+5801G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70329944 | |||||||
chr9:70330038 | A | C | 1 | a0001c0005t0003g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+5895A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330038 | |||||||
chr9:70330076 | T | C | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2397+5933T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330076 | |||||||
chr9:70330145 | A | T | 1 | a0003c0003t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2397+6002A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330145 | |||||||
chr9:70330286 | T | C | 1 | a0001c0001t0002g0292 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2397+6143T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330286 | |||||||
chr9:70330548 | C | CT | 62 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0105 others(59): Show |
67 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2397+6423dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70330548 | ||||||
chr9:70330548 | CT | C | 113 | a0001c0001t0002g0131 a0001c0001t0002g0213 a0001c0001t0007g0283 others(110): Show |
121 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2397+6423delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70330548 | ||||||
chr9:70330548 | CTT | C | 7 | a0002c0002t0001g0033 a0002c0002t0004g0087 a0002c0009t0006g0009 others(4): Show |
7 | HG01070.hp2 HG01891.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2397+6422_2397+642 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70330548 | ||||||
chr9:70330567 | C | T | 1 | a0001c0005t0003g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+6424C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330567 | |||||||
chr9:70330568 | A | C | 1 | a0001c0005t0003g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+6425A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330568 | |||||||
chr9:70330646 | G | A | 1 | a0002c0002t0001g0046 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2397+6503G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330646 | |||||||
chr9:70330657 | C | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+6514C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70330657 | |||||||
chr9:70331095 | G | A | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2397+6952G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331095 | |||||||
chr9:70331175 | T | A | 5 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+7032T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331175 | |||||||
chr9:70331241 | T | C | 1 | a0001c0001t0002g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2397+7098T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331241 | |||||||
chr9:70331413 | A | T | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2397+7270A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331413 | |||||||
chr9:70331415 | AAAAC | A | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397+7274_2397+727 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70331415 | ||||||
chr9:70331419 | CAG | C | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+7277_2397+727 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331419 | |||||||
chr9:70331471 | G | A | 331 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(328): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.2397+7328G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331471 | |||||||
chr9:70331471 | G | T | 1 | a0001c0005t0003g0029 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2397+7328G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331471 | |||||||
chr9:70331495 | A | G | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397+7352A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331495 | |||||||
chr9:70331505 | G | GT | 120 | a0001c0001t0002g0281 a0002c0002t0001g0002 a0002c0002t0001g0003 others(117): Show |
128 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2397+7372dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70331505 | ||||||
chr9:70331519 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+7376C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331519 | |||||||
chr9:70331777 | G | A | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+7634G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331777 | |||||||
chr9:70331941 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+7798G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331941 | |||||||
chr9:70331960 | C | T | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2397+7817C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70331960 | |||||||
chr9:70332045 | T | C | 1 | a0003c0003t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2397+7902T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332045 | |||||||
chr9:70332101 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2397+7958C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332101 | |||||||
chr9:70332156 | C | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2397+8013C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332156 | |||||||
chr9:70332227 | A | G | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2397+8084A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332227 | |||||||
chr9:70332232 | A | G | 1 | a0005c0007t0002g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2397+8089A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332232 | |||||||
chr9:70332523 | C | CA | 55 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(52): Show |
61 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.2397+8401dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | ||||||
chr9:70332523 | C | CAA | 7 | a0002c0002t0001g0042 a0002c0002t0001g0047 a0002c0002t0001g0072 others(4): Show |
7 | HG01891.hp2 HG02080.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2397+8400_2397+840 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | ||||||
chr9:70332523 | CA | C | 66 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0122 others(63): Show |
67 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.2397+8401delA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | ||||||
chr9:70332523 | CAA | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(121): Show |
134 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.2397+8400_2397+840 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332523 | ||||||
chr9:70332660 | C | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+8517C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332660 | |||||||
chr9:70332691 | T | C | 1 | a0004c0004t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2397+8548T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332691 | |||||||
chr9:70332828 | C | CTGA | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2397+8686_2397+868 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70332828 | ||||||
chr9:70332918 | C | T | 2 | a0001c0001t0002g0122 a0001c0001t0002g0130 |
2 | HG00408.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2397+8775C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332918 | |||||||
chr9:70332994 | A | T | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2397+8851A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70332994 | |||||||
chr9:70333055 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+8912G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333055 | |||||||
chr9:70333110 | T | TA | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397+8976dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70333110 | ||||||
chr9:70333113 | A | G | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.2397+8970A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333113 | |||||||
chr9:70333290 | A | G | 1 | a0002c0002t0001g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2397+9147A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333290 | |||||||
chr9:70333303 | G | C | 4 | a0001c0001t0002g0297 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG00544.hp2 NA18965.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2397+9160G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333303 | |||||||
chr9:70333468 | G | T | 1 | a0002c0002t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2397+9325G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333468 | |||||||
chr9:70333470 | C | T | 1 | a0002c0002t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2397+9327C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333470 | |||||||
chr9:70333583 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2397+9440T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333583 | |||||||
chr9:70333601 | C | T | 1 | a0001c0010t0002g0275 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2397+9458C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333601 | |||||||
chr9:70333641 | G | T | 2 | a0001c0005t0003g0028 a0001c0005t0003g0029 |
2 | HG01496.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2397+9498G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333641 | |||||||
chr9:70333749 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2397+9606A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333749 | |||||||
chr9:70333791 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2397+9648C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333791 | |||||||
chr9:70333828 | T | A | 5 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2397+9685T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333828 | |||||||
chr9:70333893 | T | TG | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2397+9750_2397+975 others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70333893 | |||||||
chr9:70334037 | AGACATTG others(21): Show |
A | 1 | a0004c0004t0001g0336 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2397+9895_2397+992 others(32): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334037 | |||||||
chr9:70334129 | G | GT | 47 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(44): Show |
48 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.2398-9999dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70334129 | ||||||
chr9:70334132 | T | G | 8 | a0003c0003t0001g0106 a0004c0008t0005g0100 a0004c0008t0005g0101 others(5): Show |
8 | HG00738.hp2 HG01433.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2397+9989T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334132 | |||||||
chr9:70334183 | A | C | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2398-9961A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334183 | |||||||
chr9:70334252 | G | A | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2398-9892G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334252 | |||||||
chr9:70334388 | T | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-9756T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334388 | |||||||
chr9:70334418 | A | C | 4 | a0002c0002t0001g0077 a0002c0002t0001g0078 a0002c0002t0001g0083 others(1): Show |
4 | HG00673.hp2 NA18967.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.2398-9726A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334418 | |||||||
chr9:70334439 | C | T | 1 | a0004c0004t0001g0318 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2398-9705C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334439 | |||||||
chr9:70334557 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2398-9587A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334557 | |||||||
chr9:70334724 | G | T | 1 | a0003c0003t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2398-9420G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334724 | |||||||
chr9:70334736 | A | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0042 |
2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.2398-9408A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334736 | |||||||
chr9:70334746 | C | T | 1 | a0001c0005t0003g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2398-9398C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334746 | |||||||
chr9:70334752 | A | G | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2398-9392A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334752 | |||||||
chr9:70334868 | C | G | 1 | a0001c0001t0002g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2398-9276C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334868 | |||||||
chr9:70334877 | C | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2398-9267C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334877 | |||||||
chr9:70334949 | G | A | 1 | a0003c0003t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2398-9195G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70334949 | |||||||
chr9:70335238 | T | G | 25 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(22): Show |
27 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.2398-8906T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335238 | |||||||
chr9:70335316 | T | C | 1 | a0002c0002t0001g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2398-8828T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335316 | |||||||
chr9:70335330 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-8814G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335330 | |||||||
chr9:70335408 | A | G | 338 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(335): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2398-8736A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335408 | |||||||
chr9:70335452 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-8692G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335452 | |||||||
chr9:70335462 | A | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398-8682A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335462 | |||||||
chr9:70335526 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2398-8618C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335526 | |||||||
chr9:70335536 | T | A | 2 | a0001c0001t0002g0252 a0001c0001t0002g0309 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2398-8608T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335536 | |||||||
chr9:70335589 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2398-8555A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335589 | |||||||
chr9:70335696 | A | G | 1 | a0002c0002t0019g0048 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2398-8448A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335696 | |||||||
chr9:70335713 | A | G | 117 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(114): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2398-8431A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70335713 | |||||||
chr9:70336207 | TGTA | T | 31 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(28): Show |
33 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.2398-7935_2398-793 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70336207 | ||||||
chr9:70336213 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2398-7931C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336213 | |||||||
chr9:70336501 | A | G | 38 | a0001c0001t0002g0010 a0001c0001t0002g0110 a0001c0001t0002g0111 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.2398-7643A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336501 | |||||||
chr9:70336703 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2398-7441A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336703 | |||||||
chr9:70336855 | A | G | 1 | a0002c0002t0022g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2398-7289A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336855 | |||||||
chr9:70336909 | G | A | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398-7235G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336909 | |||||||
chr9:70336938 | C | T | 25 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0122 others(22): Show |
26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2398-7206C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70336938 | |||||||
chr9:70337118 | C | T | 52 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(49): Show |
54 | HG00140.hp2 HG00673.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.2398-7026C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337118 | |||||||
chr9:70337173 | C | T | 1 | a0003c0003t0001g0172 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2398-6971C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337173 | |||||||
chr9:70337206 | T | G | 2 | a0004c0008t0005g0101 a0004c0008t0005g0104 |
2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2398-6938T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337206 | |||||||
chr9:70337373 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2398-6771A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337373 | |||||||
chr9:70337438 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2398-6706G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337438 | |||||||
chr9:70337450 | GT | G | 81 | a0001c0001t0002g0110 a0001c0001t0002g0124 a0001c0001t0002g0125 others(78): Show |
84 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2398-6670delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | ||||||
chr9:70337450 | GTT | G | 86 | a0001c0001t0002g0010 a0001c0001t0002g0111 a0001c0001t0002g0121 others(83): Show |
91 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.2398-6671_2398-667 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | ||||||
chr9:70337450 | GTTT | G | 27 | a0002c0002t0001g0007 a0002c0002t0001g0050 a0002c0002t0001g0073 others(24): Show |
29 | HG00673.hp2 HG01256.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.2398-6672_2398-667 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | ||||||
chr9:70337450 | GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0002g0237 a0001c0001t0002g0259 a0001c0001t0002g0288 |
3 | HG01891.hp1 NA18991.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2398-6683_2398-667 others(18): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | ||||||
chr9:70337450 | GTTTTTTT others(8): Show |
G | 106 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(103): Show |
116 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2398-6684_2398-667 others(19): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337450 | ||||||
chr9:70337519 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-6625A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337519 | |||||||
chr9:70337589 | G | T | 1 | a0004c0004t0001g0319 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2398-6555G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337589 | |||||||
chr9:70337772 | A | T | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2398-6372A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337772 | |||||||
chr9:70337788 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2398-6356G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337788 | |||||||
chr9:70337814 | T | G | 1 | a0003c0003t0008g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2398-6330T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337814 | |||||||
chr9:70337851 | A | AT | 177 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(174): Show |
192 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.2398-6279dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337851 | ||||||
chr9:70337851 | A | ATT | 8 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(5): Show |
8 | HG01433.hp2 HG01928.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2398-6280_2398-627 others(6): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337851 | ||||||
chr9:70337851 | AT | A | 56 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(53): Show |
61 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.2398-6279delT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70337851 | ||||||
chr9:70337958 | G | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(101): Show |
114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2398-6186G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337958 | |||||||
chr9:70337973 | G | T | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2398-6171G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70337973 | |||||||
chr9:70338053 | C | T | 2 | a0003c0003t0001g0012 a0003c0003t0001g0164 |
3 | NA18987.hp2 NA19055.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2398-6091C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338053 | |||||||
chr9:70338126 | C | T | 3 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0274 |
3 | HG01928.hp2 HG02148.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2398-6018C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338126 | |||||||
chr9:70338444 | G | A | 26 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(23): Show |
28 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.2398-5700G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338444 | |||||||
chr9:70338568 | A | C | 104 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(101): Show |
114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.2398-5576A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338568 | |||||||
chr9:70338576 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2398-5568A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338576 | |||||||
chr9:70338605 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2398-5539A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338605 | |||||||
chr9:70338752 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-5392C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338752 | |||||||
chr9:70338836 | A | G | 1 | a0001c0005t0003g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2398-5308A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338836 | |||||||
chr9:70338840 | C | T | 1 | a0004c0004t0018g0338 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2398-5304C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338840 | |||||||
chr9:70338843 | T | C | 1 | a0001c0001t0016g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2398-5301T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338843 | |||||||
chr9:70338867 | T | A | 1 | a0002c0002t0019g0048 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2398-5277T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70338867 | |||||||
chr9:70339066 | A | C | 2 | a0003c0003t0001g0174 a0003c0003t0001g0182 |
2 | NA18961.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2398-5078A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339066 | |||||||
chr9:70339225 | C | T | 1 | a0016c0016t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2398-4919C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339225 | |||||||
chr9:70339360 | C | T | 148 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(145): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2398-4784C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339360 | |||||||
chr9:70339361 | G | A | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2398-4783G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339361 | |||||||
chr9:70339423 | C | T | 1 | a0016c0016t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2398-4721C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339423 | |||||||
chr9:70339662 | A | G | 1 | a0001c0001t0021g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2398-4482A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339662 | |||||||
chr9:70339914 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2398-4230G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339914 | |||||||
chr9:70339986 | C | CGTT | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2398-4158_2398-415 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339986 | |||||||
chr9:70339987 | C | A | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2398-4157C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339987 | |||||||
chr9:70339992 | C | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-4152C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70339992 | |||||||
chr9:70340288 | C | CT | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2398-3846dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70340288 | ||||||
chr9:70340324 | A | G | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2398-3820A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340324 | |||||||
chr9:70340559 | AATG | A | 25 | a0001c0001t0002g0010 a0001c0001t0002g0121 a0001c0001t0002g0122 others(22): Show |
26 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.2398-3581_2398-357 others(7): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70340559 | ||||||
chr9:70340727 | T | C | 2 | a0003c0003t0001g0146 a0003c0003t0001g0307 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2398-3417T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340727 | |||||||
chr9:70340815 | G | A | 3 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0230 |
3 | HG00642.hp1 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2398-3329G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340815 | |||||||
chr9:70340841 | G | C | 334 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2398-3303G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340841 | |||||||
chr9:70340846 | G | A | 1 | a0015c0017t0002g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2398-3298G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340846 | |||||||
chr9:70340931 | G | C | 2 | a0003c0003t0001g0146 a0003c0003t0001g0307 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2398-3213G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70340931 | |||||||
chr9:70341027 | G | A | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2398-3117G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341027 | |||||||
chr9:70341135 | G | T | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2398-3009G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341135 | |||||||
chr9:70341174 | G | T | 1 | a0001c0001t0002g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2398-2970G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341174 | |||||||
chr9:70341251 | C | T | 114 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(111): Show |
122 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2398-2893C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341251 | |||||||
chr9:70341371 | A | G | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2398-2773A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341371 | |||||||
chr9:70341542 | A | G | 61 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(58): Show |
63 | HG00140.hp2 HG00673.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.2398-2602A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341542 | |||||||
chr9:70341598 | C | A | 116 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(113): Show |
124 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2398-2546C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341598 | |||||||
chr9:70341607 | C | A | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2398-2537C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341607 | |||||||
chr9:70341642 | T | G | 54 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(51): Show |
60 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2398-2502T>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341642 | |||||||
chr9:70341781 | A | G | 159 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(156): Show |
170 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2398-2363A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341781 | |||||||
chr9:70341841 | A | G | 114 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(111): Show |
122 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2398-2303A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341841 | |||||||
chr9:70341944 | A | G | 116 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(113): Show |
124 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2398-2200A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341944 | |||||||
chr9:70341952 | C | T | 151 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(148): Show |
162 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2398-2192C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341952 | |||||||
chr9:70341953 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-2191G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70341953 | |||||||
chr9:70342057 | C | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2398-2087C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342057 | |||||||
chr9:70342092 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-2052A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342092 | |||||||
chr9:70342116 | A | G | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2398-2028A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342116 | |||||||
chr9:70342224 | G | C | 275 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(272): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2398-1920G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342224 | |||||||
chr9:70342230 | G | A | 3 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 |
3 | HG02572.hp1 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2398-1914G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342230 | |||||||
chr9:70342253 | G | T | 1 | a0010c0022t0012g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2398-1891G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342253 | |||||||
chr9:70342320 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1824C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342320 | |||||||
chr9:70342407 | A | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1737A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342407 | |||||||
chr9:70342440 | C | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2398-1704C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342440 | |||||||
chr9:70342625 | C | G | 57 | a0003c0003t0001g0004 a0003c0003t0001g0012 a0003c0003t0001g0013 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2398-1519C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342625 | |||||||
chr9:70342696 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2398-1448A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342696 | |||||||
chr9:70342770 | G | T | 3 | a0001c0001t0002g0233 a0001c0001t0002g0246 a0001c0001t0002g0281 |
3 | NA18961.hp1 NA18994.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2398-1374G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342770 | |||||||
chr9:70342846 | G | A | 2 | a0002c0002t0001g0090 a0002c0002t0001g0091 |
2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2398-1298G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342846 | |||||||
chr9:70342884 | T | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1260T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342884 | |||||||
chr9:70342909 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-1235G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70342909 | |||||||
chr9:70343147 | C | CT | 92 | a0001c0001t0021g0310 a0002c0002t0001g0002 a0002c0002t0001g0003 others(89): Show |
98 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2398-983dupT | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70343147 | ||||||
chr9:70343147 | C | CTT | 27 | a0002c0002t0001g0007 a0002c0002t0001g0063 a0002c0002t0001g0073 others(24): Show |
29 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.2398-984_2398-983d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70343147 | ||||||
chr9:70343149 | T | C | 2 | a0001c0001t0002g0262 a0001c0001t0002g0273 |
2 | HG00741.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2398-995T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343149 | |||||||
chr9:70343262 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-882C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343262 | |||||||
chr9:70343263 | G | A | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2398-881G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343263 | |||||||
chr9:70343321 | T | A | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2398-823T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343321 | |||||||
chr9:70343331 | G | A | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2398-813G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343331 | |||||||
chr9:70343680 | G | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2398-464G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343680 | |||||||
chr9:70343722 | G | A | 156 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(153): Show |
167 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2398-422G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343722 | |||||||
chr9:70343777 | C | A | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2398-367C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | chr9 | 70343777 | |||||||
chr9:70343872 | AGCTAGAC others(12): Show |
A | 1 | a0007c0012t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2398-269_2398-251d others(21): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr9 | 70343872 | ||||||
chr9:70344361 | A | G | 1 | a0004c0004t0018g0338 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2523+92A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344361 | |||||||
chr9:70344390 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2523+121T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344390 | |||||||
chr9:70344407 | AAT | A | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2523+154_2523+155d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 70344407 | ||||||
chr9:70344499 | G | A | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2523+230G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344499 | |||||||
chr9:70344512 | C | A | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2523+243C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344512 | |||||||
chr9:70344597 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2523+328T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344597 | |||||||
chr9:70344627 | T | C | 1 | a0001c0001t0002g0010 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2523+358T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344627 | |||||||
chr9:70344774 | G | A | 5 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+505G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344774 | |||||||
chr9:70344776 | T | A | 1 | a0004c0004t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2523+507T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344776 | |||||||
chr9:70344818 | A | G | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2523+549A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344818 | |||||||
chr9:70344840 | C | T | 1 | a0002c0002t0010g0059 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2523+571C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70344840 | |||||||
chr9:70345140 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2523+871T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345140 | |||||||
chr9:70345171 | TCTA | T | 108 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(105): Show |
118 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2523+906_2523+908d others(5): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr9 | 70345171 | ||||||
chr9:70345174 | ACT | A | 3 | a0001c0001t0002g0234 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG02129.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2523+906_2523+907d others(4): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345174 | |||||||
chr9:70345178 | A | T | 3 | a0001c0001t0002g0234 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG02129.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2523+909A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345178 | |||||||
chr9:70345565 | A | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2524-1040A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345565 | |||||||
chr9:70345875 | T | C | 334 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2524-730T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70345875 | |||||||
chr9:70346407 | C | T | 1 | a0002c0002t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2524-198C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346407 | |||||||
chr9:70346412 | C | T | 1 | a0001c0001t0002g0264 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2524-193C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346412 | |||||||
chr9:70346429 | G | A | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2524-176G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346429 | |||||||
chr9:70346487 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2524-118G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346487 | |||||||
chr9:70346514 | T | A | 1 | a0004c0006t0001g0333 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2524-91T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 18/24 | chr9 | 70346514 | |||||||
chr9:70346668 | T | A | 1 | a0001c0001t0002g0231 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2568+19T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346668 | |||||||
chr9:70346729 | C | T | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2568+80C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346729 | |||||||
chr9:70346905 | C | T | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2569-161C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346905 | |||||||
chr9:70346946 | C | A | 1 | a0001c0001t0002g0209 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2569-120C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 19/24 | chr9 | 70346946 | |||||||
chr9:70347179 | T | C | 7 | a0003c0003t0001g0156 a0003c0003t0001g0157 a0003c0003t0001g0159 others(4): Show |
7 | HG02080.hp2 HG02129.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.2664+18T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 20/24 | chr9 | 70347179 | |||||||
chr9:70347238 | G | C | 1 | a0004c0004t0001g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2664+77G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 20/24 | chr9 | 70347238 | |||||||
chr9:70347277 | C | T | 1 | a0001c0005t0003g0027 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2664+116C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 20/24 | chr9 | 70347277 | |||||||
chr9:70347900 | A | G | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2770-19A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 21/24 | chr9 | 70347900 | |||||||
chr9:70348125 | T | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+87T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348125 | |||||||
chr9:70348252 | T | A | 109 | a0001c0001t0002g0001 a0001c0001t0002g0015 a0001c0001t0002g0017 others(106): Show |
119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2889+214T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348252 | |||||||
chr9:70348305 | G | A | 13 | a0001c0001t0002g0120 a0001c0001t0002g0238 a0001c0001t0002g0239 others(10): Show |
13 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.2889+267G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348305 | |||||||
chr9:70348429 | C | T | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(50): Show |
59 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2889+391C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348429 | |||||||
chr9:70348430 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+392G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348430 | |||||||
chr9:70348486 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2889+448G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348486 | |||||||
chr9:70348535 | A | C | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+497A>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348535 | |||||||
chr9:70348553 | C | T | 1 | a0004c0004t0001g0331 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2889+515C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348553 | |||||||
chr9:70348626 | G | A | 2 | a0002c0002t0001g0036 a0002c0002t0001g0037 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2889+588G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348626 | |||||||
chr9:70348652 | C | T | 32 | a0002c0002t0001g0007 a0002c0002t0001g0073 a0002c0002t0001g0074 others(29): Show |
34 | HG00673.hp2 HG00741.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.2889+614C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348652 | |||||||
chr9:70348667 | G | T | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2889+629G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348667 | |||||||
chr9:70348698 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2889+660A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348698 | |||||||
chr9:70348723 | A | G | 2 | a0007c0012t0001g0107 a0007c0012t0001g0175 |
2 | HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2889+685A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348723 | |||||||
chr9:70348780 | A | G | 1 | a0005c0007t0002g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2889+742A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70348780 | |||||||
chr9:70349034 | A | G | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2889+996A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349034 | |||||||
chr9:70349048 | TTTAA | T | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2889+1014_2889+101 others(8): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 70349048 | ||||||
chr9:70349127 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2890-987C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349127 | |||||||
chr9:70349128 | G | A | 3 | a0003c0003t0001g0153 a0003c0003t0001g0155 a0003c0003t0001g0197 |
3 | HG01496.hp2 HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2890-986G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349128 | |||||||
chr9:70349131 | A | G | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2890-983A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349131 | |||||||
chr9:70349177 | C | T | 1 | a0011c0021t0001g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2890-937C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349177 | |||||||
chr9:70349181 | T | C | 1 | a0002c0002t0001g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2890-933T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349181 | |||||||
chr9:70349193 | A | G | 1 | a0010c0022t0012g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2890-921A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349193 | |||||||
chr9:70349221 | C | T | 1 | a0016c0016t0002g0294 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2890-893C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349221 | |||||||
chr9:70349227 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2890-887C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349227 | |||||||
chr9:70349239 | G | T | 1 | a0002c0002t0019g0048 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2890-875G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349239 | |||||||
chr9:70349346 | C | T | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2890-768C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349346 | |||||||
chr9:70349407 | A | G | 1 | a0002c0002t0001g0047 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2890-707A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349407 | |||||||
chr9:70349414 | CATAGAAG others(19): Show |
C | 1 | a0002c0002t0001g0031 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2890-698_2890-673d others(28): Show |
SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr9 | 70349414 | ||||||
chr9:70349623 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2890-491G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349623 | |||||||
chr9:70349672 | A | G | 8 | a0001c0005t0003g0023 a0001c0005t0003g0024 a0001c0005t0003g0025 others(5): Show |
8 | HG01496.hp1 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2890-442A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349672 | |||||||
chr9:70349826 | C | G | 7 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0235 others(4): Show |
7 | HG01099.hp2 HG01261.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2890-288C>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349826 | |||||||
chr9:70349851 | A | G | 25 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(22): Show |
25 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2890-263A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349851 | |||||||
chr9:70349972 | A | G | 1 | a0012c0020t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2890-142A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70349972 | |||||||
chr9:70350092 | T | A | 1 | a0001c0010t0002g0258 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2890-22T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 22/24 | chr9 | 70350092 | |||||||
chr9:70350341 | G | C | 1 | a0001c0001t0002g0291 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3070-35G>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 23/24 | chr9 | 70350341 | |||||||
chr9:70350361 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3070-15G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 23/24 | chr9 | 70350361 | |||||||
chr9:70350522 | A | G | 334 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.3165+51A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350522 | |||||||
chr9:70350704 | T | C | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.3165+233T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350704 | |||||||
chr9:70350723 | T | C | 156 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(153): Show |
167 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.3165+252T>C | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350723 | |||||||
chr9:70350797 | T | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3165+326T>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70350797 | |||||||
chr9:70351054 | A | G | 1 | a0010c0022t0012g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3165+583A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351054 | |||||||
chr9:70351146 | G | A | 2 | a0006c0011t0009g0303 a0006c0011t0009g0304 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3165+675G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351146 | |||||||
chr9:70351227 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3165+756G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351227 | |||||||
chr9:70351353 | C | CA | 8 | a0001c0001t0002g0126 a0001c0001t0002g0206 a0001c0001t0017g0214 others(5): Show |
8 | HG00741.hp1 HG01256.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.3166-822dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr9 | 70351353 | ||||||
chr9:70351703 | A | T | 1 | a0009c0015t0011g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3166-488A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351703 | |||||||
chr9:70351803 | C | T | 119 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(116): Show |
127 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.3166-388C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351803 | |||||||
chr9:70351853 | A | T | 1 | a0002c0002t0013g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3166-338A>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351853 | |||||||
chr9:70351869 | A | G | 26 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(23): Show |
26 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.3166-322A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351869 | |||||||
chr9:70351882 | C | T | 5 | a0002c0009t0006g0009 a0002c0009t0006g0097 a0002c0009t0014g0099 others(2): Show |
5 | HG01891.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3166-309C>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351882 | |||||||
chr9:70351941 | A | G | 215 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0015 others(212): Show |
231 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.3166-250A>G | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70351941 | |||||||
chr9:70352017 | G | T | 6 | a0004c0008t0005g0100 a0004c0008t0005g0101 a0004c0008t0005g0102 others(3): Show |
6 | HG00738.hp2 HG01433.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.3166-174G>T | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70352017 | |||||||
chr9:70352036 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3166-155G>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70352036 | |||||||
chr9:70352070 | G | GA | 27 | a0004c0004t0001g0313 a0004c0004t0001g0314 a0004c0004t0001g0315 others(24): Show |
27 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.3166-112dupA | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr9 | 70352070 | ||||||
chr9:70352148 | C | A | 1 | a0004c0004t0018g0338 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3166-43C>A | SMC5 | ENSG00000198887.9 | transcript | ENST00000361138.7 | protein_coding | 24/24 | chr9 | 70352148 |